CCR5 Haplotypes and Mother-to-Child HIV Transmission in Malawi

被引:19
作者
Pedersen, Bonnie R. [1 ]
Kamwendo, Deborah [1 ]
Blood, Melinda [2 ]
Mwapasa, Victor [3 ]
Molyneux, Malcolm [3 ]
North, Kari [1 ]
Rogerson, Stephen J. [4 ]
Zimmerman, Peter [2 ]
Meshnick, Steven R. [1 ]
机构
[1] Univ N Carolina, Chapel Hill, NC 27515 USA
[2] Case Western Reserve Univ, Sch Med, Cleveland, OH USA
[3] Univ Malawi, Coll Med, Blantyre, Malawi
[4] Univ Melbourne, Melbourne, Vic, Australia
来源
PLOS ONE | 2007年 / 2卷 / 09期
关键词
D O I
10.1371/journal.pone.0000838
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background. CCR5 and CCR2 gene polymorphisms (SNPs) have been associated with protection against HIV transmission in adults and with delayed progression to AIDS. The CCR5 Delta 32 deletion and SNP -2459G are associated with reduced expression of the CCR5 protein. Methodology/Principal Findings. We investigated the association between infant CCR2/CCR5 diplotype and HIV mother to child transmission (MTCT) in Malawi. Blood samples from infants (n = 552) of HIV positive women who received nevirapine were genotyped using a post-PCR multiplex ligase detection reaction and haplotypes were identified based on 8 CCR2/CCR5 SNPs and the open reading frame 32 base pair deletion. Following verification of Hardy-Weinberg equilibrium, log linear regression was performed to examine the association between mutations and MTCT. Overall, protection against MTCT was weakly associated with two CCR5 SNPs, -2459G (Risk ratio [RR], 0.78; confidence interval [CI], 0.54-1.12), and the linked CCR5 -2135T (RR, 0.78; CI, 0.54-1.13). No child carried the CCR5 D32 SNP. Maternal Viral Load (MVL) was found to be an effect measure modifier. Among mothers with low MVL, statistically significant protection against MTCT was observed for -2459G (RR, 0.50; CI, 0.27-0.91), and -2135T (RR, 0.51; CI, 0.28-0.92). Statistically significant protection was not found at high MVL. Conclusions/Significance. Results from this study suggest that CCR5 SNPs -2459G and -2135T associated with reduced receptor expression protect against MTCT of HIV at low MVLs, whereas high MVLs may over-ride differences in coreceptor availability.
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页数:8
相关论文
共 44 条
[1]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[2]  
[Anonymous], AIDS EP UPD
[3]   CCR2-64I allele and genotype association with delayed AIDS progression in African women [J].
Anzala, AO ;
Ball, TB ;
Rostron, T ;
O'Brien, SJ ;
Plummer, FA ;
Rowland-Jones, SL .
LANCET, 1998, 351 (9116) :1632-1633
[4]   Genetics of resistance to HIV infection: Role of co-receptors and co-receptor ligands [J].
Arenzana-Seisdedos, Fernando ;
Parmentier, Marc .
SEMINARS IN IMMUNOLOGY, 2006, 18 (06) :387-403
[5]   Mechanism of transdominant inhibition of CCR5-mediated HIV-1 infection by ccr5Δ32 [J].
Benkirane, M ;
Jin, DY ;
Chun, RF ;
Koup, RA ;
Jeang, KT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30603-30606
[6]   Estimating the timing of mother-to-child transmission of human immunodeficiency virus in a breast-feeding population in Kinshasa, Zaire [J].
Bertolli, J ;
StLouis, ME ;
Simonds, RJ ;
Nieburg, P ;
Kamenga, M ;
Brown, C ;
Tarande, M ;
Quinn, T ;
Ou, CY .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (04) :722-726
[7]  
BRUSE S, 2006, MULTIPLEX LIGASE DET
[8]   The beta-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates [J].
Choe, H ;
Farzan, M ;
Sun, Y ;
Sullivan, N ;
Rollins, B ;
Ponath, PD ;
Wu, LJ ;
Mackay, CR ;
LaRosa, G ;
Newman, W ;
Gerard, N ;
Gerard, C ;
Sodroski, J .
CELL, 1996, 85 (07) :1135-1148
[9]   CCR5 promoter polymorphisms, CCR5 59029A and CCR5 59353C, are under represented in HIV-1-infected long-term non-progressors [J].
Clegg, AO ;
Ashton, LJ ;
Biti, RA ;
Badhwar, P ;
Williamson, P ;
Kaldor, JM ;
Stewart, GJ .
AIDS, 2000, 14 (02) :103-108
[10]   Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene [J].
Dean, M ;
Carrington, M ;
Winkler, C ;
Huttley, GA ;
Smith, MW ;
Allikmets, R ;
Goedert, JJ ;
Buchbinder, SP ;
Vittinghoff, E ;
Gomperts, E ;
Donfield, S ;
Vlahov, D ;
Kaslow, R ;
Saah, A ;
Rinaldo, C ;
Detels, R ;
OBrien, SJ .
SCIENCE, 1996, 273 (5283) :1856-1862