James Roger
| Title | Senior Instructor |
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| Institution | School of Medicine and Dentistry |
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| Department | Dentistry in the Center for Oral Biology |
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| Address | University of Rochester Medical Center School of Medicine and Dentistry 601 Elmwood Ave, Box 611 Rochester NY 14642
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| 2005 |
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| Recipient of the Robert Burkhardt Memorial Scholarship | Pennsylvania Academy of Stomatology | | 2006 |
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| Best Manuscript, Journal of Dental Education | | 2006 |
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| 2007 | Academic Dental Careers Fellowship Program Fellow | ADEA | | 2006 |
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| 1st Prize Dental Research Division, Poster Presentation | Marquette University Research Day | | 2007 |
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| Dentsply/SCADA Student Clinician Research Program, Marquette representative at the ADA Annual Meeting | | 2007 |
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| 2008 | Sjögren's Syndrome Foundation Fellowship; "Autoantibody characterization in salivary gland B cells in primary Sjögren' | | 2008 |
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| 2008 Volpe Prize for Periodontal Research, Finalist | The Ohio State University, Columbus, OH |
B cells have been implicated as central players in the autoimmune diseases Sjögren's Syndrome (SS), Systemic Lupus Erythematosus (SLE), and Rheumatoid Arthritis (RA). While it has been reported that B cells participate in both immune and autoimmune response through their traditional role of antibody (and auto-antibody) production--B cells are also known to participate, possibly pathologically, through antibody independent functions such as cytokine production and antigen presentation. It has long been reported that B cells are capable of cytokine production; B cells activated through the B cell Receptor (BCR) or Toll-Like Receptors (TLR) produce cytokines such as IL-10, IL-6 and TNFa. Preliminary data has shown that B cells produce a large and diverse array of cytokines in biologically significant quantities. Further data has shown that B cells can be induced to make pro-inflammatory cytokines (IFNg, IL-12p40, and TNFa) when stimulated by Th1 cells, or cytokines associated with allergic responses (IL-4) when stimulated by Th2 cells. This B / T cell communication indicates potentially complex effector roles when considering cytokine-producing B cells. In mice, IL-10 producing B cells seem to ameliorate symptoms of autoimmune diseases of RA and Inflammatory Bowel Disease. While the observation that B cells are capable of producing a variety of effector cytokines under differing stimulation conditions is tantalizing, a systematic approach to dissect the function of these cytokine producing B cells is necessary to elucidate their effector functions in both health and autoimmune disease. The immuno-modulatory effects of the cytokines produced and the hypothesis that cytokine-producing B cells contribute in both the healthy state as well as the autoimmune conditions of Sjögren's Syndrome, Lupus and Rheumatoid, through systemic inflammatory modulation and target-tissue influences are being evaluated.
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Barr PM, Wei C, Roger J, Schaefer-Cutillo J, Kelly JL, Rosenberg AF, Jung J, Sanz I, Friedberg JW. Syk inhibition with fostamatinib leads to transitional B lymphocyte depletion. Clin Immunol. 2012 Mar; 142(3):237-42.
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Rogér JM. The Academic Dental Careers Fellowship Program: a pilot program to introduce dental students to academia. J Dent Educ. 2008 Apr; 72(4):438-47.
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Rogér JM, Wehmeyer MM, Milliner MS. Reflections on academic careers by current dental school faculty. J Dent Educ. 2008 Apr; 72(4):448-57.
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Rogér JM, Javarone JA, Ealba EL, Markiewicz MR, Morlandt AB. The National Student Research Group of the AADR--an introduction. J Dent Res. 2007 May; 86(5):388-91.
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Rogér JM. A survey of dual-degree training opportunities at US dental schools. J Dent Educ. 2006 Sep; 70(9):909-17.
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