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Home > About BNE > Press Room > 2011 Archive > October > JOURNAL OF IMMUNOLOGY PUBLISHES STUDY OF CLEVELAND BIOLABS’ DRUG CBLB502 IN ACUTE RENAL ISCHEMIC FAILURE JOURNAL OF IMMUNOLOGY PUBLISHES STUDY OF CLEVELAND BIOLABS’ DRUG CBLB502 IN ACUTE RENAL ISCHEMIC FAILURE
Buffalo, NY – October 3, 2011 -- Cleveland BioLabs, Inc. (NASDAQ:CBLI) )today announced that a study demonstrating CBLB502’s ability to inhibit acute renal ischemic failure was published in the October 1, 2011 issue of The Journal of Immunology (J Immunol 2011 187:3831-3839; doi:10.4049/jimmunol.1003238). The study, conducted by scientists at Cleveland Clinic, Roswell Park Cancer Institute and Hokkaido University, analyzed the ability of CBLB502 to attenuate injury in a murine model of acute ischemic renal failure, a potentially fatal and poorly treatable disease that is frequently developed as a result of decreased blood flow through the kidneys. CBLB502, given 30 minutes before bilateral renal pedicle occlusion, provided marked protection against the renal dysfunction and inflammation that follows reperfusion of ischemic kidneys. CBLB502 administration caused marked decreases in leukocyte infiltration, pro-inflammatory cytokine production, and tubular injury and resulted in significant improvement of animal survival. Importantly, CBLB502 given within 30 minutes after ischemic kidney reperfusion reproduced the protective effects of pretreatment with the same compound, indicating a window following reperfusion in which CBLB502 administration may mitigate against acute renal ischemic failure. These results indicate the potential for use of TLR5 (toll-like receptor 5) agonists, such as CBLB502, as both mitigators and protectors against acute renal ischemic failure. Andrei Gudkov, Ph.D., D. Sci., Chief Scientific Officer of Cleveland BioLabs, and Senior Vice President of Basic Science at Roswell Park Cancer Institute, commented, “The spectrum of pathologies that may be addressed by CBLB502’s mechanism of action continues to expand. Ischemia-reperfusion injury continues to be a major clinical problem causing significant morbidity and mortality in transplantation as well as in other surgeries. This study and previously collected data on CBLB502’s efficacy against tourniquet-induced injury in animal models further reinforces our belief that CBLB502 may be broadly efficacious in protecting against ischemic injury.” CBLB502 is currently at an advanced stage of development for biodefense applications as a medical radiation countermeasure. In January 2011, preclinical data regarding direct anticancer effects of CBLB502 in several mouse and rat models of colon and lung cancer, lymphoma, melanoma, and head and neck cancer was reported. The Journal of Immunology publication may be found online at: http://www.jimmunol.org/content/early/2011/08/29/jimmunol.1003238 About Cleveland BioLabs, Inc. |