| Literature DB >> 22289890 |
Douglas W McMillin1, Jake Delmore, Joseph M Negri, Matthew Vanneman, Shohei Koyama, Robert L Schlossman, Nikhil C Munshi, Jacob Laubach, Paul G Richardson, Glenn Dranoff, Kenneth C Anderson, Constantine S Mitsiades.
Abstract
Conventional assays evaluating antitumor activity of immune effector cells have limitations that preclude their high-throughput application. We adapted the recently developed Compartment-Specific Bioluminescence Imaging (CS-BLI) technique to perform high-throughput quantification of innate antitumor activity and to show how pharmacologic agents (eg, lenalidomide, pomalidomide, bortezomib, and dexamethasone) and autologous BM stromal cells modulate that activity. CS-BLI-based screening allowed us to identify agents that enhance or inhibit innate antitumor cytotoxicity. Specifically, we identified compounds that stimulate immune effector cells against some tumor targets but suppressed their activity against other tumor cells. CS-BLI offers rapid, simplified, and specific evaluation of multiple conditions, including drug treatments and/or cocultures with stromal cells and highlights that immunomodulatory pharmacologic responses can be heterogeneous across different types of tumor cells. This study provides a framework to identify novel immunomodulatory agents and to prioritize compounds for clinical development on the basis of their effect on antitumor immunity.Entities:
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Year: 2012 PMID: 22289890 PMCID: PMC3325048 DOI: 10.1182/blood-2011-04-348490
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113