IMMUNOREGULATORY ROLE OF TRANSFORMING GROWTH-FACTOR-BETA (TGF-BETA) IN DEVELOPMENT OF KILLER-CELLS - COMPARISON OF ACTIVE AND LATENT TGF-BETA-1

被引:146
作者
WALLICK, SC
FIGARI, IS
MORRIS, RE
LEVINSON, AD
PALLADINO, MA
机构
[1] GENENTECH INC, DEPT CELL GENET, SAN FRANCISCO, CA 94080 USA
[2] STANFORD UNIV, MED CTR, DEPT CARDIOVASC SURG, TRANSPLANTAT IMMUNOL, STANFORD, CA 94305 USA
关键词
D O I
10.1084/jem.172.6.1777
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Using recombinant DNA technology, we have generated Chinese hamster ovary (CHO) cell lines that synthesize latent transforming growth factor β1 (TGF-β1) to study immune regulation by TGF-β1. In vitro, latent TGF-β1 synthesized by transfectants or added exogenously as a purified complex after activation inhibited CTL generation to a similar extent as seen with acid-activated recombinant human (rHu) TGF-β1. In vivo, serum from nu/nu mice bearing CHO/TGF-β1 tumors contained significant levels of latent TGF-β1 in addition to depressed natural killer (NK) activity in spleens which paralleled that seen in C3H/HeJ mice treated with acid-activated rHuTGF-β1. rHuTGF-β1 treatment of mice receiving heart allografts resulted in significant enhancement of organ graft survival. Because of possible regulated tissue-specific activation, administration oflatent rather than active TGF-β may provide a better route to deliver this powerful immunosuppressive agent in vivo. © 1990, Rockefeller University Press., All rights reserved.
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页码:1777 / 1784
页数:8
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