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The Journal of Immunology, 2004, 172: 1508-1514.
Copyright © 2004 by The American Association of Immunologists

Tumor-Infiltrating Lymphocyte Secretion of IL-6 Antagonizes Tumor-Derived TGF-{beta}1 and Restores the Lymphokine-Activated Killing Activity1

Ya-Wen Hsiao, Kuang-Wen Liao2, Shao-Wen Hung and Rea-Min Chu3

Department of Veterinary Medicine, National Taiwan University, Taipei, Taiwan, Republic of China

IL-6 is a multifunctional cytokine that regulates cell growth, differentiation, and cell survival. Many tumor cells produce TGF-{beta}1, which allows them to evade CTL-mediated immune responses. IL-6 antagonizes TGF-{beta}1 inhibition of CD3 cell activation. However, whether IL-6 restores NK activity, which also is suppressed by TGF-{beta}1, is not known. We used canine transmissible venereal tumor (CTVT), which produces TGF-{beta}1, as a model to determine whether IL-6 restores lymphokine-activated killer (LAK) activity. During the progression phase, CTVT cells stop expressing MHC molecules. During the regression phase, the number of surface MHC molecules increases dramatically on about one-third of tumor cells. Tumor cells that stop expressing MHC should be targeted by NK cells. In this study, we found that TGF-{beta}1 secreted by CTVT cells suppressed LAK cytotoxicity. Interestingly, tumor-infiltrating lymphocytes (TIL) isolated from regressing CTVT secrete high concentrations of IL-6 and antagonize the anti-LAK activity of tumor cell TGF-{beta}1. TIL also produce IL-6 during progression phase, but the concentration is too low to block the anti-LAK activity of TGF-{beta}1. There is probably a threshold concentration of IL-6 needed to reverse TGF-{beta}1-inhibited LAK activity. In addition, in the absence of TGF-{beta}1, IL-6 derived from TIL does not promote the activity of LAK. This new mechanism, in which TIL manufacture high concentrations of IL-6 to block tumor TGF-{beta}1 anti-LAK activity, has potential applications in cancer immunotherapy and tumor prognosis.




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