HIV-1 vaccine design: harnessing diverse lymphocytes to conquer a diverse pathogen.

Sherri L Surman, Robert Sealy, Bart G Jones, Julia L Hurwitz

Journal: Human vaccines 2009;5(4):268-71

PMID: 19684481

Abstract

In the fall of 2007, the HIV-1 research field received news that their front-runner vaccine was not protective. In response to this disappointment, scientists are now reviewing the intricacies of the immune response toward HIV-1 to develop new and better strategies for vaccine development. Decades ago, researchers recognized the impressive amino acid and carbohydrate diversity of HIV-1, and the associated obstacles to vaccine development. At first glance, the diversity and other unique features of HIV-1 may seem insurmountable, but attention to vaccine successes in other fields serves to renew optimism. The newly-licensed rotavirus and papillomavirus cocktail vaccines remind scientists that diverse pathogens can be conquered and that the chronic nature of a virus infection need not thwart successful vaccine design. Here we describe current efforts to gain insights from other vaccine fields and to adopt a cocktail vaccine approach for the prevention of HIV-1 infections in humans.

Address: Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
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