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Spontaneously Induced Suppressor Cells In Vitro : Nonspecific Suppression of In Vitro Antibody Formation
Author(s) -
Kodama Kazue,
Kurashige Satonori,
Mitsuhashi Susumu
Publication year - 1981
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.1981.tb00125.x
Subject(s) - biology , concanavalin a , myeloid derived suppressor cell , microbiology and biotechnology , in vitro , suppressor , lipopolysaccharide , immune system , antigen , population , antibody , cd40 , cell culture , cytotoxic t cell , immunology , biochemistry , medicine , gene , genetics , environmental health
Nonspecific suppressor cells were induced during in vitro culture of normal mouse spleen cells (SPC) using the Marbrook culture system. The suppressor cells inhibited both the primary and secondary antibody‐formation responses antigen nonspecifically in vitro , and both IgM‐ and IgG‐responses were inhibited. The supernatants from suppressive precultured cells were not suppressive. The suppressor cells also inhibited the response of allogeneic SPC beyond H‐2 compatibility. The induction of the suppressor cells did not require the presence of antigen but required fetal calf serum (FCS) or both FCS and 2‐mercaptoethanol (2‐ME). The suppressor cells were generated from the nylon‐wool adherent, radiation‐sensitive T cell population. On the other hand, the suppressor cells were nylon‐wool nonadherent, relatively radiation‐sensitive T cells. Actively antibody‐producing cells were not affected by the suppressor cells. The suppressor cells inhibited the mitogenic responses of normal SPC to phytohemagglutinin‐P (PHA), bacterial lipopolysaccharide (LPS) and concanavalin A (Con A). The suppressor cells themselves inhibited the growth of EL4 cells (T‐cell leukemia of C57BL/6 mouse origin) and MOPCll cells (B cells, plasmacytoma of BALB/c mouse origin) even at a low effector‐to‐target cell ratio (E:T ratio = 1:1), but did not kill these tumor cells. These results indicate that the target cells of the suppressor cells are both T and B cells, and that the mechanism of action of the suppression is either inhibition of proliferation or inhibition of early events in the course of the immune response.