Delineation of canine parvovirus T cell epitopes with peripheral blood mononuclear cells and T cell clones from immunized dogs

1 Laboratory of Immunobiology, National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven 2 Central Veterinary Institute, P.O. Box 65, Lelystad, The Netherlands and 3 Department of Microbiology, Colorado State University, Fort Collins, Colorado 80523, U.S.A. Thre...

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Veröffentlicht in:Journal of general virology 1990-10, Vol.71 (10), p.2321-2329
Hauptverfasser: Rimmelzwaan, G.F, Poelen, M.C.M, Meloen, R.H, Carlson, J, Uytde-Haag, F.G.C.M, Osterhaus, A.D.M.E
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Sprache:eng
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Zusammenfassung:1 Laboratory of Immunobiology, National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven 2 Central Veterinary Institute, P.O. Box 65, Lelystad, The Netherlands and 3 Department of Microbiology, Colorado State University, Fort Collins, Colorado 80523, U.S.A. Three synthetic peptides derived from the amino acid sequence of VP 2 of canine parvovirus (CPV) which were recently shown to represent three distinct T cell epitopes for BALB/c mice could prime BALB/c mice for a CPV-specific proliferative T cell response upon immunization. Proliferative responses of peripheral blood mononuclear cells (PBMC) from CPV-immunized dogs upon stimulation with these and other peptides, covering the major part of the sequence of VP 2 ', identified the presence of T cell epitopes for this species. Most of these epitopes were recognized by PBMC from only a minority of the dogs tested. With three newly generated canine Thyl + T cell clones, which recognized CPV antigen in association with major histocompatibility complex class II molecules, two distinct T cell epitopes were identified within the unique sequence of VP 1 . Received 16 March 1990; accepted 28 June 1990.
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-71-10-2321