Heterosexual intercourse now accounts for the majority of HIV transmission
within sub-Saharan Africa. The generation of microbicides and vaccines, therefore, requires a better understanding of the mucosal correlates of protection, including the role of HIV-specific IgA.
It is now accepted that not all individuals are equally susceptible to HIV-1 infection, as exemplified by the HIV Exposed Seronegative (HESN) women of the Pumwani Cohort in Nairobi, Kenya. To assess whether mucosal IgA responses contribute to this protection, 3 novel IgA variable genes were cloned from HESN cervical B-cell cDNA.
Nine monoclonal IgA Abs were produced, two of which were properly produced
from cell culture. The HESN-derived A6/30L and A9/30L variants had a greater specificity for gp120IIIB than their A6/4L and A9/4L counterparts, while the A6 variant recognizes a distinct gp120 epitope compared to the broadly neutralizing antibody IgGb12. Further characterization of these IgA chains may suggest their suitability for use in microbicides or mucosal vaccines.
| Identifer | oai:union.ndltd.org:MANITOBA/oai:mspace.lib.umanitoba.ca:1993/4589 |
| Date | 14 April 2011 |
| Creators | Sarna, Caitlin S. |
| Contributors | Plummer, Francis A. (Medical Microbiology), Fowke, Keith R. (Medical Microbiology) Berry, Jody D. (Immunology) |
| Source Sets | University of Manitoba Canada |
| Language | en_US |
| Detected Language | English |
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