Cancer Research AACR Conference on Molecular Diagnostics - 2008  Tumor Immunology: New Perspectives
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[Cancer Research 41, 1451-1459, April 1, 1981]
© 1981 American Association for Cancer Research

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Use of Monoclonal Antibodies to Define the Diversity of Mammary Tumor Viral Gene Products in Virions and Mammary Tumors of the Genus Mus1

D. Colcher, P. Horan Hand, Y. A. Teramoto, D. Wunderlich and J. Schlom2

Laboratory of Cellular and Molecular Biology, National Cancer Institute, NIH, Bethesda, Maryland 20205

Monoclonal antibodies have been generated against disrupted mammary tumor viruses isolated from Mus musculus, Mus cervicolor, and Mus cookii. Monoclonal antibodies directed against the M.W. 36,000 external glycoproteins of these viruses demonstrate the presence of multiple epitopes, i.e., distinct antigenic determinants, within these glycoproteins. These epitopes represent type, group, and interspecies determinants. Monoclonal antibodies have also been used to define multiple epitopes on the M.W. 28,000 major internal polypeptides of murine mammary tumor viruses that exhibit both type- and group-specific determinants. The monoclonal antibodies to the M.W. 36,000 glycoprotein and the M.W. 28,000 polypeptide have been used to distinguish all six mammary tumor virus isolates of M. musculus from each other, including both endogenous and exogenous viruses from the same strain, and a new virus isolate from BALB/c mice. With the use of the immunoperoxidase technique, the monoclonal antibodies generated have been used to demonstrate a heterogeneity of expression of mammary tumor virus gene products in primary mammary tumors of three Mus species. These studies have revealed that a given antigenic determinant may be expressed differentially in mammary tumors of two different Mus species, among mammary tumors of the same Mus species, and, at times, in different areas of the same mammary tumor.

1 These studies were supported in part by Contract NO1-CP-01018 from the National Cancer Institute.

2 To whom requests for reprints should be addressed.

Received 10/ 1/80. Accepted 1/13/81.







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Molecular Cancer Research Cancer Prevention Research
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Copyright © 1981 by the American Association for Cancer Research.