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array:23 [ "pii" => "S0301054615000531" "issn" => "03010546" "doi" => "10.1016/j.aller.2015.01.010" "estado" => "S300" "fechaPublicacion" => "2016-01-01" "aid" => "679" "copyright" => "SEICAP" "copyrightAnyo" => "2014" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Allergol Immunopathol (Madr). 2016;44:23-31" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 418 "formatos" => array:3 [ "EPUB" => 7 "HTML" => 258 "PDF" => 153 ] ] "itemSiguiente" => array:18 [ "pii" => "S0301054615000579" "issn" => "03010546" "doi" => "10.1016/j.aller.2015.01.012" "estado" => "S300" "fechaPublicacion" => "2016-01-01" "aid" => "683" "copyright" => "SEICAP" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Allergol Immunopathol (Madr). 2016;44:32-40" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 428 "formatos" => array:3 [ "EPUB" => 10 "HTML" => 185 "PDF" => 233 ] ] "en" => array:12 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Analysis of <span class="elsevierStyleItalic">FOXP3</span> gene in children with allergy and autoimmune diseases" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "32" "paginaFinal" => "40" ] ] "contieneResumen" => array:1 [ "en" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 455 "Ancho" => 3247 "Tamanyo" => 48864 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">FOXP3</span> gene scheme. Numbers indicate exonic regions and arrows represent primers employed in this study.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "R.M. Pacheco-Gonzalez, C. Avila, I. Dávila, A. García-Sánchez, L. Hernández-Hernández, D. Benito-Pescador, R. Torres, P. Prieto-Matos, M. Isidoro-Garcia, F. Lorente, C. Sanz" "autores" => array:11 [ 0 => array:2 [ "nombre" => "R.M." "apellidos" => "Pacheco-Gonzalez" ] 1 => array:2 [ "nombre" => "C." "apellidos" => "Avila" ] 2 => array:2 [ "nombre" => "I." "apellidos" => "Dávila" ] 3 => array:2 [ "nombre" => "A." "apellidos" => "García-Sánchez" ] 4 => array:2 [ "nombre" => "L." "apellidos" => "Hernández-Hernández" ] 5 => array:2 [ "nombre" => "D." "apellidos" => "Benito-Pescador" ] 6 => array:2 [ "nombre" => "R." "apellidos" => "Torres" ] 7 => array:2 [ "nombre" => "P." "apellidos" => "Prieto-Matos" ] 8 => array:2 [ "nombre" => "M." "apellidos" => "Isidoro-Garcia" ] 9 => array:2 [ "nombre" => "F." "apellidos" => "Lorente" ] 10 => array:2 [ "nombre" => "C." "apellidos" => "Sanz" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0301054615000579?idApp=UINPBA00004N" "url" => "/03010546/0000004400000001/v1_201601070106/S0301054615000579/v1_201601070106/en/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S0301054615000543" "issn" => "03010546" "doi" => "10.1016/j.aller.2015.03.001" "estado" => "S300" "fechaPublicacion" => "2016-01-01" "aid" => "680" "copyright" => "SEICAP" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Allergol Immunopathol (Madr). 2016;44:18-22" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 451 "formatos" => array:3 [ "EPUB" => 10 "HTML" => 192 "PDF" => 249 ] ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Molecular-based diagnosis of respiratory allergic diseases in children from Curitiba, a city in Southern Brazil" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "18" "paginaFinal" => "22" ] ] "contieneResumen" => array:1 [ "en" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "L.M.L. Araujo, N.A. Rosario, A. Mari" "autores" => array:3 [ 0 => array:2 [ "nombre" => "L.M.L." "apellidos" => "Araujo" ] 1 => array:2 [ "nombre" => "N.A." "apellidos" => "Rosario" ] 2 => array:2 [ "nombre" => "A." "apellidos" => "Mari" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0301054615000543?idApp=UINPBA00004N" "url" => "/03010546/0000004400000001/v1_201601070106/S0301054615000543/v1_201601070106/en/main.assets" ] "en" => array:19 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Amelioration of some immunological disorders caused by the faeces of the dominant true house dust mites in El-Minia Governorate, Egypt" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "23" "paginaFinal" => "31" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Bahaa K.A. Abdel-Salam, Nagiba I.A. Shoker, Ahmed M.R. Mohamad" "autores" => array:3 [ 0 => array:4 [ "nombre" => "Bahaa K.A." "apellidos" => "Abdel-Salam" "email" => array:1 [ 0 => "Bahaa.abdelsalam@science.miniauniv.edu.eg" ] "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "Nagiba I.A." "apellidos" => "Shoker" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "Ahmed M.R." "apellidos" => "Mohamad" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Zoology Department, Faculty of Science, El-Minia University, 61519 El-Minia, Egypt" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Biology Department, College of Science and Humanities in Quwiaya, Shaqra University, 11961 Shaqra, Saudi Arabia" "etiqueta" => "b" "identificador" => "aff0010" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 893 "Ancho" => 1584 "Tamanyo" => 80592 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">TNF-α levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated with either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Mite faeces are small airborne particles (about 20<span class="elsevierStyleHsp" style=""></span>μm). They have great allergenic potential due to protein residues, and inhalation of faecal particles is the main way of exposure.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">1</span></a> Most allergens are biochemically active molecules and include enzymes, enzyme inhibitors, and proteins involved in molecular transport, regulation and cell and tissue structure.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">2</span></a> The majority of works on mite allergens referred to species of the family Pyroglyphidae.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">2</span></a> This family has five genera, of which the genus <span class="elsevierStyleItalic">Dermatophagoides</span> is the most important one from a medical point of view. The European house dust mite (HDM), <span class="elsevierStyleItalic">D. pteronyssinus</span>, and the American HDM, <span class="elsevierStyleItalic">D. farinae</span>, are distributed all over the world.<a class="elsevierStyleCrossRefs" href="#bib0245"><span class="elsevierStyleSup">3,4</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The optimal environmental temperature for these mites is 18–27<span class="elsevierStyleHsp" style=""></span>°C. Proper indoor relative humidity, temperature and enough food are the key factors determining their survival and development.<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">5</span></a> Their major food source is skin scales, hair and wool of pets, fungi, plant pollen and organic debris. The highest HDM densities have been found in bedrooms and living rooms because these indoor spaces usually have large areas covered by textile materials.<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">4</span></a> In recent years, lifestyle changes including central heating systems in homes provide suitable conditions for growth and reproduction of HDMs.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">1</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Allergic diseases such as asthma are amongst the most common chronic diseases affecting people in developed countries.<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">6</span></a> Asthma is a chronic and complex inflammatory disease of the airways with symptoms including excess mucus production, wheeze, dyspnoea, cough, fatigue, anxiety, tachycardia, and chest tightness.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">7</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Relationships between HDMs and asthma are ambiguous. For example, atopy is not necessarily related to house dust mite allergens and also allergens may not be associated with atopy. Skin-prick test is the routine diagnostic method for atopy-related allergens. The population fraction of asthma attributable to atopy can be calculated when the proportion of people with asthma who have specific IgE or positive skin-prick tests is known.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">8</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Many scientific reports suggest that asthma involves the activation of many inflammatory cells like mast cells, macrophages/monocytes, eosinophils, T-helper type-2 lymphocytes (Th2), dendritic cells, basophils, neutrophils and platelets.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">9</span></a> These cells may also be important sources of mediators in asthma. Cytokines, the main important one of these mediators, can synergise or antagonise the effects of other cytokines and regulated in a complex manner and function via cytokine cascade.<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">10</span></a> The major groups of cytokines are lymphokines, pro-inflammatory cytokines, inhibitory cytokines, growth factors and chemokines. Asthmatic inflammatory cells are involved in the production of different cytokines such as Tumour necrosis factor (TNF)-α, Interleukin (IL)-1β, IL-4 and IL-13.</p><p id="par0030" class="elsevierStylePara elsevierViewall">TNF-α and IL-1β are pro-inflammatory cytokines.<a class="elsevierStyleCrossRefs" href="#bib0275"><span class="elsevierStyleSup">9,10,12</span></a> Two major forms of TNF are TNF-α and TNF-β. TNF-α is produced by many cells including macrophages, T-lymphocytes, mast cells, and epithelial cells, but the principal source is the macrophage. The secretion of TNF-α by monocytes/macrophages is greatly enhanced by other cytokines such as IL-1, granulocyte macrophage-colony stimulating factor (GM-CSF) and interferon (IFN)-γ. Devalia et al. showed that human eosinophils are also capable of releasing TNF-α, together with airway epithelial cells.<a class="elsevierStyleCrossRef" href="#bib0285"><span class="elsevierStyleSup">11</span></a> For IL-1, there are also two distinct forms (α and β). The major cellular sources of IL-1 are monocytes, macrophages, neutrophils, eosinophils, mast cells, platelets, lymphocytes, NK cells, endothelial cells, airway smooth muscle cells and vascular smooth muscle cells.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">12</span></a> Air pollutants like nitrogen dioxide can stimulate epithelial cells express IL-1β while eosinophils can produce IL-1α.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">13</span></a> A wide variety of stimuli including IL-1 itself TNF-α, GM-CSF, endotoxin and phagocytosis can increase the expression of IL-1 in monocytes/macrophages.<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">10</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">IL-4 and IL-13 are anti-inflammatory lymphokines.<a class="elsevierStyleCrossRefs" href="#bib0275"><span class="elsevierStyleSup">9,10,12</span></a> IL-4, a type-2 T-helper cell derived cytokine, is thought to be an upstream cytokine that regulates allergic inflammation by promoting Th2 cell differentiation and IgE synthesis.<a class="elsevierStyleCrossRef" href="#bib0300"><span class="elsevierStyleSup">14</span></a> Synthesis of IL-4 can be induced by stimulation of the antigen receptors on T-lymphocytes and by IgE-Fc receptor cross linking in mast cells and basophils. IL-13 is produced by activated T-lymphocytes, B-lymphocytes and mast cells. In the mouse, almost exclusively Th2 clones express IL-13, however, in humans it can be expressed in both Th1 and Th2 lymphocyte clones.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">15</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Immunoglobulin (Ig) E is a class of antibody isotype that has been found only in mammals. It plays an essential role in type I hypersensitivity,<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">16</span></a> which manifests various allergic diseases, such as allergic asthma. Diagnosis of allergy is most often done when a physician reviews a patient's history and finds a positive result for the presence of allergen specific IgE when conducting a skin or blood test.<a class="elsevierStyleCrossRef" href="#bib0315"><span class="elsevierStyleSup">17</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Oxidative stress plays a role in asthma aetiology due to activation of various inflammatory cells of the respiratory tract such as neutrophils, eosinophils, mast cells and lymphocytes.<a class="elsevierStyleCrossRef" href="#bib0320"><span class="elsevierStyleSup">18</span></a> The continuous exposure of the respiratory tract to environmental oxidants and airway inflammatory cell-generated reactive oxygen species (ROS) creates a high level of oxidative stress in the lung.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">7</span></a> Many studies have shown that cells involved in an asthmatic inflammatory process have a capacity for producing ROS. Activated eosinophils, neutrophils, monocytes, and macrophages generate superoxide (O<span class="elsevierStyleInf">2</span><span class="elsevierStyleSup">−</span>) via a membrane associated NADPH-dependent complex. The subsequent dismutation of O<span class="elsevierStyleInf">2</span><span class="elsevierStyleSup">−</span> can result in the formation of hydrogen peroxide (H<span class="elsevierStyleInf">2</span>O<span class="elsevierStyleInf">2</span>). O<span class="elsevierStyleInf">2</span><span class="elsevierStyleSup">−</span> and H<span class="elsevierStyleInf">2</span>O<span class="elsevierStyleInf">2</span> are moderate oxidants and both of them are critical in the formation of potent cytotoxic free radicals in biological systems through their interactions with other molecules.<a class="elsevierStyleCrossRef" href="#bib0325"><span class="elsevierStyleSup">19</span></a> This process is involved in asthmatic inflammation; moreover, the concentration of nitric oxide (NO) is increased in airways of asthmatic subjects.<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">20</span></a> In addition to the recruited inflammatory cells, epithelial airway cells are potential sources of ROS production.<a class="elsevierStyleCrossRef" href="#bib0335"><span class="elsevierStyleSup">21</span></a> Several asthma mediators, such as platelet activating factor, chemokines, adhesion molecules, and eosinophilic granule proteins<a class="elsevierStyleCrossRef" href="#bib0340"><span class="elsevierStyleSup">22</span></a> are potential promoters of ROS production. In addition to these endogenous sources, environmental factors linked to asthma, such as air pollutants, are important.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">23</span></a> Increased production of ROS is deleterious because free radical-induced oxidation of proteins, DNA, and lipids can cause direct tissue damage and evoke cellular responses through the generation of secondary reactive species.<a class="elsevierStyleCrossRef" href="#bib0350"><span class="elsevierStyleSup">24</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Medicinal plants have been used to cure human illness since ancient times. Certain types of these plants are believed to promote positive health and maintain organism resistance against infection by re-establishing body equilibrium and conditioning the body tissues.<a class="elsevierStyleCrossRef" href="#bib0355"><span class="elsevierStyleSup">25</span></a> Curcuma (<span class="elsevierStyleItalic">Curcuma longa</span>, Linn) is a rhizomatous perennial herb that belongs to the family Zingiberaceae. It is used as a herbal remedy due to the prevalent belief that the plant has medical properties. <span class="elsevierStyleItalic">C. longa</span> also acts as an antioxidant and used in the treatment of many diseases such as asthma.<a class="elsevierStyleCrossRef" href="#bib0360"><span class="elsevierStyleSup">26</span></a> Karkade (<span class="elsevierStyleItalic">Hibiscus sabdariffa</span>, Linn), a member of the Malvaceae family, is one of these medicinal plant originated from Egypt. All parts of <span class="elsevierStyleItalic">H. sabdariffa</span> are used for medicinal purposes, especially in alternative medicine. <span class="elsevierStyleItalic">H. sabdariffa</span> is taken in many parts of the world for the treatment or management of many diseases. It is used as anti-inflammatory and antioxidant.<a class="elsevierStyleCrossRef" href="#bib0365"><span class="elsevierStyleSup">27</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Therefore, the present work aims to study the curcuma and karkade amelioration of the allergenic immunological disorder caused by the faeces of two mite species, <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> that were recorded as the dominant true HDM in the valley and desert houses of asthmatic patients in EL-Minia Governorate, respectively.<a class="elsevierStyleCrossRef" href="#bib0370"><span class="elsevierStyleSup">28</span></a></p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Materials and methods</span><p id="par0060" class="elsevierStylePara elsevierViewall">The dominant allergenic mite species, <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span>, recorded in the valley and desert houses were used for experiments.<a class="elsevierStyleCrossRef" href="#bib0370"><span class="elsevierStyleSup">28</span></a> Mites were isolated from the collected dust samples by Berlese–Tullgren method, preserved and mounted on microscope slides for identification according to Colloff.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">2</span></a><span class="elsevierStyleItalic">D. pteronyssinus</span> photos were captured by light microscopy at 100× and 400× magnifications.</p><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Preparation of extracts</span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Mite faeces extract</span><p id="par0065" class="elsevierStylePara elsevierViewall">Isolated male and female individuals, in copulation state, of <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> were cultured and grown in small Petri dishes with paper tissues under their covers. Cultures were kept at 25<span class="elsevierStyleHsp" style=""></span>°C, 75<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5% relative humidity and fed on a mixture of Aquarium gold fish flakes (Mars Ireland, Dublin4, Mars Fishcare Europe) and dry yeast granules<a class="elsevierStyleCrossRef" href="#bib0375"><span class="elsevierStyleSup">29</span></a> with 1:1 ratio in complete darkness. When the population density was sufficiently high, <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> crude faeces were isolated by the Berlese–Tullgren method. Five grams from these faeces pellets were used for each inhalation.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Medicinal plant extracts</span><p id="par0070" class="elsevierStylePara elsevierViewall">Curcuma and karkade were purchased from the local market in El-Minia Governorate, Egypt. A fresh sample of 50<span class="elsevierStyleHsp" style=""></span>g plant species was sterilised, dried and ground into powder. Each sample (50<span class="elsevierStyleHsp" style=""></span>g) was extracted twice with 300<span class="elsevierStyleHsp" style=""></span>ml ethanol at room temperature for two days and filtered. The filtrate of each plant was concentrated by a rotary evaporation (Büchner rotary evaporate) at 40<span class="elsevierStyleHsp" style=""></span>°C. The ethanol extract was weighed and stored at 4<span class="elsevierStyleHsp" style=""></span>°C until used. Doses 250<span class="elsevierStyleHsp" style=""></span>mg curcuma and 500<span class="elsevierStyleHsp" style=""></span>mg karkade extracts per kg albino rat body weight (b.wt.) were used.<a class="elsevierStyleCrossRefs" href="#bib0360"><span class="elsevierStyleSup">26,30</span></a></p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Experimental animals</span><p id="par0075" class="elsevierStylePara elsevierViewall">Male albino rats, <span class="elsevierStyleItalic">Rattus norvegicus</span> (6–8 weeks old, weight 100–120<span class="elsevierStyleHsp" style=""></span>g) were purchased from the Biological Supply Center, Theodore Bilharz Research Institute, TBRI, Cairo, Egypt and housed under specific pathogen-free conditions and maintained on a 12-h light–dark cycle, with food and water ad libitum. Animals were classified into three groups (five animals each). The first group (control) was untreated. The second group was intranasal inhaled daily with either <span class="elsevierStyleItalic">D. pteronyssinus</span> or <span class="elsevierStyleItalic">D. farinae</span> faeces extract daily for 4 weeks. The third and the fourth groups were oral treated daily with curcuma and karkade extracts at a dose of 250 and 500<span class="elsevierStyleHsp" style=""></span>mg/kg b.wt., respectively, and intranasal inhaled daily with faeces extract daily for the same period.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Cytokines, immunoglobulin and ROS in serum</span><p id="par0080" class="elsevierStylePara elsevierViewall">After 72<span class="elsevierStyleHsp" style=""></span>h from the last treating, animals from each group were sacrificed under chloroform anaesthesia. Blood samples were taken from the heart and centrifuged at 3000<span class="elsevierStyleHsp" style=""></span>rpm for 30<span class="elsevierStyleHsp" style=""></span>min. Sera were removed and kept at −20<span class="elsevierStyleHsp" style=""></span>°C for the assessments of TNF-α, IL-1β, IL-4, IL-13, IgE antibody levels by ELISA using kits purchased from R&D Systems (Minneapolis, MN, USA). ROS kit was obtained from Elaab (Wuhan, China).</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Statistical analysis</span><p id="par0085" class="elsevierStylePara elsevierViewall">SPSS program version 18.0 was used to analyse the data. Statistical analysis of the obtained data was performed using one way analysis of variance (ANOVA) test followed by least square differences (LSD) analysis for comparison between means. Results were expressed as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>standard error (SE). Values of <span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05 were considered statistically non-significant, while <span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05 value were statistically significant.</p></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Results</span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">The main characteristics of the dominant true house dust mite species in the valley and desert houses</span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Dermatophagoides pteronyssinus</span><p id="par0090" class="elsevierStylePara elsevierViewall">Both sexes of <span class="elsevierStyleItalic">D. pteronyssinus</span> are feebly sclerotised mites, with striated cuticle and chelate chelicerae (ch) and without vertical setae.</p><p id="par0095" class="elsevierStylePara elsevierViewall">In the male, the first and second pairs of legs are almost equal in length and width and the first apodemes (ap I) are always widely separated from one another and do not meet to form a sternum (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>A). The anus is encircled by an oval perianal ring which also encloses prominent anal suckers (a.s) (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>B).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0100" class="elsevierStylePara elsevierViewall">In the female, the genital opening is λ-shaped and bounded anteriorly by a crescent epigynium (ep) (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>C). The apex of bursa copulatrix is flower-shaped when viewed dorsally (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>D, arrow).</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Dermatophagoides farinae</span><p id="par0105" class="elsevierStylePara elsevierViewall">Similar to <span class="elsevierStyleItalic">D. pteronyssinus</span>, both sexes of <span class="elsevierStyleItalic">D. farinae</span> are feebly sclerotised mites, with striated cuticle and chelate chelicerae and without vertical setae.</p><p id="par0110" class="elsevierStylePara elsevierViewall">In the male, the first legs are thickened and the first apodemes (ap I) mostly fuse in the middle to form a short sternum (st), while the third apodemes (ap III) are long and bent sharply at a right angle. The anus is encircled by an oval perianal ring which also encloses prominent anal suckers (a.s) (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>A). The hysterosomal shield (h.s), as long as broad terminates posterior of the second dorsal setae (d2) (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>B).</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0115" class="elsevierStylePara elsevierViewall">In the female, the genital opening is λ-shaped and bounded anteriorly by a short crescent epigynium (ep) (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>C). Bursa copulatrix (b.c) has a flask-shape (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>D).</p></span></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Immunological studies</span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Assessments of TNF-α</span><p id="par0120" class="elsevierStylePara elsevierViewall">Results of ELISA in <a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a> showed that TNF-α in control groups of <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> recorded 14.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.27<span class="elsevierStyleHsp" style=""></span>pg/ml and 31.08<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.359<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively. Inhaled groups with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces counted higher level of TNF-α (61.9<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.973<span class="elsevierStyleHsp" style=""></span>pg/ml and 71.55<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.074<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) than those recorded in the inhaled groups treated with the curcuma (38.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.247<span class="elsevierStyleHsp" style=""></span>pg/ml and 50.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.147<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the karkade (57.3<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.343<span class="elsevierStyleHsp" style=""></span>pg/ml and 38.73<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.338<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively). Statistical analysis showed a significant difference in TNF-α levels between the curcuma- and karkade-treated groups and either control or faeces-treated groups, <span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05.</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Assessments of IL-1β</span><p id="par0125" class="elsevierStylePara elsevierViewall">The IL-1β ELISA values demonstrated that the curcuma-treated groups for <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> (30<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.767<span class="elsevierStyleHsp" style=""></span>pg/ml and 38.55<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.403<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively), the karkade-treated groups (52.3<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.206<span class="elsevierStyleHsp" style=""></span>pg/ml and 25.53<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.446<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the control groups (10.46<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.751<span class="elsevierStyleHsp" style=""></span>pg/ml and 18<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.357<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) are lower than the groups inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces (58.3<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.907<span class="elsevierStyleHsp" style=""></span>pg/ml and 59.63<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.593<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>). This study also showed that there is a significant difference in IL-1β level between the curcuma-and karkade-treated group and either native or faeces-treated group (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05).</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Assessments of IL-4</span><p id="par0130" class="elsevierStylePara elsevierViewall">In parallel to TNF-α and IL-1β, results of IL-4 indicated that the groups inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces (61.3<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.572<span class="elsevierStyleHsp" style=""></span>pg/ml and 76.45<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.074<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) are higher than the curcuma-treated groups (32.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.313<span class="elsevierStyleHsp" style=""></span>pg/ml and 45.48<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.708<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the karkade-treated groups (56.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.108<span class="elsevierStyleHsp" style=""></span>pg/ml and 39.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.58<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the control groups (13.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.873<span class="elsevierStyleHsp" style=""></span>pg/ml and 24.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.357<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>). In addition, a significant difference in IL-4 levels between the curcuma- and the karkade-treated groups and either control or faeces-treated group was monitored (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05).</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Assessments of IL-13</span><p id="par0135" class="elsevierStylePara elsevierViewall">ELISA data of the fourth cytokine, IL-13, showed that both the control groups for <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> (16.73<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.121<span class="elsevierStyleHsp" style=""></span>pg/ml and 30.13<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.125<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the inhaled groups treated with either the curcuma (42<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.514<span class="elsevierStyleHsp" style=""></span>pg/ml and 51.43<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.704<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) or the karkade (63.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.252<span class="elsevierStyleHsp" style=""></span>pg/ml and 47.43<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) (<a class="elsevierStyleCrossRef" href="#fig0030">Fig. 6</a>) are lower than the inhaled groups with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces (64.3<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.325<span class="elsevierStyleHsp" style=""></span>pg/ml and 74.13<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.858<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively). Statistical analysis showed a significant difference in IL-13 between the curcuma- and the karkade-treated groups and either control or faeces-treated groups, <span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05.</p><elsevierMultimedia ident="fig0030"></elsevierMultimedia></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Assessments of IgE</span><p id="par0140" class="elsevierStylePara elsevierViewall">Total IgE ELISA data indicated that both the treated groups with curcuma for <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> (11.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.435<span class="elsevierStyleHsp" style=""></span>pg/ml and 12.23<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.351<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the karkade-treated groups for the same two species (14.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.183<span class="elsevierStyleHsp" style=""></span>pg/ml and 11.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.461<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) are lower than the groups inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces (15.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.851<span class="elsevierStyleHsp" style=""></span>pg/ml and 16.46<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.702<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively), while the control groups counted 5.63<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.433<span class="elsevierStyleHsp" style=""></span>pg/ml for <span class="elsevierStyleItalic">D. pteronyssinus</span> and 8.13<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.563<span class="elsevierStyleHsp" style=""></span>pg/ml for <span class="elsevierStyleItalic">D. farinae</span> (<a class="elsevierStyleCrossRef" href="#fig0035">Fig. 7</a>). This study also showed that there is a significant difference in IgE levels between the curcuma- and the karkade-treated groups and the faeces-inhaled groups (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05).</p><elsevierMultimedia ident="fig0035"></elsevierMultimedia></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Assessments of ROS</span><p id="par0145" class="elsevierStylePara elsevierViewall">The ROS in serum had high levels in group inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces (57.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.764<span class="elsevierStyleHsp" style=""></span>pg/ml and 59.78<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.492<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) than the curcuma- (28.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.285<span class="elsevierStyleHsp" style=""></span>pg/ml and 46.80<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.285<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and karkade-treated groups (53.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.217<span class="elsevierStyleHsp" style=""></span>pg/ml and 29.76<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.447<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) and the control groups (25.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.738<span class="elsevierStyleHsp" style=""></span>pg/ml and 21.52<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.131<span class="elsevierStyleHsp" style=""></span>pg/ml, respectively) (<a class="elsevierStyleCrossRef" href="#fig0040">Fig. 8</a>). In addition, a significant difference in ROS levels between the curcuma- and the karkade-treated group and either control or faeces group was detected (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05).</p><elsevierMultimedia ident="fig0040"></elsevierMultimedia></span></span></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Discussion</span><p id="par0150" class="elsevierStylePara elsevierViewall">Asthmatic disorders have been rising in recent years. So, the first factor to be considered related to these disorders is the cytokine production. Cytokines are small, extracellular signalling mediators playing an important role in the co-ordination and persistence of inflammation in asthma.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">12</span></a> They possess overlapping biological activities, exert different effects at different concentrations, can synergise or antagonise the effects of other cytokines and regulate in a complex manner and function via cytokine cascade.<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">10</span></a></p><p id="par0155" class="elsevierStylePara elsevierViewall">The high level of TNF-α in our results in the inhaled group with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces confirms the previous experiments, where TNF-α is present abundantly in asthmatic airways. There is evidence that IgE triggering in sensitised lungs leads to increased TNF-α expression in epithelial cells in both rat and human.<a class="elsevierStyleCrossRef" href="#bib0385"><span class="elsevierStyleSup">31</span></a> It is reported that TNF-α is also released from alveolar macrophages of asthmatic patients after allergen challenge.<a class="elsevierStyleCrossRef" href="#bib0390"><span class="elsevierStyleSup">32</span></a> Furthermore, both monocytes and alveolar macrophages show increased gene expression of TNF-α after IgE triggering in vitro that is enhanced by INF-γ. In vitro studies also indicate that TNF-α plays a role in bronchial hyperresponsiveness and airway remodelling in asthma.<a class="elsevierStyleCrossRef" href="#bib0395"><span class="elsevierStyleSup">33</span></a></p><p id="par0160" class="elsevierStylePara elsevierViewall">Asthmatic patients show an increased level of IL-1β.<a class="elsevierStyleCrossRef" href="#bib0400"><span class="elsevierStyleSup">34</span></a> In addition, increased expression of IL-1β in asthmatic airway epithelium has been reported, together with an increased number of macrophages expressing IL-1β.<a class="elsevierStyleCrossRef" href="#bib0405"><span class="elsevierStyleSup">35</span></a> The high level of IL-1β is parallel to our measured results.</p><p id="par0165" class="elsevierStylePara elsevierViewall">Another cytokine (IL-4) plays an important role in the pathogenesis of allergic disorders.<a class="elsevierStyleCrossRef" href="#bib0410"><span class="elsevierStyleSup">36</span></a> Additional effects that seem of particular importance for asthma include stimulation of mucus producing cells and fibroblast, thus also implicating IL-4 in the pathogenesis of airway remodelling.<a class="elsevierStyleCrossRef" href="#bib0415"><span class="elsevierStyleSup">37</span></a> Numerous in vivo studies highlighted its role in IgE production.<a class="elsevierStyleCrossRef" href="#bib0420"><span class="elsevierStyleSup">38</span></a> Over expression of IL-4 in lungs leads to a lymphocytic and eosinophilic inflammation, but without airway hyperreactivity.<a class="elsevierStyleCrossRef" href="#bib0425"><span class="elsevierStyleSup">39</span></a> IL-4 appears to play an important role in Th2 cell development and recruitment to the airways.<a class="elsevierStyleCrossRef" href="#bib0430"><span class="elsevierStyleSup">40</span></a> These properties of IL-4 ensure our results, where we found that high levels of IL-4 were detected in inhaled groups.</p><p id="par0170" class="elsevierStylePara elsevierViewall">The fourth cytokine, IL-13, has a very similar biological activity to IL-4. The levels of IL-13 together with IL-4 are increased after allergen challenge of patients with asthma.<a class="elsevierStyleCrossRef" href="#bib0435"><span class="elsevierStyleSup">41</span></a> In allergen-induced airway changes, it has been hypothesised that IL-4 is crucial for the initial Th2 development during primary sensitisation but IL-13 release might prove more important during secondary antigen exposure.<a class="elsevierStyleCrossRef" href="#bib0440"><span class="elsevierStyleSup">42</span></a> Our data of IL-13 are in accordance with the above reviews, where we recorded a lower level in the control group and groups treated with medicinal plants than the inhaled group.</p><p id="par0175" class="elsevierStylePara elsevierViewall">In addition to the above cytokines, IgE antibodies play an important role in mediating type I hypersensitivity in humans. In both food and inhalant allergy it is accepted that HDM-specific IgE binds to high-affinity Fc RI on mast cells, basophils, macrophages, and dendritic cells, as well as to low-affinity Fc RII on macrophages, monocytes, lymphocytes, eosinophils, and platelets.<a class="elsevierStyleCrossRef" href="#bib0445"><span class="elsevierStyleSup">43</span></a> When mite allergens penetrate mucosal barriers of the respiratory tract and contact IgE antibodies bound to mast cells or basophils, histamine and other mediators that induce symptoms of immediate hypersensitivity are released.<a class="elsevierStyleCrossRef" href="#bib0450"><span class="elsevierStyleSup">44</span></a></p><p id="par0180" class="elsevierStylePara elsevierViewall">The other factor to be considered related to asthma disorder is the reactive oxygen species (ROS). The lungs have endogenous antioxidant mechanisms to combat the damaging effects of ROS.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">8</span></a> Many studies have reported increased indices of oxidative stress in the blood and airways of asthmatic subjects, where airway inflammation in asthmatic patients is associated with increased production of ROS (superoxide anion, hydrogen peroxide and hydroxyl radicals) by peripheral blood eosinophils, neutrophils, and alveolar macrophages.<a class="elsevierStyleCrossRef" href="#bib0455"><span class="elsevierStyleSup">45</span></a></p><p id="par0185" class="elsevierStylePara elsevierViewall">Curcuma is used as a food additive, while karkade is a herbal tea consumed both hot and cold by people around the world. Oral administration of curcumin in instances of acute inflammation was found to be as effective as cortisone or phenylbutazone, and one-half as effective in cases of chronic inflammation.<a class="elsevierStyleCrossRef" href="#bib0460"><span class="elsevierStyleSup">46</span></a> In this study we found that some allergenic disorder could be highly modulated in some cytokines, IgE and ROS by curcuma than karkade. The low amelioration caused by karkade might be due to the interplay effect of the karkade extract between humoral (B-cells) and cell-mediated (T-cells) immunity since the administration of the extracts led to changes in the production of cytokines (cell mediated immunity) and antibodies titre (humoral immunity).<a class="elsevierStyleCrossRef" href="#bib0365"><span class="elsevierStyleSup">27</span></a></p><p id="par0190" class="elsevierStylePara elsevierViewall">The data conclusion showed that repeated exposure to <span class="elsevierStyleItalic">D. pteronyssinus</span> or <span class="elsevierStyleItalic">D. farinae</span> faeces caused an increase in some cytokines (TNF-α, IL-1β, IL-4 and IL-13), immunoglobulin IgE and ROS. The high level of these mediators may participate in airway disorder. These disorders were ameliorated with a medicinal plant (curcuma and karkade) treatment. This ensures that curcuma and karkade may play an important role in the amelioration of the airway immune response.</p></span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Conflict of interest</span><p id="par0195" class="elsevierStylePara elsevierViewall">The authors have no conflict of interest to declare.</p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Ethical disclosures</span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Protection of human and animal subjects</span><p id="par0200" class="elsevierStylePara elsevierViewall">The procedures followed were in accordance with the regulations of the responsible Clinical Research Ethics Committee and in accordance with those of the World Medical Association and the Helsinki Declaration</p></span><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Confidentiality of data</span><p id="par0205" class="elsevierStylePara elsevierViewall">No patient data appears in this article.</p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Right to privacy and informed consent</span><p id="par0210" class="elsevierStylePara elsevierViewall">No patient data appears in this article.</p></span></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:10 [ 0 => array:3 [ "identificador" => "xres594873" "titulo" => "Abstract" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "abst0005" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abst0010" "titulo" => "Objective" ] 2 => array:2 [ "identificador" => "abst0015" "titulo" => "Methods" ] 3 => array:2 [ "identificador" => "abst0020" "titulo" => "Results" ] 4 => array:2 [ "identificador" => "abst0025" "titulo" => "Conclusions" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec609799" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 3 => array:3 [ "identificador" => "sec0010" "titulo" => "Materials and methods" "secciones" => array:4 [ 0 => array:3 [ "identificador" => "sec0015" "titulo" => "Preparation of extracts" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0020" "titulo" => "Mite faeces extract" ] 1 => array:2 [ "identificador" => "sec0025" "titulo" => "Medicinal plant extracts" ] ] ] 1 => array:2 [ "identificador" => "sec0030" "titulo" => "Experimental animals" ] 2 => array:2 [ "identificador" => "sec0035" "titulo" => "Cytokines, immunoglobulin and ROS in serum" ] 3 => array:2 [ "identificador" => "sec0040" "titulo" => "Statistical analysis" ] ] ] 4 => array:3 [ "identificador" => "sec0045" "titulo" => "Results" "secciones" => array:2 [ 0 => array:3 [ "identificador" => "sec0050" "titulo" => "The main characteristics of the dominant true house dust mite species in the valley and desert houses" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0055" "titulo" => "Dermatophagoides pteronyssinus" ] 1 => array:2 [ "identificador" => "sec0060" "titulo" => "Dermatophagoides farinae" ] ] ] 1 => array:3 [ "identificador" => "sec0065" "titulo" => "Immunological studies" "secciones" => array:6 [ 0 => array:2 [ "identificador" => "sec0070" "titulo" => "Assessments of TNF-α" ] 1 => array:2 [ "identificador" => "sec0075" "titulo" => "Assessments of IL-1β" ] 2 => array:2 [ "identificador" => "sec0080" "titulo" => "Assessments of IL-4" ] 3 => array:2 [ "identificador" => "sec0085" "titulo" => "Assessments of IL-13" ] 4 => array:2 [ "identificador" => "sec0090" "titulo" => "Assessments of IgE" ] 5 => array:2 [ "identificador" => "sec0095" "titulo" => "Assessments of ROS" ] ] ] ] ] 5 => array:2 [ "identificador" => "sec0100" "titulo" => "Discussion" ] 6 => array:2 [ "identificador" => "sec0105" "titulo" => "Conflict of interest" ] 7 => array:3 [ "identificador" => "sec0110" "titulo" => "Ethical disclosures" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0115" "titulo" => "Protection of human and animal subjects" ] 1 => array:2 [ "identificador" => "sec0120" "titulo" => "Confidentiality of data" ] 2 => array:2 [ "identificador" => "sec0125" "titulo" => "Right to privacy and informed consent" ] ] ] 8 => array:2 [ "identificador" => "xack200112" "titulo" => "Acknowledgements" ] 9 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2014-09-30" "fechaAceptado" => "2015-01-14" "PalabrasClave" => array:1 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec609799" "palabras" => array:6 [ 0 => "HDMs" 1 => "TNF-α" 2 => "IL-4" 3 => "IL-1β" 4 => "IL-13" 5 => "IgE and ROS" ] ] ] ] "tieneResumen" => true "resumen" => array:1 [ "en" => array:3 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Background</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">House dust mites (HDMs) faeces are the main factor involved in respiratory disorder. The true HDMs, <span class="elsevierStyleItalic">Dermatophagoides pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span>, detected in the samples collected from the house dust are the most important causes of allergic disorders such as asthma.</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Objective</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">The aim of this investigation was to study the curcuma and karkade amelioration of the allergenic immunological disorder, especially some cytokines, IgE and ROS, caused by the faeces of the dominant true HDM, <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> in valley and desert houses in EL-Minia Governorate, respectively.</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Methods</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">HDM cultures, faeces isolation, plant extraction and ELISA techniques were used. Male albino rats were classified into control, inhaled, and treated groups.</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Results</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">The present immunological study on the dominant allergenic true HDMs, <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span>, revealed that significantly higher serum levels of TNF-α, IL-1β, IL-4, IL-13 and IgE were found in rats treated with both <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> faeces than the other groups. In addition, statistical analysis of ROS data showed significant difference between the curcuma- and karkade-treated groups and either the control or the faeces-treated groups (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05).</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conclusions</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Some immunological disturbances caused by repeated exposure to the faeces of two dominant allergenic true HDM species (<span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span>) in the valley and desert houses could be ameliorated by curcuma and karkade.</p></span>" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "abst0005" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abst0010" "titulo" => "Objective" ] 2 => array:2 [ "identificador" => "abst0015" "titulo" => "Methods" ] 3 => array:2 [ "identificador" => "abst0020" "titulo" => "Results" ] 4 => array:2 [ "identificador" => "abst0025" "titulo" => "Conclusions" ] ] ] ] "multimedia" => array:8 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 2592 "Ancho" => 2167 "Tamanyo" => 564891 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">D. pteronyssinus</span>. (A) Ventral view of male. (B) Dorsal view of male. (C) Ventral view of female. (D) Flower-shaped apex of bursa copulatrix. Chelate chelicera (ch), apodem1 (ap1), anal suckers (a.s), oblong hysterosomal shield (h.s, arrows), dorsal seta (d2), crescentic epigynium (ep).</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 2416 "Ancho" => 2167 "Tamanyo" => 462550 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">D. farinae</span>. (A) Ventral view of male. (B) Dorsal view of male. (C) Ventral view of female. (D) Flask-shape bursa copulatrix (b.c). Chelate chelicera (ch), apodem I (apI), apodem III (apIII), anal suckers (a.s), hysterosomal shield (h.s, arrows), dorsal seta (d2), crescentic epigynium (ep), sternum (st).</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 893 "Ancho" => 1584 "Tamanyo" => 80592 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">TNF-α levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated with either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] 3 => array:7 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 875 "Ancho" => 1594 "Tamanyo" => 82208 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">IL-1β levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated with either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] 4 => array:7 [ "identificador" => "fig0025" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 900 "Ancho" => 1585 "Tamanyo" => 85662 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">IL-4 levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated with either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] 5 => array:7 [ "identificador" => "fig0030" "etiqueta" => "Figure 6" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr6.jpeg" "Alto" => 923 "Ancho" => 1590 "Tamanyo" => 89697 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">IL-13 levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated with either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] 6 => array:7 [ "identificador" => "fig0035" "etiqueta" => "Figure 7" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr7.jpeg" "Alto" => 857 "Ancho" => 1561 "Tamanyo" => 81720 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">IgE levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated with either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] 7 => array:7 [ "identificador" => "fig0040" "etiqueta" => "Figure 8" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr8.jpeg" "Alto" => 907 "Ancho" => 1591 "Tamanyo" => 80295 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">ROS levels in male albino rats untreated (control), inhaled with <span class="elsevierStyleItalic">D. pteronyssinus</span> and <span class="elsevierStyleItalic">D. farinae</span> mite faeces and treated either curcuma or karkade. * shows the significance of treated rates with curcuma in comparison to the inhaled rates. ** shows the significance of treated rates with karkade in comparison to the inhaled rates.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => 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Year/Month | Html | Total | |
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2024 May | 30 | 8 | 38 |
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2023 December | 90 | 10 | 100 |
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2023 October | 104 | 19 | 123 |
2023 September | 63 | 3 | 66 |
2023 August | 66 | 7 | 73 |
2023 July | 82 | 7 | 89 |
2023 June | 66 | 34 | 100 |
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2023 April | 107 | 23 | 130 |
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2020 December | 2 | 2 | 4 |
2020 November | 0 | 6 | 6 |
2020 October | 1 | 3 | 4 |
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2020 May | 0 | 8 | 8 |
2020 April | 0 | 2 | 2 |
2020 March | 0 | 5 | 5 |
2020 February | 0 | 1 | 1 |
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2019 December | 0 | 3 | 3 |
2019 November | 0 | 4 | 4 |
2019 October | 0 | 2 | 2 |
2019 September | 0 | 4 | 4 |
2019 August | 0 | 4 | 4 |
2019 July | 0 | 8 | 8 |
2019 June | 0 | 1 | 1 |
2019 May | 0 | 16 | 16 |
2018 February | 10 | 4 | 14 |
2018 January | 23 | 0 | 23 |
2017 December | 10 | 3 | 13 |
2017 November | 14 | 7 | 21 |
2017 October | 11 | 3 | 14 |
2017 September | 13 | 11 | 24 |
2017 August | 6 | 5 | 11 |
2017 July | 6 | 2 | 8 |
2017 June | 20 | 7 | 27 |
2017 May | 26 | 10 | 36 |
2017 April | 38 | 13 | 51 |
2017 March | 9 | 27 | 36 |
2017 February | 14 | 3 | 17 |
2017 January | 9 | 1 | 10 |
2016 December | 20 | 5 | 25 |
2016 November | 24 | 3 | 27 |
2016 August | 0 | 1 | 1 |
2016 June | 0 | 2 | 2 |
2016 March | 1 | 1 | 2 |
2016 February | 2 | 1 | 3 |
2016 January | 2 | 0 | 2 |