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New method shortens dendritic cell preparation time.

Vaccine Weekly

| October 23, 2002 | COPYRIGHT 2002 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2002 OCT 23 - (NewsRx.com & NewsRx.net) -- by Maria G. Essig, MS, ELS, senior medical writer - A research team from the University of Antwerp in Belgium have developed a new and faster methods method of generating mature, viable, and highly active CD83+ dendritic cells.

"Dendritic cells are professional antigen-capturing and -presenting cells of the immune system," explained Peter Ponsaerts and his colleagues. "Because of their exceptional capability of activating tumor-specific T cells, cancer vaccination research is now shifting toward the formulation of a clinical human DC vaccine."

The investigators cultured human monocytes in serum-free AIM-V medium and allowed them to mature via polyriboinosinic polyribocytidylic acid (polyI:C) for 24 hours. The resulting DCs exhibited typical mature DC markers and high stimulatory potential. In an influenza model, peptide-pulsed DCs showed a large autologous stimulatory capacity (Messenger RNA electroporation of human monocytes, followed by rapid in vitro differentiation, leads to highly stimulatory antigen-loaded mature dendritic cells. Journal of Immunology, 2002;169(4):1669-1675).

Antigen loading was accomplished by electroporation of mRNA that encoded the enhanced green fluorescent protein (EGFP). After electroporation and a short period of serum-free maturation, the resulting cells showed typical mature DC characteristics and positive EGFP fluorescence. Autologous T cell activation studies demonstrated that ...

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Source: HighBeam Research, New method shortens dendritic cell preparation time.

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