Source:http://linkedlifedata.com/resource/pubmed/id/14522934
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
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pubmed:dateCreated |
2003-10-2
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pubmed:abstractText |
We investigate here whether P1A, which was the first CTL-recognized and unmutated tumor antigen to be identified, is a tumor rejection antigen for J558 plasmacytoma in mice with an unperturbed T-cell repertoire. We show that although transgenic mice expressing P1A in the thymus have almost complete deletion of P1A-reactive T cells, they reject the B7-1-transfected J558 at a rate comparable with wild-type mice. Thus, P1A is not a necessary tumor rejection antigen for the J558 tumor cells. On the other hand, if anti-P1A CTL response is sufficient for tumor rejection, tumor cells must lose the antigenic epitope to evade CTL destruction. To test this, we analyze whether tumor cells escaping J558-B7 immune spleen cells harbor mutations in the P1A epitope. We find that although the spleen contained a high proportion of P1A-reactive T cells, the recurrent tumor cells have no mutation in the P1A antigenic epitope and remain susceptible to lysis by P1CTL. Thus, the antigen-bearing tumor cells can evade immune destruction in the presence of a high number of P1A-reactive T cells. Taken together, our results demonstrate that in mice with a normal TCR repertoire, substantial numbers of P1A-reactive T cells are neither necessary nor sufficient for tumor rejection and raise interesting questions regarding the significance of T-cell response against unmutated tumor antigens.
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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:month |
Sep
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pubmed:issn |
0008-5472
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
63
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6051-5
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:14522934-Animals,
pubmed-meshheading:14522934-Antigens, Neoplasm,
pubmed-meshheading:14522934-Epitopes, T-Lymphocyte,
pubmed-meshheading:14522934-Immune Tolerance,
pubmed-meshheading:14522934-Lymphocyte Activation,
pubmed-meshheading:14522934-Mice,
pubmed-meshheading:14522934-Mice, Inbred BALB C,
pubmed-meshheading:14522934-Mice, Transgenic,
pubmed-meshheading:14522934-Neoplasms, Experimental,
pubmed-meshheading:14522934-T-Lymphocytes,
pubmed-meshheading:14522934-Transfection
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pubmed:year |
2003
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pubmed:articleTitle |
On the role of unmutated antigens in tumor rejection in mice with unperturbed T-cell repertoires.
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pubmed:affiliation |
Division of Cancer Immunology, Department of Pathology, Ohio State University Medical Center, Columbus, Ohio 43210, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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