AI Article Synopsis

  • A study tested neutralization effectiveness of clade-specific plasma against primary HIV-1 viruses and pseudoviruses from different strains, using two neutralization platforms.
  • In the PBMC assay, the strongest neutralizing antibody responses were observed when the antibody pool matched the virus clade, demonstrating significant cross-recognition in certain clade pairs.
  • The pseudovirus assay showed less cross-clade neutralization, but the clade C antibody pool was notably effective, suggesting the need for more research on clade C envelopes to develop broadly neutralizing antibodies.

Article Abstract

A panel of paired primary virus isolates and envelope pseudoviruses from sixty strains representing six HIV-1 clades was tested for neutralization using pooled, clade-specific plasma in two prominently utilized neutralization platforms: a primary isolate assay using peripheral blood mononuclear cells (PBMC) and a pseudovirus assay using a reporter epithelial cell line. Using the PMBC assay, pairing of the antibody pool against homologous clade viruses generated the highest geometric mean neutralizing antibody titer in 4 out of 6 clades tested, and neutralization patterns showed numerous examples of reciprocal cross-recognition between antibody and viruses of specific clade pairs. In the pseudovirus assay, cross-clade neutralization was more limited, with fewer distinct cross-clade relationships evident. The clade C antibody pool was broadly cross-reactive, neutralizing the greatest number of viruses in both assays. These data highlight the importance of the neutralization assay format employed and suggest that clade C envelopes merit further evaluation for the elicitation of broadly neutralizing antibodies.

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http://dx.doi.org/10.1016/j.virol.2008.02.022DOI Listing

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