z-logo
open-access-imgOpen Access
CTLA-4 expressed by human dendritic cells modulates thei cytokine secretion and induction of T cell proliferation
Author(s) -
Stefania Laurent,
Paolo Carrega,
Danièle Saverino,
Patrizia Piccioli,
M. Camoriamo,
Anna Morabito,
Béatrice Dozin,
Vanessa Fontana,
Rita Simone,
Lorenzo Mortara,
M. C. Mingari,
Guido Ferlazzo,
Maria Pia Pistillo
Publication year - 2011
Publication title -
journal of biological research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.218
H-Index - 6
eISSN - 2284-0230
pISSN - 1826-8838
DOI - 10.4081/jbr.2011.4651
Subject(s) - secretion , microbiology and biotechnology , biology , t cell , downregulation and upregulation , ctla 4 , cytokine , immune system , monocyte , cell growth , immunology , endocrinology , gene , biochemistry , genetics

CTLA-4 is the major nefative regulator of T cell response. We have analyzed the expression of CTLA-4 in human monocytes and monocyte-derived DCs and the effects of its engagement on cytokine production and T cell stimulatory activity by mature DCs (mDCs). We found the CTLA-4 was highly expressed on freshly isolated monocytes, then down-modulated on the immature DCs (iDCs) and upregulated on mDCs. Treatment of mDCS with an agonistic anti-CTLA-4 m Ab enhanced secretion of IL-10 but reduced secretion of IL-8 and IL-12, as well as autologous CD4* T-cell proliferation in response to simulation with PPD recall antigenloaded-DCs. Neutralization of IL-10 with an anti-IL-10 antibody partially restored the ability of anti-CTLA-4-treated mDCs to stimulate T cell proliferation in response to PPD. Our data provide the first evidence that CTLA-4 receptor is expressed by human mDCs and exerts immune modulatory effects in these cells.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here