nef gene sequence variation among HIV-1-infected African children

被引:6
作者
Chakraborty, R
Reinis, M
Rostron, T
Philpott, S
Dong, T
D'Agostino, A
Musoke, R
de Silva, E
Stumpf, M
Weiser, B
Burger, H
Rowland-Jones, SL
机构
[1] Nyumbani Childrens Home, Nairobi, Kenya
[2] Univ Oxford, Weatherall Inst Mol Med, MRC, Human Immunol Unit, Oxford, England
[3] New York City Dept Hlth, Wadsworth Ctr, Albany, NY USA
[4] Acad Sci Czech Republ, Inst Mol Genet, Prague, Czech Republic
[5] Univ London Imperial Coll Sci Technol & Med, Dept Sci Biol, Ctr Bioinformat Biochem Bldg, London, England
基金
英国医学研究理事会;
关键词
Africa; AIDS; children; coreceptor polymorphisms; disease progression; host immunogenetics; nef gene;
D O I
10.1111/j.1468-1293.2006.00341.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background There are few data on African children infected with nonclade B HIV-1 in endemic settings, which limits generalizations about pathogenesis and progression. Genotypic and phenotypic variations in host immunogenetics and HIV-1 negative factor (nef) accessory protein may influence disease progression and have frequently been characterized in subjects infected with clade B HIV-1. Methods In this descriptive study, we report nef gene sequence variation and host genetic polymorphisms in 32 Kenyan children, including 12 slow progressors. Results Phylogenetic analysis identified HIV-1 clades A, C and D and a recombinant A/D subtype. Grossly defective nef genes or significant changes from relevant clade reference sequences were not identified in children with delayed disease progression. Conclusions nef sequence variations may not be common in perinatally infected African children. Further studies are warranted in HIV-1-infected subjects in settings where infection is endemic.
引用
收藏
页码:75 / 84
页数:10
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