Literature DB >> 886185

Transient suppression of the humoral immune response mediated by a factor derived from specifically activated, doubly primed lymphoid cells.

K E Kempf, A S Rubin.   

Abstract

In cultures of sheep erythrocyte- (SRBC) stimulated spleen cells from mice immunized with tetanus toxoid (TT) and horse erythrocytes (HRBC) 30 to 90 days earlier, the addition of both HRBC (day 0) and TT (day 2) resulted in significant suppression of the anti-SRBC plaque-forming cell (PFC) response compared to the response of similar cultures maintained without the priming antigens. The observed inhibition was due to the presence of a soluble factor that was released into the supernatant fluid of the specifically stimulated, primed population of lymphoid cells between 72 and 120 hr after culture initiation. The active mediator, a macromolecule of approximately 24,000 daltons as determined by gel filtration over Sephadex G-150 and Ultrogel AcA 44, was suppressive when added within 24 hr, but not 48 hr, of assay for PFC against the reference SRBC antigen. The transiently acting soluble suppressor (TASS) was not overtly cytotoxic since total cell recovery and viability were unaffected in its presence. The results presented here are discussed in relation to a possible mechanism of action in which the negative regulation of immunoglobulin production is favored once a minimum level of immune reactivity is reached.

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Year:  1977        PMID: 886185

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  3 in total

1.  The conversion of an enhancing factor to a suppressor factor by the formation of an aggregate molecule.

Authors:  H L Mulcahy; A S Rubin; A B MacDonald
Journal:  Immunology       Date:  1981-01       Impact factor: 7.397

2.  Suppressive effect of alcoholic liver disease sera on lymphocyte transformation.

Authors:  G P Young; F J Dudley; M B Van Der Weyden
Journal:  Gut       Date:  1979-10       Impact factor: 23.059

3.  Purification and properties of a factor from leukaemic T cells which non-specifically enhances the antibody response.

Authors:  H L Mulcahy; A S Rubin; A B MacDonald
Journal:  Immunology       Date:  1981-01       Impact factor: 7.397

  3 in total

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