IFNL4 genotype influences the rate of HIV-1 seroconversion in men who have sex with men

Virulence. 2022 Dec;13(1):757-763. doi: 10.1080/21505594.2022.2066612.

Abstract

Individuals lacking interferon lambda 4 (IFNL4) protein due to a common null mutation (rs368234815) in the IFNL4 gene display higher resistance against several infections. The influence of IFNL4 on HIV-1 infection is still under discussion and conflicting results have been reported. This study intended to corroborate or refute the association of the null allele of IFNL4 and HIV-1 predisposition in a cohort of men who have sex with men (MSM). IFNL4 null genotype was assessed on 619 HIV-1-seronegative MSM who were followed for 36 months during a trial of a prophylactic vaccine against HIV-1. Of those, 257 individuals seroconverted during this period. A logistic regression model was constructed including demographic and IFNL4 genotype. In addition, a meta-analysis using data from the current study and other European populations was conducted. The null IFNL4 genotypes were correlated with lower HIV-1 seroconversion (Adjusted OR = 0.4 [95%CI: 0.2-0.8], P = 0.008) and longer time to seroconversion (889 vs. 938 days, P= 0.01). These results were validated by a meta-analysis incorporating data from other European populations and the result yielded a significant association of the IFNL4 null genotype under a dominant model with a lower probability of HIV-1 infection (OR=0.4 [95% CI: 0.3-0.6]; P= 1.3 x 10E-5).

Keywords: HESN; HIV exposed seronegative; HIV-1; IFNL4; IL28B.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genotype
  • HIV Infections* / genetics
  • HIV-1* / genetics
  • Homosexuality, Male
  • Humans
  • Interferons
  • Interleukins / genetics
  • Male
  • Seroconversion
  • Sexual and Gender Minorities*

Substances

  • IFNL4 protein, human
  • Interleukins
  • Interferons

Grants and funding

Funding, this work was supported by grants [SAF2016-80125-R] (Ministerio de Economía, Industria y Competitividad, Spain) to A. Caruz and FJ. Marquez; grant [1381073-2020] from European Regional Development Fund. G. Meza and C. Jaimes-Bernal are recipients of a grant from AUIP (Asociación Universitaria Iberoamericana de Postgrado).