New CCR5 variants associated with reduced HIV coreceptor function in southeast Asia

被引:22
作者
Capoulade-Métay, C
Ma, LY
Truong, LX
Dudoit, Y
Versmisse, P
Nguyen, NV
Nguyen, M
Scott-Algara, D
Barré-Sinoussi, F
Debré, P
Bismuth, G
Pancino, G
Theodorou, I
机构
[1] CHU Pitie Salpetriere, INSERM, U543, F-75013 Paris, France
[2] Inst Pasteur, Unite Biol Retrovirus, Paris, France
[3] Inst Cochin, INSERM, U567, Paris, France
[4] Inst Pasteur, Ho Chi Minh City, Vietnam
[5] Hop Binh Trieu, Ho Chi Minh City, Vietnam
[6] Inst Pasteur, Phnom Penh, Cambodia
关键词
HIV-1; infection; Vietnam; Cambodia; CCR5; chemokine; polymorphisms;
D O I
10.1097/00002030-200411190-00004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Despite multiple exposure to HIV-1, some individuals remain uninfected. This resistance has been associated with homozygosity for a 32 base pair deletion in the gene for the CCR5 receptor. This variant occurs frequently in Caucasians but is extremely rare in Asians or Africans. Objective: To identify variations in CCR5 receptor gene that affect susceptibility to HIV infection in non-Caucasians. Methods: CCR5 coding region polymorphisms were screened in three groups of Vietnamese subjects: 47 HIV-1 infected intravascular drug users, 50 highly HIV-1-exposed but seronegative intravascular drug users and 37 HIV-1-unexposed seronegative individuals. DNA was analysed by denaturing high performance liquid chromatography; this was followed by examination of the biochemical and HIV coreceptor properties of the coding regions. Results: Five CCR5 coding region variants were identified in this Vietnamese population. The S185R, 1254T and C269F mutations have not been previously described; G106R and R223Q have already been found in other Asian populations, but the functional properties of G106R is not known. These variants differed in biochemical and HIV coreceptor properties. S185R and 1254T variants had receptor and coreceptor activities comparable to that of the wild type, whereas C269F and G106R behaved differently. This latter pair are poorly expressed at the cell surface, weakly bind macrophage inflammatory protein 1beta (CCL4) and RANTES (CCL5), and display reduced HIV-1 coreceptor efficiency. Conclusions: Among the five CCR5 variants found in this Vietnamese population, G106R and C269F displayed significant modifications of their receptor and coreceptor properties, which may contribute to susceptibility to HIV-1 infection and/or disease progression within this population. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:2243 / 2252
页数:10
相关论文
共 45 条
[1]   The extent of genetic variation in the CCR5 gene [J].
AnsariLari, MA ;
Liu, XM ;
Metzker, ML ;
Rut, AR ;
Gibbs, RA .
NATURE GENETICS, 1997, 16 (03) :221-222
[2]   Epidemiologic and biologic characterization of a cohort of human immunodeficiency virus type I highly exposed, persistently seronegative female sex workers in northern Thailand [J].
Beyrer, C ;
Artenstein, AW ;
Rugpao, S ;
Stephens, H ;
VanCott, TC ;
Robb, ML ;
Rinkaew, M ;
Birx, DL ;
Khamboonruang, C ;
Zimmerman, PA ;
Nelson, KE ;
Natpratan, C .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (01) :59-67
[3]   Multiple nonfunctional alleles of CCR5 are frequent in various human populations [J].
Blanpain, C ;
Lee, B ;
Tackoen, M ;
Puffer, B ;
Boom, A ;
Libert, F ;
Sharron, M ;
Wittamer, V ;
Vassart, G ;
Doms, RW ;
Parmentier, M .
BLOOD, 2000, 96 (05) :1638-1645
[4]   Extracellular cysteines of CCR5 are required for chemokine binding, but dispensable for HIV-1 coreceptor activity [J].
Blanpain, C ;
Lee, B ;
Vakili, J ;
Doranz, BJ ;
Govaerts, C ;
Migeotte, I ;
Sharron, M ;
Dupriez, V ;
Vassart, G ;
Doms, RW ;
Parmentier, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :18902-18908
[5]   Genetics of HIV-1 infection: chemokine receptor CCR5 polymorphism and its consequences [J].
Carrington, M ;
Dean, M ;
Martin, MP ;
O'Brien, SJ .
HUMAN MOLECULAR GENETICS, 1999, 8 (10) :1939-1945
[6]   Novel alleles of the chemokine-receptor gene CCR5 [J].
Carrington, M ;
Kissner, T ;
Gerrard, B ;
Ivanov, S ;
O'Brien, SJ ;
Dean, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (06) :1261-1267
[7]   Cloning and functional expression of CC CKR5, a human monocyte CC chemokine receptor selective for MIP-1 alpha, MIP-1 beta, and RANTES [J].
Combadiere, C ;
Ahuja, SK ;
Tiffany, HL ;
Murphy, PM .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 60 (01) :147-152
[8]   Natural proteolytic processing of hemofiltrate CC chemokine 1 generates a potent CC chemokine receptor (CCR)1 and CCR5 agonist with anti-HIV properties [J].
Detheux, M ;
Ständker, L ;
Vakili, J ;
Münch, J ;
Forssmann, U ;
Adermann, K ;
Pöhlmann, S ;
Vassart, G ;
Kirchhoff, F ;
Parmentier, M ;
Forssmann, WG .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (10) :1501-1508
[9]   Differential tropism and chemokine receptor expression of human immunodeficiency virus type 1 in neonatal monocytes, monocyte-derived macrophages, and placental macrophages [J].
Fear, WR ;
Kesson, AM ;
Naif, H ;
Lynch, GW ;
Cunningham, AL .
JOURNAL OF VIROLOGY, 1998, 72 (02) :1334-1344
[10]  
Follézou JY, 1999, AM J TROP MED HYG, V61, P420