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Published on: May 31, 2018
Release of the serum immunosuppressive factor by monocytes in patients with Crohn's disease
1Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Insights
Sera from Crohn's disease patients suppressed mouse spleen cell proliferation. Monocytes may release this immunosuppressive factor, potentially contributing to abnormal immune responses in the gut.
Area of Science:
- Immunology
- Gastroenterology
Background:
- Crohn's disease is an inflammatory bowel disease characterized by an abnormal immune response.
- The immunosuppressive effects of Crohn's disease sera and peripheral blood mononuclear cells (PBMCs) are not fully understood.
Purpose of the Study:
- To investigate the in vitro immunosuppressive effect of sera and PBMCs from Crohn's disease patients.
- To identify the cellular source of immunosuppressive factors in Crohn's disease.
Main Methods:
- Sera and culture supernatants of PBMCs (adherent and non-adherent fractions) from Crohn's disease patients and controls were analyzed for immunosuppressive activity.
- Mouse spleen cell proliferation assays were used to assess immunosuppressive effects.
- Fractionization of culture supernatants was performed to characterize the immunosuppressive factor.
Main Results:
- Sera from Crohn's disease patients significantly suppressed mouse spleen cell proliferation compared to controls.
- Culture supernatants from adherent PBMCs of Crohn's disease patients exhibited potent immunosuppressive activity (96 +/- 1%).
- Fractionization revealed that the immunosuppressive factor shares biochemical properties with previously identified serum immunosuppressive fractions.
Conclusions:
- Monocytes in Crohn's disease patients may release a serum immunosuppressive factor.
- This factor could contribute to impaired immune reactivity at mucosal lesions and sustained abnormal immune responses in the intestinal wall.
Abstract:
We investigated the in vitro immunosuppressive effect of the sera and the culture supernatants of the peripheral blood mononuclear cells obtained from patients with Crohn's disease. Sera from Crohn's disease markedly suppressed the proliferative response of mouse spleen cells, compared with sera from ulcerative colitis, intestinal tuberculosis and normal controls. The culture supernatants of the adherent mononuclear cells from Crohn's disease showed a remarkable suppressive effect (96 +/- 1%), while the culture supernatants of the non-adherent mononuclear cells had no suppressive activity (-10 +/- 16%). The culture supernatants of the adherent and non-adherent mononuclear cells from normal controls had no suppressive activity. The fractionization of the culture supernatants of the adherent cells from the Crohn's disease patients demonstrated that the fractions with high suppressive activity had similar or identical biochemical properties to the serum immunosuppressive fractions which has been reported previously. These results indicate that monocytes may release the serum immunosuppressive factor in Crohn's disease. This factor may contribute to the depression of the immune reactivity in the mucosal lesion and to the persistence of the stimulation of abnormal immune response in the intestinal wall.
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