: 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. This article is protected by copyright. All rights reserved.
Follicular helper T cell signature of replicative exhaustion, apoptosis and senescence in common variable immunodeficiency / Milardi, Giulia; Di Lorenzo, Biagio; Gerosa, Jolanda; Barzaghi, Federica; Di Matteo, Gigliola; Omrani, Maryam; Jofra, Tatiana; Merelli, Ivan; Barcella, Matteo; Filippini, Matteo; Conti, Anastasia; Ferrua, Francesca; Giuffrida, Francesco Pozzo; Dionisio, Francesca; Rovere-Querini, Patrizia; Marktel, Sarah; Assanelli, Andrea; Piemontese, Simona; Brigida, Immacolata; Zoccolillo, Matteo; Cirillo, Emilia; Giardino, Giuliana; Danieli, Maria Giovanna; Specchia, Fernando; Pacillo, Lucia; Di Cesare, Silvia; Giancotta, Carmela; Romano, Francesca; Matarese, Alessandro; Chetta, Alfredo Antonio; Trimarchi, Matteo; Laurenzi, Andrea; De Pellegrin, Maurizio; Darin, Silvia; Montin, Davide; Marinoni, Maddalena; Dellepiane, Rosa Maria; Sordi, Valeria; Lougaris, Vassilios; Vacca, Angelo; Melzi, Raffaella; Nano, Rita; Azzari, Chiara; Bongiovanni, Lucia; Pignata, Claudio; Cancrini, Caterina; Plebani, Alessandro; Piemonti, Lorenzo; Petrovas, Constantinos; Di Micco, Raffaella; Ponzoni, Maurilio; Aiuti, Alessandro; Cicalese, Maria Pia; Fousteri, Georgia. - In: EUROPEAN JOURNAL OF IMMUNOLOGY. - ISSN 0014-2980. - (2022). [Epub ahead of print] [10.1002/eji.202149480]
Follicular helper T cell signature of replicative exhaustion, apoptosis and senescence in common variable immunodeficiency
Ferrua, Francesca;Rovere-Querini, Patrizia;Trimarchi, Matteo;Laurenzi, Andrea;Bongiovanni, Lucia;Piemonti, Lorenzo;Ponzoni, Maurilio;Aiuti, Alessandro;Cicalese, Maria Pia;
2022-01-01
Abstract
: 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. This article is protected by copyright. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.