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Journal of Virology, June 2000, p. 5736-5739, Vol. 74, No. 12
Departments of Medicine, Epidemiology, and
Biostatistics, University of Washington,1 and
Division of Human Biology, Fred Hutchinson Cancer Research
Center,3 Seattle, Washington;
Departments of Medical Microbiology and Paediatrics,
University of Nairobi, Nairobi, Kenya2; and
Institute of Molecular Medicine, Oxford University, Oxford,
United Kingdom4
Received 28 July 1999/Accepted 22 March 2000
Genetic polymorphisms in chemokine and chemokine receptor genes
influence susceptibility 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
breastmilk 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 suggest 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. This suggests that a genetic
polymorphism in a gene encoding a chemokine receptor ligand may be
associated with increased infectivity of the index case and highlights
the importance of considering transmission as well as clinical outcome
in designing chemokine-based therapies for HIV-1.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Maternal SDF1 3'A Polymorphism Is Associated with Increased
Perinatal Human Immunodeficiency Virus Type 1 Transmission
*
Corresponding author. Mailing address: IARTP, Box
359909, University of Washington, Seattle, WA 98195. Phone: (206)
731-2822. Fax: (206) 731-2427. E-mail:
gjohn{at}u.washington.edu.
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