Maternal SDF1 3 ' A polymorphism is associated with increased perinatal human immunodeficiency virus type 1 transmission

Citation
Gc. John et al., Maternal SDF1 3 ' A polymorphism is associated with increased perinatal human immunodeficiency virus type 1 transmission, J VIROLOGY, 74(12), 2000, pp. 5736-5739
Citations number
23
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF VIROLOGY
ISSN journal
0022538X → ACNP
Volume
74
Issue
12
Year of publication
2000
Pages
5736 - 5739
Database
ISI
SICI code
0022-538X(200006)74:12<5736:MS3'AP>2.0.ZU;2-U
Abstract
Genetic polymorphisms in chemokine and chemokine receptor genes influence s usceptibility to human immunodeficiency virus type 1 (HIV-1) infection and disease progression, but little is known regarding the association between these allelic variations and the ability of the host to transmit virus. In this study, we show that the maternal heterozygous SDF1 genotype (SDF1 3'A/ wt) is associated with perinatal transmission of HIV-1 (risk ratio [RR], 1. 8; 95% confidence interval [CI], 1.0 to 3.3) and particularly postnatal bre astmilk transmission (RR, 3.1; 95% CI, 1.1 to 8.6), In contrast, the infant SDF1 genotype had no effect on mother-to-infant transmission. These data s uggest that SDF1, which is a ligand for the T-tropic HIV-1 coreceptor CXCR4 , may affect the ability of a mother to transmit the virus to her infant. T his suggests that a genetic polymorphism in a gene encoding a chemokine rec eptor ligand may be associated with increased infectivity of the index case and highlights the importance of considering transmission as well as clini cal outcome in designing chemokine-based therapies for HIV-1.