HIV-1 movement across genital tract cells surprisingly enhanced by usurping antibody response

UCI-led study results have important implications for HIV vaccine development

2013-12-04

(Press-News.org) Contact information: Tom Vasich
tmvasich@uci.edu
949-824-6455
University of California - Irvine
HIV-1 movement across genital tract cells surprisingly enhanced by usurping antibody response UCI-led study results have important implications for HIV vaccine development Irvine, Calif., Dec. 3, 2013 — Infectious disease researchers have identified a novel mechanism wherein HIV-1 may facilitate its own transmission by usurping the antibody response directed against itself. These results have important implications for HIV vaccine development and for understanding the earliest events in HIV transmission.

In a study appearing in the November issue of PLoS Pathogens, Dr. Donald Forthal of UC Irvine and colleagues studied the mechanisms employed by the virus to cross genital tract tissue and establish infection. Since cervicovaginal fluid is acidic and HIV-1 in cervicovaginal fluid is likely coated with antibodies, they explored the effect of low pH and HIV-1-specific antibodies on transcytosis, the movement of HIV-1 across tight-junctioned epithelial cells.

The researchers found that the combination of HIV-1-specific antibodies and low pH enhanced transcytosis as much as 20-fold.

Virus that underwent transcytosis under these conditions was infectious, and infectivity was highly influenced by whether or not the antibody neutralized the virus. They observed enhanced transcytosis using antibody from cervicovaginal and seminal fluids and using transmitted/founder strains of HIV-1. Enhanced transcytosis was due to the Fc neonatal receptor (FcRn), which binds immune complexes at acidic pH and releases them at neutral pH. Finally, staining of human tissue revealed abundant FcRn expression on columnar epithelial cells of penile urethra and endocervix.

### The study is accessible at PLoS Pathogens at: http://www.plospathogens.org/article/info%3Adoi%2F10.1371%2Fjournal.ppat.1003776

The work was supported by the National Institute of Allergy and Infectious Diseases (awards R01AI102715 and U19 AI096398).

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