Abstract: |
A tumor-specific antigen (TSA) expressed on the chemically induced BALB/c Meth A sarcoma and one of 22 other BALB/c sarcomas tested, CMS 13, was detected in in vitro cellular and humoral assays. The distribution pattern of the TSA defined in a complement-dependent microcytoxicity assay by cytotoxic antibodies present in CMS13 antisera was similar to that detected by a cytotoxic T-cell clone, designated CTLL-MA10B, in an 18-h cell-mediated cytotoxicity assay. The serologically defined TSA was shown to be expressed on gp96, a M, 96,000 glycoprotein isolated from Meth A cytosol with immunoprotective activity in in vivo tumor rejection assays. Immunization of BALB/c mice with Meth A, CMS 13, or preparations of gp96 isolated from these sarcomas induced tumor resistance in these mice to Meth A and CMS13 but not CMS5, an antigenically unrelated sarcoma. These results suggest that the shared TSA is expressed on gp96 and is functional in tumor rejection assays. © 1987, American Association for Cancer Research. All rights reserved. |
Keywords: |
nonhuman; mouse; animal; mice; animal experiment; tumor antigen; mice, inbred balb c; sarcoma; antibodies, monoclonal; antigens, neoplasm; cytotoxic t lymphocyte; t-lymphocytes, cytotoxic; tumor immunity; cytotoxicity, immunologic; glycoprotein; therapy; interleukin-2; immunization; sarcoma, experimental; immune sera; cross reactions; h-2 antigens; female; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; blood and hemopoietic system; cell strain meth a
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