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Cross-clade neutralization patterns among HIV-1 strains from the six major clades of the pandemic evaluated and compared in two different models.
- Source :
-
Virology [Virology] 2008 Jun 05; Vol. 375 (2), pp. 529-38. Date of Electronic Publication: 2008 Apr 22. - Publication Year :
- 2008
-
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.
- Subjects :
- Antibody Specificity
Cells, Cultured
Cross Reactions
Disease Outbreaks
HIV Antibodies blood
HIV Infections prevention & control
HIV-1 classification
HeLa Cells
Humans
Leukocytes, Mononuclear
Neutralization Tests standards
Sensitivity and Specificity
AIDS Vaccines immunology
HIV Antibodies immunology
HIV Infections immunology
HIV-1 immunology
Neutralization Tests methods
Subjects
Details
- Language :
- English
- ISSN :
- 0042-6822
- Volume :
- 375
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Virology
- Publication Type :
- Academic Journal
- Accession number :
- 18433824
- Full Text :
- https://doi.org/10.1016/j.virol.2008.02.022