In Vitro Effect of Cyclosporine on Interleukin-2 Receptor Expression Stimulated by Cryptococcus neoformans
In the experiments reported here, the authors found that CsA inhibited proliferative responses of nonimmune controls at doses as low as 5 ng/ml, a level well below the concentration required to inhibit responses to antigens of the major histocompatibility complex. The concentration required to inhib...
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Published in | The Journal of infectious diseases Vol. 155; no. 4; pp. 799 - 802 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
01.04.1987
University of Chicago Press |
Subjects | |
Online Access | Get full text |
ISSN | 0022-1899 1537-6613 |
DOI | 10.1093/infdis/155.4.799 |
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Abstract | In the experiments reported here, the authors found that CsA inhibited proliferative responses of nonimmune controls at doses as low as 5 ng/ml, a level well below the concentration required to inhibit responses to antigens of the major histocompatibility complex. The concentration required to inhibit secondary responses of immune subjects and to inhibit production of IL-2 was higher (30 ng/ml) but still below the typical serum trough concentrations used clinically. In addition to inhibiting IL-2 production, CsA depressed IL-2 receptor expression during in vitro primary responses. |
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AbstractList | In the experiments reported here, the authors found that CsA inhibited proliferative responses of nonimmune controls at doses as low as 5 ng/ml, a level well below the concentration required to inhibit responses to antigens of the major histocompatibility complex. The concentration required to inhibit secondary responses of immune subjects and to inhibit production of IL-2 was higher (30 ng/ml) but still below the typical serum trough concentrations used clinically. In addition to inhibiting IL-2 production, CsA depressed IL-2 receptor expression during in vitro primary responses. |
Author | Miller, G. P. G. Lewis, Dorothy E. |
Author_xml | – sequence: 1 givenname: G. P. G. surname: Miller fullname: Miller, G. P. G. organization: Program in Infectious Diseases and Clinical Microbiology, Department of Medicine, University of Texas Health Science Center at Houston, Houston, Texas – sequence: 2 givenname: Dorothy E. surname: Lewis fullname: Lewis, Dorothy E. organization: Program in Infectious Diseases and Clinical Microbiology, Department of Medicine, University of Texas Health Science Center at Houston, Houston, Texas |
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Keywords | Lymphokine Immunosuppressive agent Interleukin 2 In vitro Biological receptor |
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Notes | istex:DFFC132650EAB3D0556D0DF611159F9E28AD83BB ark:/67375/HXZ-8WLBJ33W-7 Please address requests for reprints to Dr. Geraldine Miller, Program in Infectious Diseases, P.O. Box 20708, Houston, Texas 77030. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
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Snippet | In the experiments reported here, the authors found that CsA inhibited proliferative responses of nonimmune controls at doses as low as 5 ng/ml, a level well... |
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SubjectTerms | Antigens Biological and medical sciences Cell lines Cells, Cultured Concise Laboratory and Clinical Communications Cryptococcosis - immunology Cryptococcus - immunology Cryptococcus neoformans Cryptococcus neoformans - immunology Cultured cells cyclosporin A Cyclosporins Cyclosporins - pharmacology Cytometry Humans Immunomodulators Infectious diseases interleukin-2 Interleukin-2 - biosynthesis Lymphocyte Activation Lymphocytes Medical sciences Messenger RNA Pharmacology. Drug treatments Receptors Receptors, Immunologic - drug effects Receptors, Interleukin-2 T lymphocytes |
Title | In Vitro Effect of Cyclosporine on Interleukin-2 Receptor Expression Stimulated by Cryptococcus neoformans |
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