Literature DB >> 9396769

Self-reactive B cells are not eliminated or inactivated by autoantigen expressed on thyroid epithelial cells.

S Akkaraju1, K Canaan, C C Goodnow.   

Abstract

Graves' Disease results from the production of autoantibodies against receptors for thyroid stimulating hormone (TSH) on thyroid epithelial cells, and represents the prototype for numerous autoimmune diseases caused by autoantibodies that bind to organ-specific cell membrane antigens. To study how humoral tolerance is normally maintained to organ-specific membrane antigens, transgenic mice were generated selectively expressing membrane-bound hen egg lysozyme (mHEL) on the thyroid epithelium. In contrast to the deletion of autoreactive B cells triggered by systemic mHEL (Hartley, S.B., J. Crosbie, R. Brink, A.B. Kantor, A. Basten, and C.C. Goodnow. 1991. Nature. 353:765-769), selective expression of mHEL autoantigen on thyroid cells did not trigger elimination or inactivation of circulating HEL-reactive B cells. These results provide evidence that tolerance is not actively acquired to organ-specific antigens in the preimmune B cell repertoire, underscoring the importance of maintaining tolerance to such antigens by other mechanisms. The role of an intact endothelial barrier in sequestering organ-specific antigens from circulating preimmune B cells is discussed.

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Year:  1997        PMID: 9396769      PMCID: PMC2199176          DOI: 10.1084/jem.186.12.2005

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  33 in total

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Authors:  I Okayasu; Y Hara; K Nakamura; N R Rose
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4.  Unaltered thyroid function in mice responding to a highly immunogenic thyrotropin receptor: implications for the establishment of a mouse model for Graves' disease.

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Journal:  Clin Exp Immunol       Date:  1995-02       Impact factor: 4.330

Review 5.  Myasthenia gravis: pathogenesis and treatment.

Authors:  D P Richman; M A Agius
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Review 6.  Autoimmune thyroid disease: further developments in our understanding.

Authors:  A P Weetman; A M McGregor
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7.  Nonimmune thyroid destruction results from transgenic overexpression of an allogeneic major histocompatibility complex class I protein.

Authors:  A G Frauman; P Chu; L C Harrison
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Review 8.  Goodpasture syndrome: molecular and clinical advances.

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9.  Censoring of self-reactive B cells with a range of receptor affinities in transgenic mice expressing heavy chains for a lysozyme-specific antibody.

Authors:  S B Hartley; C C Goodnow
Journal:  Int Immunol       Date:  1994-09       Impact factor: 4.823

10.  Expression and function of multiple regulators of complement activation in autoimmune thyroid disease.

Authors:  N Tandon; S L Yan; B P Morgan; A P Weetman
Journal:  Immunology       Date:  1994-04       Impact factor: 7.397

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  17 in total

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4.  Critical Differences between Induced and Spontaneous Mouse Models of Graves' Disease with Implications for Antigen-Specific Immunotherapy in Humans.

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Review 5.  Role of inhibitory signaling in peripheral B cell tolerance.

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Review 6.  Breaking tolerance to thyroid antigens: changing concepts in thyroid autoimmunity.

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7.  Censoring of self-reactive B cells by follicular dendritic cell-displayed self-antigen.

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8.  Peripheral deletion of mature alloreactive B cells induced by costimulation blockade.

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9.  Liver-expressed Igkappa superantigen induces tolerance of polyclonal B cells by clonal deletion not kappa to lambda receptor editing.

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10.  Gene dosage--limiting role of Aire in thymic expression, clonal deletion, and organ-specific autoimmunity.

Authors:  Adrian Liston; Daniel H D Gray; Sylvie Lesage; Anne L Fletcher; Judith Wilson; Kylie E Webster; Hamish S Scott; Richard L Boyd; Leena Peltonen; Christopher C Goodnow
Journal:  J Exp Med       Date:  2004-10-18       Impact factor: 14.307

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