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Extracorporeal Photopheresis Promotes IL-1β Production
Author(s) -
Erhan Yakut,
Christopher Jakobs,
Adriana Peric,
Gabriela Michel,
Nelli Baal,
Gregor Bein,
Bernhard Brüne,
Veit Hornung,
Holger Hackstein
Publication year - 2015
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1400694
Subject(s) - extracorporeal photopheresis , leukapheresis , photopheresis , immunology , medicine , inflammasome , cytokine , immune system , cutaneous t cell lymphoma , context (archaeology) , dendritic cell , biology , lymphoma , transplantation , graft versus host disease , microbiology and biotechnology , mycosis fungoides , cd34 , inflammation , stem cell , paleontology
Extracorporeal photopheresis (ECP) is a widely used clinical cell-based therapy exhibiting efficacy in heterogenous immune-mediated diseases such as cutaneous T cell lymphoma, graft-versus-host disease, and organ allograft rejection. Despite its documented efficacy in cancer immunotherapy, little is known regarding the induction of immunostimulatory mediators by ECP. In this article, we show that ECP promotes marked release of the prototypic immunostimulatory cytokine IL-1β. ECP primes IL-1β production and activates IL-1β maturation and release in the context of caspase-1 activation in monocytes and myeloid dendritic cells. Of interest, IL-1β maturation by ECP was fully intact in murine cells deficient in caspase-1, suggesting the predominance of an inflammasome-independent pathway for ECP-dependent IL-1β maturation. Clinically, patient analysis revealed significantly increased IL-1β production in stimulated leukapheresis concentrates and peripheral blood samples after ECP. Collectively, these results provide evidence for promotion of IL-1β production by ECP and offer new insight into the immunostimulatory capacity of ECP.

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