Literature DB >> 4623608

Immunosuppression of mice injected with heterologous anti-immunoglobulin heavy chain antisera.

D D Manning, J W Jutila.   

Abstract

Neonatal injection of mice with rabbit anti-micro antiserum has been shown to produce complete loss of direct and indirect plaque-forming responses to sheep erythrocytes as well as loss of serum IgM and severe depressions of all other serum immunoglobulins. Similar injection of anti-gamma1gamma2 or anti-gamma1 antibodies effects a loss of the indirect response but induces relatively minor alterations in serum Ig levels. Delaying initiation of anti-micro treatment until young adulthood results in a somewhat diminished effect on plaque-forming responses and serum Ig levels but triggers the release of high serum levels of an aberrant micro-bearing protein. Anti-micro suppression of genetically thymusless mice indicates that at least part of the target cells for suppression are bone marrow derived. A working hypothesis for the maturation of humoral antibody-producing cell lines as it relates to these data is discussed.

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Year:  1972        PMID: 4623608      PMCID: PMC2139172          DOI: 10.1084/jem.135.6.1316

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


  38 in total

1.  Surface immunoglobulins on mouse lymphoid cells.

Authors:  A D Bankhurst; N L Warner
Journal:  J Immunol       Date:  1971-08       Impact factor: 5.422

2.  Antigen receptor molecules: inhibition by antiserum against kappa light chains.

Authors:  J Lesley; R W Dutton
Journal:  Science       Date:  1970-07-31       Impact factor: 47.728

3.  The induction of haemolysin producing cells in vitro: inhibition by antiglobulin antisera.

Authors:  K U Hartmann; S Reeg; C Mehner
Journal:  Immunology       Date:  1971-01       Impact factor: 7.397

4.  Immunological responses of 'nude' mice.

Authors:  H H Wortis
Journal:  Clin Exp Immunol       Date:  1971-02       Impact factor: 4.330

5.  The comparative immunosuppressive effects of heterologous antisera to various C3H mouse tissues.

Authors:  A E Sloboda; J Landes
Journal:  J Immunol       Date:  1970-01       Impact factor: 5.422

6.  Absence of thymus in a mouse mutant.

Authors:  E M Pantelouris
Journal:  Nature       Date:  1968-01-27       Impact factor: 49.962

7.  Incidence of cells simultaneously secreting IgM and IgG antibody to sheep erythrocytes.

Authors:  G J Nossal; N L Warner; H Lewis
Journal:  Cell Immunol       Date:  1971-02       Impact factor: 4.868

8.  Effect of blocking cell receptors on an immune response resulting from in vitro cooperation between thymocytes and thymus-independent cells.

Authors:  G Doria; G Agarossi; S Di Pietro
Journal:  J Immunol       Date:  1971-11       Impact factor: 5.422

9.  Suppression of immunoglobulin class synthesis in mice. I. Effects of treatment with antibody to -chain.

Authors:  A R Lawton; R Asofsky; M B Hylton; M D Cooper
Journal:  J Exp Med       Date:  1972-02-01       Impact factor: 14.307

10.  Demonstration of heavy and light chain antigenic determinants on the cell-bound receptor for antigen. Similarities between membrane-attached and humoral antibodies produced by the same cell.

Authors:  C S Walters; H Wigzell
Journal:  J Exp Med       Date:  1970-12-01       Impact factor: 14.307

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  24 in total

1.  T cell-dependent helper and suppressive influences in an adoptive IgG antibody response.

Authors:  S Arrenbrecht; G F Mitchell
Journal:  Immunology       Date:  1975-03       Impact factor: 7.397

2.  Central B-cell tolerance: where selection begins.

Authors:  Roberta Pelanda; Raul M Torres
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-04-01       Impact factor: 10.005

3.  Peripheral B cell tolerance and function in transgenic mice expressing an IgD superantigen.

Authors:  Bao Hoa Duong; Takayuki Ota; Djemel Aït-Azzouzene; Miyo Aoki-Ota; José Luis Vela; Christoph Huber; Kevin Walsh; Amanda L Gavin; David Nemazee
Journal:  J Immunol       Date:  2010-03-15       Impact factor: 5.422

4.  Control of proliferation and differentiation in B lymphocytes by anti-Ig antibodies and a serum-derived cofactor.

Authors:  C L Sidman; E R Unanue
Journal:  Proc Natl Acad Sci U S A       Date:  1978-05       Impact factor: 11.205

5.  Induction of high titers of anti-IgE by immunization of inbred mice with syngeneic IgE.

Authors:  S Haba; A Nisonoff
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

6.  Induction of an auto-anti-IgE response in rats. III. Inhibition of a specific IgE response.

Authors:  J S Marshall; E B Bell
Journal:  Immunology       Date:  1989-03       Impact factor: 7.397

7.  Failure of central axonal regeneration after immunosuppressive treatment.

Authors:  M Berry; A C Riches; J Knowles; P Willis; D Steers
Journal:  J Anat       Date:  1979-09       Impact factor: 2.610

Review 8.  Immunoglobulin profiles of the chronic antibody response: discussion in relation to brucellosis infections.

Authors:  R G White
Journal:  Postgrad Med J       Date:  1978-09       Impact factor: 2.401

9.  Development of plasmacytoid cells with Russell bodies in autoimmune "viable motheaten" mice.

Authors:  L D Shultz; D R Coman; B L Lyons; C L Sidman; S Taylor
Journal:  Am J Pathol       Date:  1987-04       Impact factor: 4.307

10.  Specific suppression of the antibody response by antibodies to receptors.

Authors:  H Cosenza; H Köhler
Journal:  Proc Natl Acad Sci U S A       Date:  1972-09       Impact factor: 11.205

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