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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-3-14
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pubmed:abstractText |
Murine anti-reovirus cytotoxic T lymphocytes (CTLs) were analyzed for H-2 restricted recognition of virus infected target cells and for potential cross-reactivity with cells infected by reovirus serotype 1 (T1; Lang strain) or by serotype 3 (T3; Dearing strain). Anti-reovirus CTL specifically lysed virus infected cells and lysis was shown to be H-2 restricted by the H-2Dd, H-2Ld, H-2Kd, H-2Kb, and H-2Kk antigens. No H-2 antigens were identified which failed to restrict virus recognition by anti-reovirus CTL. Anti-T1 and anti-T3 CTLs were also shown to crossreact completely with cells infected with the opposite virus serotype. Thus, anti-reovirus CTLs are restricted by a broad spectrum of H-2 antigens and they detect common rather than unique structural components of these two viral serotypes.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0882-8245
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
77-87
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2297393-Animals,
pubmed-meshheading:2297393-Cell Line, Transformed,
pubmed-meshheading:2297393-Chromium Radioisotopes,
pubmed-meshheading:2297393-Cross Reactions,
pubmed-meshheading:2297393-Cytotoxicity, Immunologic,
pubmed-meshheading:2297393-Female,
pubmed-meshheading:2297393-H-2 Antigens,
pubmed-meshheading:2297393-Male,
pubmed-meshheading:2297393-Mice,
pubmed-meshheading:2297393-Mice, Inbred BALB C,
pubmed-meshheading:2297393-Mice, Inbred C57BL,
pubmed-meshheading:2297393-Reoviridae
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pubmed:year |
1990
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pubmed:articleTitle |
H-2 restriction and serotype crossreactivity of anti-reovirus cytotoxic T lymphocytes (CTL).
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pubmed:affiliation |
Department of Immunology, Scripps Clinic and Research Foundation, La Jolla, CA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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