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TCR- and IL-1-mediated co-stimulation reveals an IL-4-independent way of Th2 cell proliferation
Author(s) -
Magdalena Huber,
Andreas Rutherford,
Wolfgang Meister,
Angela Weiss,
Martin Röllinghotf,
Michael Lohoff,
Klaus Eichmann
Publication year - 1996
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/8.8.1257
Subject(s) - clone (java method) , t cell receptor , cell growth , t cell , biology , microbiology and biotechnology , interleukin 4 , interleukin 2 , in vitro , chemistry , immunology , cytokine , gene , biochemistry , immune system
Previously, it has been shown that Th1 cells, when triggered solely via their TCR, are blocked from proliferation in response to IL-2. Herein, we describe a similar characteristic for Th2 cells in that immobilized mAb directed to the TCR blocked proliferation of Th2 cells in response to IL-4. This "proliferative block' was observed in all four Th2 cell clones tested, but not in a subline of one of the clones which has been cultured in vitro for several years. Addition of IL-1 neutralized the proliferative block in all four Th2 cell clones. Surprisingly, blocking experiments with sIL-4R and anti-IL-4 mAb revealed that in three out of four Th2 cell clones this effect of IL-1 was IL-4-independent and could also not be blocked by cyclosporin A (CsA). In contrast, the proliferation of one Th2 cell clone in response to the TCR- and IL-1-mediated signals was indeed inhibited by sIL-4R, anti-IL-4 mAb and CsA. Thus, our data illustrate that in addition to the well-known IL-4-dependent proliferation, there also exists an IL-4-independent, IL-1-mediated way of Th2 cell proliferation.

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