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M Kohyama

Publications and source records attributed to M Kohyama.

22 records · Page 2Linked to original sources

Autoreactive CD8+ T cell clones producing immune suppressive lymphokines IL-10 and interferon-gamma.

Highly purified CD8+ T cells were stimulated repeatedly by syngeneic irradiated spleen cells. From separate cloning experiments, we succeeded in isolating two CD8+ clones, 4B4 and D2, which proliferated in response to autologous antigen-presenting cells (APC) completely in the absence of fetal calf serum. A T cell proliferation assay, using congenic strain of mice, indicates that both autoreactive clones were restricted to self-Db molecules. Our study is the first report of establishing murine autoreactive CD8+ clones restricted to self MHC class I molecules. To assess the immune suppressive activity of each autoreactive clone, we measured the production of IL-10 and interferon-gamma, which have specific immune suppressive activity toward type 1 helper T cell (Th1) proliferation and IgE synthesis, respectively. In response to autologous APC, both D2 and 4B4 produced considerable amounts of interferon-gamma and a low but significant level of IL-10. Each supernatant of D2 and 4B4 significantly suppressed IgE synthesis. These results strongly suggest the existence of CD8+ autoreactive T cells with immune suppressive activity.

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Anti-IL-10 antibody enhances the proliferation of CD8+ T cell clones: autoregulatory role of murine IL-10 in CD8+ T cells.

All CD8+ T cell clones used in this study secreted IL-10, and their proliferation was inhibited by exogenous IL-10. This study addresses the question of whether IL-10 produced by responding T cell clones would inhibit proliferation of the secreting T cells themselves. Anti-IL-10 antibodies enhanced the proliferative response of the CD8+ T cell clones, the enhancing effect appearing in the late period of proliferation. However, the proliferation of both CD4+ Th1 and Th2 clones was not affected by anti-IL-10 throughout the culture. In addition to that of the cloned T cells, the proliferative response of a primary culture of CD8+ T cells was enhanced by the anti-IL-10 antibody. This is the first report on a lymphokine which has an autoregulatory role in inhibiting T cell proliferation.

Animals↗

Endoscopic laser therapy in the curative and palliative treatment of upper gastrointestinal cancer.

Endoscopic laser treatment was initially applied for gastrointestinal bleeding, but has been actively extended, especially in Japan, to the curative treatment of early upper gastrointestinal cancers. We have treated 10 cases of early gastric cancer and 1 case of early esophageal cancer by Nd-YAG laser radiation, and 2 cases of early gastric cancer by photochemical therapy (PCT) with argon laser + hematoporphyrin derivative. Also, 62 cases of advanced cancer were treated, 10 of the esophagus and 52 of the stomach, for bleeding (18 cases) or stenosis (34 cases). The cases were nonresectable or they were patients who refused surgery. Satisfactory results were obtained by treatment with YAG laser, but have not yet been obtained with PCT. In order to find indications for the possible extension of endoscopic laser therapy to operable cases of early gastric cancer, we studied lymph node metastases in 200 cases of early gastric cancer surgically treated by us. It was found that early gastric cancers (both mucosal and submucosal) measuring less than 2 cm in diameter, of type I, IIa, and IIc (without ulcer scar), had no lymph node metastases and such cases can be treated by local therapy--such as endoscopic laser therapy. In palliative endoscopic laser therapy for complications of advanced gastrointestinal cancers, there are no major problems with active performance. We obtained a high (90%) hemostatic rate in bleeding cases of upper gastrointestinal cancer and a satisfactory (65%) rate of dilating effect in cases of cancerous stenosis at the esophagus and cardia.(ABSTRACT TRUNCATED AT 250 WORDS)

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