Literature DB >> 87431

The expression of Ia antigenic determinants on macrophages required for the in vitro antibody response.

J E Niederhuber, P Allen, L Mayo.   

Abstract

A subpopulation of antigen-presenting macrophages required for an in vitro antibody response to burro erythrocytes was deleted by pretreating the splenic macrophages with anti-Ia serum and complement (C). The in vitro response of the macrophage depleted T-B cell population could not be restored by the addition of macrophages resistant to anti-Ia antibodies and C (Ia-). The response of Ia- macrophages and the macrophage-depleted T-B cells was only reconstituted by the addition of Ia+ macrophages. Macrophages pretreated with anti-Ia antibodies restricted to react with determinants of one I subregion could not support the in vitro antibody response when added to cultures whose macrophages were pretreated with anti-Ia serum and C specific for the I-J subregion. These results confirmed that Ia determinants of the I-A, the I-E, and the I-C subregions were all expressed on the I-J+ macrophage required for an in vitro antibody response.

Mesh:

Substances:

Year:  1979        PMID: 87431

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


  21 in total

1.  Involvement of I-J epitopes in the self- and allo-recognition sites of T cells: blocking of syngeneic and allogeneic mixed lymphocyte reaction-responder cells by monoclonal anti-I-J antibodies.

Authors:  W Uracz; R Abe; T Tada
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

2.  Visualization of anti-I-J antibody binding sites on bone marrow-derived macrophages.

Authors:  R M Nakamura; K Kitamura
Journal:  Immunol Res       Date:  1987       Impact factor: 2.829

3.  Anti-I-J alloantisera elicited by immunization of B10.A(3R) (I-Jb) mice with bone marrow-derived macrophages from B10.A(5R) (I-Jk) mice.

Authors:  L M Bradley; S M Shiigi; A Malley
Journal:  Immunology       Date:  1986-03       Impact factor: 7.397

4.  A non-T:non-B cell bears I-A, I-E, I-J, and Tla (Qa-1?) determinants.

Authors:  S Habu; K Yamauchi; R K Gershon; D B Murphy
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

5.  Ly-1 inducer and Ly-1,2 acceptor T cells in the feedback suppression circuit bear an I-J-subregion controlled determinant.

Authors:  D D Eardley; D B Murphy; J D Kemp; F W Shen; H Cantor; R K Gershon
Journal:  Immunogenetics       Date:  1980       Impact factor: 2.846

6.  The use of a monoclonal i-j-specific antibody to distinguish cells in the feedback suppression circuit from those in the contrasuppressor circuit.

Authors:  K Yamauchi; M Taniguchi; D Green; R K Gershon
Journal:  Immunogenetics       Date:  1982       Impact factor: 2.846

7.  Characterization of responding cells in oxidative mitogen stimulation. III. Presence of I-A- and I-J, E, C-subregion gene products on the surface of required cells.

Authors:  M L Phillips; S W Hill; J W Parker; R L O'Brien; J A Frelinger
Journal:  Immunogenetics       Date:  1980       Impact factor: 2.846

Review 8.  Surface receptors on lymphoreticular cells: sensory devices for host recognition of foreign antigens and neoplasia.

Authors:  B E Elliott; R S Kerbel; Z A Nagy
Journal:  Can Med Assoc J       Date:  1980-06-21       Impact factor: 8.262

9.  Increased Ia expression, T lymphocyte subset abnormalities and autoimmunity in murine strains bearing the lpr gene.

Authors:  M J Dauphinée; N Talal
Journal:  Clin Exp Immunol       Date:  1984-10       Impact factor: 4.330

10.  Accessory cell function of liver granuloma macrophages of Schistosoma mansoni-infected mice.

Authors:  L B Schook; S R Wellhausen; D L Boros; J E Niederhuber
Journal:  Infect Immun       Date:  1983-12       Impact factor: 3.441

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