Literature DB >> 5528413

Induction and reversal of immune paralysis in vitro.

V S Byers, E E Sercarz.   

Abstract

Induction of the immune response can only be completed after antigen is removed from the cellular environment. Primed rabbit lymph node fragments were cultured in vitro with 5 mg/ml BSA. If antigen was removed from the fragments 2 hr later, they produced a normal anti-BSA response, which was first evident 5 days later. If antigen removal was delayed for 3 days, the onset of the response was postponed for 2 to 3 days. Pulses with BUDR marked the periods of cell proliferation in both sets of cultures, and established that the postponement of antibody production was preceded by a postponement in the wave of proliferation among precursors of antibody forming cells. The similarity in avidity of antibody-containing fluids from normal and postponed cultures support the idea that the same cell population produced the response in each case. It was concluded that a reversible state of paralysis could be instituted in antigen-responsive cells, and this state did not depend upon cell-killing. The widespread incidence of temporary paralysis as an early aspect of the immune response was discussed.

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Year:  1970        PMID: 5528413      PMCID: PMC2138880          DOI: 10.1084/jem.132.5.845

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


  17 in total

1.  A method of trace iodination of proteins for immunologic studies.

Authors:  P J McConahey; F J Dixon
Journal:  Int Arch Allergy Appl Immunol       Date:  1966

2.  Mechanism of immunologic tolerance. I. Induction of tolerance to bovine gamma-globulin by injection of antigen into intact organs in vitro.

Authors:  D W Scott; B H Waksman
Journal:  J Immunol       Date:  1969-02       Impact factor: 5.422

Review 3.  The mechanism of immunological paralysis.

Authors:  D W Dresser; N A Mitchison
Journal:  Adv Immunol       Date:  1968       Impact factor: 3.543

4.  The suppressive effect of supraoptimum doses of antigen on the secondary antibody-forming response of spleen cells cultured in cell-impermeable diffusion chambers.

Authors:  T Makinodan; I Hoppe; T Sado; E E Capalbo; M R Leonard
Journal:  J Immunol       Date:  1965-09       Impact factor: 5.422

5.  Determination of avidity of anti-albumin antibodies in the mouse. Influence of the number of cells transferred on the quality of the secondary adoptive response.

Authors:  F Celada; D Schmidt; R Strom
Journal:  Immunology       Date:  1969-08       Impact factor: 7.397

6.  Recovery from immunological paralysis in relation to age and residual antigen.

Authors:  N A Mitchison
Journal:  Immunology       Date:  1965-08       Impact factor: 7.397

7.  The X-Y-Z scheme of immunocyte maturation. II. The effect of antigen on spontaneous escape from immune paralysis.

Authors:  S J Dowden; E E Sercarz
Journal:  J Immunol       Date:  1967-04       Impact factor: 5.422

8.  High-dose delay of the immune response. Effect of actinomycin D on continuation of the immune response in vitro.

Authors:  J Iványi; M Maler; L Wudl; E Sercarz
Journal:  J Exp Med       Date:  1968-06-01       Impact factor: 14.307

9.  The X-Y-Z scheme of immunocyte maturation. V. Paralysis of memory cells.

Authors:  V S Byers; E E Sercarz
Journal:  J Exp Med       Date:  1968-10-01       Impact factor: 14.307

10.  The relative affinity of antibodies synthesized in the secondary response.

Authors:  L A Steiner; H N Eisen
Journal:  J Exp Med       Date:  1967-12-01       Impact factor: 14.307

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  10 in total

1.  The adoptive secondary response to human serum albumin under conditions of high antigen pressure. The response of high and low avidity B cell subsets.

Authors:  E B Bell; F L Shand
Journal:  Immunology       Date:  1977-10       Impact factor: 7.397

2.  Antibody response to a protein antigen (ovalbumin) in dissociated spleen cell cultures from primed mice. Evidence for a suppressive effect of antigen.

Authors:  M R Salaman; S Britton
Journal:  Immunology       Date:  1973-01       Impact factor: 7.397

3.  In vitro antibody response to a distinct antigenic determinant of Escherichia coli beta-D-galactosidase. Effect of antigen dosage and co-cultivation of lymph node fragments on peak titres and duration of antibody synthesis.

Authors:  A J Macario; E Conway de Macario
Journal:  Immunology       Date:  1974-07       Impact factor: 7.397

4.  Reversibility of high dose unresponsiveness to concanavalin A in thymus lymphocytes.

Authors:  J Andersson; O Sjöberg; G Möller
Journal:  Immunology       Date:  1972-10       Impact factor: 7.397

5.  Cellular mechanisms of escape from immunological tolerance.

Authors:  J Ivanyi; A Salerno
Journal:  Immunology       Date:  1972-02       Impact factor: 7.397

6.  Rapid breaking of tolerance against Escherichia coli lipopolysaccharide in vivo and in vitro.

Authors:  O Sjöberg
Journal:  J Exp Med       Date:  1972-04-01       Impact factor: 14.307

7.  Regulation of autosensitization. The immune activation and specific inhibition of self-recognizing thymus-derived lymphocytes.

Authors:  I R Cohen; H Wekerle
Journal:  J Exp Med       Date:  1973-02-01       Impact factor: 14.307

8.  The in vitro induction of immunological tolerance in the B lymphocyte by oligovalent thymus-dependent antigens.

Authors:  J W Schrader
Journal:  J Exp Med       Date:  1975-05-01       Impact factor: 14.307

9.  Immunological tolerance in bone marrow-derived lymphocytes. I. Evidence for an intracellular mechanism of inactivation of hapten-specific precursors of antibody-forming cells.

Authors:  D H Katz; T Hamaoka; B Benacerraf
Journal:  J Exp Med       Date:  1972-12-01       Impact factor: 14.307

10.  Autosensitization in vitro.

Authors:  I R Cohen; A Globerson; M Feldman
Journal:  J Exp Med       Date:  1971-04-01       Impact factor: 14.307

  10 in total

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