Impact of IL-6 and IL-6r variants on HIV-1 susceptibility and progression to AIDS: a case-control study in a Moroccan population

被引:1
作者
Haddaji, Asmaa [1 ,2 ]
Ouladlahsen, Ahd [3 ,4 ]
Lkhider, Mustapha [2 ]
Tanouti, Ikram-Allah [1 ]
Abbadi, Islam [1 ]
Hilmi, Soufiane [1 ]
Bensghir, Rajaa [4 ]
Guessous, Fadila [5 ,6 ]
Pineau, Pascal [7 ]
El Filali, Kamal Marhoum [3 ,4 ]
Ezzikouri, Sayeh [1 ]
机构
[1] Inst Pasteur Maroc, Virol Unit, Viral Hepatitis Lab, 1 Pl Louis Pasteur, Casablanca 20360, Morocco
[2] Hassan II Univ Casablanca, Fac Sci & Tech Mohammedia, Lab Virol Oncol Biosci Environm & New Energies, Casablanca, Morocco
[3] Univ Hassan 2, Fac Med & Pharm, Casablanca, Morocco
[4] CHU Ibn Rochd, Serv Malad Infect, Casablanca, Morocco
[5] Mohammed VI Univ Hlth Sci UM6SS, Casablanca, Morocco
[6] Univ Virginia, Sch Med, Dept Microbiol Immunol & Canc Biol, Charlottesville, VA USA
[7] Inst Pasteur, Unite Org Nucl & Oncogenese, INSERM U993, Paris, France
关键词
IL6; IL6R; AIDS; HIV; variants; CORONARY-HEART-DISEASE; PROMOTER POLYMORPHISM; GENETIC-VARIANTS; INTERLEUKIN-6; RECEPTOR; RISK; ASSOCIATION; RS2228145; SARCOMA; RATES;
D O I
10.1080/15257770.2024.2359593
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-6 (IL-6), a pro-inflammatory cytokine, is an important regulator of the inflammatory immune response. We aimed to assess the association of common single nucleotide polymorphisms (SNPs) in IL-6 (rs1800795 G > C, rs1800797 A > G) and interleukin-6 receptor (IL-6R) (rs2228145 A > C) genes with HIV-1 infection, AIDS progression, and response to treatment. In this case-control study involving 199 individuals living with HIV-1 and 200 HIV-uninfected controls, we conducted genotyping of IL-6/IL-6R SNPs using TaqMan real-time PCR assays. Soluble IL-6 levels were measured using ELISA. No associations were found between the investigated SNPs and HIV infection. However, a significant association was noted between the C-G and G-A haplotypes and susceptibility to HIV-1 infection. Additionally, a significant association was revealed between HIV-1 RNA viral loads and IL-6 SNP G > C in the post-treatment HIV group. Interestingly, we observed a significant association between the investigated SNPs and protection against progression to AIDS, namely the IL-6 G > A SNP in its recessive model and the IL-6R A > C SNP in its codominant and dominant models. Nevertheless, we found no significant differences between IL-6 levels and the different genotypes and alleles of the IL-6 gene either before or after combination antiretroviral therapy. IL-6 promoter haplotypes are associated with susceptibility to HIV-1 infection. Furthermore, IL-6 A > G and IL-6R A > C polymorphisms have been associated with protection against AIDS progression. Interestingly, the IL-6 G > C SNP may affect the response to treatment in people living with HIV-1.
引用
收藏
页码:1045 / 1064
页数:20
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