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Journal of General Virology, Vol 80, 1609-1615, Copyright © 1999 by Society for General Microbiology
ARTICLES |
J Marttila, J Ilonen, E Norrby and A Salmi
Turku Immunology Centre and Department of Virology, University of Turku, Kiinamyllynkatu 13, FIN-20520 Turku, Finland
T cell epitopes of the measles virus (MV) nucleoprotein were studied by synthesizing overlapping 20 aa peptides over the known sequence of the protein and analysing the proliferation responses of a panel of MV-specific T cell lines and clones against these peptides. T cell lines were established from eleven healthy controls and seven multiple sclerosis patients, all with a history of past MV infection. The epitopes recognized by these lines were concentrated in a few regions of the polypeptide chain. Overlapping peptides containing aa 321--340 and 331--350 were most often recognized. Other epitopes were detected close to the amino-terminal end of the polypeptide chain as each of the peptides 1--20, 21--40, 31--50 and 51--70 contained stimulating moieties. Some responses were also detected towards peptides 151--200 and 221--250, but the carboxy-terminal end of the polypeptide was not recognized by any of the tested T cell lines. The amino acid sequences of the peptides that stimulated the T cell clones and lines, as a rule, contained binding motifs described for HLA-DR alleles found in T cell donors. The regions of protein sequence which did not reveal any T cell epitopes were, instead, relatively free of binding motifs. The results suggest that only a few epitopes of the MV nucleoprotein are important in establishing T cell immunity.
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