covid
Buscar en
Medicina Universitaria
Toda la web
Inicio Medicina Universitaria Probiotics and Helicobacter pylori infection
Journal Information
Vol. 14. Issue 57.
Pages 217-223 (October 2012)
Share
Share
Download PDF
More article options
Vol. 14. Issue 57.
Pages 217-223 (October 2012)
Full text access
Probiotics and Helicobacter pylori infection
Probióticos e infección por Helicobacter pylori
Visits
19244
Massimiliano Praitano Ma, Salvatore Iaconob, Ruggiero Francavillaa
a Interdisciplinary Department of Medicine, University of Bari, Italy.
b Department of Medicine, University of Palermo, Italy.
This item has received
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Tables (1)
Table 1. Summary of clinical trials of probiotics in Helicobacter pylori infection in children: effects on eradication rates.

Aproximadamente un 50% de la población mundial está infectada con Helicobacter pylori (H. pylori), con una tasa de prevalencia muy elevada en los países en desarrollo. Los lineamientos actuales sugieren el uso de la terapia triple como primer tratamiento de elección, para tratar la infección por H. pylori. Aunque la tasa de falla en erradicarla es más de un 30%. El actual interés en los probióticos como un agente terapéutico contra H. pylori es incentivada por el incremento en la resistencia de esta bacteria patógena a los antibióticos. Por lo tanto, el incremento en el interés en terapias alternativas es un tópico actual. Los datos disponibles en niños indican que los probióticos parecen ser eficaces en la prevención de los efectos colaterales de los antibióticos. También pueden ser de ayuda en la prevención de las complicaciones del H. pylori, al disminuír su densidad y gastritis, además de prevenir la colonización o reinfección de la misma al inhibir la adhesión a las celulas epiteliales gástricas. No hay una clara evidencia que los probióticos puedan incrementar la tasa de erradicación del H. pylori.

Palabras clave:
Probióticos, Helicobacter pylori, recolonización, Italia

Approximately 50% of the world population is infected with Helicobacter pylori (H. pylori), with the highest prevalence rates in developing countries. The current guidelines suggest the use of triple therapy as first choice treatment of H. pylori infection, although the eradication failure rate is more than 30%. Current interest in probiotics as therapeutic agents against H. pylori is stimulated by the increasing resistance of pathogenic bacteria to antibiotics, thus the interest for alternative therapies is a real actual topic. Available data in children indicate that probiotics seems to be efficacious for the prevention of antibiotic associated side-effects, and might be helpful for the prevention of H. pylori complications by decreasing H. pylori density, gastritis, and for the prevention of H. pylori colonization or re-infection by inhibiting adhesion to gastric epithelial cells. There is no clear evidence that probiotics may increase the H. pylori eradication rate.

Keywords:
Probiotics, Helicobacter pylori, recolonization, Italy
Full Text

Introduction

Probiotics have recently been defined by FAO/WHO as "live microorganisms which when administered in adequate amounts confer a health benefit on the host".1 Several controlled clinical trials have shown beneficial outcomes in children for the use of probiotics in some different conditions as rotavirus infections, antibiotic-associated diarrhea, irritable bowel syndrome.2-4

Most of commonly used microorganism in clinical practice are lactic acid-producing bacteria such as Lactobacillus spp, and microrganisms belonging to genus Bifidobacterium and Bacillus. Other less commonly used probiotic microorganisms are strains of Streptococcus, Escherichia coli, and Saccharomyces.3 Different biological effects have been described for probiotics, including the synthesis of antimicrobial substances as lactic acid, hydrogen peroxide and bacteriocins, the competitive interaction with pathogens for microbial adhesion sites, and finally the modulation of the host immune response.5,6 Research efforts into the clinical effects of probiotics in man are rapidly increasing. A field in which particular interest is arising represents the Helicobacter pylori (H. pylori) infection.

Helicobacter pylori

The Gram-negative, spiral-shaped bacterium H. pylori is a common human pathogen and a public health problem that causes gastritis and peptic ulcers both in adults7 and children8 and it is considered an important cofactor in the development of gastric cancer.9 It is well known that childhood is an important period for acquisition of H. pylori infection although several recent articles have reported a decline in the prevalence of H. pylori infection in children over the last 10 years.10 Intrafamiliar transmission of the infection, especially from mother to child, has been hypothesized as the major mode of dissemination.11 Poor socioeconomic conditions remain a significant risk factor for infection, while exclusive breast-feeding (longer than four months) and higher socioeconomic status have been reported as protective factors against the infection.8

Recent evidence-based guidelines from ESPGHAN and NASPGHAN recommend, as first choice treatment, a triple therapy using a proton pump inhibitor (PPi) with amoxicillin and clarythromycin or imidazole given twice daily for 7-14 days.12 These regimens have the disadvantages of being expensive, risking poor compliance, causing side-effects and in particular encouraging resistance emergence, both in H. pylori and commensal organisms exposed gratuitously.13 Moreover, as most of the colonized children remain asymptomatic, the administration of antibiotic treatments is not ethically acceptable. Other factors limiting the administration of such treatments in developing countries are their high cost for the families from the low socio-economic stratum (the most affected by the infections) and the relative inefficiency of the antibiotics due to the fact that, when treated, children tend to be rapidly re-colonized.8

Therefore, recent review studies report eradication rates of standard triple therapy in children below 75%.14,15 It has been recently shown that a novel 10 day sequential regimen, characterized by the sequential administration of three antibiotics, is highly efficacious in eradicating H. pylori infection both in adults and children.16,17 Our group recorded in children an eradication rate significantly higher than that achieved by the standard triple therapy,18,19 even in H. pylori clarithromycin resistant strain.19 This treatment is now considered a good option for H. pylori infection accordingly to ESPGHAN and NASPGHAN guidelines.12

Nowadays, there is considerable interest in alternative therapies (e.g. targeting urease, a known virulence factor) or adjunctive treatment against Helicobacter pylori20 to reduce some of the drawbacks associated with the antibiotic consumption. To these aims, probiotics have been included as "possible" tools for management of the infection21 and a considerable amount of reports have currently been carried out on their possible role in the treatment and prophylaxis of H. pylori infection.

Material and methods

Several in vitro studies have shown that various lactobacilli can inhibit H. pylori growth. Strains with this ability include Lactobacillus acidophilus: L. acidophilus strain CRL 639,22L. acidophilus in a liophilized culture (lactisyn),23L. acidophilus LB,24L. acidophilus strain NAS and DDS-1;25L. casei rhamnosus dairy starter;26L. johnsonii La1;27L. salivarius WB 1004.28 Lactobacilli are known to produce by catabolism relatively large amounts of lactate, and this has been considered as the inhibitory and/ or the bactericidal factor by some authors.26,29 Indeed, lactic acid could inhibit the H. pylori urease30 and in addition could exert its antimicrobial effect resulting from the lowering of the pH. Other authors have clearly shown that for some strains a substance other than lactate also contributes to the antibacterial effects. 22,24,27,31-33

Some probiotic strains such as L. reuteri34 or Weissellaconfusa35 can inhibit H. pylori growth by competing with adhesion sites. A probiotic that shares glycolipid-binding specificity with H. pylori may compete with pathogens for the receptor site making it possible to hypothesize a future application as anti-adhesion drugs.36 We have recently shown that, two years after H. pylori eradication, 30% of children became re-infected37 therefore the possibility to reduce this phenomenon by the simple administration of a probiotic is fascinating.

In vitro studies have shown that L. plantarumstrain 299v and L. rhamnosus GG increase the expression of MUc2 and MUc3 genes38 and the subsequent extracellular secretion of mucin by colon cell cultures.39 This property can mediate the ability of these strains to restore the mucosal permeability of gastric mucosa or inhibit the adherence of pathogenic bacteria, including H. pylori.30

Probiotics could also modify the host immune response.30L. salivarius wB 1004 has shown in vitro to reduce IL-8 secretion by gastric epithelial cells29 and in animal studies certain lactic acid bacteria (L. casei, L. acidophilus, L. rhamnosus, L. delbrueckiisubsp. bulgaricus, L. plantarum, Lactococcuslactis and Streptococcus thermophilus) have been able to increase the number of iga producing cells associated to the lamina propria of small intestine.40 However, the specific interaction of probiotics with the immune system and the mechanism by which they can exert a beneficial effect are still unclear. Moreover, the immunoadjuvant capacity observed would be a property of the strain assayed and cannot be generalized to genus or species.

Recent studies have defined potentially new probiotic strains of L. reuteri, a small minority of which showed strong anti-inflammatory combined with anti-pathogen effects. L. reuteri atcc Pta 6475 produces and exports substances that can interfere with TNFα production in human macrophages41 and suppresses NF-KB activation affecting apoptosis42 whilst still retaining its basic anti-pathogen activity during both planktonic and biofilm growth.43

Results

Probiotics and H. pylori loads: 13 C-urea breath test

In most human studies, the effect of probiotic treatment on the level of H. pylori infection has been estimated indirectly by the 13C-urea breath test (13c-UBT) delta over baseline value, a well-known semi quantitative measurement of the bacterial load.44

In children two studies have been performed (by the same investigators) to evaluate the ability of probiotics to interfere with the intra-gastric bacterial load. First, cruchet et al. performed a randomized, double blind, controlled study on asymptomatic children screened for H. pylori by the 13c-UBT;45H. pylori-colonized subjects were distributed into five groups to receive a product containing live L. johnsonii La1 or L. paracasei St11, heat-killed La1 or L. paracasei St11, or just vehicle every day for four weeks. A second 13c-UBT was carried out at the end of this period. The authors detected a moderate but significant difference in 13c-UBT values in children receiving live La1, whereas no differences were observed in the other groups. Subsequently, in a randomized open trial, Gotteland et al.46 Randomized asymptomatic H. pylori-positive children to receive either 7-day triple therapy, or Saccharomyces boulardii as a symbiotic simultaneously with inulin or L. acidophilus LB daily for eight weeks. An additional group of asymptomatic H. pylori-positive children was followed for eight weeks without any treatment. A significant decrease in 13c-UBT values (repeated after eight weeks) was observed in the antibiotic group and in the Saccharomyces boulardii group but not in the L. acidophilus LB group. No changes in 13c-UBT values were observed in untreated children. These results suggest that anti-H. pylori activity is species and strain specific, with some probiotics, such as Saccharomyces boulardii and L. johnsonii La1, interfering with H. pylori in vivo more actively than others (L. acidophilus LB, L. paracasei St11). This ability of some probiotics strains may represent an interesting alternative to modulate H. pylori colonization in children infected by this pathogen through a regular ingestion of the beneficial microorganisms.

Probiotics alone and H. pylori eradication rate Table 1 summarizes the clinical trials performed in children on the effect of probiotics on H. pylori eradication rates alone or as an adjuvant to eradicating regimens. In children, two studies evaluated whether probiotics may eradicate alone the H. pylori infection. Gotteland et al. Showed that H. pylori eradication was successful in 66% of children treated with antibiotic, in 12% of the Saccharomyces boulardii plus inulin and in 6.5% of L. acidophilus LB group; no spontaneous clearance was observed in children without treatment.46 The fact that the 13c-UBT was carried out immediately after treatment (in the case of probiotic supplementation) limits the conclusion on a real eradication of the bacterium. A further multicentre randomized, controlled, double-blind trial has been recently carried out in asymptomatic H. pylori positive children.50 Subjects have been allocated into four groups to receive one of the following dietary daily treatments for three weeks: cranberry juice and La1 (CB/La1), placebo juice and La1 (La1), cranberry juice and heat-killed La1 (CB), or placebo juice and heat-killed La1 (control). After treatment, H. pylori eradication rates significantly differed in the four groups: 1.5% in the control group compared with 14.9%, 16.9%, and 22.9% in the La1, CB, and CB/La1 groups, respectively; the latter group showed the highest eradication rate. However, a third 13c-UBT performed after a one month washout showed a recrudescence of the infection in 80% of those children who had resulted negative, suggesting just a temporary inhibition of H. pylori that disappeared once the administration of the inhibiting factors was interrupted.50 In a recent study Lactobacillus gasseri Oll2716 (LG21) was administered in cheese to pre-school children for one year.53 As a result, 24 of 82 subjects who completed the study (29.3%) were considered to be cured after treatment according to the HpSA test, whereas no eradication was observed in the six subjects in the placebo group consuming ordinary cheese. Spontaneous eradication was found in one of 18 children (5.6%) who represented the control group. The difference in the rate of eradication between the active and control groups was statistically significant. However, HpSA test was repeated in 12 of 24 subjects who were HpSA-negative after undergoing the LG21 treatment, but found that five of those 12 (41.7%) had reversed to be HpSA-positive. Therefore, a final eradication rate was around 17%.53

Probiotics plus antibiotic treatment and H. pylori eradication rate

It has been suggested that the use of probiotics as an adjuvant to eradicating regimens could improve the success of H. pylori eradication. Several clinical trials have been carried out both in adults and children, providing conflicting results. Table 1 summarizes the clinical trials performed in children on the effect of probiotics on H. pylori eradication rates. Sykora et al. supplemented a standard triple therapy with fermented milk containing L. casei DN-114 001 for 14 days in H. pylori positive patients and showed a significantly higher eradication rate in the probiotic as compared to the placebo group.47

Hurduc et al. demonstrated that the addition of Saccharomyces boulardii to a standard triple therapy in symptomatic children confers a 12% non-significant enhanced therapeutic benefit on H. pylori eradication.51

In contrast, Goldman et al. tested the efficacy of a commercial yogurt containing B. animalis and L. casei as an adjuvant to triple therapy and found no difference in H. pylori eradication rates between probiotic and placebo group.48 In a study of our group, aimed to evaluate the efficacy of probiotics to reduce antibiotic side effects, we found no differences in the eradication rates according to the presence/absence of the probiotic L. reuteri atcc 55730 (SD2112).49

Recently, in a double-blind placebo-controlled randomized clinical trial no difference was found with respect to H. pylori eradication rates between children receiving standard triple therapy supplemented with L. rhamnosus GG or placebo.52

These data do not represent convincing evidence to support the use of probiotics as an adjunct with the aim of increasing the H. pylori eradication rate in children. Nevertheless, further studies are needed to clarify their role in this particular issue. The major limit to establish whether a probiotic is able to significantly increase the eradication rate is represented by the power of the study. Indeed, due to the high eradication rates that we mostly achieve with standard antibiotic treatment, to detect a 10% increase in eradication (secondary to the use of a probiotic strain), given a power of al least 80% and an alpha error level of 5%, 150 patients in each arm are needed to be enrolled.

Probiotics and antibiotic-associated gastrointestinal side effects during H. pylori eradication therapy

Bacterial resistance and antibiotic' side-effects represent the most frequent cause for anti-H. pylori treatment failure in clinical practice.13

Several studies evaluated whether probiotic supplementation might help to prevent or reduce drug-related side effects during H. pylori eradication therapy.

The rationale of coupling a probiotic to any antibiotic treatment stem from the result of a recent study showing that daily supplementation with viable probiotic bacteria during and post antibiotic therapy reduces the extent of disruption of the intestinal microbiota as well as the incidence and total numbers of antibiotic-resistant strains in the re-growth population, suggesting that a probiotic should be always associated to an antibiotic.54

Our group has performed the first trial in children to determine whether adding probiotics to an anti-H. pylori regimen could be of help to prevent or minimize the gastrointestinal side-effects burden.49 Forty H. pylori-positive children were consecutively treated with 10-day sequential therapy, and were blindly randomized to receive either L. reuteri atcc 55730 (SD2112) or placebo (maltodextrin) for 20 days starting from the first day of the anti-H. pylori regimen. Overall, in all probiotic-supplemented children as compared to those receiving placebo, there was a significant reduction in the gastrointestinal symptom rating scale score during eradication therapy, which became markedly evident at the end of follow-up. In detail, children receiving L. reuteri complained of epigastric pain less frequently during eradicating treatment as well as abdominal distension, belching, disorders of defecation and halitosis thereafter. In a randomized open trial performed in symptomatic H. pylori positive children the occurrence of antibiotic associated side effects was significantly reduced by the addition of Saccharomyces boulardii compared with the placebo-supplemented group.51 However, the authors concluded that it could not be excluded that the incidence and interpretation of side effects was influenced by the fact that it was an open trial.

Finally, in a double-blind placebo-controlled randomized clinical trial preformed by Szayeska et al. The supplementation of standard triple therapy with L. rhamnosus GG did not significantly alter the incidence of antibiotic associated side-effects.52

Given the results from these studies, probiotic treatment seems to be able to reduce H. pylori therapy associated side-effects; however, it is evident that not all probiotics are created equal, that the beneficial effects are strain specific, and each strain must be evaluated individually.

Probiotics and H. pylori infection prevention

Many preliminary studies have been done concerning therapeutic or prophylactic vaccination against H. pylori with a promising effect,55 but the translation to a human vaccine remains difficult, in part because the immunology of the stomach is still poorly understood. Considering that primary H. pylori infection occurs predominantly in early childhood, prophylaxis of the infection will be almost accomplished by administering probiotics to children for a couple of years while at risk for the primary infection. A pilot study for primary prevention has been recently performed:53 308 H. pylori-negative children have been randomized to receive LG21 containing cheese or ordinary cheese. In the per-protocol analysis, the rates of H. pylori infection were 4.1% and 8.1% in the active and placebo groups, respectively. There was no statistically significant difference between those two groups, although the incidence of the infection was reduced by approximately 50% by the LG21-cheese treatment.53

Discussion

Probiotics seem to represent a novel approach to the management of H. pylori infection. Despite the fact that there is no clear evidence that the addition of probiotics to the eradicating therapy increases the eradication rates in children, it seems to be efficacious for the prevention of antibiotic associated side effects. Results so far are encouraging and further clinical trials are called for. The design of such studies should be such as to clarify which probiotic strains are suitable, in what form, in what dose and for how long. Another important issue will be to address the cost-effectiveness of using probiotics in different clinical conditions.

As a perspective the persistent strains specific ability, although weak in some cases, of some probiotics to decrease H. pylori density and gastritis could be of help in reducing the risk of H. pylori-associated complication later in life by attenuating level of infection;56 further studies are needed to evaluate whether this effect is sustained over time. It is also fascinating the hypothesis of using probiotics to inhibiting H. pylori adhesion to gastric epithelial cells thus preventing H. pylori colonization especially in young children or H. pylori re-infection in high-risk patients. Finally, clinical studies on a combination of the anti-inflammatory effects of some probiotics strains with the earlier known anti-H. pylori effect are claimed for clinical application.

Conflict of interest

The authors declare that there is no conflict of interest.

Financial disclosure

No financial support was received in relation to this article.


Corresponding author:

Ruggiero Francavilla MD, PhD.

E-mail:
rfrancavilla@me.com

Received: October 2012.

Accepted: October 2012

Bibliography
[1]
Accessed on October 25, 2012..
ftp://ftp.fao..
org/es/esn/food/probio_report_en. , (pdf),
[2]
Sullivan A, Nord CE..
Probiotics and gastrointestinal diseases..
, 257 (J Intern Med 2005), pp. 78-92
[3]
Romano C, Ferrau'' V, Cavataio, et al..
lactobacillus reuteri in children with functional abdominal pain (FAP)..
[4]
Francavilla R, Miniello VL, Magistà AM, et al..
A randomized controlled trial of lactobacillus rhamnosus strain GG in children with functional abdominal pain..
, 126 (Pediatrics 2010), pp. e1445-1452
[5]
Fuller R..
Probiotics in human medicine..
, 32 (Gut 1991), pp. 439-442
[6]
Franceschi F, Cazzato A, Nista, et al..
Role of probiotics in patients with Helicobacter pylori infection..
, 12 (Helicobacter 2007), pp. 59-63
[7]
No authors listed..
Helicobacter pylori in Peptic Ulcer Disease..
, 12 (NIH consensus Statement 1994), pp. 1-23
[8]
Elitsur Y, Yahav J..
Helicobacter pylori infection in pediatrics..
, 10:S47-53.ESPGHAN (Helicobacter 2005),
[9]
Uemura N, Okamoto S, Yamamoto S, et al..
Helicobacter pylori infection and the development of gastric cancer..
, 345 (N Engl J Med 2001), pp. 784-789
[10]
Daugule I, Rowland M..
Helicobacter pylori infection in children..
, 13 (Helicobacter 2008), pp. S41-46
[11]
Kivi M, Tindberg Y, Sörberg M, et al..
Concordance of Helicobacter pylori strains within families..
, 41 (J ClinMicrobiol 2003), pp. 5604-5608
[12]
Koletzko S, Jones NL, Goodman KJ, et al..
H pylori working Groups of ESPGHAN and NASPGHAN..
evidence-based guidelines from ESPGHAN and NASPGHAN for Helicobacter pylori infection in children. , 53 (J PediatrGastroenterolNutr 2011), pp. 230-243
[13]
Deltenre M, Ntounda R, Jonas C, et al..
Eradication of Helicobacter pylori: why does it fail? Ital J GastroenterolHepatol 1998..
, 30 pp. S326-328
[14]
Oderda G, Shcherbakov P, Bontems P, et al..
European Pediatric Task Force on Helicobacter pylori..
Results from the pediatric european register for treatment of Helicobacter pylori (PERTH). , 12 (Helicobacter 2007), pp. 150-156
[15]
Kato S, Konno M, Maisawa S, et al..
Results of triple eradication therapy in Japanese children: a retrospective multi-center study..
, 39 (J Gastroenterol 2004), pp. 838-843
[16]
Vaira D, Zullo A, Vakil N, et al..
Sequential therapy versus standard triple-drug therapy for Helicobacter pylori eradication: a randomized trial..
, 146 (Ann Intern Med 2007), pp. 556-563
[17]
Francavilla R, Lionetti E, Castellaneta SP, et al..
Improved efficacy of 10-Day sequential treatment for Helicobacter pylori eradication in children: a randomized trial..
, 129 (Gastroenterology 2005), pp. 1414-1419
[18]
Francavilla R, Lionetti E, Cavallo L..
Sequential treatment for Helicobacter pylori eradication in children..
, 57 (Gut 2008), pp. 1178
[19]
Francavilla R, Lionetti E, Castellaneta, et al..
Clarithromycin-resistant genotypes and eradication of Helicobacter pylori..
, 157 (J Pediatr 2010), pp. 228-232
[20]
Hamilton-Miller JM..
The role of probiotics in the treatment and prevention of Helicobacter pylori infection..
, 22 (Int J antimicrob Agents 2003), pp. 360-366
[21]
Malfertheiner P, Mégraud F, O''Morain C, et al..
European Helicobacter Pylori Study Group (EHPSG)..
Current concepts in the management of Helicobacter pylori infection--the Maastricht 2-2000 Consensus Report. , 16 (Aliment Pharmacolther 2002), pp. 167-180
[22]
Lorca Gl, Wadström T, Valdez GF, et al..
Lactobacillus acidophilus autolysins inhibit Helicobacter pylori in vitro..
, 42 (CurrMicrobiol 2001), pp. 39-44
[23]
Bhatia SJ, Kochar N, Abraham P, et al..
Lactobacillus acidophilus inhibits growth of campylobacter pylori in vitro..
, 27 (J ClinMicrobiol 1989), pp. 2328-2330
[24]
Coconnier MH, Lievin V, Hemery E, et al..
Antagonistic activity against Helicobacter infection in vitro and in vivo by the human lactobacillus acidophilus strain LB..
, 64 (Aappl environ Microbiol 1998), pp. 4573-4580
[25]
Rasic J, Klem I, Jovanic D, Ac M..
Antimicrobial effect of lactobacillus acidophilus and lactobacillus delbrueckii subsp..
Bulgaricus against Helicobacter pylori in vitro. , 14 (Arch Gastroenterohepatol 1995), pp. 158-160
[26]
Midolo PD, Lambert JR, Hull R, et al..
In vitro inhibition of Helicobacter pylori Nctc 11637 by organic acids and lactic acid bacteria..
, 79 (J ApplBacteriol 1995), pp. 475-479
[27]
Michetti P, Dorta G, Wiesel PH, et al..
Effect of whey-based culture supernatant of lactobacillus acidophilus (johnsonii) La1 on Helicobacter pylori infection in humans..
, 60 (Digestion 1999), pp. 203-209
[28]
Aiba Y, Suzuki N, Kabir AM, et al..
Lactic acid-mediated suppression of Helicobacter pylori by the oral administration of lactobacillus salivarius as a probiotic in a gnotobiotic murine model..
, 93 (Am J Gastroenterol 1998), pp. 2097-2101
[29]
Borruel N, Casellas F, Antolín M, et al..
Effects of nonpathogenic bacteria on cytokine secretion by human intestinal mucosa..
, 98 (Am J Gastroenterol 2003), pp. 865-870
[30]
Lesbros-Pantoflickova D, Corthésy-Theulaz I, Blum AL..
Helicobacter pylori and probiotics..
, 137 (J Nutr 2007), pp. S812-818
[31]
Johnson C, Dicksved J Jonsson H, et al..
Anti Helicobacter pylori activity among lactic acid bacteria isolated from gastric biopsies and strains of lactobacillus reuteri (abstract)..
, 8 (Helicobacter 2003), pp. 473
[32]
Pinchuk IV, Bressollier P, Verneuil B, et al..
In vitro anti-Helicobacter pylori activity of the probiotic strain Bacillus subtilis 3 is due to secretion of antibiotics..
, 45 (Antimicrob Agents Chemother 2001), pp. 3156-3161
[33]
Cats A, Kuipers EJ, Bosschaert MA, et al..
Effect of frequent consumption of a lactobacillus casei-containing milk drink in Helicobacter pylori-colonized subjects..
, 17 (Aliment Pharmacolther 2003), pp. 429-435
[34]
Mukai T, Asasaka T, Sato E, et al..
Inhibition of binding of Helicobacter pylori to the glycolipid receptors by probiotic lactobacillus reuteri..
, 32 (FEMS Immunol Med Microbiol 2002), pp. 105-110
[35]
Nam H, Ha M, Bae O, et al..
Effect of Weissellaconfusa strain PL9001 on the adherence and growth of Helicobacter pylori..
, 68 (Appl Environ Microbiol 2002), pp. 4642-4645
[36]
Felley C, Michetti P..
Probiotics and Helicobacter pylori..
, 17 (Best Pract Res Clin Gastroenterol 2003), pp. 785-791
[37]
Magistà AM, Ierardi E, Castellaneta S, et al..
Helicobacter pylori status and symptom assessment two years after eradication in pediatric patients from a high prevalence area..
, 40 (J Pediatr Gastroenterol Nutr 2005), pp. 312-318
[38]
Mack DR, Michail S, Wei S, et al..
Probiotics inhibit enteropathogenic E..
coli adherence in vitro by inducing intestinal mucin gene expression. , 276 (Am J Physiol 1999), pp. 941-950
[39]
Mack DR, Ahrne S, Hyde L, et al..
Extracellular MUc3 mucin secretion follows adherence of lactobacillus strains to intestinal epithelial cells in vitro..
, 52 (Gut 2003), pp. 827-833
[40]
Vitini E, Alvarez S, Medina M, et al..
Gut mucosal immunostimulation by lactic acid bacteria..
, 24 (Biocell 2000), pp. 223-232
[41]
Lin YP, Thibodeaux CH, Penã Ja, et al..
Probiotic lactobacillus reuteri suppress proinflammatory cytokines via c-Jun..
, 14 (Inflamm Bowel Dis 2008), pp. 1068-1083
[42]
Iyer C, Kosters A, Sethi G, et al..
Probiotic lactobacillus reuteri promotes TNF-induced apoptosis in human myeloid leukemia-derived cells by modulation of NF-kappaB and MAPK signalling..
, 10 (cell Microbiol 2008), pp. 1442-1452
[43]
Jones SE, Versalovic J..
Probiotic lactobacillus reuteri bio-films produce antimicrobial and anti-inflammatory factors..
, 9 (BMC Microbiol 2009), pp. 35
[44]
Chang MC, Chang YT, Sun CT, et al..
Quantitative correlation of Helicobacter pylori stool antigen (HpSA) test with 13curea breath test (13c-UBT) by the updated Sydney grading system of gastritis..
, 49 (Hepatogastroenterology 2002), pp. 576-579
[45]
Cruchet S, Obregon MC, Salazar G, et al..
Effect of the ingestion of a dietary product containing Lactobacillus johnsonii La1 on Helicobacter pylori colonization in children..
, 19 (Nutrition 2003), pp. 716-721
[46]
Gotteland M, Poliak L, Cruchet S, et al..
Effect of regular ingestion of Saccharomyces boulardii plus inulin or lactobacillus acidophilus LB in children colonized by Helicobacter pylori..
, 94 (ActaPaediatr 2005), pp. 1747
[47]
Sykora J, Valeckova K, Amlerova J, et al..
Effects of a specially designed fermented milk product containing probiotic lactobacillus casei DN-114 001 and the eradication of Helicobacter pylori in children: a prospective randomized, double-blind study..
, 39 (J ClinGastroenterol 2005), pp. 692-698
[48]
Goldman CG, Barrado DA, Balcarce N, et al..
Effect of a pro-biotic food as an adjuvant to triple theeradication of Helicobacter pylori infection in children..
, 22 (Nutrition 2006), pp. 984-988
[49]
Lionetti E, Miniello VL, Castellaneta S, et al..
Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial..
, 24 (Aliment Pharmacol Ther 2006), pp. 1461-1468
[50]
Gotteland M, Andrews M, Toledo M, et al..
Modulation of Helicobacter pylori colonization with cranberry juice and lactobacillus johnsonii La1 in children..
, 24 (Nutrition 2008), pp. 421-426
[51]
Hurduc V, Plesca D, Dragomir D, et al..
A randomized, open trial evaluating the effect of Saccharomyces boulardii on the eradication rate of Helicobacter pylori infection in children..
, 98 (Acta Paediatr 2009), pp. 127-131
[52]
Szajewska H, Albrecht P, Topczewska-Cabanek A..
Randomized, double-blind, placebo-controlled trial: effect of lacto-bacillus GG supplementation on Helicobacter pylori eradication rates and side effects during treatment in children..
, 48 (J Pediatr Gastroenterol Nutr 2009), pp. 431-436
[53]
Boonyaritichaikij S, Kuwabara K, Nagano J, et al..
Long-term administration of probiotics to asymptomatic pre-school children for either the eradication or the prevention of Helicobacter pylori infection..
, 14 (Helicobacter 2009), pp. 202-207
[54]
Plummer SF, Garaiova I, Sarvotham T, et al..
Effects of probiotics on the composition of the intestinal microbiota following antibiotic therapy..
, 26 (Int J Antimicrob Agents 2005), pp. 69-74
[55]
Permin H, Andersen LP..
Inflammation, immunity, and vaccines for Helicobacter infection..
, 10 (Helicobacter 2005), pp. 21-25
[56]
Yamaoka Y, Kodama T, Kita M, et al..
Relation between clinical presentation, Helicobacter pylori density, interleukin 1beta and 8 production, and caga status..
, 45 (Gut 1999), pp. 804-811
Article options