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J. Virol. doi:10.1128/JVI.01348-06
Copyright (c) 2006, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Modulation of DNA Vaccine-Elicited CD8⁺ T Lymphocyte Epitope Immunodominance Hierarchies

Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA

^* To whom correspondence should be addressed. Email: dbarouch{at}bidmc.harvard.edu.

	Abstract

Generating broad cellular immune responses against a diversity of viral epitopes is a major goal of current vaccine strategies for both HIV-1 and other pathogens. Virus-specific CD8⁺ T lymphocyte responses, however, are often highly focused on a very limited number of immunodominant epitopes. For an HIV-1 vaccine, the breadth of CD8⁺ T lymphocyte responses may prove critical as a result of the need to cover a wide diversity of viral isolates in the population and to limit viral escape from dominant epitope-specific T lymphocytes. Here we show that epitope modification strategies can alter CD8⁺ T lymphocyte epitope immunodominance hierarchies elicited by a DNA vaccine in mice. Mice immunized with a DNA vaccine expressing SIV Gag lacking the dominant D^b-restricted AL11 epitope generated a marked and durable augmentation of responses specific for the subdominant D^b-restricted KV9 epitope. Moreover, anatomic separation strategies and heterologous prime-boost regimens generated codominant responses against both epitopes. These data demonstrate that dominant epitopes can dramatically suppress the immunogenicity of subdominant epitopes in the context of gene-based vaccines and that epitope modification strategies can be utilized to enhance responses to subdominant epitopes.

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