Previous Article | Next Article ![]()
Journal of Virology, October 2009, p. 10280-10285, Vol. 83, No. 19
0022-538X/09/$08.00+0 doi:10.1128/JVI.00138-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Department of Pathology and Laboratory Medicine, University of Wisconsin—Madison, Madison, Wisconsin 53706
Received 21 January 2009/ Accepted 2 July 2009
Understanding the correlates of immune protection against human immunodeficiency virus and simian immunodeficiency virus (SIV) will require defining the entire cellular immune response against the viruses. Here, we define two novel translation products from the SIV env mRNA that are targeted by the T-cell response in SIV-infected rhesus macaques. The shorter product is a subset of the larger product, which contains both the first exon of the Rev protein and a translated portion of the rev intron. Our data suggest that the translation of viral alternate reading frames may be an important source of T-cell epitopes, including epitopes normally derived from functional proteins.
Published ahead of print on 15 July 2009.
This article has been cited by other articles:
Copyright © 2010 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»