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
. 2007;39(1-3):62-78.
doi: 10.1007/s12026-007-0064-5.

Natural Tregs, CD4+CD25+ inhibitory hybridomas, and their cell contact dependent suppression

Affiliations

Natural Tregs, CD4+CD25+ inhibitory hybridomas, and their cell contact dependent suppression

Elizabeth H Field et al. Immunol Res. 2007.

Abstract

The natural CD4+CD25+ T regulatory (Treg) lymphocyte has emerged as a critical cell for controlling immune responses to self, foreign proteins, and pathogens. Identified initially by the constitutive expression of CD4 and CD25, natural Tregs suppress a variety of immune cells and responses, including CD4+CD25- proliferation and IL-2 production, and CD8 cell proliferation, IFNgamma production and CTL activity. Although natural Tregs require activation with specific antigen to attain their suppressive phenotype, once activated they execute inhibition in an antigen specific as well as non-specific (bystander) fashion. Treg suppression depends on IL-2, CD25, and cell:cell contact. The use of live cell imaging in vivo and in vitro to visualize the dynamic cell:cell interactions involving natural Tregs as well as the CD4+CD25+ Treg inhibitory hybridoma RD6 has refined the mechanistic models of contact dependent Treg suppression.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Eur J Immunol. 2004 Sep;34(9):2480-8 - PubMed
    1. Nat Immunol. 2006 Jan;7(1):83-92 - PubMed
    1. Mol Hum Reprod. 2004 May;10(5):347-53 - PubMed
    1. J Exp Med. 1990 Jan 1;171(1):141-57 - PubMed
    1. Int Immunol. 1998 Dec;10(12):1969-80 - PubMed

MeSH terms

LinkOut - more resources