Literature DB >> 6966663

Antigen-antibody complexes generate Lyt 1 inducers of suppressor cells.

V S Rao, J A Bennett, F W Shen, R K Gershon, M S Mitchell.   

Abstract

Pretreatment of H-2b mice with KCl-extracts of an H-2d tumor (L1210) together with L1210 antibody rendered the mice incapable of mounting an effective immune response to viable L1210 tumor cells. This specific immunosuppression was associated with inhibition of macrophage functions, which could be used to quantitate the level of suppression. Lyt 1 cells (but not Lyt 2 cells) from either the spleen or thymus of mice pretreated with antigen-antibody complexes could adoptively transfer the suppressed state to normal mice. The Lyt 1 cells that transferred the suppression were resistant to low (20 mg/kg) doses of cyclophosphamide (Cy) but required a Cy-sensitive precursor and/or amplifier cell to be activated. Once activated, they required a Cy-sensitive Lyt 1 2 3 acceptor cell in the normal recipient to effectively suppress the adoptive host's macrophages. Our results indicative that immune complexes in concert with a Cy-sensitive T cell generate Cy-resistant Lyt 1 inducers of suppression. These in turn activate normal thymic or peripheral Lyt 1 2 3 acceptor cells, resulting in the generation of effector suppressor T cells. These suppressor cells are most likely the proximate cause of the inhibition of macrophages we have observed in vivo.

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Year:  1980        PMID: 6966663

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


  10 in total

1.  Induction of antigen-specific suppression by circulating Cryptococcus neoformans antigen.

Authors:  J W Murphy; R A Cox
Journal:  Clin Exp Immunol       Date:  1988-08       Impact factor: 4.330

Review 2.  Suppressor mechanisms in tumor immunity.

Authors:  G T Nepom; I Hellström; K E Hellström
Journal:  Experientia       Date:  1983-03-15

3.  Immunological agnosis: a state that derives from T suppressor cell inhibition of antigen-presenting cells.

Authors:  W Ptak; R K Gershon
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

4.  Surgery, trauma and immune suppression. Evolving the mechanism.

Authors:  J Lundy; C M Ford
Journal:  Ann Surg       Date:  1983-04       Impact factor: 12.969

5.  Functional deletion of different Ly-1 T-cell-inducer subset activities by Ly-2 suppressor T lymphocytes.

Authors:  D R Green; R K Gershon; D D Eardley
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

6.  Regulation of macrophage phagocytosis of syngeneic erythrocytes by T-cell subsets from NZB mice: differential effects of T cells from young and old mice.

Authors:  K Nakamura; A Yoshii; T Akahoshi; S Kashiwazaki; M Kawakami
Journal:  Immunology       Date:  1982-07       Impact factor: 7.397

7.  Cell surface phenotypes of radiolabeled immune long-lived lymphocytes that selectively localize in syngeneic tumours.

Authors:  J J Mulé; I Hellström; K E Hellström
Journal:  Am J Pathol       Date:  1982-05       Impact factor: 4.307

8.  Serum-mediated suppression of lymphocyte transformation responses in coccidioidomycosis.

Authors:  R A Cox; R M Pope
Journal:  Infect Immun       Date:  1987-05       Impact factor: 3.441

9.  Effects of pulse cyclophosphamide on NZB/W disease.

Authors:  D Chia; L Levy; E V Barnett; W H Carnes
Journal:  Immunology       Date:  1981-05       Impact factor: 7.397

10.  Two Ly-2 T helper cell subsets distinguished by Qa-1 phenotype. The priming environment determines whether one or both subsets will be generated.

Authors:  J S McDougal; F W Shen; S P Cort; J Bard
Journal:  J Exp Med       Date:  1982-03-01       Impact factor: 14.307

  10 in total

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