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Featured researches published by Tadashi Sudo.


Immunobiology | 1987

Inhibitory effects of tunicamycin on the mixed lymphocyte reaction and mitogen-induced lymphocyte blastogenesis

Minoru Irahara; Masaharu Kamada; Takahide Mori; Tadashi Sudo; Tsuneatsu Mori

The role of asparagine(Asn)-linked saccharides on the surface of lymphocytes in cellular interactions was examined by performing studies on the effects of tunicamycin (TM), which inhibits the glycosylation of proteins N-glycosylated at asparagine residues, on the mixed lymphocyte reaction (MLR) and mitogen-induced lymphocyte blastogenesis of human lymphocytes by measuring 3H-thymidine (TdR) incorporation. Responses were expressed as percentages of that of the control (MLR without TM). The lymphocyte blastogenesis in the one- and two-way MLR were, respectively, 43.1% and 48.0% of the control at 0.1 microgram/ml of TM, and 5.5% and 7.2% at 1 microgram/ml of TM. The inhibitory effect of TM on the one-way MLR was shown using TM-pretreated stimulator cells, TM-pretreated responder cells or both. TM blocked lymphocyte blastogenesis in the secondary as well as in the primary MLR. The inhibitory effect of TM on the two-way MLR was observed when TM was added on day 0 to day 2, but not on day 4 of incubation. TM blocked mitogen-induced lymphocyte blastogenesis by phytohemagglutinin, concanavalin A or by pokeweed mitogen. As TM had no cytotoxic effect on cultured cells, these inhibitory effects of TM were thought to be due to the loss of Asn-linked saccharides from glycoprotein of the surface of lymphocytes. These findings indicated that Asn-linked saccharides of glycoprotein on the surface of lymphocytes were important in cellular interactions that are necessary for the cellular immune response.


Journal of the National Cancer Institute | 1984

Antitumor Activity of Deoxyribonucleic Acid Fraction From Mycobacterium bovis BCG. I. Isolation, Physicochemical Characterization, and Antitumor Activity

Tohru Tokunaga; Hiroshi Yamamoto; Shizuo Shimada; Hayao Abe; Tamotsu Fukuda; Yoshikazu Fujisawa; Yoshio Furutani; Osamu Yano; Tetsuro Kataoka; Tadashi Sudo; Nobuyoshi Makiguchi; Toshio Suganuma


Archive | 1981

Bacterial cell extract, process for preparing same, antitumor preparation containing same, and adjuvant preparation containing same

Shizuo Shimada; Tadashi Sudo; Hitoshi Inoue; Yoshio Furutani; Yoshikazu Fujisawa


Endocrine Journal | 1994

IMMUNOMOLECULAR MECHANISMS IN MAMMALIAN IMPLANTATION

Tsuneatsu Mori; Mao Wu Guo; Wei Yu Shen; Etsuko Mori; Tadashi Sudo


Journal of the National Cancer Institute | 1984

Expression of Heterophil Forssman Antigen as Glycoprotein on Transformed Rat Cell Lines: Shedding of the Antigen From the Cells

Tsuneatsu Mori; Etsuko Mori; Tadashi Sudo; Kyoichi Kano


Journal of the National Cancer Institute | 1986

Heterophil Forssman Glycoprotein and Adenovirus 12: Transformed Rat Cell Lines

Tsuneatsu Mori; Etsuko Mori; Yuji Shigyo; Tadashi Sudo; Kyoichi Kano


Journal of the National Cancer Institute | 1983

Expression of Heterophil Forssman Antigen on Cultured Malignant Cell Lines

Tsuneatsu Mori; Tadashi Sudo; Kyoichi Kano


Archive | 1990

Common antigen (PSC-A) to Pseudomonas aeruginosa which acts as an agent for protecting Pseudomonas aeruginosa infection

Tamotsu Fukuda; Shiro Shigeta; Hiroaki Okuya; Yasuyuki Kuroiwa; Tadashi Sudo


Journal of Biochemistry | 1984

Purification and Characterization of a Tuberculin-Active Substance from Mycobacterium bovis BCG

Osamu Yano; Tamotsu Fukuda; Hayao Abe; Tadashi Sudo


Archive | 1993

Monoclonal anti-asialo GM1 antibody

Shizuo Shimada; Tadashi Sudo; Daiji Iwata

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Shiro Shigeta

Fukushima Medical University

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Tetsuro Kataoka

National Institutes of Health

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