Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1998;17(1-2):13-22.
doi: 10.1007/BF02786426.

Role of gamma delta T cells in immunity to infectious diseases and the regulation of hematolymphoid cell development

Affiliations
Review

Role of gamma delta T cells in immunity to infectious diseases and the regulation of hematolymphoid cell development

S R Carding. Immunol Res. 1998.

Abstract

My research interests are twofold. The first is to define the biochemical and molecular mechanisms that regulate hematopoietic cell development. In particular, the role that the cytokine interleukin-2 (IL2) plays in regulating the development and selection of lymphocyte progenitor cells, and in myelopoiesis are primary areas of research. The second is to understand the role that gamma delta T cells play in pathogen-induced immune responses and autoimmunity. Their involvement in the immune response to the intracellular bacteria Listeria monocytogenes in mice and Mycobacteria tuberculosis (Mtb) in humans, in T cell-mediated inflammatory bowel disease in humans, and the nature of the antigens they recognize during these responses are major areas of interest. Research material includes patient-derived tissues as well as both conventional and genetically engineered (transgenic) strains of mice.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Immunol. 1994 Jun 1;152(11):5392-7 - PubMed
    1. J Immunol. 1995 Feb 1;154(3):998-1006 - PubMed
    1. J Clin Invest. 1988 Dec;82(6):1877-83 - PubMed
    1. J Exp Med. 1990 Oct 1;172(4):1225-31 - PubMed
    1. Mol Med. 1997 Mar;3(3):183-203 - PubMed

Substances

LinkOut - more resources