Using a molecular switch to turn on cancer vaccines
In this paper, David Spencer and colleagues, of Baylor University in Houston, Texas, addressed this problem by looking to the adaptor molecule downstream of the TLR, MyD88. They engineered a form of MyD88 that could induce downstream signaling in response to a drug, and expressed this inducible MyD88 (iMyD88) in DCs. Further, the researchers combined iMyD88 with a second pathway required for optimal activation of DCs- CD40 signaling- so that they could control both pathways with administration of a single drug. This combination improved DC-mediated tumor antigen-specific T cell responses in mouse cancer models and T cell responses to human tumor antigens. The researchers hope that this "switch" might be broadly applicable to the design of DC vaccines.
INFORMATION:
TITLE:
A composite MyD88/CD40 "switch" synergistically activates mouse and human dendritic cells for enhanced antitumor efficacy
AUTHOR CONTACT:
David Spencer
Baylor College of Medicine, Houston, TX, USA
Phone: 713-798-6475; Fax: 713-798-3033; E-mail: dspencer@bcm.tmc.edu
View this article at: http://www.jci.org/articles/view/44327?key=56347f1f6448c0426b53
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