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[Cancer Research 35, 164-171, January 1, 1975]
© 1975 American Association for Cancer Research

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Assessment of Reactivities of Natural Antibodies to Endogenous RNA Tumor Virus Envelope Antigens and Virus-induced Cell Surface Antigens1

M. G. Hanna, Jr., James N. Ihle, Barry L. Batzing2, Raymond W. Tennant and Cynthia K. Schenley

Carcinogenesis Program, Biology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830

The autogenous humoral immune response of mice to their endogenous leukemia virus (MuLV) has been examined with respect to the reactivities of natural antibodies to MuLV envelope antigens and virus-induced cell surface antigens. The natural reactivity of MuLV envelope antigens was evaluated by means of a radioimmune precipitation assay of intact and disrupted virus, as well as by virus neutralization tests. The specificity of natural antibody for MuLV envelope antigens was determined by immunoelectron microscopy and radioimmune precipitation. Antibody reactivity to virus-induced cell-surface antigens was evaluated by immunoelectron microscopy and a complement-dependent cytotoxicity test. The strains of mice selected for study were C57BL/6, C3H/Anf, and the C57BL/6 x C3H/Anf F1 hybrid. Although there were quantitative differences in the antibody levels among these various strains, the naturally recognized antigenic determinants of the virus were consistent, i.e., gp68, gp43, and p15. High levels of neutralizing antibody against the xenotropic BALB:virus-2 were detected in these various normal sera with the focus reduction assay; however, only marginal levels of neutralizing activity against Moloney leukemia virus were detected with the XC virus assay. No anticellular antibody could be detected in these normal sera with the complement-dependent cytotoxicity assay.

1 Research supported jointly by the Carcinogenesis Program of the National Cancer Institute and by the United States Atomic Energy Commission under contract with Union Carbide Corporation. One of a series of papers on autogenous immunity to endogenous tumor virus.

2 Postdoctoral investigator, University of Tennessee-Oak Ridge Graduate School of Biomedical Sciences, Oak Ridge, Tenn. 37830. Present address: State University of New York, Cortland, N. Y. 13045.

Received 7/18/74. Accepted 9/24/74.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1975 by the American Association for Cancer Research.