| Robert H. Swanborg, Ph.D., is Professor of Immunology and Microbiology, and Associate in Neurology. He received his Ph.D. from the State University of New York at Buffalo in 1965, followed by a postdoctoral year, also in Buffalo. Dr. Swanborg joined the Department of Microbiology at Wayne State University in 1966. He spent a sabbatical year at the WennerGren Institute, Stockholm, in 1975-1976. Dr. Swanborg is the recipient of a Javits Neuroscience Investigator Award from the National Institute of Neurological Disorders and Stroke, NIH.
Dr. Swanborg is studying autoimmune encephalomyelitis, which provides a model for the human demyelinating disease, multiple sclerosis. Autoreactive T lymphocytes specific for myelin exist in the normal host. Although these have the potential to invade the central nervous system to induce autoimmune disease, they are usually inactive. Current studies are addressing the mechanisms by which these autoreactive T cells might inadvertently become activated to induce encephalomyelitis. Other studies relate to mechanisms by which other lymphocytes regulate the activation of the autoreactive T cells. Immunological and molecular biological approaches are being employed in these studies. The long-term objective of Dr. Swanborg's ongoing investigation is to elucidate the mechanisms that govern the induction and regulation of autoimmune disease with the hope of gaining insight into the etiology of human demyelinating diseases.
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Selected Publications
| Lighvani S., Huang X., Trivedi P.P., Swanborg R.H., Hazlett L.D. Substance P regulates natural killer cell interferon-gamma production and resistance to Pseudomonas aeruginosa infection. Eur. J. Immunol., 35:1567-1575, 2005. Medline |
| Trivedi P.P., Roberts P.C., Wolf N.A., Swanborg R.H. NK cells inhibit T cell proliferation via p21-mediated cell cycle arrest. J. Immunol., 174:4590-4597, 2005. Medline |
| Conant S.B., Swanborg R.H. Autoreactive T cells persist in rats protected against experimental autoimmuneencephalomyelitis and can be activated through stimulation of innate immunity. J. Immunol., 172:5322-5328, 2004. Medline |
| Conant S.B., Swanborg R.H. MHC class II peptide flanking residues of exogenous antigens influencerecognition by autoreactive T cells. Autoimmun. Rev., 2:8-12, 2003. Medline |
| Swanborg R.H., Whittum-Hudson J.A., Hudson A.P. Infectious agents and multiple sclerosis--are Chlamydia pneumoniae and humanherpes virus 6 involved? J. Neuroimmunol., 136:1-8, 2003. Medline |
| Swanborg R.H., Whittum-Hudson J.A., Hudson A.P. Human herpesvirus 6 and Chlamydia pneumoniae as etiologic agents in multiple sclerosis - a critical review. Microbes. Infect., 4:1327-1333, 2002. Medline |
| Swanborg, R.H., Experimental autoimmune encephalomyelitis in the rat: lessons in T-cell immunology and autoreactivity, Immunol. Rev., 184:129-135, 2001. Medline |
| Wolf, N.A. and Swanborg, R.H., DA rat NK+CD3- cells inhibit autoreactive T-cell responses, J. Neuroimmunol., 119:81-87, 2001. Medline |
| Lenz, D.C., Lu, L., Conant, S.B., Wolf, N.A., Gerard, H.C., Whittum-Hudson, J.A., Hudson, A.P. and Swanborg, R.H. A Chlamydia pneumoniae-specific peptide induces experimental autoimmune encephalomyelitis in rats. J. Immunol., 167:1803-1808, 2001. Medline |
| Lenz, D.C., Wolf, N.A. and Swanborg, R.H. Parental genes do not codominantly confer susceptibility to experimental autoimmune encephalomyelitis in F1 rats. J. Neuroimmunol., 114:181-187, 2001. Medline |
| Lenz, D.C., and Swanborg, R.H. Suppressor cells in demyelinating disease: a new paradigm for the new millennium. J. Neuroimmunol., 100:53-57, 1999. Medline |
| Lenz, D.C., Wolf, N.A., and Swanborg, R.H. Strain variation in autoimmunity: attempted tolerization of DA rats results in the induction of experimental autoimmune encephalomyelitis. J. Immunol., 163:1763-1768, 1999. Medline |
| Smeltz, R.B., Wolf, N.A., and Swanborg, R.H. Inhibition of autoimmune T cell responses in the DA rat by bone marrow-derived natural killer cells in vitro: implications for autoimmunity. J. Immunol., 163:1390-1399, 1999. Medline |
| Smeltz,, R.B., Wauben, M.H.M., Wolf, N.A. and Swanborg. R.H. Critical requirement for aspartic acid at position 82 of myelin basic protein 73-86 for recruitment of Vb8.2+ T cells and encephalitogenicity in the Lewis rat. J. Immunol., 162:829-836, 1999. Medline |
| Swanborg, R.H. Experimental autoimmune encephalomyelitis, Encyclopedia of Immunology. 2nd edition, I.M. Roitt and P.J. Delves, eds., Academic Press, London, 856-860, 1998. |
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