Interferon lambda rs368234815 ΔG/ΔG is associated with higher CD4+:CD8+ T-cell ratio in treated HIV-1 infection

被引:4
作者
Freitas, Ines T. [1 ]
Tinago, Willard [1 ]
Sawa, Hirofumi [2 ,3 ]
McAndrews, Julie [4 ]
Doak, Brenda [4 ]
Prior-Fuller, Charlotte [4 ]
Sheehan, Gerard [1 ,7 ]
Lambert, John S. [1 ,7 ]
Muldoon, Eavan [7 ]
Cotter, Aoife G. [1 ,3 ,7 ]
Hall, William W. [1 ,2 ,3 ]
Mallon, Patrick W. G. [1 ,6 ]
Carr, Michael J. [2 ,5 ]
机构
[1] Univ Coll Dublin, Sch Med, Ctr Expt Pathogen Host Res, Dublin 4, Ireland
[2] Hokkaido Univ, Global Stn Zoonosis Control, Global Inst Collaborat Res & Educ GI CoRE, Kita Ku, N20,W10, Sapporo, Hokkaido 0010020, Japan
[3] GVN, 801 W Baltimore St, Baltimore, MD 21201 USA
[4] Mater Misericordiae Univ Hosp, Dept Immunol, Dublin 7, Ireland
[5] Univ Coll Dublin, Sch Med, Natl Virus Reference Lab, Dublin 4, Ireland
[6] St Vincents Univ Hosp, Dept Infect Dis, Dublin 4, Ireland
[7] Mater Misericordiae Univ Hosp, Dept Infect Dis, Dublin 7, Ireland
基金
英国惠康基金;
关键词
HIV; Interferon lambda; T-cells; CD4(+); CD8(+); ANTIRETROVIRAL THERAPY; GENETIC-VARIATION; CD4/CD8; RATIO; IL28B; VIRUS; POLYMORPHISMS; NORMALIZATION; INDIVIDUALS; CONTRIBUTES; CLEARANCE;
D O I
10.1186/s12981-020-00269-0
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background The objectives of this study were to investigate the relationships between polymorphisms at the interferon lambda (IFNL) locus and CD4(+):CD8(+) ratio normalisation in people living with HIV (PLWH) on effective antiretroviral therapy (ART); and to examine whether these polymorphisms influence the composition of T lymphocyte compartments in long-term treated HIV-1 infection. Methods A cross-sectional study in PLWH enrolled into the Mater Immunology study. We performed IFNL genotyping on stored samples and evaluated the association of IFNL single-nucleotide polymorphisms (rs368234815 and rs12979860) with CD4(+):CD8(+) ratio normalization (> 1) and expanded CD4(+) and CD8(+) T-cell subsets; CD45RO(+)CD62L(+) (central-memory), CD45RO(+) CD62L(-)(effector-memory) and CD45RO(-)CD62L(+) (naive), using logistic and linear regression models, respectively. Results 190 ambulatory PLWH recruited to the main study, 143 were included in the analysis (38 had no stored DNA and 9 no T-lymphocyte subpopulation). Of 143 included, the median age (IQR) was 45(39-48) years, 64% were male and 66% were of Caucasian ethnicity. Heterosexual-contact (36%), injecting drug-use (33%) and men who have sex with men (24%) were the most presented HIV-transmission risk groups. The majority of subjects (90.2%) were on ART with 79% of the cohort having an undetectable HIV-RNA (< 40 copies/ml) and the time since ART initiation was 7.5 (3.7-10.4) year. rs368234815 and rs12979860 displayed similar allelic frequencies, with minor alleles Delta G and T representing 39% and 42%, respectively, of circulating alleles. rs368234815 Delta G/Delta G minor homozygotes were significantly associated with increased odds for attaining a normalised CD4(+):CD8(+) ratio compared to rs368234815 T/T major homozygotes in PLWH virologically suppressed on effective ART (OR = 3.11; 95% CI [1.01:9.56]). rs368234815 Delta G/Delta G homozygosity was also significantly associated with lower levels of CD4(+) effector memory T-cells (regression coefficient: - 7.1%, p = 0.04) and CD8(+) naive T-cell subsets were significantly higher in HIV-1 mono-infected PLWH with rs368234815 Delta G/Delta G (regression coefficient: + 7.2%, p = 0.04). Conclusions In virally-suppressed, long-term ART-treated PLWH, rs368234815 Delta G/Delta G homozygotes were more likely to have attained normalisation of their CD4(+):CD8(+) ratio, displayed lower CD4(+) effector memory and higher naive CD8(+) T-cells. Further studies are needed to replicate our findings in other, larger and more diverse cohorts and to determine the impact of IFNL genetic-variation on CD4(+):CD8(+) ratio normalisation and clinical outcomes in PLWH.
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