Literature DB >> 6131747

Cellular origin of blocking factors from cultured spleen cells of tumor-bearing mice.

T A Koppi, W J Halliday.   

Abstract

Spleen cells from mice bearing methylcholanthrene-induced tumors were cultured for 2 days without further stimulation. Blocking factors were consistently detected in culture supernatants by their ability to suppress leukocyte adherence inhibition reactions between soluble tumor antigens and peritoneal cells of tumor-bearing mice. The blocking factors were specific for individual tumors. The cellular origin of these factors was investigated by depleting the spleen cell population of various cell types before culturing. The cells involved were removed by treatment with antibodies to certain membrane markers (Thy-1, Ly-2, Ia, I-J) but not by anti-Ly-1 antibodies. Removal of adherent cells also prevented production of blocking factors, which was restored by reconstitution with syngeneic but not allogeneic cells from normal mice. The normal reconstituting cells were shown to bear Ia, but not I-J or IgM. This indicates that blocking factors (previously shown to have I-J determinants in their molecules) originate from suppressor T lymphocytes (Thy-1+, Ly-1-2+, I-J+), with macrophages (I-J-, Ia+) in the role of accessory cells.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6131747     DOI: 10.1016/0008-8749(83)90345-3

Source DB:  PubMed          Journal:  Cell Immunol        ISSN: 0008-8749            Impact factor:   4.868


  7 in total

1.  Effects of anti-idiotype vaccine on tumour growth and on production of soluble factors modulating cell-mediated immunity in vitro.

Authors:  J M Greer; W J Halliday
Journal:  Cancer Immunol Immunother       Date:  1991       Impact factor: 6.968

2.  Cellular requirements for the suppression of leucocyte adherence inhibition reactions by serum factors from tumour-bearing mice.

Authors:  V K Kuchroo; W J Halliday
Journal:  Immunology       Date:  1986-04       Impact factor: 7.397

3.  Suppression of contact hypersensitivity by short-term ultraviolet irradiation: I. Immunosuppression by serum from irradiated mice.

Authors:  T G Harriott-Smith; W J Halliday
Journal:  Clin Exp Immunol       Date:  1988-01       Impact factor: 4.330

4.  Comparison of T suppressor factors from tumour-bearing mice and mice immunized with a monoclonal anti-idiotypic antibody.

Authors:  J M Greer; W J Halliday
Journal:  Cancer Immunol Immunother       Date:  1990       Impact factor: 6.968

5.  Effect of monoclonal antibodies to early pregnancy factor (EPF) on the in vivo growth of transplantable murine tumours.

Authors:  K A Quinn; H Morton
Journal:  Cancer Immunol Immunother       Date:  1992       Impact factor: 6.968

6.  Monoclonal antibodies to early pregnancy factor perturb tumour cell growth.

Authors:  K A Quinn; S Athanasas-Platsis; T Y Wong; B E Rolfe; A C Cavanagh; H Morton
Journal:  Clin Exp Immunol       Date:  1990-04       Impact factor: 4.330

7.  The absence of delayed-type hypersensitivity reactivity in a syngeneic murine tumour system.

Authors:  G Los; R A De Weger; R M Moberts; H Van Loveren; R J Sakkers; W Den Otter
Journal:  Immunology       Date:  1987-09       Impact factor: 7.397

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.