AI Article Synopsis

  • The study focuses on identifying broadly cross-reactive neutralizing (BCN) antibodies, which are crucial for creating a universally effective HIV vaccine.
  • A total of 117 serum samples from HIV-1 (CRF07_BC) individuals were tested, revealing that 18 samples could neutralize all three primary HIV-1 strains, with BCN sera showing a stronger neutralizing response compared to non-BCN sera.
  • Additionally, sera from asymptomatic individuals were more effective at neutralizing key HIV strains than those from symptomatic individuals, suggesting that BCN responses could play a role in protecting against HIV infection and disease progression.

Article Abstract

The identification of broadly cross-reactive neutralizing (BCN) antibodies is essential for the development of a more universally effective vaccine for human immunodeficiency virus (HIV). In this study, CRF07_BC serum was analyzed for cross-clade antibody reactivity and neutralization. A total of 117 HIV-1 sera (CRF07_BC) were screened for their capacity to neutralize three primary HIV-1 isolates. A total of 18 out of 117 sera cross-neutralized all three viruses, and were tested along with eight randomly selected non-BCN sera against seven primary HIV-1 isolates and two laboratory strains that represented different clades and tropisms. BCN sera neutralized eight or all nine of these primary isolates. Non-BCN sera did not display any broadly cross-reactive neutralizing responses. BCN sera neutralized with higher frequency and geometric mean titers compared to non-BCN sera. Sera from asymptomatic individuals on average neutralized a significantly greater number of the three key isolates than sera from symptomatic individuals. Our data indicate that the three HIV-1 isolated strains are sufficient to screen broad cross-neutralizing sera, and that BCN responses may contribute to protection from infection and disease progression. The neutralizing antibody response demonstrated extensive cross-neutralization, suggesting that neutralizing antibodies induced by vaccines will have a relatively low epitope diversity to overcome in patients infected with HIV-1 B'/C recombinant (CRF07_BC).

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Source
http://dx.doi.org/10.3892/mmr.2012.790DOI Listing

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