端粒酶
端粒
CD8型
外周血单个核细胞
流式细胞术
T细胞
生物
分子生物学
医学
端粒酶逆转录酶
细胞毒性T细胞
病毒学
免疫学
免疫系统
男科
癌症研究
DNA
基因
遗传学
体外
作者
Javier Rodríguez-Centeno,Andrés Esteban-Cantos,Rocío Montejano,Natalia Stella-Ascariz,Rosa de Miguel Buckley,Beatriz Mena-Garay,Gabriel Saiz-Medrano,Belén Alejos,María Jiménez-González,José I. Bernardino,Julen Cadiñanos,Juan Miguel Castro-Álvarez,Berta Rodés,José Ramón Arribas
摘要
To evaluate whether the negative impact of tenofovir on telomere length (TL) is due to immune reconstitution interference or inhibition of telomerase.One hundred and twenty-eight long-term aviraemic HIV adults treated with tenofovir-containing (n = 79) or tenofovir-sparing regimens (n = 49) were recruited to compare the following: TL in whole blood, PBMCs, CD4+ T cells and CD8+ T cells by quantitative PCR (qPCR); telomerase activity in PBMCs, CD4+ cells and CD8+ T cells using the TRAPeze RT Telomerase Detection Kit; and T cell maturational subset distribution by flow cytometry.In an adjusted analysis, participants treated with tenofovir for at least 4 years had shorter TL in CD8+ T cells (P = 0.04) and lower telomerase activity in CD4+ (P = 0.012) and CD8+ T cells (P = 0.023). Tenofovir treatment was also associated with lower proportions of recent thymic emigrant (RTE) CD4+ cells (P = 0.031) and PD1 marker expression (P = 0.013).In long-term aviraemic HIV adults, the inhibition of telomerase by tenofovir could explain telomere shortening in CD8+ T cells. There is no telomere shortening in the CD4+ compartment and the decrease in telomerase activity could be explained both by the inhibition by tenofovir and by the lower proportion of RTE CD4+cells.
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