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炎症性肠病患者对 SARS-CoV-2 疫苗接种的细胞和体液免疫反应。

Cellular and Humoral Immune Responses to SARS-CoV-2 Vaccination in Inflammatory Bowel Disease Patients.

机构信息

Clinical and Research Centre for Inflammatory Bowel Disease ISCARE and First Faculty of Medicine, Charles University, Prague, Czech Republic.

GENNET Prague, Czech Republic.

出版信息

J Crohns Colitis. 2022 Sep 8;16(9):1347-1353. doi: 10.1093/ecco-jcc/jjac048.

DOI:10.1093/ecco-jcc/jjac048
PMID:35358307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8992348/
Abstract

BACKGROUND AND AIMS

Knowledge on the immunogenicity of anti-SARS-CoV-2 vaccines in inflammatory bowel disease [IBD] patients is limited. Therefore, SARS-CoV-2-specific T-cell responses and antibodies were analysed in 60 IBD vaccine recipients and 30 controls.

METHODS

SARS-CoV-2 IgG antibodies against the viral spike protein were measured at baseline and at 8 and 26 weeks after the second vaccine dose. SARS-CoV-2 IgG antibodies against the nucleocapsid antigens were measured at week 26. A SARS-CoV-2 interferon-gamma released assay [IGRA] was performed in all vaccinees at week 26.

RESULTS

At weeks 0 and 8, no differences were found in anti-spike antibodies between cohorts. At week 26, the decrease in antibody levels was more significant in the IBD cohort compared to the healthy cohort, and anti-nucleocapsid antibodies were not detected in either group. At week 26, 16 of 90 [18%] vaccinated individuals had a negative IGRA test result, seven of 90 [8%] were borderline and 67 [74%] had a positive IGRA result; 22 of the 23 individuals with negative or borderline IGRA results belonged to the IBD cohort. However, the overall functional ability of T-lymphocytes to produce interferon-gamma after the unspecific mitogen stimulation was lower in IBD patients. In vaccinated individuals with low or borderline IGRA, treatment with tumour necrosis factor-alpha inhibitors was the most frequent. In individuals with a significant drop in anti-spike antibody levels, plasmatic interferon-gamma concentrations after the specific SARS-CoV-2 stimulation were also insufficient.

CONCLUSIONS

Simple humoral and cellular post-vaccination monitoring is advisable in IBD patients so that repeated vaccine doses may be scheduled.

摘要

背景与目的

目前对于炎症性肠病(IBD)患者接种抗 SARS-CoV-2 疫苗后的免疫原性知之甚少。因此,本研究分析了 60 例 IBD 疫苗接种者和 30 名对照者的 SARS-CoV-2 特异性 T 细胞反应和抗体。

方法

在接种第 2 剂疫苗后 8 周和 26 周时,检测血清中针对病毒刺突蛋白的 SARS-CoV-2 IgG 抗体。在第 26 周时检测针对核衣壳抗原的 SARS-CoV-2 IgG 抗体。在所有接种者中,第 26 周时还进行了 SARS-CoV-2 干扰素-γ释放试验(IGRA)。

结果

在第 0 周和第 8 周时,两组间针对刺突蛋白的抗体无差异。第 26 周时,与健康对照组相比,IBD 组的抗体水平下降更显著,且两组均未检测到针对核衣壳的抗体。第 26 周时,90 例接种者中有 16 例(18%)IGRA 检测结果为阴性,7 例(8%)为临界值,67 例(74%)为阳性;23 例 IGRA 检测结果为阴性或临界值的个体中,22 例来自 IBD 组。然而,IBD 患者外周血 T 淋巴细胞在非特异性丝裂原刺激下产生干扰素-γ的整体功能较低。在 IGRA 检测结果为阴性或临界值的接种者中,TNF-α 抑制剂的使用率最高。在抗刺突抗体水平显著下降的个体中,特异性 SARS-CoV-2 刺激后血浆中干扰素-γ的浓度也不足。

结论

在 IBD 患者中,建议进行简单的体液和细胞免疫后监测,以便安排重复接种疫苗。