Cancer Research  09 AM Call for Abstracts
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 40, 1125-1129, April 1, 1980]
© 1980 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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Durden, D. L.
Right arrow Articles by Distasio, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Durden, D. L.
Right arrow Articles by Distasio, J. A.

Comparison of the Immunosuppressive Effects of Asparaginases from Escherichia coli and Vibrio succinogenes1

Donald L. Durden and John A. Distasio2

Department of Microbiology D4-4, University of Miami School of Medicine, Miami, Florida 33101

The immunosuppressive effects of antileukemic asparaginases isolated from Escherichia coli and Erwinia carotovora are well documented, but the basis for the immunosuppression is unclear. In addition to catalyzing the deamination of L-asparagine, the E. coli and E. carotovora enzymes also deaminate L-glutamine (glutaminase activity). Many investigators have suggested that this glutaminase activity may be the cause of immunosuppression. The role of glutaminase activity in this immunosuppression has been difficult to evaluate, largely because the lack of a glutaminase-free asparaginase obtainable in significant quantity has precluded any rigorous in vivo experimentation. This laboratory has isolated an asparaginase from Vibrio succinogenes which has potent antilymphoma activity and lacks glutaminase activity. In the present communication, we report the effects of treatment with E. coli and V. succinogenes asparaginases on specialized immune responses in BALB/cCrgl mice.

The immunosuppressive effects of E. coli and V. succinogenes asparaginase on the humoral response of mice during sheep red blood cell (SRBC) immunization were investigated using the plaque-forming cell assay. There was a marked reduction in the number of IgM and IgG plaque-forming cells in the E. coli asparaginase-treated group. No reduction in the plaque-forming cell response was observed in the V. succinogenes asparaginase-treated mice. Levels of antibody against SRBC as determined by hemagglutination were also depressed in E. coli asparaginase-treated mice. Splenocytes isolated from mice immunized with SRBC and simultaneously treated with asparaginase were tested for their capability to serve as effector cells in a direct-target killing assay using 51Cr-labeled SRBC's. At all concentrations tested, the E. coli enzyme significantly suppressed the cytotoxic response of splenocytes, while splenocytes from mice treated with V. succinogenes asparaginase maintained control levels of cytotoxicity. The data provide evidence that a glutaminase-free asparaginase from V. succinogenes does not suppress the in vivo immune response of mice to SRBC as compared to the pronounced immunosuppressive effects observed in mice treated with E. coli asparaginase.

1 Supported by Grants IN-51P and IN-51Q from the American Cancer Society, Grant F79UM-1 from the Florida Division of the American Cancer Society (Jeffrey Frohman Research Grant), and grants from the United Way and the Women's Cancer Association of the University of Miami.

2 To whom requests for reprints should be addressed.

Received 10/15/79. Accepted 1/ 2/80.




This article has been cited by other articles:


Home page
J. Nutr.Home page
P. Bunpo, B. Murray, J. Cundiff, E. Brizius, C. J. Aldrich, and T. G. Anthony
Alanyl-Glutamine Consumption Modifies the Suppressive Effect of L-Asparaginase on Lymphocyte Populations in Mice
J. Nutr., February 1, 2008; 138(2): 338 - 343.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
P. N.-M. Cheng, T.-L. Lam, W.-M. Lam, S.-M. Tsui, A. W.-M. Cheng, W.-H. Lo, and Y.-C. Leung
Pegylated Recombinant Human Arginase (rhArg-peg5,000mw) Inhibits the In vitro and In vivo Proliferation of Human Hepatocellular Carcinoma through Arginine Depletion
Cancer Res., January 1, 2007; 67(1): 309 - 317.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. B. Reinert, L. M. Oberle, S. A. Wek, P. Bunpo, X. P. Wang, I. Mileva, L. O. Goodwin, C. J. Aldrich, D. L. Durden, M. A. McNurlan, et al.
Role of Glutamine Depletion in Directing Tissue-specific Nutrient Stress Responses to L-Asparaginase
J. Biol. Chem., October 20, 2006; 281(42): 31222 - 31233.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
C. M. Ensor, F. W. Holtsberg, J. S. Bomalaski, and M. A. Clark
Pegylated Arginine Deiminase (ADI-SS PEG20,000 mw) Inhibits Human Melanomas and Hepatocellular Carcinomas in Vitro and in Vivo
Cancer Res., October 1, 2002; 62(19): 5443 - 5450.
[Abstract] [Full Text] [PDF]




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 © 1980 by the American Association for Cancer Research.