Literature DB >> 5554099

Further studies of antigenic competition. 3. A model to account for the phenomenon based on a deficiency of cell-to-cell interaction in immune lymphoid cell populations.

R S Kerbel, D Eidinger.   

Abstract

A striking correlation between the capacity of an antigen to nonspecifically suppress humoral immune responses of subsequently administered antigens which are non-cross-reacting, i.e. to manifest antigenic competition and produce enlargement of spleen size through cell proliferation, was found. Increase in spleen size was always accompanied by a drop in the normal proportion of thymus-derived cells to non-thymus-derived cells. Various means of altering the immune response to the initial antigen, and hence, the capacity of that antigen to suppress in a model of antigenic competition were performed and correlated with changes in spleen size and in the proportion of theta-positive cells in the spleen. In all instances, when the experimental condition reduced or abolished antigenic competition, the increase in spleen size and reduction in the proportion of theta-positive cells in the spleen was reduced or abolished. Furthermore, under conditions in which the suppressive capacity of the initial antigen was unaltered, the increase in spleen size and reduction in theta-proportion occurred normally. Finally, the better the suppression in a model of antigenic competition, the greater the increase in spleen size and reduction in the proportion of theta-positive cells. On the basis of these observations, it appears that there is a relationship between spleen enlargement through clonally restricted cell proliferation and the expression of antigenic competition; one cannot have the latter without the former. It is postulated that the immunological lesion associated with antigenic competition resides at the level of interference with cell interaction between thymus-derived antigen-reactive cells and marrow-derived antibody-forming cells. This occurs as a result of a relative "diluting out" of cells of both populations carrying antigenic specificity differing from the one(s) which induced the dilution effect in the first place. The net effect of this is to decrease the chance of a "hit" or interaction between a marrow-derived and thymus-derived cell of the same specificities. This mechanism, which is compatible with theories of clonal selection, and which in fact is dependent upon them, supports the view that the term "antigenic competition" is a misnomer; there is no competition by the antigens for anything. The term "antigen-induced suppression" is suggested as a more suitable alternative.

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Year:  1971        PMID: 5554099      PMCID: PMC2138918          DOI: 10.1084/jem.133.5.1043

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


  21 in total

1.  Antigenic competition: cellular or humoral.

Authors:  J Radovich; D W Talmage
Journal:  Science       Date:  1967-10-27       Impact factor: 47.728

2.  Inhibitory effect of a tolerated antigen on antibody production to a second antigen.

Authors:  P Liacopoulos; S G Herlem
Journal:  Int Arch Allergy Appl Immunol       Date:  1968

3.  The effect of antigen competition on both the primary and secondary immune capacity in mice.

Authors:  M G Hanna; L C Peters
Journal:  J Immunol       Date:  1970-01       Impact factor: 5.422

4.  Antigen competition: antigens compete for a cell occurring with limited frequency.

Authors:  J F Albright; T F Omer; J W Deitchman
Journal:  Science       Date:  1970-01-09       Impact factor: 47.728

5.  Immunocompetence of transferred thymus-marrow cell combinations.

Authors:  H N Claman; E A Chaperon; R F Triplett
Journal:  J Immunol       Date:  1966-12       Impact factor: 5.422

6.  Specific tolerance to sheep erythrocytes in mouse bone marrow cells.

Authors:  J H Playfair
Journal:  Nature       Date:  1969-05-31       Impact factor: 49.962

7.  Mouse thymic iso-antigens.

Authors:  A E Reif; J M Allen
Journal:  Nature       Date:  1966-01-29       Impact factor: 49.962

8.  Antigenic changes in lymph-node cells after administration of antiserum to thymus cells.

Authors:  M Schlesinger; I Yron
Journal:  Science       Date:  1969-06-20       Impact factor: 47.728

9.  Cell to cell interaction in the immune response. II. The source of hemolysin-forming cells in irradiated mice given bone marrow and thymus or thoracic duct lymphocytes.

Authors:  G F Mitchell; J F Miller
Journal:  J Exp Med       Date:  1968-10-01       Impact factor: 14.307

10.  Antigen-reactive cells in normal, immunized, and tolerant mice.

Authors:  W D Armstrong; E Diener; G R Shellam
Journal:  J Exp Med       Date:  1969-02-01       Impact factor: 14.307

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  10 in total

1.  Properties of a subpopulation of T cells bearing histamine receptors.

Authors:  M Plaut; L M Lichtenstein; C S Henney
Journal:  J Clin Invest       Date:  1975-04       Impact factor: 14.808

2.  In vitro studies of 'antigenic competition'. II. Reconstitution of the immune defect and the relationship between antigen-induced suppression and non-specific enhancement.

Authors:  H Pross; D Eidinger
Journal:  Immunology       Date:  1973-08       Impact factor: 7.397

3.  Increased production of plaque-forming cells in mouse lymph nodes following regional injection of a second antigen.

Authors:  S E Sher; T N Harris
Journal:  Immunology       Date:  1972-07       Impact factor: 7.397

4.  Cell interactions in the immune response in vitro. V. Specific collaboration via complexes of antigen and thymus-derived cell immunoglobulin.

Authors:  M Feldmann
Journal:  J Exp Med       Date:  1972-10-01       Impact factor: 14.307

5.  Studies on antigenic competition. 3. Effect on antigenic competition on antibody affinity.

Authors:  Y T Kim; N Merrifield; T Zarchy; N I Brody; G W Siskind
Journal:  Immunology       Date:  1974-05       Impact factor: 7.397

6.  Antigenic competition between minor (non-H-2) histocompatibility antigens.

Authors:  L L Johnson; D W Bailey; L E Mobraaten
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

7.  Blastogenic response of Toxoplasma-infected mouse spleen cells to T- and B-cell mitogens.

Authors:  G T Strickland; A Ahmed; K W Sell
Journal:  Clin Exp Immunol       Date:  1975-10       Impact factor: 4.330

8.  Depression of the plaque-forming cells to sheep red blood cells by the new-born larvae of Trichinella spiralis.

Authors:  G M Faubert
Journal:  Immunology       Date:  1976-04       Impact factor: 7.397

9.  Cortisone-induced immunotolerance to nematode infection in CBA/Ca mice. II. A model for human chronic trichuriasis.

Authors:  T D Lee; D Wakelin
Journal:  Immunology       Date:  1983-03       Impact factor: 7.397

10.  A cellular deficit in the reconstitutive capacity of immune populations of lymphoid cells demonstrable in studies of delayed hypersensitivity in mice. Evidence for thymus-bone marrow cell synergism.

Authors:  D Eidinger; A Ackerman
Journal:  J Exp Med       Date:  1971-05-01       Impact factor: 14.307

  10 in total

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