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The Journal of Immunology, Vol 149, Issue 9 3120-3126, Copyright © 1992 by American Association of Immunologists
ARTICLES |
WC Jones, AL Barnard, A Slade and KH Mills
National Institute for Biological Standards and Control, South Mimms, Potters Bar, Herts, UK.
CD4+ T cell recognition of the simian immunodeficiency virus (SIV) surface envelope (env) glycoprotein was examined by using a panel of 10 T cell lines and 4 T cell clones derived from 10 individual macaques immunized with inactivated SIV or recombinant SIV env proteins. The results demonstrated that CD4+ T cells from each animal recognized between 1 and 7 peptides in 4 distinct regions of the protein including both variable and conserved domains. MLR of PBMC from selected macaques together with RFLP analysis by using the HLA DR beta probes suggested that animals of distinct MHC class II haplotypes can recognize identical peptides. These T cell epitopes within conserved regions of the envelope protein, together with identified linear B cell epitopes recognized by neutralizing antibodies, may be relevant in vaccine design.
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N. Almond, A. Jenkins, S. Jones, C. Arnold, P. Silvera, K. Kent, K. H. G. Mills, and E. J. Stott The appearance of escape variants in vivo does not account for the failure of recombinant envelope vaccines to protect against simian immunodeficiency virus J. Gen. Virol., September 1, 1999; 80(9): 2375 - 2382. [Abstract] [Full Text] |
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