Division of Immunology, Transplantation, and Infectious Diseases, Diabetes Research Institute, IRCCS San Raffaele Hospital, Via Olgettina 60, Milan, 20132, Italy.
Pediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Hospital, Via Olgettina 60, Milan, 20132, Italy.
Eur J Immunol. 2022 Jul;52(7):1171-1189. doi: 10.1002/eji.202149480. Epub 2022 May 29.
Common variable immunodeficiency (CVID) is the most frequent primary antibody deficiency whereby follicular helper T (Tfh) cells fail to establish productive responses with B cells in germinal centers. Here, we analyzed the frequency, phenotype, transcriptome, and function of circulating Tfh (cTfh) cells in CVID patients displaying autoimmunity as an additional phenotype. A group of patients showed a high frequency of cTfh1 cells and a prominent expression of PD-1 and ICOS as well as a cTfh mRNA signature consistent with highly activated, but exhausted, senescent, and apoptotic cells. Plasmatic CXCL13 levels were elevated in this group and positively correlated with cTfh1 cell frequency and PD-1 levels. Monoallelic variants in RTEL1, a telomere length- and DNA repair-related gene, were identified in four patients belonging to this group. Their blood lymphocytes showed shortened telomeres, while their cTfh were more prone to apoptosis. These data point toward a novel pathogenetic mechanism in CVID, whereby alterations in DNA repair and telomere elongation might predispose to antibody deficiency. A Th1, highly activated but exhausted and apoptotic cTfh phenotype was associated with this form of CVID.
普通可变免疫缺陷(CVID)是最常见的原发性抗体缺陷,滤泡辅助 T(Tfh)细胞无法在生发中心与 B 细胞建立有效的反应。在这里,我们分析了表现出自免疫为附加表型的 CVID 患者循环滤泡辅助 T(cTfh)细胞的频率、表型、转录组和功能。一组患者表现出 cTfh1 细胞的高频率和 PD-1 和 ICOS 的显著表达,以及与高度激活、耗尽、衰老和凋亡细胞一致的 cTfh mRNA 特征。该组患者的血浆 CXCL13 水平升高,并与 cTfh1 细胞频率和 PD-1 水平呈正相关。属于该组的四名患者中鉴定出 RTEL1(与端粒长度和 DNA 修复相关的基因)的单等位基因变体。他们的血液淋巴细胞显示出缩短的端粒,而他们的 cTfh 细胞更容易凋亡。这些数据表明 CVID 存在一种新的发病机制,其中 DNA 修复和端粒延长的改变可能导致抗体缺陷。Th1、高度激活但耗尽和凋亡的 cTfh 表型与这种形式的 CVID 相关。