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A clinical grade cocktail of cytokines and PGE2 results in uniform maturation of human monocyte-derived dendritic cells: implications for immunotherapy
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY, USA.
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY , USA.
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY, USA.
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY, USA.
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2002 (English)In: Vaccine, ISSN 0264-410X, E-ISSN 1873-2518, Vol. 20, no Suppl. 4, p. A8-A22Article in journal (Refereed) Published
Abstract [en]

Dendritic cells (DCs) can induce tumor- or pathogen-specific T cell responses in humans. We comprehensively compared the clinically available DC maturation stimuli for their ability to promote uniformly mature DCs that elicit higher levels of T cell responses. We compared the standard maturation stimulus, autologous monocyte-conditioned medium (MCM), with a synthetic double stranded RNA (poly I:C), soluble CD40 ligand trimer, and a defined cocktail of cytokines (TNF-α, IL-1β, IL-6) and PGE2 to promote mature phenotype and function in human monocyte-derived DCs. The cocktail was the most efficient despite the lack of induction of IL-12p70. While these results support the use of the MCM-mimic cocktail in clinical DC immunotherapy trials, the roles of it’s individual constituents remain to be completely defined.

Place, publisher, year, edition, pages
Elsevier BV , 2002. Vol. 20, no Suppl. 4, p. A8-A22
Keywords [en]
Dendritic cells, T cell activation, Vaccination, Immunotherapy
National Category
Immunology
Identifiers
URN: urn:nbn:se:liu:diva-202163DOI: 10.1016/s0264-410x(02)00382-1OAI: oai:DiVA.org:liu-202163DiVA, id: diva2:1889314
Available from: 2024-08-15 Created: 2024-08-15 Last updated: 2024-08-15

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Larsson, Marie

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