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Letter to the Editor
Autoimmune diseases and vaccines against COVID-19. Decision-making in uncertain scenarios
Enfermedades autoinmunes y vacunas contra la COVID-19. Toma de decisiones en escenarios de incertidumbre
Alberto E. Calvo Elíasa, Lucía Pérez Casadob, José Luis Callejas Rubioc
a Servicio de Medicina Interna, Hospital Clínico San Carlos, Madrid, Spain
b Servicio de Medicina Interna, Hospital Universitario de Cabueñes, Gijón, Spain
c Unidad de Enfermedades Autoinmunes Sistémicas, Servicio de Medicina Interna, Hospital Clínico Universitario San Cecilio, Granada, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We have read the special article that was recently published in your journal by Cairoli and Espinosa regarding vaccines against the 2019 coronavirus disease &#40;COVID-19&#41; in patients with systemic autoimmune diseases &#40;SADs&#41;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a>&#46; We greatly appreciate the authors&#8217; clarity in presenting such a complex situation from a clinical point of view for physicians who work with these conditions&#44; including their contribution of responses to when&#44; how&#44; whom&#44; and with what to vaccinate patients with SADs&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A key issue is to determine whether patients with SADs develop immunity against the severe acute respiratory syndrome coronavirus 2 &#40;SARS-CoV-2&#41; and what factors have an impact on this response&#46; As discussed in the paper&#44; this problem is even more important in patients under treatment with rituximab&#44; as this drug is linked to a decline in immunoglobulin production and&#44; therefore&#44; to lower post-vaccination antibody levels&#46; Although we believe that we are all clear on this&#44; the question is whether the risk of infection is greater as a result of this treatment&#46; This stems from the possibility that rituximab induces a decrease in humoral response&#44; but not in cellular response&#46; The data available in the literature in this regard are scarce and yield inconclusive results&#46; Ferguson et al&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> published the case of a patient treated with rituximab who received two doses of a messenger ribonucleic acid &#40;mRNA&#41; vaccine and failed to produce antibodies&#44; but did have a positive interferon-gamma release assay &#40;IGRA&#41; after receiving the second dose&#46; This suggests that it could be advisable to study this group of patients with an IGRA whenever individuals with B-cell depletion have a negative serology test<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a>&#46; Bonelli et al&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> described five cases of patients under treatment with rituximab who were vaccinated with BNT162b2 &#40;Pfizer&#47;BioNTech&#41;&#44; with only two cases exhibiting a serological response concurring with a recovery of their levels of CD19<span class="elsevierStyleSup">&#43;</span> B-cells&#44; although the IGRA was positive in five cases&#46; Along these lines&#44; Prendecki et al&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> evaluated subjects&#8217; serological responses with an enzyme linked immunosorbent assay &#40;ELISA&#41; and their T-cell response with an IGRA after receiving both a first and second dose of mRNA vaccines BNT162b2 and ChAdOx1 in a cohort of 161 patients under treatment with rituximab and other immunosuppressive drugs used to treat different SADs&#46; They included a total of 114 patients who had received treatment with rituximab at some point of the clinical evolution of their disease&#46; Of these&#44; 64 &#40;56&#37;&#41; patients received the vaccine earlier than 6 months since the administration of rituximab and 69 &#40;60&#46;5&#37;&#41; had a B-cell count &#60;10 cells&#47;&#956;l at the time of vaccination&#46; As expected&#44; those vaccinated over 6 months after receiving the last dose of rituximab had higher seroconversion rates &#40;71&#37; vs&#46; 49&#37;&#41;&#46; The IGRA was positive in 38 &#40;82&#46;6&#37;&#41; of the 46 patients in which it was performed&#46; Most significantly&#44; 15 patients had a positive IGRA and a negative serology test&#44; with B-cell levels &#60;10 cells&#47;&#956;l&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">From a clinical point of view&#44; although the significance of potential protection against a SARS-CoV-2 infection in this subgroup of patients is unknown&#44; it is possible that they may have some degree of protection compared with those who fail to develop any response&#46; More studies must be carried out to answer these questions&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Calvo El&#237;as AE&#44; P&#233;rez Casado L&#44; Callejas Rubio JL&#46; Enfermedades autoinmunes y vacunas contra la COVID-19&#46; Toma de decisiones en escenarios de incertidumbre&#46; Med Clin &#40;Barc&#41;&#46; 2022&#59;159&#58;e3&#46;</p>"
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ISSN: 23870206
Original language: English
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