Literature DB >> 6213552

The in vitro generation of suppressor lymphocytes involves interactions between PNA+ and PNA- thymocyte populations.

A Eisenthal, D Nachitgal, M Feldman.   

Abstract

Employing cell fractionation with the aid of peanut agglutinin, it was found that at least two subpopulations of T cells are required for the generation of suppressor T lymphocytes in culture. The co-operation of these two subpopulations, the medullary and the cortical types of thymocytes, is required for the induction phase but it apparently plays no role in the expression of the suppressive effect. With the aid of genetic markers, it was found that in medullary-type, cortisone-resistant, PNA-negative T cell was the progenitor of the suppressor lymphocytes, while the cortical type cells performed an accessory (regulatory?) function. Finally, it was observed that allostimulation of T cells in culture give rise to both 'helper' and suppressor cells. The generation of 'helper' lymphocytes requires allostimulation for less than 24 hr while the induction of suppressor cells requires a longer period of stimulation which leads in the end to predominance of the suppressor effect.

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Year:  1982        PMID: 6213552      PMCID: PMC1555484     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  29 in total

Review 1.  The role of specific suppressor T cells in immune tolerance.

Authors:  D Nachtigal; I Zan-Bar; M Feldman
Journal:  Transplant Rev       Date:  1975

2.  A procedure for removing red cells and dead cells from lymphoid cell suspensions.

Authors:  W F Davidson; C R Parish
Journal:  J Immunol Methods       Date:  1975-06       Impact factor: 2.303

Review 3.  T cell control of antibody production.

Authors:  R K Gershon
Journal:  Contemp Top Immunobiol       Date:  1974

4.  Role of the thymus in tolerance. 8. Relative effectiveness of nonaggregated and heat-aggregated bovine gamma globulin, injected directly into lymphoid organs of normal rats, in suppressing immune responsiveness.

Authors:  A Horiuchi; B H Waksman
Journal:  J Immunol       Date:  1968-12       Impact factor: 5.422

5.  Cell interactions in the induction of tolerance: the role of thymic lymphocytes.

Authors:  R K Gershon; K Kondo
Journal:  Immunology       Date:  1970-05       Impact factor: 7.397

6.  In vitro stimulation of mouse thymus cells by PHA and allogeneic cells.

Authors:  H Blomgren; E Svedmyr
Journal:  Cell Immunol       Date:  1971-08       Impact factor: 4.868

7.  Evidence for a small pool of immunocompetent cells in the mouse thymus.

Authors:  H Blomgren; B Andersson
Journal:  Exp Cell Res       Date:  1969-10       Impact factor: 3.905

8.  Amplifying and suppressive effect of thymus cells.

Authors:  W Droege
Journal:  Nature       Date:  1971-12-31       Impact factor: 49.962

9.  Infectious immunological tolerance.

Authors:  R K Gershon; K Kondo
Journal:  Immunology       Date:  1971-12       Impact factor: 7.397

10.  Cell-mediated immune responses in vitro. I. Suppression of the generation of cytotoxic lymphocytes by concanavalin A and concanavalin A-activated spleen cells.

Authors:  D L Peavy; C W Pierce
Journal:  J Exp Med       Date:  1974-08-01       Impact factor: 14.307

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  2 in total

1.  Analysis of electrophoretic mobility histogram of mouse thymocytes during tumour development.

Authors:  T Iwaguchi; M Shimizu; T Mori; T Nakajima
Journal:  Immunology       Date:  1984-06       Impact factor: 7.397

2.  Colony formation by subpopulations of T lymphocytes. IV. Inhibitory effect of hydrocortisone on human and murine T cell subsets.

Authors:  M H Claësson; C Röpke
Journal:  Clin Exp Immunol       Date:  1983-11       Impact factor: 4.330

  2 in total

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