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Interference of the CD30–CD30L Pathway Reduces Atherosclerosis Development
Author(s) -
Amanda C. Foks,
Ilze Bot,
Vanessa Frodermann,
Saskia C.A. de Jager,
Mariëtte ter Borg,
Peter J. van Santbrink,
Hideo Yagita∥,
Johan Kuiper,
Gijs H.M. van Puijvelde
Publication year - 2012
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.112.300509
Subject(s) - tumor necrosis factor alpha , cd30 , splenocyte , immune system , t cell , biology , cell growth , immunology , endocrinology , medicine , biochemistry , immunohistochemistry
Costimulatory molecules tightly control immune responses by providing positive signals that promote T-cell activation or by transducing inhibitory signals that limit T-cell responses. CD30 and CD30L are members of the tumor necrosis factor receptor superfamily and are involved in the activation and proliferation of T and B cells, which have been implicated in the initiation and progression of atherosclerosis. In the present study, we thus aimed to determine the role of the CD30-CD30L pathway in the development of atherosclerosis.

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