Literature DB >> 4038633

Specific anti-erythrocyte focus formation as a measure of autoantibody secreting cells in NZB mice.

J Moore, C Calkins.   

Abstract

Using a modification of the antibody forming cell (AFC) focus assay, it is possible to quantitate the spontaneous anti-erythrocyte autoantibody response of New Zealand Black (NZB) mice at the level of the autoantibody secreting cell. This complement independent assay is specific for an antigen(s) present on unmodified mouse erythrocytes. A comparison with the direct Coombs' test showed that the focus assay detected autoantibody responses earlier and demonstrated a wide range of AFC levels in responding mice. The focus assay provides a method for evaluating autoimmunity at the cellular level and for investigating the activities of cells responding to autoantigens.

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Year:  1985        PMID: 4038633      PMCID: PMC1577159     

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  18 in total

1.  The secretion of antibody by isolated lymph node cells.

Authors:  E HELMREICH; M KERN; H N EISEN
Journal:  J Biol Chem       Date:  1961-02       Impact factor: 5.157

2.  Formation of antigen specific foci as a complement independent assay for individual antibody-secreting cells.

Authors:  J Moore; C Calkins
Journal:  J Immunol Methods       Date:  1983-10-28       Impact factor: 2.303

3.  In vitro generation of cells producing antierythrocyte autoantibodies in normal mice.

Authors:  M Levy; W H Fridman; C Neauport-Sautes
Journal:  Cell Immunol       Date:  1982-08       Impact factor: 4.868

4.  Cellular assay for measuring anti-erythrocyte antibody responses.

Authors:  B Leshem; D Naor
Journal:  J Immunol Methods       Date:  1978       Impact factor: 2.303

5.  Polyclonal B-cell activators induce immunological response to autologous serum proteins.

Authors:  D Primi; C I Smith; L Hammarström; G Möller
Journal:  Cell Immunol       Date:  1977-12       Impact factor: 4.868

6.  Radioimmunoassay for immunoglobulin G autoantibody on the surface of mouse erythrocytes.

Authors:  C E Jones; C T Lee; W Skinner; J A Lamott; H H Koyama; K W Maxwell; H H Fudenberg
Journal:  Clin Immunol Immunopathol       Date:  1983-11

7.  Natural antibodies against tubulin, actin myoglobin, thyroglobulin, fetuin, albumin and transferrin are present in normal human sera, and monoclonal immunoglobulins from multiple myeloma and Waldenström's macroglobulinemia may express similar antibody specificities.

Authors:  S Avrameas; B Guilbert; G Dighiero
Journal:  Ann Immunol (Paris)       Date:  1981 Mar-Apr

8.  Organ-specific IgM autoantibodies to liver, heart and brain in man: generalized occurrence and possible functional significance in normal individuals, and studies in patients with multiple sclerosis.

Authors:  A S Daar; J W Fabre
Journal:  Clin Exp Immunol       Date:  1981-07       Impact factor: 4.330

9.  CBA/N X-linked B-cell defect prevents NZB B-cell hyperactivity in F1 mice.

Authors:  J D Taurog; H M Moutsopoulos; Y J Rosenberg; T M Chused; A D Steinberg
Journal:  J Exp Med       Date:  1979-07-01       Impact factor: 14.307

10.  Immunization of dissociated spleen cell cultures from normal mice.

Authors:  R I Mishell; R W Dutton
Journal:  J Exp Med       Date:  1967-09-01       Impact factor: 14.307

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  2 in total

1.  Active role of T cells in promoting an in vitro autoantibody response to self erythrocytes in NZB mice.

Authors:  R D Miller; C E Calkins
Journal:  Immunology       Date:  1988-04       Impact factor: 7.397

Review 2.  Regulatory T cells essential to prevent the loss of self-tolerance in murine models of erythrocyte-specific autoantibody responses.

Authors:  Catherine E Calkins
Journal:  Immunol Res       Date:  2011-12       Impact factor: 2.829

  2 in total

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