Literature DB >> 109503

Induction of suppressor cells in rat spleen: influence of microbial stimulation.

J A Mattingly, D D Eardley, J D Kemp, R K Gershon.   

Abstract

The role of the products of prostaglandin synthetase in the suppression of in vitro secondary antibody responses by rat spleen cells was examined. By including cells from both germfree and conventional rats in these studies, the effect of in vivo microbial stimulation on this suppression was also determined. We found that 1) the suppression that is normally present in the spleen cells of rats can be eliminated by the use of glass wool or indomethacin; 2) germfree rats do not display this suppressor activity, and 3) this "deficit" in the germfree rat may be due to a lack of a microbial-induced signal from a nonadherent cell to an adherent prostaglandin-containing macrophage, implying that at least two cells are involved in the prostaglandin-synthetase dependent suppressor effect. It is possible that large amounts of some or all microbial products activate "suppressor" macrophages and that inbred rats behave like "chronically infected" mice because of an inability to regulate their "normal" microbial flora.

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Year:  1979        PMID: 109503

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


  17 in total

Review 1.  Antigen recognition in the gastrointestinal tract: death to the dogma.

Authors:  L Mayer; A Panja; Y Li
Journal:  Immunol Res       Date:  1991       Impact factor: 2.829

2.  Glucocorticoids enhance concanavalin A-induced mitogenic response through the inhibition of nitric oxide production.

Authors:  F Ramírez; A Silva
Journal:  Immunology       Date:  1997-01       Impact factor: 7.397

3.  Induction of antigen-specific T suppressor cells by soluble Paracoccidioides brasiliensis antigen.

Authors:  B E Jimenez-Finkel; J W Murphy
Journal:  Infect Immun       Date:  1988-04       Impact factor: 3.441

4.  Maturation of the rat small intestine at weaning: changes in epithelial cell kinetics, bacterial flora, and mucosal immune activity.

Authors:  A G Cummins; T W Steele; J T LaBrooy; D J Shearman
Journal:  Gut       Date:  1988-12       Impact factor: 23.059

5.  Immunosuppressive macrophages induced by arthropathic peptidoglycan-polysaccharide polymers from bacterial cell walls.

Authors:  D R Regan; P L Cohen; W J Cromartie; J H Schwab
Journal:  Clin Exp Immunol       Date:  1988-12       Impact factor: 4.330

6.  Hypothalamic-immune interactions. II. The effect of hypothalamic lesions on the ability of adherent spleen cells to limit lymphocyte blastogenesis.

Authors:  T L Roszman; R J Cross; W H Brooks; W R Markesbery
Journal:  Immunology       Date:  1982-04       Impact factor: 7.397

7.  Alveolar macrophages. VI. Regulation of alveolar macrophage-mediated suppression of lymphocyte proliferation by a putative T cell.

Authors:  L A Warner; P G Holt; G Mayrhofer
Journal:  Immunology       Date:  1981-01       Impact factor: 7.397

8.  Suppressor cell regulation of cell-mediated immune responses in renal infection in vitro modulation of suppressor cell activity.

Authors:  T Miller; E Marshall
Journal:  J Clin Invest       Date:  1980-10       Impact factor: 14.808

9.  Proliferative responses of central and peripheral rat lymphocytes elicited by cord factor (trehalose 6,6'-dimycolate).

Authors:  F Kierszenbaum; D R Walz
Journal:  Infect Immun       Date:  1981-07       Impact factor: 3.441

10.  Effect of indomethacin treatment upon actively-induced and transferred experimental allergic encephalomyelitis (EAE) in Lewis rats.

Authors:  H Ovadia; P Y Paterson
Journal:  Clin Exp Immunol       Date:  1982-08       Impact factor: 4.330

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