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Human Thymic Stromal Lymphopoietin Preferentially Stimulates Myeloid Cells
Author(s) -
Pedro A. Reche,
Vassili Soumelis,
Daniel M. Gorman,
Teresa Clifford,
Man-Ru Liu,
Marilyn Travis,
Sandra Zurawski,
Jim Johnston,
Yong-Jun Liu,
Hergen Spits,
René de Waal Malefyt,
Robert A. Kastelein,
J. Fernando Bazán
Publication year - 2001
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.167.1.336
Subject(s) - thymic stromal lymphopoietin , cd80 , biology , microbiology and biotechnology , chemokine , cytokine , cd11c , immunology , cd40 , immune system , cytotoxic t cell , genetics , in vitro , phenotype , gene
The sequence of a novel hemopoietic cytokine was discovered in a computational screen of genomic databases, and its homology to mouse thymic stromal lymphopoietin (TSLP) suggests that it is the human orthologue. Human TSLP is proposed to signal through a heterodimeric receptor complex that consists of a new member of the hemopoietin family termed human TSLP receptor and the IL-7R alpha-chain. Cells transfected with both receptor subunits proliferated in response to purified, recombinant human TSLP, with induced phosphorylation of Stat3 and Stat5. Human TSLPR and IL-7Ralpha are principally coexpressed on monocytes and dendritic cell populations and to a much lesser extent on various lymphoid cells. In accord, we find that human TSLP functions mainly on myeloid cells; it induces the release of T cell-attracting chemokines from monocytes and, in particular, enhances the maturation of CD11c(+) dendritic cells, as evidenced by the strong induction of the costimulatory molecules CD40 and CD80 and the enhanced capacity to elicit proliferation of naive T cells.

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