Distribution of CCR5Δ32 in human immunodeficiency virus-infected children and its relationship to disease course

被引:13
作者
Bakshi, SS
Zhang, LQ
Ho, D
Than, S
Pahwa, SG
机构
[1] NYU, Sch Med, N Shore Univ Hosp, Dept Pediat,Div Immunol, Manhasset, NY USA
[2] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
关键词
D O I
10.1128/CDLI.5.1.38-40.1998
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Homozygosity for a 32-bp deletion in the CCR5 gene (CCR5 Delta 32) has been shown to confer resistance to infection with the macrophage-tropic strain of human immunodeficiency virus (HIV) type 1, We examined the distribution of CCR5 Delta 32 in 47 children (age range, 1.5 to 19 years), of whom 43 were infected with HN, by the perinatal route (n = 41) or by the intravenous route (n = 2). The infected patients were classified as rapid progressors (RP) (n = 7) (CDC category C3 or death by 2 years of age), non-rapid progressors (NRP) (n = 17) (survival for greater than or equal to 8 years after infection), or intermediate (n = 19), CCR5 Delta 32 heterozygosity was found in two HIV-infected children, both NRP, None of the subjects were homozygous for CCR5 Delta 32, and the remaining children had no evidence of CCR5 Delta 32. The presence of CCR5 Delta 32 heterozygosity in 4.8% of this, predominantly non-Caucasian population is consistent with the published distribution of the mutation, The finding that CCR5 Delta 32 was present only in NRP and not in any RP is in agreement with previous reports suggesting that heterozygosity for CCR5 Delta 32 may confer limited protection from disease progression.
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页码:38 / 40
页数:3
相关论文
共 17 条
[11]   The role of a mutant CCR5 allele in HIV-1 transmission and disease progression [J].
Huang, YX ;
Paxton, WA ;
Wolinsky, SM ;
Neumann, AU ;
Zhang, LQ ;
He, T ;
Kang, S ;
Ceradini, D ;
Jin, ZQ ;
Yazdanbakhsh, K ;
Kunstman, K ;
Erickson, D ;
Dragon, E ;
Landau, NR ;
Phair, J ;
Ho, DD ;
Koup, RA .
NATURE MEDICINE, 1996, 2 (11) :1240-1243
[12]   Relative resistance to HIV-1 infection of CD4 lymphocytes from persons who remain uninfected despite multiple high-risk sexual exposures [J].
Paxton, WA ;
Martin, SR ;
Tse, D ;
OBrien, TR ;
Skurnick, J ;
VanDevanter, NL ;
Padian, N ;
Braun, JF ;
Kotler, DP ;
Wolinsky, SM ;
Koup, RA .
NATURE MEDICINE, 1996, 2 (04) :412-417
[13]   Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene [J].
Samson, M ;
Libert, F ;
Doranz, BJ ;
Rucker, J ;
Liesnard, C ;
Farber, CM ;
Saragosti, S ;
Lapoumeroulie, C ;
Cognaux, J ;
Forceille, C ;
Muyldermans, G ;
Verhofstede, C ;
Burtonboy, G ;
Georges, M ;
Imai, T ;
Rana, S ;
Yi, YJ ;
Smyth, RJ ;
Collman, RG ;
Doms, RW ;
Vassart, G ;
Parmentier, M .
NATURE, 1996, 382 (6593) :722-725
[14]   LOWER PREVALENCE AND INCIDENCE OF HIV-1 SYNCYTIUM-INDUCING PHENOTYPE AMONG INJECTING DRUG-USERS COMPARED WITH HOMOSEXUAL MEN [J].
SPIJKERMAN, IJB ;
KOOT, M ;
PRINS, M ;
KEET, IPM ;
VANDENHOEK, AJAR ;
MIEDEMA, F ;
COUTINHO, RA .
AIDS, 1995, 9 (09) :1085-1092
[15]   Expression pattern of HIV-1 coreceptors on T cells: Implications for viral transmission and lymphocyte homing [J].
Unutmaz, D ;
Littman, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1615-1618
[16]   MACROPHAGE-TROPIC VARIANTS INITIATE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION AFTER SEXUAL, PARENTERAL, AND VERTICAL TRANSMISSION [J].
VANTWOUT, AB ;
KOOTSTRA, NA ;
MULDERKAMPINGA, GA ;
ALBRECHTVANLENT, N ;
SCHERPBIER, HJ ;
VEENSTRA, J ;
BOER, K ;
COUTINHO, RA ;
MIEDEMA, F ;
SCHUITEMAKER, H .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :2060-2067
[17]   Adaptive evolution of human immunodeficiency virus-type 1 during the natural course of infection [J].
Wolinsky, SM ;
Korber, BTM ;
Neumann, AU ;
Daniels, M ;
Kunstman, KJ ;
Whetsell, AJ ;
Furtado, MR ;
Cao, YZ ;
Ho, DD ;
Safrit, JT ;
Koup, RA .
SCIENCE, 1996, 272 (5261) :537-542