TY - JOUR
T1 - Cytokine signature in convalescent SARS-CoV-2 patients with inflammatory bowel disease receiving vedolizumab
AU - Dallari, Simone
AU - Martinez Pazos, Vicky
AU - Munoz Eusse, Juan
AU - Wellens, Judith
AU - Thompson, Craig
AU - Colombel, Jean Frederic
AU - Satsangi, Jack
AU - Cadwell, Ken
AU - Wong, Serre Yu
AU - Neil, Jessica Anne
AU - Sota, Stela
AU - Jang, Kyung Ku
AU - Ching, Krystal
AU - Venzon, Mericien
AU - Yao, Xiaomin
AU - Bernard, Lucie
AU - Chen, Xin
AU - Tankelevich, Michael
AU - Navalurkar, Reema
AU - Dixon, Rebekah
AU - Helmus, Drew S.
AU - Lange, Marcia Mukanga
AU - Spiera, Emily
AU - Sangmo, Lodoe
N1 - Publisher Copyright:
© 2024, The Author(s).
PY - 2024/12
Y1 - 2024/12
N2 - While differential antibody responses SARS-CoV-2 in patients with inflammatory bowel disease (IBD) receiving infliximab and vedolizumab are well-characterized, the immune pathways underlying these differences remain unknown. Prior to COVID-19 vaccine development, we screened 235 patients with IBD receiving biological therapy for antibodies to SARS-CoV-2 and measured serum cytokines. In seropositive patients, we prospectively collected clinical data. We found a cytokine signature in patients receiving vedolizumab who are seropositive compared with seronegative for SARS-CoV-2 antibodies that may be linked to repeated SARS-CoV-2 infections. However, there were no differences between seropositive and seronegative patients receiving infliximab. In this single-center cohort of patients with IBD with anti-SARS-CoV-2 antibodies at the onset of the COVID-19 pandemic, and therefore without influence of vaccination, there is a cytokine signature in patients receiving vedolizumab but not infliximab. These findings lay the groundwork for further studies on immune consequences of viral infection in patients with IBD, which is postulated to evolve from aberrant host-microbe responses.
AB - While differential antibody responses SARS-CoV-2 in patients with inflammatory bowel disease (IBD) receiving infliximab and vedolizumab are well-characterized, the immune pathways underlying these differences remain unknown. Prior to COVID-19 vaccine development, we screened 235 patients with IBD receiving biological therapy for antibodies to SARS-CoV-2 and measured serum cytokines. In seropositive patients, we prospectively collected clinical data. We found a cytokine signature in patients receiving vedolizumab who are seropositive compared with seronegative for SARS-CoV-2 antibodies that may be linked to repeated SARS-CoV-2 infections. However, there were no differences between seropositive and seronegative patients receiving infliximab. In this single-center cohort of patients with IBD with anti-SARS-CoV-2 antibodies at the onset of the COVID-19 pandemic, and therefore without influence of vaccination, there is a cytokine signature in patients receiving vedolizumab but not infliximab. These findings lay the groundwork for further studies on immune consequences of viral infection in patients with IBD, which is postulated to evolve from aberrant host-microbe responses.
UR - https://www.scopus.com/pages/publications/85181233073
U2 - 10.1038/s41598-023-50035-1
DO - 10.1038/s41598-023-50035-1
M3 - Article
AN - SCOPUS:85181233073
SN - 2045-2322
VL - 14
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 186
ER -