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INFLUENZA-VIRUS INFECTION ELICITS CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX-RESTRICTED T-CELLS SPECIFIC FOR AN EPITOPE IDENTIFIED IN THE NS1 NONSTRUCTURAL PROTEIN
被引:12
作者:
HACKETT, CJ
HOROWITZ, D
WYSOCKA, M
DILLON, SB
机构:
[1] WISTAR INST, PHILADELPHIA, PA 19104 USA
[2] SMITHKLINE BEECHAM PHARMACEUT, KING OF PRUSSIA, PA 19406 USA
关键词:
D O I:
10.1099/0022-1317-73-6-1339
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
A T cell epitope of the influenza virus NS1 molecule was identified and shown to be a determinant used in class II major histocompatibility complex-restricted T cell responses to infectious virus. An I-E(d)-restricted BALB/c mouse T hybridoma clone recognizing influenza virus A/Puerto Rico/8/34 (PR8; subtype H1N1) but not A/Udorn/72 (subtype H3N2) secreted lymphokines in response to purified recombinant NS1 or fusion proteins containing amino acids 1 to 81 or 1 to 42 of NS1. As expected for recognition of a non-virion protein, the clone failed to respond to u.v.-inactivated virus. The antigenic determinant was localized by synthetic peptides to amino acids 13 to 32 of NS1, explaining the lack of recognition of A/Udorn/72 virus which has an alanine to valine substitution at position 23 within the determinant. A single intranasal dose of infectious PR8 virus was found to elicit T cells that responded to peptide NS1 13-32, suggesting that this determinant is a significant target of T cells in normal infections. To stimulate helper T cell responses similar to those achieved with infectious virus, influenza virus vaccines may therefore have to include NS1 in addition to virion components.
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页码:1339 / 1343
页数:5
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