The evolutionary history of the CCR5-Δ32 HIV-resistance mutation

被引:101
作者
Galvani, AP [1 ]
Novembre, J
机构
[1] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
[2] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
关键词
CCR5; evolution; HIV; population genetics;
D O I
10.1016/j.micinf.2004.12.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The CCR5 chemokine receptor is exploited by HIV-1 to gain entry into CD4(+)T cells. A deletion mutation (Delta 32) confers resistance against HIV by obliterating the expression of the receptor on the cell surface. Intriguingly, this allele is young in evolutionary time, yet it has reached relatively high frequencies in Europe. These properties indicate that the mutation has been under intense positive selection. HIV-1 has not exerted selection for long enough on the human population to drive the CCR5-Delta 32 allele to current frequencies, fueling debate regarding the selective pressure responsible for rise of the allele. The allele exists at appreciable frequencies only in Europe, and within Europe, the frequency is higher in the north. Here we review the population genetics of the CCR5 locus, the debate over the historical selective pressure acting on CCR5-Delta 32, the inferences that can potentially be drawn from the geographic distribution of CCR5-Delta 32 and the role that other genetic polymorphisms play in conferring resistance against HIV. We also discuss parallel evolution that has occurred at the CCR5 locus of other primate species. Finally, we highlight the promise that therapies based on interfering with the CCR5 receptor could have in the treatment of HIV. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:302 / 309
页数:8
相关论文
共 78 条
[1]   CCR5 provides a signal for microbial induced production of IL-12 by CD8α+ dendritic cells [J].
Aliberti, J ;
Sousa, CRE ;
Schito, M ;
Hieny, S ;
Wells, T ;
Huffnagle, GB ;
Sher, A .
NATURE IMMUNOLOGY, 2000, 1 (01) :83-87
[2]   Influence of CCR5 promoter haplotypes on AIDS progression in African-Americans [J].
An, P ;
Martin, MP ;
Nelson, GW ;
Carrington, M ;
Smith, MW ;
Gong, K ;
Vlahov, D ;
O'Brien, SJ ;
Winkler, CA .
AIDS, 2000, 14 (14) :2117-2122
[3]  
ANDERSON R M, 1991
[4]  
[Anonymous], 1998, Viruses, Plagues, and History
[5]   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
[6]   A strong signature of balancing selection in the 5′ cis-regulatory region of CCR5 [J].
Bamshad, MJ ;
Mummidi, S ;
Gonzalez, E ;
Ahuja, SS ;
Dunn, DM ;
Watkins, WS ;
Wooding, S ;
Stone, AC ;
Jorde, LB ;
Weiss, RB ;
Ahuja, SK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10539-10544
[7]   Contrasting frequencies of CCR5Δ32 and CCR2-64I alleles in the Tunisian population [J].
Barbouche, RM ;
Hong, L ;
Dellagi, K ;
Kostrikis, LG .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2001, 26 (03) :298-299
[8]  
BEAN JMW, 1963, LATER MIDDLE AGES, pR15
[9]   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
[10]   Chemokines and HIV-1 second receptors: The therapeutic connection [J].
Cairns, JS ;
D'Souza, MP .
NATURE MEDICINE, 1998, 4 (05) :563-568