T cell responses to repeated SARS-CoV-2 vaccination and breakthrough infections in patients on TNF inhibitor treatment: a prospective cohort study.

IF 9.7 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2024-09-10 DOI:10.1016/j.ebiom.2024.105317
Asia-Sophia Wolf,Kristin H Bjørlykke,Hilde S Ørbo,Sabin Bhandari,Guri Solum,Ingrid Fadum Kjønstad,Ingrid Jyssum,Unni C Nygaard,Anja Bråthen Kristoffersen,Ingrid E Christensen,Sarah E Josefsson,Katrine Persgård Lund,Adity Chopra,Julie Røkke Osen,Viktoriia Chaban,Anne T Tveter,Joseph Sexton,Tore K Kvien,Jørgen Jahnsen,Espen A Haavardsholm,Gunnveig Grødeland,John Torgils Vaage,Sella A Provan,Hassen Kared,Fridtjof Lund-Johansen,Ludvig A Munthe,Silje Watterdal Syversen,Guro Løvik Goll,Kristin Kaasen Jørgensen,Siri Mjaaland
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Abstract

BACKGROUND Understanding cellular responses to SARS-CoV-2 immunisations is important for informing vaccine recommendations in patients with inflammatory bowel disease (IBD) and other vulnerable patients on immunosuppressive therapies. This study investigated the magnitude and quality of T cell responses after multiple SARS-CoV-2 vaccine doses and COVID-19 breakthrough infection. METHODS This prospective, observational study included patients with IBD and arthritis on tumour necrosis factor inhibitors (TNFi) receiving up to four SARS-CoV-2 vaccine doses. T cell responses to SARS-CoV-2 peptides were measured by flow cytometry before and 2-4 weeks after vaccinations and breakthrough infection to assess the frequency and polyfunctionality of responding cells, along with receptor-binding domain (anti-RBD) antibodies. FINDINGS Between March 2, 2021, and December 20, 2022, 143 patients (118 IBD, 25 arthritis) and 73 healthy controls were included. In patients with either IBD or arthritis, humoral immunity was attenuated compared to healthy controls (median anti-RBD levels 3391 vs. 6280 BAU/ml, p = 0.008) after three SARS-CoV-2 vaccine doses. Patients with IBD had comparable quantities (median CD4 0.11% vs. 0.11%, p = 0.26, CD8 0.031% vs. 0.047%, p = 0.33) and quality (polyfunctionality score: 0.403 vs. 0.371, p = 0.39; 0.105 vs. 0.101, p = 0.87) of spike-specific T cells to healthy controls. Patients with arthritis had lower frequencies but comparable quality of responding T cells to controls. Breakthrough infection increased spike-specific CD8 T cell quality and T cell responses against non-spike peptides. INTERPRETATION Patients with IBD on TNFi have T cell responses comparable to healthy controls despite attenuated humoral responses following three vaccine doses. Repeated vaccination and breakthrough infection increased the quality of T cell responses. Our study adds evidence that, in the absence of other risk factors, this group may in future be able to follow the general recommendations for COVID-19 vaccines. FUNDING South-Eastern Norway Regional Health Authority, Coalition for Epidemic Preparedness Innovations (CEPI), Norwegian Institute of Public Health, Akershus University Hospital, Diakonhjemmet Hospital.
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TNF抑制剂治疗患者对重复SARS-CoV-2疫苗接种和突破性感染的T细胞反应:一项前瞻性队列研究。
背景了解细胞对 SARS-CoV-2 免疫接种的反应对于为炎症性肠病 (IBD) 患者和其他接受免疫抑制疗法的易感患者提供疫苗建议非常重要。本研究调查了多次接种SARS-CoV-2疫苗和COVID-19突破性感染后T细胞反应的程度和质量。方法这项前瞻性观察研究纳入了接受最多四次SARS-CoV-2疫苗接种的使用肿瘤坏死因子抑制剂(TNFi)的IBD和关节炎患者。在 2021 年 3 月 2 日至 2022 年 12 月 20 日期间,共纳入了 143 名患者(118 名 IBD 患者,25 名关节炎患者)和 73 名健康对照者。与健康对照组相比,IBD 或关节炎患者在接种三剂 SARS-CoV-2 疫苗后,体液免疫力下降(抗 RBD 水平中位数为 3391 对 6280 BAU/ml,p = 0.008)。IBD 患者尖峰特异性 T 细胞的数量(中位数 CD4 0.11% 对 0.11%,p = 0.26;CD8 0.031% 对 0.047%,p = 0.33)和质量(多功能性评分:0.403 对 0.371,p = 0.39;0.105 对 0.101,p = 0.87)与健康对照组相当。关节炎患者的应答T细胞频率较低,但质量与对照组相当。突破性感染提高了尖峰特异性 CD8 T 细胞的质量和针对非尖峰肽的 T 细胞应答。重复接种疫苗和突破性感染可提高 T 细胞应答的质量。我们的研究提供了更多证据,表明在没有其他风险因素的情况下,该群体今后可以按照一般建议接种COVID-19疫苗。
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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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