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Robert E. Cone

Professor of Immunology
cone@uchc.edu

  • Ph.D., University of Michigan 
  • Member, Walter and Eliza Hall Institute for Medical Research (Melbourne Australia (1971-1972)
  • Member, Basel Institute for Immunology, Basel, Switzerland (1973-1974)
  • Immunology Graduate Program
  • Accepting Lab Rotation Students: Summer '09
 
Areas of Interest

No Rolls Royce is built without brakes! The immune system is highly regulated to protect the host from the "collateral damage" of an immune response that protects from foreign invaders. A failure of this complex regulatory system can lead to autoimmune disease, a "fifth column" attack against self , damage to tissue and/or to a loss or deficiency in immunity resulting in susceptibility to infection or cancer. The overall objective of our laboratory is to understand immunoregulation at the cellular and molecular level. To achieve this goal we analyze the induction and function of antigen-specific regulatory T lymphocytes stimulated by cells from the eye. This mechanism "protects" the eye from damage by the immune response. Molecular and cell-based mechanisms of regulation of T lymphocytes that effect cell-mediated immunity and autoimmune disease is under analysis. The biochemical properties , molecular/genetic origin and functional properties of soluble, antigen-specific T cell proteins that regulate some aspects of immunity but may also cause some aspects of food allergies, chemical sensitivities and Inflammatory Bowel Syndrome is also being investigated.

Lab Rotation Projects
  • The role of the thymus in adult mice as a mechanism that supplies regulatory cells that induce splenic suppressor T cells: how does this happen?
  • The mechanism of suppression and induction by splenic suppressor T cells. These investigations are done with the examination of the immune response to foreign antigens and the prevention of autoimmune disease.
  • The nature and migration of regulatory dendritic cells from the eye that induce regulatory T cells.
  • The cellular basis of the regulation of T cells by the central nervous system.
Publications

Selected Publications

Cone RE, Chattopadhyay S, Sharafieh R, Lemire Y, O'Rourke J. The suppression of hypersensitivity by ocular-induced CD8(+) T cells requires compatibility in the Qa-1 haplotype. Immunol Cell Biol. 2009 Jan 13. [Epub ahead of print]

Cone RE, Chattopadhyay S, O'Rourke J. Control of delayed-type hypersensitivity by ocular- induced CD8+ regulatory T cells.
Chem Immunol Allergy. 2008;94:138-49.

Chattopadhyay S, O'Rourke J, Cone RE. Implication for the CD94/NKG2A-Qa-1 system in the generation and function of ocular-induced splenic CD8+ regulatory T cells. Int Immunol. 2008 Apr;20(4):509-16.

Cone RE, Li X, Sharafieh R, O'Rourke J, Vella AT. The suppression of delayed-type hypersensitivity by CD8+ regulatory T cells requires interferon-gamma. Immunology. 2007 Jan;120(1):112-9. Epub 2006 Oct 18.

Li X, Shen S, Urso D, Kalique S, Park SH, Sharafieh R, O'Rourke J, Cone RE. Phenotypic and immunoregulatory characteristics of monocytic iris cells. Immunology. 2006 Apr;117(4):566-75

Li X, Wang Y, Urso D, O'Rourke J, Cone RE. Thymocytes induced by antigen injection into the anterior chamber activate splenic CD8+ suppressor cells and enhance the antigen-induced production of immunoglobulin G1 antibodies. Immunology. 2004 Sep;113(1):44-56.

Li X, Taylor S, Zegarelli B, Shen S, O'Rourke J, Cone RE. The induction of splenic suppressor T cells through an immune-privileged site requires an intact sympathetic nervous system. J Neuroimmunol. 2004 Aug;153(1-2):40-9.

Paper icon View more publications, see Pubmed listing.

rev. 3/09

  
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