共 27 条
CXCR4 and CCR5 genetic polymorphisms in long-term nonprogressive human immunodeficiency virus infection:: Lack of association with mutations other than CCR5-Δ32
被引:57
作者:

Cohen, OJ
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Paolucci, S
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Bende, SM
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Daucher, M
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Moriuchi, H
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Moriuchi, M
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Cicala, C
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Davey, RT
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Baird, B
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h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA

Fauci, AS
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA
机构:
[1] NIAID, Immunoregulat Lab, Bethesda, MD 20892 USA
关键词:
D O I:
10.1128/JVI.72.7.6215-6217.1998
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Polymorphisms in the coding sequences of CCR5 and CXCR4 were studied in a group of human immunodeficiency virus (HIV)-infected long-term nonprogressors. Two different point mutations were found in the CXCR4 coding sequence. One of these CXCR4 mutations was silent, and each was unique to two nonprogressors. The well described 32-bp deletion within the CCR5 coding sequence (CCR5-Delta 32) was found in 4 of 13 nonprogressors, and 12 different point mutations were found scattered over the CCR5 coding sequence from 8 nonprogressors. Most of the mutations created either silent or conservative changes in the predicted amino acid sequence: only one of these mutations was found in more than a single nonprogressor. All nonsilent mutations were tested in an HIV envelope-dependent fusion assay, and all functioned comparably to wild-type controls. Polymorphisms in the CXCR4 and CCR5 coding sequences other than CCR5-Delta 32 do not appear to play a dominant mechanistic role in nonprogression among HIV-infected individuals.
引用
收藏
页码:6215 / 6217
页数:3
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[J].
Doranz, BJ
;
Rucker, J
;
Yi, YJ
;
Smyth, RJ
;
Samson, M
;
Peiper, SC
;
Parmentier, M
;
Collman, RG
;
Doms, RW
.
CELL,
1996, 85 (07)
:1149-1158

Doranz, BJ
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Rucker, J
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Yi, YJ
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Smyth, RJ
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Samson, M
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Peiper, SC
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Parmentier, M
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Collman, RG
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机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104

Doms, RW
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h-index: 0
机构: UNIV PENN,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104