Cancer Research CTRC-AACR San Antonio Breast Cancer Symposium
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

[Cancer Research 31, 1383-1388, October 1, 1971]
© 1971 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Glynn, J. P.
Right arrow Articles by Kende, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Glynn, J. P.
Right arrow Articles by Kende, M.

Treatment of Moloney Virus-induced Leukemia with Cyclophosphamide and Specificially Sensitized Allogeneic Cells1

John P. Glynn2 and Meir Kende

Drug Evaluation Branch, Drug Research and Development, Chemotherapy, National Cancer Institute [J. P. G.], and Microbiological Associates, Inc. [M. K.], Bethesda, Maryland 20014

Allogeneic but H-2-compatible spleen cells (DBA/2) were used in conjunction with cyclophosphamide in the treatment of transplantable Moloney virus-induced leukemia of BALB/c mice. Treatment was withheld to within 2 to 6 days of the median survival time of the untreated controls. Cyclophosphamide therapy was followed within 4 to 6 hr by DBA/2 spleen cells either from animals sensitized to Moloney sarcoma virus, C57BL spleen cells, or BALB/c spleen cells or from nonsensitized animals. With Moloney sarcoma virus-sensitized cells, 44/69 animals were long-term survivors, whereas no survivors were obtained with other forms of therapy. All the survivors were stable chimeras as judged by the persistent production of DBA/2 {gamma}-globulin allotype.

1 Supported in part by Contract PH-43-68-1283 with Microbiological Associates, Inc.

2 Deceased May 7, 1971. Direct reprint requests to M. Kende, Microbiological Associates, Inc., Bethesda Md. 20014.

Received 1/21/71. Accepted 5/20/71.







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 © 1971 by the American Association for Cancer Research.