Logo do repositório
 
A carregar...
Miniatura
Publicação

Correlation between anti-gp41 antibodies and virus infectivity decay during primary HIV-1 infection

Utilize este identificador para referenciar este registo.
Nome:Descrição:Tamanho:Formato: 
Anti_gp41.pdf1 MBAdobe PDF Ver/Abrir

Orientador(es)

Resumo(s)

Recent experiments have suggested that the infectivity of simian immunodeficiency virus (SIV) and human immunodeficiency virus type-1 (HIV-1) in plasma decreases over time during primary infection. Because anti-gp41 antibodies are produced early during HIV-1 infection and form antibody-virion complexes, we studied if such early HIV-1 specific antibodies are correlated with the decay in HIV-1 infectivity. Using a viral dynamic model that allows viral infectivity to decay and frequent early viral load data obtained from 6 plasma donors we estimate that HIV-1 infectivity begins to decay after about 2 weeks of infection. The length of this delay is consistent with the time before antibody-virion complexes were detected in the plasma of these donors and is correlated (p = 0.023, r = 0.87) with the time for antibodies to be first detected in plasma. Importantly, we identify that the rate of infectivity decay is significantly correlated with the rate of increase in plasma anti-gp41 IgG concentration (p = 0.046, r = 0.82) and the increase in IgM+IgG anti-gp41 concentration (p = 8.37 × 10-4, r = 0.98). Furthermore, we found that the viral load decay after the peak did not have any significant correlation with the rate of anti-gp41 IgM or IgG increase. These results indicate that early anti-gp41 antibodies may cause viral infectivity decay, but may not contribute significantly to controlling post-peak viral load, likely due to insufficient quantity or affinity. Our findings may be helpful to devise strategies, including antibody-based vaccines, to control acute HIV-1 infection.

Descrição

Copyright © 2018 Vaidya, Ribeiro, Liu, Haynes, Tomaras and Perelson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

Palavras-chave

Antibodies Primary HIV-1 infection Viral dynamics model Viral load Virus infectivity

Contexto Educativo

Citação

Frontiers in Microbiology 1 June 2018 | Volume 9 | Article 1326

Projetos de investigação

Unidades organizacionais

Fascículo

Editora

Frontiers

Licença CC

Métricas Alternativas