HIV

HIV uses protein interaction pathways to force host cells to make more HIV copies. Judith Klein of Carnegie Mellon University aims to use advanced computational methods to predict parallel pathways that can be found and used to circumvent the points of HIV interception.

Olaf Kutsch of the University of Alabama proposes that HIV latency is controlled by host-gene promoter interference, a mechanism that prevents the initiation of viral gene expression. Understanding how host-gene promoter interference controls latent HIV-1 infection may aid development of therapies to deplete latent HIV in patients.

Claudia Pastori of Fondazione S. Raffaele del Monte Tabor in Italy seeks to induce mucosal immunity against HIV by using a bacterial adhesive protein to target antigens to specific cells. The goal of this approach is to present conserved epitopes of HIV in their natural form to elicit the production of protective antibodies in the tissues where these antibodies will be effective.

Emmanuel Ho of the University of Manitoba in Winnipeg, Canada will develop a polyether urethane (PU) intra-vaginal ring designed to slowly release the HIV peptide gp120, as well as the cytokine IL-12 as an adjuvant, directly into the vaginal mucosa to stimulate a sustained mucosal immune response.

Edward Dolk of Utrecht University in the Netherlands proposes using two-sided antibodies, which bind to HIV and to transport receptors in the epithelium. Binding these receptors will cause excretion of the HIV particles outside of the body, thereby reducing viral load.

David Schwartz of Hackensack University Medical Center in the U.S. will test an intradermal injection that increases levels of vitamin A and blocks vitamin D3 metabolism. These important mechanisms can "educate" B cells to home to the gut and to make mucosal antibodies against many viruses, including HIV.

Charani Ranasinghe of The Australian National University will test a new vaccine technology that modulates a host cytokine response to HIV vaccines. If successful, this "cytokine trap" technology may also enhance T-cell mediated immunity to other vaccine antigens, such as Tuberculosis.

Ann Kurth of New York University in the U.S. will test the hypothesis that eliminating intra-vaginal practices such as douching will allow the return of healthy vaginal flora conditions which includes ideal pH and an intact vaginal mucosa. By restoring and maintaining this healthy environment, Kurth proposes that incidences of pelvic inflammatory disease and HIV infection can be reduced.

BK virus is a very common and non-pathogenic virus that persists in specific organs for long periods of time. Simon Lacey of Beckman Research Institute of the City of Hope in the U.S. proposes using an engineered BK virus as a vaccine vector to introduce HIV polyepitope sequences in hopes of inducing a strong and long- lasting immune response against HIV.

Samuel Landry of Tulane University will research the use of immune tolerance of dominant HIV epitopes prior to conventional vaccination with an HIV protein in order to stimulate a broader immune response.