TY - JOUR
T1 - SARS-CoV-2 vaccination for patients with inflammatory bowel disease
T2 - a British Society of Gastroenterology Inflammatory Bowel Disease section and IBD Clinical Research Group position statement
AU - Inflammatory Bowel Disease section of the British Society of Gastroenterology and the the Inflammatory Bowel Disease Clinical Research Group
AU - Alexander, James L
AU - Moran, Gordon W
AU - Gaya, Daniel R
AU - Raine, Tim
AU - Hart, Ailsa
AU - Kennedy, Nicholas A
AU - Lindsay, James O
AU - MacDonald, Jonathan
AU - Segal, Jonathan P
AU - Sebastian, Shaji
AU - Selinger, Christian P
AU - Parkes, Miles
AU - Smith, Philip J
AU - Dhar, Anjan
AU - Subramanian, Sreedhar
AU - Arasaradnam, Ramesh
AU - Lamb, Christopher A
AU - Ahmad, Tariq
AU - Lees, Charlie W
AU - Dobson, Liz
AU - Wakeman, Ruth
AU - Iqbal, Tariq H
AU - Arnott, Ian
AU - Powell, Nick
AU - Din, Shahida
N1 - Copyright © 2021 Elsevier Ltd. All rights reserved.
PY - 2021/3
Y1 - 2021/3
N2 - SARS-CoV-2 has caused a global health crisis and mass vaccination programmes provide the best opportunity for controlling transmission and protecting populations. Despite the impressive clinical trial results of the BNT162b2 (Pfizer/BioNTech), ChAdOx1 nCoV-19 (Oxford/AstraZeneca), and mRNA-1273 (Moderna) vaccines, important unanswered questions remain, especially in patients with pre-existing conditions. In this position statement endorsed by the British Society of Gastroenterology Inflammatory Bowel Disease (IBD) section and IBD Clinical Research Group, we consider SARS-CoV-2 vaccination strategy in patients with IBD. The risks of SARS-CoV-2 vaccination are anticipated to be very low, and we strongly support SARS-CoV-2 vaccination in patients with IBD. Based on data from previous studies with other vaccines, there are conceptual concerns that protective immune responses to SARS-CoV-2 vaccination may be diminished in some patients with IBD, such as those taking anti-TNF drugs. However, the benefits of vaccination, even in patients treated with anti-TNF drugs, are likely to outweigh these theoretical concerns. Key areas for further research are discussed, including vaccine hesitancy and its effect in the IBD community, the effect of immunosuppression on vaccine efficacy, and the search for predictive biomarkers of vaccine success.
AB - SARS-CoV-2 has caused a global health crisis and mass vaccination programmes provide the best opportunity for controlling transmission and protecting populations. Despite the impressive clinical trial results of the BNT162b2 (Pfizer/BioNTech), ChAdOx1 nCoV-19 (Oxford/AstraZeneca), and mRNA-1273 (Moderna) vaccines, important unanswered questions remain, especially in patients with pre-existing conditions. In this position statement endorsed by the British Society of Gastroenterology Inflammatory Bowel Disease (IBD) section and IBD Clinical Research Group, we consider SARS-CoV-2 vaccination strategy in patients with IBD. The risks of SARS-CoV-2 vaccination are anticipated to be very low, and we strongly support SARS-CoV-2 vaccination in patients with IBD. Based on data from previous studies with other vaccines, there are conceptual concerns that protective immune responses to SARS-CoV-2 vaccination may be diminished in some patients with IBD, such as those taking anti-TNF drugs. However, the benefits of vaccination, even in patients treated with anti-TNF drugs, are likely to outweigh these theoretical concerns. Key areas for further research are discussed, including vaccine hesitancy and its effect in the IBD community, the effect of immunosuppression on vaccine efficacy, and the search for predictive biomarkers of vaccine success.
KW - COVID-19/epidemiology
KW - COVID-19 Vaccines/pharmacology
KW - Disease Transmission, Infectious/prevention & control
KW - Gastroenterology/methods
KW - Humans
KW - Immunocompromised Host
KW - Inflammatory Bowel Diseases/immunology
KW - SARS-CoV-2
KW - Societies, Medical
KW - United Kingdom
KW - Vaccination/methods
U2 - 10.1016/S2468-1253(21)00024-8
DO - 10.1016/S2468-1253(21)00024-8
M3 - Review article
C2 - 33508241
SN - 2468-1253
VL - 6
SP - 218
EP - 224
JO - The Lancet Gastroenterology & Hepatology
JF - The Lancet Gastroenterology & Hepatology
IS - 3
ER -