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
. 2005 Mar;26(4):463-84.
doi: 10.1007/s00281-004-0190-2.

B cell superantigens: a microbe's answer to innate-like B cells and natural antibodies

Affiliations
Review

B cell superantigens: a microbe's answer to innate-like B cells and natural antibodies

Carl S Goodyear et al. Springer Semin Immunopathol. 2005 Mar.

Abstract

Marginal zone B cells and B-1 cells have been termed innate-like B cells as they express limited repertoires that play special roles in immune defenses against common infections. These B cells are the sources of natural antibodies and are capable of highly accelerated clonal responses that help counter blood-borne infections. We have characterized a class of microbial product with highly adapted binding interactions with host immunoglobulins/B cell receptors (BCRs), which enable the targeting of large supra-clonal sets of B cells for activation-associated apoptotic death. In recent studies, we have shown that all B cells with V region-targeted BCRs are susceptible. However, compared to follicular B cells, in vivo exposure preferentially causes innate-like B cells to undergo induced death with subsequent long-lasting supra-clonal depletion and immune tolerance. Based on these properties, it is likely that B cell superantigens influence the pathogenesis of some common infections, but also may provide novel therapeutic opportunities to treat B cell neoplastic and autoimmune diseases.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Exp Med. 2002 Mar 18;195(6):771-80 - PubMed
    1. Eur J Immunol. 2001 Apr;31(4):1017-28 - PubMed
    1. J Immunol. 1991 Sep 15;147(6):1877-83 - PubMed
    1. J Biol Chem. 1984 Feb 10;259(3):1695-702 - PubMed
    1. J Immunol. 2003 Jan 1;170(1):84-90 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources