Chemokine receptor gene polymorphisms and risk of human T lymphotropic virus type I infection in Jamaica

Abstract

Polymorphisms of some chemokine receptor genes and their ligands are associated with susceptibility and progression of human immunodeficiency virus infection. This study assessed whether these variants are also responsible for susceptibility to infection with human T lymphotropic virus (HTLV) type I. Frequencies of CCR5-Δ32, CCR2-641, and SDF-1-3′A genotype among 116 HTLV-I-positive and 126 HTLV-I-negative persons of African descent in Jamaica were 1.0%, 14.9%, and 5.4%, respectively. The association of HTLV-I infection with the most common variant, CCR2-641, was examined in 532 subjects. Thirteen (5.4%) of 241 HTLV-I-negative subjects were homozygous for CCR2-641, versus 3 (1.0%) of 291 HTLV-I-positive subjects (P = .005). Among HTLV-I carriers, provirus load and antibody titer were not significantly different in persons with CCR2-+/641 or CCR2-+/+. These findings suggest that CCR2-641, or alleles in linkage disequilibrium with it, may affect the risk of HTLV-I infection in a recessive manner.