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Departments of Biochemistry and Surgery, The University of Texas Health Science Center, Houston, Texas 77030, and The University of Texas Science Park, Smithville, Texas 78957 [J. P. A.]
Extracts of viable 3-methylcholanthrene-induced murine sarcoma cells (MCA-F and MCA-2A) prepared using single-phase (2.5%) 1-butanol significantly retarded the outgrowth of the homotypic, but not the heterotypic, tumor of syngeneic C3H/HeJ mice. Butanol extracts specifically evoked a delayed hypersensitivity response in tumor-immune syngeneic mice, but not in alloimmune DBA/2J mice. Crude butanol extracts of MCA-F cells did not contain alloantigenic activity, as shown by their inability to block H-2 or la-specific antibodies in a complement-dependent cytotoxicity assay. Absorption of these same allospecific reagents with untreated or with butanol-extracted cells indicated that H-2 antigens remain associated with the cell surface during extraction. Thus, butanol appears to release tumor antigens, but not alloantigens, from the cell surface.
1 This work was supported by American Cancer Society Grant IM-62-F and by USPHS Grant CA-26321, awarded by the National Cancer Institute, Department of Health and Human Services.
2 Recipient of a National Research Service Award CA-06326 from the National Cancer Institute, Department of Health and Human Services. To whom requests for reprints should be addressed.
Received 4/13/81. Accepted 7/14/81.
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