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Mol Immunol. 2014 Dec;62(2):283-8. doi: 10.1016/j.molimm.2014.02.010. Epub 2014 Mar 14.

Do follicular dendritic cells regulate lupus-specific B cells?

Author information

1
Program in Cellular and Molecular Medicine, Childrens Hospital, Boston, MA, USA.
2
Regional Center for Biotechnology, New Delhi, India.
3
Program in Cellular and Molecular Medicine, Childrens Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA. Electronic address: Michael.carroll@Childrens.harvard.edu.

Abstract

The factors that allow self-reactive B cells to escape negative selection and become activated remain poorly defined. In this review we describe recently published results in which a B cell receptor-knock-in mouse strain specific for nucleolar self-antigens was bred with mice deficient in complement C4 and discuss the implications for the lupus field. Absence of C4 leads to a breakdown in the elimination of autoreactive B cell clones at the transitional stage. This is characterized by a relative increase in their response to a range of stimuli, entrance into follicles and a greater propensity to form self-reactive germinal centers. In this review, a model is proposed in which, in the absence of complement C4, inappropriate clearance of apoptotic debris promotes chronic activation of myeloid cells and follicular dendritic cells, resulting in secretion of Type I interferon. This allows for the maturation and activation of self-reactive B cell clones leading to increased spontaneous formation of germinal centers and subsequent generation of autoantibodies.

KEYWORDS:

Autoimmunity; Germinal center; Lupus nucleolar antigen; Negative selection

PMID:
24636642
PMCID:
PMC4160379
DOI:
10.1016/j.molimm.2014.02.010
[Indexed for MEDLINE]
Free PMC Article
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