Diversity Considerations in HIV-1 Vaccine Selection

Author:

Gaschen Brian1,Taylor Jesse1,Yusim Karina1,Foley Brian1,Gao Feng2,Lang Dorothy1,Novitsky Vladimir3,Haynes Barton2,Hahn Beatrice H.4,Bhattacharya Tanmoy1,Korber Bette15

Affiliation:

1. Los Alamos National Laboratory, Los Alamos, NM 87545, USA.

2. Duke University AIDS Center, Durham, NC 27710, USA.

3. Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.

4. University of Alabama at Birmingham, Birmingham, AL 35294, USA.

5. Santa Fe Institute, Santa Fe, NM 87501, USA.

Abstract

Globally, human immunodeficiency virus–type 1 (HIV-1) is extraordinarily variable, and this diversity poses a major obstacle to AIDS vaccine development. Currently, candidate vaccines are derived from isolates, with the hope that they will be sufficiently cross-reactive to protect against circulating viruses. This may be overly optimistic, however, given that HIV-1 envelope proteins can differ in more than 30% of their amino acids. To contend with the diversity, country-specific vaccines are being considered, but evolutionary relationships may be more useful than regional considerations. Consensus or ancestor sequences could be used in vaccine design to minimize the genetic differences between vaccine strains and contemporary isolates, effectively reducing the extent of diversity by half.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference56 articles.

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3. HIV Immunology and Sequence Databases B. Korber et al. Eds. (Los Alamos National Laboratory Los Alamos NM 2000); available at www.hiv.lanl.gov.

4. B. T. Korber B. Foley B. Gaschen C. Kuiken in Retroviral Immune Response and Restoration G. Pantaleo and B. D. Walker Eds. (Humana Press Totowa NJ 2001) pp. 1–32.

5. A. M. Schultz J. A. Bradac AIDS ( London ) 15 (suppl. 5) S147 (2001).

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