Literature DB >> 47897

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

J W Schrader.   

Abstract

B-cell tolerance has been induced by oligovalent thymus-dependent antigens in an entirely in vitro system. Dissociated spleen cells from congenitally athymic (nu/nu) mice were preincubated for 24 h with 0.1 -- 1 mg/ml of either fowl gamma globulin (FGG) of DNP-human gamma globulin (DNP-HGG). After washing, the cells were tested for the ability to mount in vitro, thymus-independent responses against FGG and DNP. A state of specific responsiveness to either FGG or DNP was thus demonstrated. Features of this wholly in vitro system that paralleled previous findings on the in vivo induction of B-cell tolerance in nu/nu mice were the kinetics, 24 h being required for tolerance induction in either case, the abrogation of tolerance induction by the presence of POL both in vivo and in vitro, and finally the observation that in neither case was there a requirement for the antigens to be deaggregated. It was shown that DNP-(Fab) 2 fragments prepared from HGG induced DNP-specific tolerance indicating that the Fc piece was not required for tolerance induction in this in vitro system. DNP-bovine serum albumin was less effective than DNP-HGG or DNP-(Fab)2. Preincubation with subtoxic concentrations of DNP-lysine of DNP-epsilon-capric acid had only a marginal effect on DNP responsiveness. Since nu/nu mice, lacking in detectable T-cell function, were used as spleen cell donors, this work provides further evidence that B-cell tolerance to thymus-dependent antigens can be induced without the participation of T cells. It is suggested that B-cell tolerance to thymus-dependent antigens occurs when the antigen in a sufficient concentration and over a sufficient period of time has direct access to the B cell. This contact with antigen must be in the absence of an additional influence provided either by adjuvants like endotoxin or POL, or by activated macrophages, which may be stimulated by activated T cells; otherwise not tolerance but B-cell activation will occur.

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Year:  1975        PMID: 47897      PMCID: PMC2189784          DOI: 10.1084/jem.141.5.962

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


  35 in total

1.  ANTIGENS IN IMMUNITY. III. DISTRIBUTION OF IODINATED ANTIGENS FOLLOWING INJECTION INTO RATS VIA THE HIND FOOTPADS.

Authors:  G L ADA; G J NOSSAL; J PYE
Journal:  Aust J Exp Biol Med Sci       Date:  1964-06

2.  TOLERANCE TO A PROTEIN ANTIGEN IN ADULT MICE AND THE EFFECT OF NONSPECIFIC FACTORS.

Authors:  H N CLAMAN
Journal:  J Immunol       Date:  1963-12       Impact factor: 5.422

3.  Properties of the major component of a peptic digest of rabbit antibody.

Authors:  A NISONOFF; F C WISSLER; L N LIPMAN
Journal:  Science       Date:  1960-12-09       Impact factor: 47.728

4.  Immunological unresponsiveness of genetically thymusless (nude) mice.

Authors:  B Kindred
Journal:  Eur J Immunol       Date:  1971-01       Impact factor: 5.532

5.  Inhibition of secondary anti-hapten responses with the hapten conjugated to type 3 pneumococcal polysaccharide.

Authors:  G F Mitchell; J H Humphrey; A R Wiliamson
Journal:  Eur J Immunol       Date:  1972-10       Impact factor: 5.532

6.  Relationship between antigen and antibody-induced suppression of immunity.

Authors:  E Diener; M Feldmann
Journal:  Transplant Rev       Date:  1972

7.  Mechanism of activation of the bone marrow-derived lymphocyte. 3. A distinction between a macrophage-produced triggering signal and the amplifying effect on triggered B lymphocytes of allogeneic interactions.

Authors:  J W Schrader
Journal:  J Exp Med       Date:  1973-12-01       Impact factor: 14.307

8.  Specific activation of the bone marrow-derived lymphocyte by antigen presented in a non-multivalent form.

Authors:  J W Schrader
Journal:  J Exp Med       Date:  1973-03-01       Impact factor: 14.307

9.  The relationship between antigenic structure and the requirement for thymus-derived cells in the immune response.

Authors:  M Feldmann; A Easten
Journal:  J Exp Med       Date:  1971-07-01       Impact factor: 14.307

10.  The ability of bacterial lipopolysaccharide to modulate the induction of unresponsiveness to a state of immunity. Cellular parameters.

Authors:  J A Louis; J M Chiller; W O Weigle
Journal:  J Exp Med       Date:  1973-12-01       Impact factor: 14.307

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  3 in total

1.  Can B-cell tolerance be induced by oligovalent thymus dependent antigens?

Authors:  H Waldmann; H Pope
Journal:  Immunology       Date:  1977-05       Impact factor: 7.397

2.  B-cell subsets responsive to fluorescein-conjugated antigens. III. Differential effect of E. Coli lipopolysaccharide on T-dependent and T-independent responses in vivo.

Authors:  M Venkataraman; D W Scott
Journal:  Immunology       Date:  1979-11       Impact factor: 7.397

3.  In vitro tolerance induction of neonatal murine B cells.

Authors:  E S Metcalf; N R Klinman
Journal:  J Exp Med       Date:  1976-06-01       Impact factor: 14.307

  3 in total

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