Cynthia L. BaldwinProfessor of Virology & Microbiology
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Cellular Immunity: Intracellular Microbes and gd
T-cells
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While macrophages are normally considered
to be a primary cell for mediating innate immune responses by phagocytosing
and destroying microbes that infect mammals, some microbial organisms
including bacteria and protozoa have specifically adapted themselves
to survive and replicate in host cells thereby "hiding" from
protective immune responses. |
Electron micrograph of a portion
of a macrophage infected with Brucella abortus. |
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Our second major area of research evaluates gd T cells, a subpopulation of T lymphocytes that comprise a major proportion of lymphocytes in mammals but whose role in mediating protective immunity is unclear at this time. Currently my lab is ascertaining whether these cells have immunological memory, how this subpopulation of T lymphocytes is activated by constitutively expressed molecules on macrophages as well as by bacterial components and how macrophages regulate their response. Finally, we interested in the role of a lineage-specific cell-surface molecule of gd T cells, known as WC1, in signal transduction and activation. Third, we are evaluating the role of cellular immune responses in protection of cattle against infections with the bacteria Leptospira borgpetersenii serovar hardjo. We are particularly interested in the unique role played by gamma delta T cells. Along with CD4 T cells, these cells exhibit recall responses in vaccinated cattle. That is, they produce interferon-gamma in response to stimulation with the bacterial antigens. Using microarray technology we are comparing genes expressed by gamma delta T cells vs CD4 T cells in response to antigen stimulation following vaccination as a mechanism to ascertain their unique role in protective immune responses. |
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Representative recent publications:Murphy E., Robertson G., Hagius S.D., Parent M., Roop M.R., Elzer P.H., and C.L. Baldwin (2002) MHC class I and II expression on macrophages containing a virulent strain of Brucella abortus measured using GFP-expressing brucellae and flow cytometry. FEMS Immunology and Medical Microbiology 33:191-200. PubMed Abstract Parent M., Bellaire B., Murphy E.A., Roop R.M., and C.L. Baldwin (2002) Role of Brucella abortus siderophore 2,3-dihydroxybenzoic acid (DHBA) for survival in macrophages, trophoblasts and in vivo. Microbial Pathogenesis 32:239-248. PubMed Abstract Sathiyaseelan T., Naimen B., Welte S., MacHugh N., Black S.J., and C.L. Baldwin (2002) Immunological characterization of a T cell stimulatory ligand on autologous monocytes. Immunology 105:181-189. PubMed Abstract Murphy E., Parent M., Sathiyaseelan J., and C.L. Baldwin (2002) Immune control of Brucella abortus 2308 infections in BALB/c mice. FEMS Immunology and Medical Microbiology 33:191-200. PubMed Abstract White A.M., Blumerman S., Naiman B., and C.L. Baldwin (2002) Expression of the bovine high affinity IL-12 receptor b2.Veterinary Immunology & Immunopathology 84:127-142. PubMed Abstract Baldwin C.L., Sathiyaseelan T., Naiman B., White A.M., Brown R., Blumerman S., Rogers A., and S.J. Black (2002) Activation of bovine peripheral blood gd T cells for cell division and IFN-g production. Veterinary Immunology & Immunopathology 87:251-259. PubMed Abstract Naiman B., Alt D., Bolin C.A., Zuerner R., and C.L. Baldwin (2001) Killed leptospira vaccine induces a potent Th1 immune response comprised of CD4 and gamma delta T lymphocytes. Infection and Immunity 69:7550-7558. PubMed Abstract Murphy E., Sathiyaseelan J., and C.L. Baldwin (2001) Interferon-gamma is crucial for surviving a Brucella abortus infection in both resistant C57BL/6 and susceptible BALB/c mice.Immunology 103:511-518. PubMed Abstract Sathiyaseelan J., Jiang X., Fernandes D., and C.L. Baldwin (2000) Growth of Brucella abortus in macrophages from resistant and susceptible mouse strains.Clinical and Experimental Immunology 121:289-294. PubMed Abstract |
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