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Circulating IFN-γ producing CD4+ T cells and IL-17A producing CD4+ T cells, HLA-shared epitope and ACPA may characterize the clinical response to therapy in rheumatoid arthritis patients

This study analyzed the association between peripheral distributions of helper T cell subsets, HLA shared-epitope (SE), anti-cyclic citrullinated peptide antibody (ACPA) and clinical response to therapy in rheumatoid arthritis (RA) patients. Frequencies of IFN-γ-producing CD4+T (Th1) and IL-17A-prod...

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Published in:Human immunology 2020-05, Vol.81 (5), p.228-236
Main Authors: Alvandpur, Niloofar, Tabatabaei, Raheleh, Tahamoli-Roudsari, Ahmad, Basiri, Zahra, Behzad, Mahdi, Rezaeepoor, Mahsa, Roshanaei, Ghodratollah, Hajilooi, Mehrdad, Solgi, Ghasem
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Language:English
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Summary:This study analyzed the association between peripheral distributions of helper T cell subsets, HLA shared-epitope (SE), anti-cyclic citrullinated peptide antibody (ACPA) and clinical response to therapy in rheumatoid arthritis (RA) patients. Frequencies of IFN-γ-producing CD4+T (Th1) and IL-17A-producing CD4+T (Th17) cells were determined by flow cytometry in 167 patients (114 cases with good-response (GR) and 53 poor-response (PR) based on DAS28). HLA-DRB1 alleles for patients and 150 healthy controls were determined by PCR-SSP. We observed that 65.2% of RA patients were SE+, 63.4%ACPA+, 43.7%SE+ACPA+ and 14.9% were SE−ACPA−. Higher significantly proportions of Th1 and Th17 cells were found in RA patients than controls (P 
ISSN:0198-8859
1879-1166
DOI:10.1016/j.humimm.2020.02.008