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. 2025 Feb:271:110404.
doi: 10.1016/j.clim.2024.110404. Epub 2024 Dec 5.

Deficient SARS-CoV-2 hybrid immunity during inflammatory bowel disease

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Free article

Deficient SARS-CoV-2 hybrid immunity during inflammatory bowel disease

Amin Alirezaylavasani et al. Clin Immunol. 2025 Feb.
Free article

Abstract

Patients with Inflammatory Bowel Disease (IBD) undergoing immunosuppressive therapies face heightened susceptibility to severe COVID-19. An in-depth understanding of systemic inflammation and cellular immune responses after SARS-CoV-2 vaccination and breakthrough infections (BTI) is required for optimizing vaccine strategies in this population. While the prevalence of high serological responders post- third COVID-19 vaccine dose was lower, and the antibody waning was higher in IBD patients than in healthy donors (HD), IBD patients showed an increase in anti-RBD Wild Type IgG levels and cross-reactive Spike -specific memory B cells following BTI. However, there was no significant enhancement in cellular immune responses against anti-SARS-CoV-2 post-BTI, with responses instead characterized by activation of SARS-CoV-2 specific and also bystander CD8 T cells. These results suggest a complex interaction between chronic inflammation in IBD and the generation of new immune responses, highlighting the need for tailored vaccine regimens and anti-inflammatory therapies to boost cellular immunity against SARS-CoV-2.

Keywords: Activation; Antibody waning; Hybrid immunity; IBD; Inflammation; TNF inhibitors.

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