Antihelminthic niclosamide modulates dendritic cells activation and function

•Effect of niclosamide on the activation of LPS-stimulated BMDCs was investigated.•Niclosamide decreased ability to stimulate antigen specific T cell proliferation.•Niclosamide attenuated hapten induced contact hypersensitivity (CHS) in vivo.•Blocking the MAPK and NF-κB contribute to the inhibitory...

Full description

Saved in:
Bibliographic Details
Published inCellular immunology Vol. 288; no. 1-2; pp. 15 - 23
Main Authors Wu, Chieh-Shan, Li, Yi-Rong, Chen, Jeremy J.W., Chen, Ying-Che, Chu, Chiang-Liang, Pan, I-Hong, Wu, Yu-Shan, Lin, Chi-Chen
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.03.2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•Effect of niclosamide on the activation of LPS-stimulated BMDCs was investigated.•Niclosamide decreased ability to stimulate antigen specific T cell proliferation.•Niclosamide attenuated hapten induced contact hypersensitivity (CHS) in vivo.•Blocking the MAPK and NF-κB contribute to the inhibitory effect of niclosamide. Dendritic cells (DCs) link the sensing of the environment by the innate immune system to the initiation of adaptive immune responses. Accordingly, DCs are considered to be a major target in the development of immunomodulating compounds. In this study, the effect of niclosamide, a Food and Drug Administration-approved antihelminthic drug, on the activation of lipopolysaccharide (LPS)-stimulated murine bone marrow-derived DCs was examined. Our experimental results show that niclosamide reduced the pro-inflammatory cytokine and chemokine expression of LPS-activated DCs. In addition, niclosamide also affected the expression of MHC and costimulatory molecules and influenced the ability of the cells to take up antigens. Therefore, in mixed cell cultures composed of syngeneic OVA-specific T cells and DCs, niclosamide-treated DCs showed a decreased ability to stimulate T cell proliferation and IFN-γ production. Furthermore, intravenous injection of niclosamide also attenuated contact hypersensitivity (CHS) in mice during sensitization with 2,4-dinitro-1-fluorobenzene. Blocking the LPS-induced activation of MAPK-ERK, JNK and NF-κB may contribute to the inhibitory effect of niclosamide on DC activation. Collectively, our findings suggest that niclosamide can manipulate the function of DCs. These results provide new insight into the immunopharmacological role of niclosamide and suggest that it may be useful for the treatment of chronic inflammatory disorders or DC-mediated autoimmune diseases.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0008-8749
1090-2163
1090-2163
DOI:10.1016/j.cellimm.2013.12.006