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Kagnoff, Martin F.

Mayo Clinic

University of California San Diego

Citations 3

Antibody biomarker discovery through in vitro directed evolution of consensus recognition epitopes
Ballew, John T., Collin, Pekka , Mäki, Markku , Kagnoff, Martin F., Kaukinen, Katri , Daugherty, Patrick S. , Murray, Joseph A.

Proceedings of the National Academy of Sciences | November 12, 2013 | Volume: 110 | Issue: 48 | Pages: 19330-19335

10.1073/pnas.1314792110 Get It

Significance The diagnosis of many diseases is dependent upon accurate detection of particular antibodies present in blood. However, the development of biochemical reagents that can reliably detect these antibodies has proved remarkably challenging. This study describes a process to create biochemical reagents that can accurately and reliably detect disease-associated antibodies, without requiring knowledge of the cause or mechanisms of disease. Simultaneously, this process enabled identification of a critical environmental agent involved in celiac disease. Thus, the process presented here may enable the development of effective diagnostic tests for other medical conditions where such tests are lacking and the identification of environmental factors involved in disease.
Antibody Repertoire Profiling Using Bacterial Display Identifies Reactivity Signatures of Celiac Disease
Spatola, Bradley N., Murray, Joseph A. , Kagnoff, Martin F., Kaukinen, Katri , Daugherty, Patrick S. , Murray, J A

Analytical Chemistry | December 12, 2012 | Volume: 85 | Issue: 2 | Pages: 1215-1222

10.1021/ac303201d Get It

IκB-kinaseβ-dependent NF-κB activation provides radioprotection to the intestinal epithelium
Egan, Laurence J. , Eckmann, Lars , Greten, Florian R. , Chae, Sung-Won, Li, Zhi-Wei, Myhre, Gennett M., Robine, Sylvie , Kagnoff, Martin F., Karin, Michael

Proceedings of the National Academy of Sciences | February 24, 2004 | Volume: 101 | Issue: 8 | Pages: 2452-2457

10.1073/pnas.0306734101 Get It

Acute injury to the intestinal mucosa is a major dose-limiting complication of abdominal radiation therapy. We studied the role of the transcription factor NF-κB in protection against radiation-induced apoptosis in the intestinal epithelium in vivo . We use mice in which NF-κB signaling through IκB-kinase (IKK)-β is selectively ablated in intestinal epithelial cells to show that failure to activate epithelial cell NF-κB in vivo results in a significant increase in radiation-induced epithelial cell apoptosis. Furthermore, bacterial lipopolysaccharide, which is normally a radioprotective agent, is radiosensitizing in IKKβ-deficient intestinal epithelial cells. Increased apoptosis in IKKβ-deficient intestinal epithelial cells was accompanied by increased expression and activation of the tumor suppressor p53 and decreased expression of antiapoptotic Bcl-2 family proteins. These results demonstrate the physiological importance of the NF-κB system in protection against radiation-induced death in the intestinal epithelium in vivo and identify IKKβ as a key molecular target for radioprotection in the intestine. Selective preactivation of NF-κB through IKKβ in intestinal epithelial cells could provide a therapeutic modality that allows higher doses of radiation to be tolerated during cancer radiotherapy.