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Production of transforming growth factor beta by human T lymphocytes and its potential role in the regulation of T cell growth.

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TLDR
TGF-beta may be an important antigen-nonspecific regulator of human T cell proliferation, and important in T cell interaction with other cell types whose cellular functions are modulated by TGF- beta.
Abstract
This study examines the potential role of transforming growth factor beta (TGF-beta) in the regulation of human T lymphocyte proliferation, and proposes that TGF-beta is an important autoregulatory lymphokine that limits T lymphocyte clonal expansion, and that TGF-beta production by T lymphocytes is important in T cell interactions with other cell types. TGF-beta was shown to inhibit IL-2-dependent T cell proliferation. The addition of picograms amounts of TGF-beta to cultures of IL-2-stimulated human T lymphocytes suppressed DNA synthesis by 60-80%. A potential mechanism of this inhibition was found. TGF-beta inhibited IL-2-induced upregulation of the IL-2 and transferrin receptors. Specific high-affinity receptors for TGF-beta were found both on resting and activated T cells. Cellular activation was shown to result in a five- to sixfold increase in the number of TGF-beta receptors on a per cell basis, without a change in the affinity of the receptor. Finally, the observations that activated T cells produce TGF-beta mRNA and that TGF-beta biologic activity is present in supernatants conditioned by activated T cells is strong evidence that T cells themselves are a source of TGF-beta. Resting T cells were found to have low to undetectable levels of TGF-beta mRNA, while PHA activation resulted in a rapid increase in TGF-beta mRNA levels (within 2 h). Both T4 and T8 lymphocytes were found to make mRNA for TGF-beta upon activation. Using both a soft agar assay and a competitive binding assay, TGF-beta biologic activity was found in supernatants conditioned by T cells; T cell activation resulted in a 10-50-fold increase in TGF-beta production. Thus, TGF-beta may be an important antigen-nonspecific regulator of human T cell proliferation, and important in T cell interaction with other cell types whose cellular functions are modulated by TGF-beta.

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REGULATION OF IMMUNE RESPONSES BY TGF-β*

TL;DR: The accumulated knowledge gained through extensive in vitro functional analyses and from in vivo animal models supports the concept that clinical therapies based on modulation of this cytokine represent an important new approach to the treatment of disorders of immune function.
References
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Journal ArticleDOI

Biological activity of recombinant human interleukin-2 produced in Escherichia coli

TL;DR: The recombinant lymphokine supports the growth of murine and human interleukin-2 dependent cell lines, enhances the generation of cytolytic cells in vitro and in vivo after alloimmunization, and generates lymphokin activated killer cells from murineand human lymphocytes.
Journal ArticleDOI

Transient expression of interleukin 2 receptors. Consequences for T cell growth.

TL;DR: The awareness of the transience and the antigen/lectin dependence of IL-2 receptor expression, together with the capacity to monitor T cell cultures for IL- 2 receptor levels, should facilitate the initiation and maintenance of cloned, antigen-specific T cells in long-term culture.
Journal Article

Effects of transforming growth factor beta on the functions of natural killer cells: depressed cytolytic activity and blunting of interferon responsiveness.

TL;DR: Results indicate that in addition to inhibitory effects on T and B cells, TGF-beta also inhibits NK cell function.
Journal ArticleDOI

Triggering of the T3-Ti antigen-receptor complex results in clonal T-cell proliferation through an interleukin 2-dependent autocrine pathway

TL;DR: The findings demonstrate that antigen-induced proliferation is mediated through an autocrine pathway involving endogenous IL-2 production, release, and subsequent binding to IL-3-Ti receptor cross-linking.
Journal ArticleDOI

Characterization of a membrane receptor for transforming growth factor-beta in normal rat kidney fibroblasts.

TL;DR: A procedure has been developed for the iodination of human transforming growth factor-beta (TGF-beta) with full retention of biological activity using the iodinated peptide, saturable receptors have been found on normal rat kidney fibroblasts, a cell line that will grow in soft agar in the presence of TGFs but not in their absence.
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