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MONOCLONAL ANTIBODY FACILITY

$98,729P30FY2016CANIH

University Of Tx Md Anderson Can Ctr, Houston TX

Investigators

Linked publications, trials & patents

Trial NCT07407920Trial NCT07349641Trial NCT06651580Trial NCT05681026Trial NCT05223036Trial NCT05078866Trial NCT05057312Trial NCT05054296Trial NCT05044546Trial NCT05023967Trial NCT05011045Trial NCT04875728Trial NCT04870645Trial NCT04810091Trial NCT04751422Trial NCT04740164Trial NCT04668300Trial NCT04615013Trial NCT04505267Trial NCT04484909Trial NCT04483349Trial NCT04481204Trial NCT04474301Trial NCT04458610Trial NCT04447222Trial NCT04435691Trial NCT04430725Trial NCT04407247Trial NCT04373720Trial NCT04317781Trial NCT04311723Trial NCT04310826Trial NCT04310397Trial NCT04265430Trial NCT04257045Trial NCT04256941Trial NCT04239989Trial NCT04239976Trial NCT04239157Trial NCT04236882Trial NCT04228042Trial NCT04220827Trial NCT04220775Trial NCT04220008Trial NCT04219969Trial NCT04219904Trial NCT04216732Trial NCT04216563Trial NCT04216524Trial NCT04216472Trial NCT04215029Trial NCT04200534Trial NCT04199026Trial NCT04196972Trial NCT04189783Trial NCT04189770Trial NCT04189757Trial NCT04188418Trial NCT04188405Trial NCT04186884Trial NCT04186832Trial NCT04185337Trial NCT04181463Trial NCT04171622Trial NCT04171219Trial NCT04171037Trial NCT04169763Trial NCT04169737Trial NCT04169542Trial NCT04160052Trial NCT04151082Trial NCT04150939Trial NCT04140487Trial NCT04135326Trial NCT04134208Trial NCT04132843Trial NCT04132505Trial NCT04132440Trial NCT04129138Trial NCT04128748Trial NCT04128501Trial NCT04127721Trial NCT04125914Trial NCT04119037Trial NCT04106843Trial NCT04106245Trial NCT04090619Trial NCT04090567Trial NCT04087057Trial NCT04083378Trial NCT04082572Trial NCT04074746Trial NCT04066894Trial NCT04062305Trial NCT04062266Trial NCT04058964Trial NCT04054245Trial NCT04054167Trial NCT04054154Trial NCT04053517

Abstract

The Monoclonal Antibody (MAb) Facility (MAF) provides non-commercially-available antibodies to MD Anderson Cancer Center investigators for specific applications. The MAF serves basic, translational and clinical researchers across the institution and is currently developing projects in each of these three areas. Although the services are based on traditional murine hybridoma technology, the MAF offers custom immunization strategies and support for functional screening in order to produce unique antibodies suitable for novel applications. The MAF occupies 726 sq. ft. in 1SCRB, home to the Center for Cancer Immunology Research (CCIR) on the South Campus. This is a state-of-the-art facility for immunology research that provides a platform for integrating basic and clinical research programs. The CCIR is equipped with customized laboratory services, centralized tissue culture rooms, liquid nitrogen tank rooms, and glassware washing and sterilization facilities, all of which are available to the MAF. The MAF has a tissue culture laboratory (SCR 4.2158), a protein chemistry area (SCR 4.2220), and space in the South Campus Vivarium that is a component of the Research Animal Support Facility shared resource. In the last 5-year period, the MAF developed three MAbs that have potential for clinical development as therapeutic agents, and several additional candidates are in preclinical assessment. Several antibodies produced by the MAF have been licensed or are in the process of being licensed for commercial development. MD Anderson members with peer-reviewed funding accounted for 97% of the usage of the resource and 30% support is requested from the CCSG. Since 2007, the MAF has supported the research of 40 MD Anderson investigators with peer reviewed funding representing 16 CCSG Programs, compared to 13 investigators in the previous grant period. Hybridoma production increased from 44 to 79 projects (a 178% increase), and total services provided increased more than 300% during this grant cycle. Publications cited using the MAF have appeared in Nature, PNAS, Blood and Nature Medicine. Future plans include the purchase of a bioreactor for large scale production to support the increasing demand for the quantities of MAbs required for preclinical development Novel methods of immunization including DNA expression will be explored. The facility also plans to explore the direct generation of fully human antibodies using humanized mice or using Phage display scFv libraries as a more rapid and direct strategy to produce antibodies for future clinical applications of newly-discovered markers.

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