期刊论文详细信息
Frontiers in Pediatrics
Protective SARS-CoV-2 Antibody Response in Children With Inflammatory Bowel Disease
article
Luca Bosa1  Costanza Di Chiara2  Paola Gaio1  Chiara Cosma3  Andrea Padoan3  Sandra Cozzani2  Giorgio Perilongo1  Mario Plebani3  Carlo Giaquinto2  Daniele Donà2  Mara Cananzi1 
[1] Unit of Pediatric Gastroenterology, Digestive Endoscopy, Hepatology and Care of the Child With Liver Transplantation, Department of Women's and Children's Health, University Hospital of Padova;Pediatric Infectious Diseases, Department of Women's and Children's Health, University Hospital of Padova;Department of Laboratory Medicine, University Hospital of Padova;Department of Medicine-DIMED, Medical School, University of Padova;Department of Women's and Children's Health, University Hospital of Padova
关键词: inflammatory bowel disease;    children;    COVID-19;    immunological response;    neutralizing antibodies;    pediatric;    SARS-CoV-2;    serology;   
DOI  :  10.3389/fped.2022.815857
学科分类:社会科学、人文和艺术(综合)
来源: Frontiers
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【 摘 要 】

Background To date, there's no evidence of an increased risk of SARS-CoV-2 infection or more severe COVID-19 in patients with inflammatory bowel disease (IBD). However, whether COVID-19 alters the clinical course of IBD or whether IBD treatment affects the immunological response to SARS-CoV-2 is still under investigation, especially in children. Aim To assess the serological response to SARS-CoV-2 in children with IBD, and to evaluate the impact of COVID-19 on the clinical course of IBD. Material and Methods This prospective study enrolled children (0–18 years) followed-up at the University Hospital of Padova for IBD, who acquired a confirmed SARS-CoV-2 infection between 02.2020 and 02.2021. The anti-SARS-CoV-2 S-RBD IgG titer was evaluated at 3 months after infection and compared to that of a control group of healthy children matched for age, sex, and COVID-19 severity. Results Twelve children with IBD ( M = 5; median age 14 years) contracted COVID-19 during the study period. 11/12 patients were under immunomodulatory treatment (4/12 steroids; 6/12 azathioprine; 3/12 anti-TNFs; 2 vedolizumab; 1 ustekinumab). SARS-CoV-2 infection remained asymptomatic in 4/12 children and caused mild COVID-19 in the remaining 8. Mean anti-SARS-CoV-2 IgG S-RBD titer was similar between IBD patients and controls (27.3 ± 43.8 vs. 36.8 ± 35.3 kAU/L, p = ns). No children experienced IBD flares nor required gastroenterological support during the infection period. Discussion Children with IBD can mount a protective humoral response against SARS-CoV-2, which is comparable to that of their healthy peers regardless of ongoing immunomodulatory treatment. This study also supports the favorable course of PIBD during COVID-19 and vice-versa.

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