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      Response to Letter to the Editor: Post-Vaccination Immunogenicity of BNT162b2 SARS-CoV-2 Vaccine and Its Predictors in Pediatric Inflammatory Bowel Disease

      letter
      , MD, PhD * ,
      Journal of Pediatric Gastroenterology and Nutrition
      Lippincott Williams & Wilkins

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          Abstract

          Dear Editor, On behalf of our research team, I would like to submit a short response to the Letter to the Editor (“Postvaccination Immunogenicity of COVID-19 Vaccine in Pediatric Inflammatory Bowel Disease.: Comment”)(1) concerning our original article published in JPGN named “Post-Vaccination Immunogenicity of BNT162b2 SARS-CoV-2 Vaccine and Its Predictors in Pediatric Inflammatory Bowel Disease.”(2) We have read with interest the letter submitted by Amnuay Kleebayoon and Viroj Wiwanitkit.(1) In this letter, the authors raise the point that higher post-vaccination levels of anti-spike S2 antibodies in inflammatory bowel disease patients compared to controls could be explained by cross-contamination with “silent COVID-19 infection” in some of the subjects who had no apparent clinical signs at the time of testing. Although this may theoretically be one plausible explanation that we would not be able to rule out (as we did not test all our subjects for SARS-CoV-2 infection along with post-vaccination antibodies), from a statistical point of view we deem unlikely that a silent SARS-CoV-2 infection would appear with different frequency (probability) in each group. Therefore, we consider this unlikely to be a true major factor underlying the difference in the antibody production between inflammatory bowel disease patients and healthy controls. We remain, however, in agreement that the possibility of a cross-contamination with undiagnosed SARS-CoV-2 infections cannot be formally ruled out.

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          Post-vaccination immunogenicity of BNT162b2 SARS-CoV-2 vaccine and its predictors in pediatric inflammatory bowel disease.

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            Postvaccination Immunogenicity of COVID-19 Vaccine in Pediatric Inflammatory Bowel Disease: Comment

            Dear Editor, We would like to share ideas on the publication “Postvaccination Immunogenicity of BNT162b2 SARS-CoV-2 Vaccine and Its Predictors in Pediatric Inflammatory Bowel Disease” (1). Bronsky et al prospectively compared the postvaccination immunity to messenger ribonucleic acid BNT162b2 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine of their pediatric patients over 12 years old with IBD to that of healthy controls and looked for predictors of its robustness (1). Bronsky et al discovered that patients with IBD had higher levels of anti-spike S2 antibodies after vaccination than controls (1). Bronsky et al concluded that prior SARS-CoV-2 infection is associated with increased postvaccination antibody production and anti-tumor necrosis factor treatment with decreased production (1). To interpret the findings correctly, a number of elements need to be taken into account. One of the potential complicating factors that could have had an impact on the outcomes of the initial booster dose would be an exceptionally mild reaction. Without specialized laboratory testing, a link between asymptomatic COVID-19 and the absence of clinical symptoms may exist (2). A silent COVID-19 must be ruled out if neither the recent clinical symptoms nor the current clinical signs are present. It is impossible to totally rule out the possibility of cross-contamination with an undiagnosed SARS-Co-V2 infection. Depending on inherited genetic variability, various people’s immune systems appear to react to COVID-19 vaccines differently (3). More clinical research is required to add further evidence addressing the findings discussed in this paper and the clinical recommendations that derive from.
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              Author and article information

              Journal
              J Pediatr Gastroenterol Nutr
              J Pediatr Gastroenterol Nutr
              MPG
              Journal of Pediatric Gastroenterology and Nutrition
              Lippincott Williams & Wilkins (Hagerstown, MD )
              0277-2116
              1536-4801
              12 March 2023
              June 2023
              12 March 2023
              : 76
              : 6
              : e90
              Affiliations
              From the [* ]Department of Paediatrics, 2nd Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
              Author notes
              Address correspondence and reprint requests to Jiri Bronsky, MD, PhD, Head, Gastroenterology and Nutrition Unit, Department of Paediatrics, University Hospital Motol, V Uvalu 84, 15006, Prague, Czech Republic (e-mail: jiri.bronsky@ 123456lfmotol.cuni.cz ).
              Article
              00030
              10.1097/MPG.0000000000003760
              10171098
              32d99f0c-22fd-4fce-8b85-2ce21ae737d2
              Copyright © 2023 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

              This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

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