Population survey of CCR5 Δ32, CCR5 m303, CCR2b 64I, and SDF1 3′A allele frequencies in indigenous Chinese healthy individuals, and in HIV-1-infected and HIV-1-uninfected individuals in HIV-1 risk groups

被引:39
|
作者
Wang, FS
Hong, WG
Cao, YZ
Liu, MX
Jin, L
Hu, LP
Wang, Z
Feng, TJ
Hou, J
Zhang, B
Shi, M
Xu, DP
Lei, ZY
Wang, B
Liu, ZD
Ye, JJ
Peng, L
Qiu, Y
Winkler, C
机构
[1] Beijing Hosp Infect Dis, Beijing Inst Infect Dis, Div Biol Engn, Beijing, Peoples R China
[2] Natl Ctr AIDS Prevent & Control, Beijing, Peoples R China
[3] Inst Med Informat, Div Med Stat, Beijing, Peoples R China
[4] Hlth & Antiepidem Ctr Henan Province, Zhengzhou, Peoples R China
[5] Shenzhen Hlth & Antiepidem Stn, Shenzhen, Guangdong Prov, Peoples R China
[6] Hlth & Antiepidem Ctr Xin Jiang Autonomous Reg, Mulomuqi, Peoples R China
[7] Sci & Technol Inst Family Planning, Kunming, Yunnan Province, Peoples R China
[8] NCI, Basic Res Program, SAIC Frederick Inc, Frederick, MD 21701 USA
关键词
coreceptors; SDF-1; CCR2; CCR5; HIV-1; allele frequency;
D O I
10.1097/00126334-200302010-00002
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 aim of this study is to determine in indigenous Chinese ethnic groups the frequencies of the chemokine (SDFI 3'A) and chemokine receptors (CCR5 Delta32, CCR5 m303, and CCR2b 641) HIV-1/AIDS restriction alleles. The study includes two cohorts; the first comprised 3165 indigenous healthy subjects representing eight ethnic groups: Han (n = 1406), Uygur (n = 316), Mongolia (n = 134), Hui (n = 386), Tibetan (n = 330), Zhuang (n = 378), Dai (n = 101), and Jingbo (n = 114). The second cohort consisted of 330 HIV-1-infected (86 subjects infected by sexual transmission and 198 subjects infected by HIV-1-contaminated blood or by sharing injection equipment; the remaining 46 subjects said nothing about HIV-1 transmission) and 474 HIV-1-uninfected Han Chinese belonging to one of two HIV-1 high-risk groups: intravenous drug users (n = 215) and individuals with sexually transmitted diseases (n = 259). Genotypes for the four genes were obtained using PCR (CCR5 Delta32) or PCR-restriction fragment length polymorphism. Randomly selected amplified PCR products were further confirmed by direct DNA sequencing. The variant allele frequencies were determined to be 0% to 3.48% for CCR5 Delta32, 0% for CCR5 m303, 16.23% to 28.79% for CCR2b 641, and 17.70% to 27.76% for SDFI 3'A in Chinese healthy individuals from eight ethnic groups. These findings show that allele frequencies differ among the eight Chinese ethnic groups for CCR5 Delta32, CCR2b 641, and SDFI 3'A and that the CCR5 m303 and CCR5 Delta32 mutant alleles were absent or infrequent in Chinese, which may be helpful for studies of specific anti-HIV-1 vaccine trials and coreceptor inhibitor drug targets in Chinese populations. Furthermore, we observed no significant differences in allele or genotypic frequencies between HIV-1-infected and HIV-1-uninfected groups from the Han ethnic group. Our finding is the first reporting that there is likely no effect of the examined polymorphisms in our study on HIV-1 transmission in the Chinese Han population, However, the genetic effects of these and other AIDS-modifying polymorphisms on the pathogenesis and clinical outcome of HIV-1/AIDS diseases is under investigation in Chinese populations.
引用
收藏
页码:124 / 130
页数:7
相关论文
共 50 条
  • [31] Protective effect of CCR2-64I and not of CCR5-Δ32 and SDF1-3′A in pediatric HIV-1 infection
    Mangano, A
    Kopka, J
    Batalla, M
    Bologna, R
    Sen, L
    JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2000, 23 (01) : 52 - 57
  • [32] Risk of mother-to-infant transmission of HIV-1 is not reduced in CCR5/Delta 32ccr5 heterozygotes
    Edelstein, RE
    Arcuino, LAM
    Hughes, JP
    Melvin, AJ
    Mohan, KM
    King, PD
    McLellan, CL
    Murante, BL
    Kassman, BP
    Frenkel, LM
    JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1997, 16 (04): : 243 - 246
  • [33] Genetic influence of CCR5, CCR2, and SDF1 variants on human immunodeficiency virus 1 (HIV-1)-related disease progression and neurological impairment, in children with symptomatic HIV-1 infection
    Singh, KK
    Barroga, CF
    Hughes, MD
    Chen, J
    Raskino, C
    McKinney, RE
    Spector, SA
    JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (10): : 1461 - 1472
  • [34] High prevalence of the CCR5Δ32 HIV-resistance mutation among Estonian HIV type 1-infected individuals
    Adojaan, Maarja
    Molder, Tarmo
    Mannik, Andres
    Kivisild, Toomas
    Villems, Richard
    Krispin, Tonu
    Ustav, Mart
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2007, 23 (02) : 193 - 197
  • [35] CCR5 Δ32 deletion and response to highly active antiretroviral therapy in HIV-1-infected patients
    Guérin, S
    Meyer, L
    Theodorou, I
    Boufassa, F
    Magierowska, M
    Goujard, C
    Rouzioux, C
    Debré, P
    Delfraissy, JF
    AIDS, 2000, 14 (17) : 2788 - 2790
  • [36] Impact of CCR5 Δ32/+ deletion on herpes zoster among HIV-1-infected homosexual men
    Krol, Anneke
    Lensen, Ruud
    Veenstra, Jan
    Prins, Maria
    Schuitemaker, Hanneke
    Coutinho, Roel A.
    EUROPEAN JOURNAL OF EPIDEMIOLOGY, 2006, 21 (06) : 469 - 473
  • [37] Impact of CCR5 Δ32/+ Deletion on Herpes Zoster Among HIV-1-Infected Homosexual Men
    Anneke Krol
    Ruud Lensen
    Jan Veenstra
    Maria Prins
    Hanneke Schuitemaker
    Roel A. Coutinho
    European Journal of Epidemiology, 2006, 21 : 469 - 473
  • [38] Protective effect of CCR5 Δ32 heterozygosity is restricted by SDF-1 genotype in children with HIV-1 infection
    Sei, S
    Boler, AM
    Nguyen, GT
    Stewart, SK
    Yang, QE
    Edgerly, M
    Wood, LV
    Brouwers, P
    Venzon, DJ
    AIDS, 2001, 15 (11) : 1343 - 1352
  • [39] Gene polymorphisms in CCR5, CCR2, CX3CR1, SDF-1 and RANTES in exposed but uninfected partners of HIV-1 infected individuals in North India (vol 26, pg 476, 2006)
    Suresh, Pallikuth
    Wanchu, Ajay
    Sachdeva, Ravinder Kaur
    Bhatnagar, Archana
    JOURNAL OF CLINICAL IMMUNOLOGY, 2007, 27 (01) : 131 - 131
  • [40] Analysis of a 32-base-pair deletion in the CCR5 chemokine receptor gene in HIV-1-infected individuals from Moscow
    Shadrina, MI
    Kopilov, VM
    Miloserdova, OV
    Slominsky, PA
    Limborska, SA
    RUSSIAN JOURNAL OF GENETICS, 2000, 36 (05) : 586 - 587