Abstract
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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 75-84 |
| Number of pages | 10 |
| Journal | HIV Medicine |
| Volume | 7 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 2006 |
| Externally published | Yes |
Keywords
- Africa
- AIDS
- Children
- Coreceptor polymorphisms
- Disease progression
- Host immunogenetics
- nef gene
ASJC Scopus subject areas
- Virology
- Medicine(all)
- Immunology