Characterization of T and B cell epitopes of a simian retrovirus (SRV-2) envelope protein. NLM AIDSLINE Important note: Information in this article was accurate in 1991. The state of the art may have changed since the publication date.

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Characterization of T and B cell epitopes of a simian retrovirus (SRV-2) envelope protein.

Symp Nonhum Primate Models AIDS. 1990 Nov 28-30;8:60 (abstract no. 44). Unique Identifier : AIDSLINE PRIM8/900044
Malley A; Werner L; Benjamini E; Leung CY; Torres J; Pangares N; Shiigi S; Axthelm M; Oregon Regional Primate Research Center, Beaverton OR


Abstract: Previously, we reported that the insoluble SRV-2 envelope peptide 92-106 represented the epitope involved in the formation of SRV-2 neutralizing antibodies. Soluble SRV-2 peptide 92-99 and peptide 100-106 were prepared and used to further define the epitope responsible for the induction of SRV-2 neutralizing antibody. SRV-2 peptide 100-106 (0.1 to 1.0 mu M) showed a dose independent inhibition of rhesus monkey neutralizing antibody, but the SRV-2 peptide 92-99 did not inhibit neutralization at any concentration tested (0.1 to 4 mu M). The T cell activating properties of SRV-2 peptides were studied by comparing SRV-2 virus and peptide induced proliferation of spleen cells from SRV-2 virus immunized mice. The optimal proliferation of T cells with the SRV-2 virus was obtained with 0.5 mu g of protein/well. T cell proliferation of SRV-2 virus primed spleen cells with unique SRV-2 envelope peptides 92-99 and 100-106 were optimal at 5 and 10 mu g/well, respectively. A peptide 233-239 common to both SRV-1 and SRV-2 also initiated T cell proliferation (optimal stimulation with 10 mu g/well). On the other hand, ovalbumin and a SIV envelope peptide 305-321 did not initiate proliferation of SRV-2 primed T cells. Specificity of the observed T cell proliferation was shown by the failure of the SRV-2 and SIV peptides to initiate proliferation of ovalbumin primed splenic T cells. The immune response of mice immunized with SRV-2 peptide 100-106 conjugated to keyhole limpet hemocyanin and the characterization of anti-peptide 100-106 monoclonal antibodies will be discussed.
Keywords: Animal Antibodies, Monoclonal/IMMUNOLOGY Antibodies, Viral/BIOSYNTHESIS B-Lymphocytes/DRUG EFFECTS/*MICROBIOLOGY Dose-Response Relationship, Drug Epitopes Lymphocyte Transformation/*DRUG EFFECTS Macaca mulatta Neutralization Tests Ovalbumin/PHARMACOLOGY Retroviruses Type D, Simian/DRUG EFFECTS/*IMMUNOLOGY Spleen/DRUG EFFECTS/MICROBIOLOGY T-Lymphocytes/DRUG EFFECTS/*MICROBIOLOGY Viral Envelope Proteins/ADMINISTRATION & DOSAGE/*PHARMACOLOGY ABSTRACTKWDanimalantibodies,monoclonal/immunologyantibodies,viral/biosynthesisb-lymphocytes/drugeffects/KWDmicrobiologydose-responserelationship,drugepitopeslymphocytetransformation/KWDdrugeffectsmacacamulattaneutralizationtestsovalbumin/pharmacologyretrovirusestyped,simian/drugeffects/KWDimmunologyspleen/drugeffects/microbiologyt-lymphocytes/drugeffects/KWDmicrobiologyviralenvelopeproteins/administration&dosage/KWDpharmacologyabstract
910730
M9170950

Copyright © 1991 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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