Lymphocytes Subsets in Correlation With Clinical Profile in Cvid Patients Without Monogenic Defects Publisher Pubmed



Tofighi Zavareh F^{1, 2, 3} ; Mirshafiey A^{1, 2} ; Yazdani R¹ ; Keshtkar AA⁴ ; Abolhassani H^{1, 5} ; Bagheri Y⁶ ; Rezaei A¹ ; Delavari S¹ ; Rezaei N^{1, 3, 7} ; Aghamohammadi A¹
Source: Expert Review of Clinical Immunology Published:2021

Abstract

Objectives: Common variable immunodeficiency (CVID) patients experience clinical manifestations rather than recurrent respiratory infections including autoimmunity, enteropathy, and lymphoproliferation. We evaluated the correlation of lymphocyte subpopulations with such manifestations. Methods: Twenty-six genetically unsolved CVID patients were subdivided into four phenotypes: infection only (IO), autoimmunity (AI), chronic enteropathy (CE), and lymphoproliferative disorders (LP) and examined for lymphocyte subsets by flow cytometry and TCD4+ proliferation by Carboxyfluorescein succinimidyl ester (CFSE) test. Results: We detected reduced memory B and increased total, effector memory (EM), cytotoxic, and activated TCD8+ in IO, AI and CE, decreased plasmablasts, total and naive TCD4+, Regulatory TCD4+ (Treg) and naive TCD8+ in IO and CE, elevated CD21low B and terminally differentiated effector memory (TEMRA) TCD8+ in IO and AI, increased helper T (Th2) and Th17 in IO, decreased Th1 in AI and defective total and naive B and central memory (CM) TCD4+ in CE. IO showed reduced TCD4+ proliferation response. Conclusions: In genetically unsolved CVID patients, increased Th2 and Th17 and reduced Treg is associated with IO, increased CD21low B and TEMRA TCD8+ and reduced Th1 is contributed to AI and reduced total and naive B, CM TCD4+ and naive TCD8+ and expanded total TCD8+ is correlated with CE. © 2021 Informa UK Limited, trading as Taylor & Francis Group.