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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Parr, T. B. Baird, S. M. Lotz, M. Kipps, T. J. Watanabe, A. Raz, E. Eisenberg, R. A. Carson, D. A. |
| Description | Author Affiliation: Raz E ( Department of Medicine, University of California, San Diego, La Jolla 92093-0663.); |
| Abstract | Somatic gene therapy is an interesting approach for the delivery of cytokines for prolonged periods. The present experiments show that direct injections into mouse skeletal muscle of cDNA expression vectors encoding interleukin 2 (IL-2), IL-4, or type beta 1 transforming growth factor (TGF-beta 1) induce biological effects characteristic of these cytokines in vivo. Mice injected intramuscularly with a vector encoding IL-2 had enhanced humoral and cellular immune responses to an exogenous antigen, transferrin, that was delivered at a separate site. These IL-2 effects were abolished by coadministration of a vector directing synthesis of TGF-beta 1. The TGF-beta 1 vector by itself depressed the anti-transferrin antibody response and caused an 8-fold increase in plasma TGF-beta 1 activity. The TGF-beta 1 plasmid injection did not cause muscle infiltration with monocytes or neutrophils and there was no evidence for fibrotic changes. Muscle injection with a cDNA encoding IL-4 selectively increased IgG1 levels but did not alter the cellular immune response to transferrin. In lupus-prone mice (MRL/lpr/lpr), injection with IL-2 expression vectors increased and TGF-beta 1 vectors decreased auto-antibodies to chromatin. These results demonstrate that intramuscular injection of cytokine genes, in the absence of infectious viral vectors, can regulate humoral and cellular immune responses in vivo. |
| ISSN | 00278424 |
| e-ISSN | 10916490 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Issue Number | 10 |
| Volume Number | 90 |
| Language | English |
| Publisher | National Academy of Sciences |
| Publisher Date | 1993-07-01 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Cytokines Genetics Muscles Physiology Transfection Animals Antibody Formation Autoantibodies Biosynthesis Gene Expression Hypersensitivity, Delayed Immunology Immunoglobulin G Metabolism Injections, Intramuscular Lymphoproliferative Disorders Mice Mice, Inbred BALB C Mice, Mutant Strains Transforming Growth Factor Beta Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Multidisciplinary |
| Content Type | Text |
| Resource Type | Article |
| Subject | Multidisciplinary |
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