4.7 Article Proceedings Paper

Complement decay accelerating factor (DAF)/CD55 in cancer

Journal

CANCER IMMUNOLOGY IMMUNOTHERAPY
Volume 55, Issue 8, Pages 987-995

Publisher

SPRINGER
DOI: 10.1007/s00262-006-0136-8

Keywords

EGF-TM7; gamma-IFN; complement; co-stimulation; extracellular matrix

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The complement system is a powerful innate mechanism involved in protection of the host against pathogens. It also has a role in the clearance of apoptotic cells and has been implicated in a range of pathologies including autoimmunity and graft rejection. The control of complement is mediated through the complement regulatory proteins (CRPs). These are present on most cells and protect normal cells from complement-mediated attack during innate activation. However, in a range of pathologies and cancer, these molecules are up or down regulated, sometimes secreted and even lost. We will review the expression of CRPs in cancer, focussing on CD55 and highlight other roles of the CRPs and their involvement in leukocyte function. We will also provide some data providing a potential mechanism by which soluble CD55 can inhibit T-cell function and discuss some of the implications of this data.

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