Mark Anderson, M.D., Ph.D.

Robert B. Friend and Michelle M. Friend Endowed Chair in Diabetes Research
Mark Anderson, M.D., Ph.D.

The main research interest of our laboratory group is to examine the genetic control of autoimmune disease to gain a better understanding of the mechanisms by which immune tolerance is broken. Recently, we generated a mouse model of a human autoimmune disease called APECED, which is classically manifested by an autoimmune attack directed at multiple endocrine organs. This disease is inherited in a monogenic autosomal recessive fashion and the causative gene was identified and is called Aire (for autoimmune regulator). Aire knockout mice, like their human counterparts, develop an autoimmune disease that is targeted to multiple organs.

Interestingly, we can ascribe one of the primary defects in these mice to the thymus gland. Specifically, it appears that Aire helps protect against autoimmunity by helping direct the ectopic transcription of multiple self-antigens in thymic medullary epithelial cells. Studies in our laboratory are ongoing on this interesting model of autoimmune disease looking in greater detail how this defect results in the breaking of immune tolerance and what genes may interact with the Aire gene to protect against or worsen autoimmunity. In addition to these ongoing studies, our laboratory is also interested in developing other models of autoimmune disease by using transgenic, knockout, and knock-in approaches.

Selected Publications

L. Zhang, J.M. Barker, S. Babu, M. Su, M. Stenerson, M. Cheng, A. Shum, E. Zamir, R. adolato, A. Law, G.S. Eisenbarth, and M.S. Anderson. A robust interferon immunassay that is highly specific for patients with Autoimmune Polyglandular Syndrome Type 1. Clinical Immunology, 125:131-137, 2007.
M.S. Anderson. Autoimmune Endocrine Disease. (2002) Current Opinion in Immunology 14, 760-764.
J. Gardner, J. DeVoss, R. Friedman, D. Wong, K.P. Johannes, Y. Tan, H. Chang., M. Krummel., and M.S.Anderson. Deletional Tolerance Mediated by Extrathymic Aire-expressing Cells. Science 321:843-847, 2008.
J. DeVoss, A.K. Shum, K.P. Johannes, W. Lu, A.K. Krawisz, T. Yang, N.P. LeClair, E. Strauss, and M.S. Anderson. Effector mechanisms of the autoimmune syndrome in the murine model of Autoimmune Polyglandular Syndrome Type 1. J Immunol 181:4072-4079, 2008.
J. Devoss., M.S.Anderson. Lessons on immune tolerance from the monogenic disease APS1. Curr Opin Genet Dev., 3:193-200, 2007.
M.A. Su, K. Giang, K. Zumer, H. Jiang, I. Oven, J.L. Rinn, J.J. Devoss, K.P. Johannes, W. Lu, J. Gardner, A. Chang, P. Bubulya, H.Y. Chang, B.M. Peterlin, and M.S. Anderson. Mechanisms of an autoimmunity syndrome in mice caused by a dominant mutation in Aire. J Clin Invest 118:1712-1726, 2008.
M.S. Anderson, E. Venanzi, L. Klein, Z. Chen, S. Berzins, S. Turley, H. von Boehmer, R. Bronson, A. Dierich, C. Benoist, and D. Mathis. Projection of an immunological self shadow within the thymus by the aire protein. (2002) Science 298, 1395-1401.
J. DeVoss, Y. Hou, K. Johannes, W. Lu, G.I. Liou, J. Rinn, H. Chang, R.R. Caspi, L. Fong, and M.S. Anderson. Spontaneous autoimmunity prevented by thymic expression of a single self-antigen. J Exp Med, 203:2727-2735, 2006.
M.S. Anderson , E. Venanzi, Z. Chen, S. Berzins, C. Benoist, and D. Mathis. The cellular mechanism of aire control of T cell tolerance. Immunity 23:227-239, 2005.
M.H. Cheng, A.K. Shum, and M.S. Anderson. What's new in the Aire? Trends in Immunology; 28:321-27, 2007.
Mark Anderson, M.D., Ph.D.

UCSF Diabetes Center 513 Parnassus Ave. HSW 1112, Box 0540 San Francisco, CA 94143

(415) 502-8052
(415) 564-5813

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