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  • Poster presentation
  • Open Access

Differential HLA-dependent HIV evolution among subtypes

  • 1,
  • 2,
  • 3 and
  • 1
Retrovirology20063 (Suppl 1) :P15

  • Published:


  • Immune Response
  • Phylogenetic Analysis
  • Consensus Sequence
  • Population Level
  • Infected Individual


Population HLA-dependent evolution has been documented over the principal HIV proteins. Effect of subtype variability is uncertain. In Argentina, B subtype and recombinant BF variants circulate in equal proportions.


Blood samples were collected from 94 drug-naive HIV infected individuals. DNA and RNA extraction were performed from PBMC and plasma, respectively. HLA-A and B genes were genotyped by PCR-SSOP. Pol and vpu genes were amplified by RT-PCR and sequenced. Aminoacidic positions were codified as 0 = "equal state" (to consensus sequence) and 1 = "variated state" (polymorphism). Phylogenetic analyses were performed by BootScanning. Statistical analysis was performed by ODDS-ratio/power calculations, Fischer exact test, Logistic regression and randomization tests. Potential new epitopes and affinities with HLA were assessed by using BIMAS software.


We found 95 polymorphisms associated with different HLA alleles. 44 out of them were inside predicted epitopes for the associated HLA allele. 13 out of them reduced the affinity for the HLA allele in the "variated" state. 5 out of them were associated with viral subtype.


Our results suggest that vpu could be undergoing adaptation to the immune response at the population level, as previously reported for pol gen. Associations with viral subtype suggest that this evolution is different among subtypes and that variants from subtype B and BF could respond differently to both natural and vaccine-induced immune response.

Authors’ Affiliations

National Reference Center for AIDS, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina
Hospital Ramos Mejia, Buenos Aires, Argentina
Nexo Asociación Civil, Buenos Aires, Argentina


© Dilernia et al; licensee BioMed Central Ltd. 2006

This article is published under license to BioMed Central Ltd.