Michael D. Robek, Ph.D.



Assistant Professor of Pathology.


Department of Pathology
Yale University School of Medicine
P.O. Box 208023
310 Cedar St., LH315A
New Haven, CT 06520-8023

Office: (203) 785-6174
Lab: (203) 785-7672
Fax: (203) 785-6127

email: michael.robek@yale.edu



Training:
B.S., Case Western Reserve University, Cleveland, OH, 1994
Ph.D., Washington University, St. Louis, MO, 2000
Postdoctoral Fellow, The Scripps Research Institute, La Jolla, CA

Expertise:
Virus-host interactions; viral immunology; hepatitis viruses; interferon.

Research Interests:
Many viruses establish chronic infections that persist for the lifetime of their hosts. Some of these viruses, including the human immunodeficiency virus and the hepatitis B (HBV) and C viruses, are associated with a large degree of worldwide morbidity and mortality. Current therapies for these diseases are only moderately effective, and are often limited by a number of variables including cost, significant side effects, and viral resistance to the drugs. Therefore, new and improved therapies for these diseases are needed. Our laboratory studies the host-pathogen interactions related to HBV infection. Approximately 350 million people worldwide are chronically infected with HBV, including an estimated 1.25 million in the United States. HBV infection leads to millions of deaths each year from liver diseases such as cirrhosis and hepatocellular carcinoma. We are exploring three unique therapeutic approaches to treat this disease. First, we are investigating the relationships between HBV and cellular regulatory pathways, as these may be exploited pharmacologically to block virus replication. Second, we are characterizing the ability of novel antiviral and immunomodulatory cytokines to inhibit HBV replication and prevent liver damage. Third, we are studying new methodologies for therapeutic vaccination to boost the immune response to HBV in people who are chronically infected. These studies have the potential to expand the repertoire of antiviral therapies beyond those currently being employed, and therefore significantly impact public health.

Professional Service:


Other Links:

Robek Lab


Selected Publications:

P. Bandi, M.L. Garcia, C.J. Booth, F.V. Chisari, and M.D. Robek. 2009. Bortezomib inhibits hepatitis B virus replication in transgenic mice. Antimicrobial Agents and Chemotherapy, in press.

Bandi, P., N.E. Pagliaccetti, and M.D. Robek. 2009. Inhibition of type III interferon activity by orthopoxvirus immunomodulatory proteins. J Interferon Cytokine Res, in press.

Garcia, M.L., R. Byfield, and M.D. Robek. 2009. Hepatitis B virus replication and release are independent of core lysine ubiquitination. J Virol, 83:4923-4933.

Pagliaccetti, N.E., R. Eduardo, S.H. Kleinstein, X.J. Mu, P. Bandi, and M.D. Robek. 2008. Interleukin-29 functions cooperatively with interferon to induce antiviral gene expression and inhibit HCV replication. J Biol Chem, 283:30079-30089.

Ying, C., Y. Li, C.H. Leung, M.D. Robek, and Y.C. Cheng. 2007. Unique antiviral mechanism discovered in anti-hepatitis B virus research with a natural product analogue. Proc. Natl. Acad. Sci. U.S.A., 104:8526-8531.

Wollmann, G., M.D. Robek, and A.N. van den Pol. 2007. Variable deficiencies in the interferon response enhance susceptibility to VSV oncolytic actions in glioblastoma but not in normal human glia. Journal of Virology, 81:1479-1491.

Robek, M.D., M.L. Garcia, B.S. Boyd, and F.V. Chisari. 2007. Role of immunoproteasome catalytic subunits in the immune response to hepatitis B virus. Journal of Virology, 81:483-491.

van den Pol, A.N., M.D. Robek, P.K. Ghosh, K. Ozduman, P. Pandi, M.D. Whim, and G. Wollmann. 2007. Cytomegalovirus induces interferon-stimulated gene expression and is attenuated by interferon in the developing brain. Journal of Virology, 81:332-348.

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This page was last modified on: 12/02/2009