Faster HIV-1 Disease Progression among Brazilian Individuals Recently Infected with CXCR4-Utilizing Strains


Autoria(s): Araripe Sucupira, Maria Cecilia; Sanabani, Sabri; Cortes, Rodrigo M.; Giret, Maria Teresa M.; Tomiyama, Helena; Sauer, Mariana M.; Sabino, Ester Cerdeira; Janini, Luiz Mario; Kallas, Esper Georges; Diaz, Ricardo Sobhie
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Introduction: Primary HIV infection is usually caused by R5 viruses, and there is an association between the emergence of CCXR4-utilizing strains and faster disease progression. We characterized HIV-1 from a cohort of recently infected individuals in Brazil, predicted the virus's co-receptor use based on the env genotype and attempted to correlate virus profiles with disease progression. Methods: A total of 72 recently infected HIV patients were recruited based on the Serologic Testing Algorithm for Recent HIV Seroconversion and were followed every three to four months for up to 78 weeks. The HIV-1 V3 region was characterized by sequencing nine to twelve weeks after enrollment. Disease progression was characterized by CD4+ T-cell count decline to levels consistently below 350 cells/mu L. Results: Twelve out of 72 individuals (17%) were predicted to harbor CXCR4-utilizing strains; a baseline CD4,350 was more frequent among these individuals (p = 0.03). Fifty-seven individuals that were predicted to have CCR5-utilizing viruses and 10 individuals having CXCR4-utilizing strains presented with baseline CD4.350; after 78 weeks, 33 individuals with CCR5 strains and one individual with CXCR4 strains had CD4.350 (p = 0.001). There was no association between CD4 decline and demographic characteristics or HIV-1 subtype. Conclusions: Our findings confirm the presence of strains with higher in vitro pathogenicity during early HIV infection, suggesting that even among recently infected individuals, rapid progression may be a consequence of the early emergence of CXCR4-utilizing strains. Characterizing the HIV-1 V3 region by sequencing may be useful in predicting disease progression and guiding treatment initiation decisions.

Brazilian Program for STD and AIDS

Brazilian Program for STD and AIDS

Ministry of Health [914/BRA/3014-UNESCO/Kallas]

Ministry of Health

Sao Paulo City Health Department

Sao Paulo City Health Department [2004-0.168.922-7/Kallas]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [04/15856-9/Diaz]

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Brazilian Ministry of Education

Brazilian Ministry of Education

Identificador

PLOS ONE, SAN FRANCISCO, v. 7, n. 1, supl. 1, Part 2, pp. 138-142, 46023, 2012

1932-6203

http://www.producao.usp.br/handle/BDPI/41165

10.1371/journal.pone.0030292

http://dx.doi.org/10.1371/journal.pone.0030292

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS ONE

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #VIRUS TYPE-1 SUBTYPES #T-CELL-ACTIVATION #HEPATITIS-G VIRUS #ANTIRETROVIRAL THERAPY #GENETIC RESTRICTION #ENZYME-IMMUNOASSAY #CORECEPTOR USAGE #PROGNOSTIC VALUE #AIDS #VARIANTS #MULTIDISCIPLINARY SCIENCES
Tipo

article

original article

publishedVersion