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CTL ontogeny and viral escape have implications for HIV vaccine design.

Vaccine Weekly

| June 02, 2004 | COPYRIGHT 2004 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2004 JUN 2 - (NewsRx.com & NewsRx.net) -- Cytotoxic T lymphocyte (CTL) ontogeny and viral escape have implications for HIV vaccine design.

According to recent research published in the journal Trends in Immunology, "The protective role of CD8+ cytotoxic T lymphocytes (CTLs) in HIV-1 infection has prompted an emphasis on generating virus-specific CTLs by vaccination, whereas the determinants of antiviral efficiency remain undefined. The general strategy of many vaccines is to maximize the breadth of CTL responses. However, patterns of changing CTL specificity and viral mutation in natural infection, in addition to data from macaque and in vitro studies, suggest that a more focused approach might optimize the activity of vaccine-generated CTLs to prevent or attenuate infection.

"CTLs recognizing early proteins (Tat and Nef) appear to exert greater antiviral pressure but might be more prone to epitope escape mutation, whereas those recognizing structural proteins (Gag and Pol) might be more likely to persist through the recognition of conserved sequences," said Otto ...

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Source: HighBeam Research, CTL ontogeny and viral escape have implications for HIV vaccine...

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