2022 - Research.com Immunology in Japan Leader Award
2020 - Paul Ehrlich and Ludwig Darmstaedter Prize
2020 - Robert Koch Prize
2015 - Canada Gairdner International Award
2012 - Member of the National Academy of Sciences
2008 - Keio Medical Science Prize, Keio University, Tokyo, Japan
Immunology, IL-2 receptor, FOXP3, Immune system and Cytotoxic T cell are his primary areas of study. His is doing research in Antigen, Autoimmunity, T cell, Immunotherapy and Self Tolerance, both of which are found in Immunology. His IL-2 receptor research incorporates themes from Interleukin 21, CD8 and Autoimmune disease.
His biological study spans a wide range of topics, including Immune homeostasis, CTLA-4, Epigenetics and Cell biology. The concepts of his Immune system study are interwoven with issues in Monoclonal antibody, Function and In vivo. His work in Cytotoxic T cell covers topics such as Molecular biology which are related to areas like Streptamer, CD1 and microRNA.
Shimon Sakaguchi mainly focuses on Immunology, FOXP3, IL-2 receptor, Immune system and Cell biology. His Immunology and T cell, Antigen, Autoimmunity, Autoimmune disease and Regulatory T cell investigations all form part of his Immunology research activities. The various areas that Shimon Sakaguchi examines in his FOXP3 study include Cancer research, Transcription factor, Immune tolerance, CTLA-4 and Epigenetics.
Shimon Sakaguchi interconnects Natural killer T cell, Interleukin 21 and Antigen-presenting cell in the investigation of issues within IL-2 receptor. He has included themes like Monoclonal antibody and Effector in his Immune system study. His studies deal with areas such as Receptor, Cell and CD40 as well as Cell biology.
FOXP3, Immunology, Immune system, Cell biology and IL-2 receptor are his primary areas of study. His FOXP3 study combines topics in areas such as Cancer research, Epigenetics, Transcription factor, Gene and Effector. His Immunology study frequently involves adjacent topics like Cell.
His work deals with themes such as Disease and Antigen, which intersect with Immune system. His Cell biology research incorporates themes from CD28, Germinal center, Immune tolerance and T-cell receptor. His studies link CD40 with IL-2 receptor.
Shimon Sakaguchi mostly deals with FOXP3, Immunology, Immune system, Autoimmunity and Cell biology. His FOXP3 study combines topics from a wide range of disciplines, such as Cancer research, T cell, CTLA-4, Transcription factor and Effector. His study in Immunology concentrates on Regulatory T cell, IL-2 receptor, Arthritis, Immune tolerance and Autoimmune disease.
In his work, Cytometry, Immunophenotyping, Immunologic Technique, Mass cytometry and Flow cytometry is strongly intertwined with Monoclonal antibody, which is a subfield of Immune system. His Autoimmunity study integrates concerns from other disciplines, such as Inflammation and Cancer. His work on Homeostasis as part of general Cell biology research is often related to Branched-chain amino acid, thus linking different fields of science.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases.
Shimon Sakaguchi;Noriko Sakaguchi;Masanao Asano;Misako Itoh.
Journal of Immunology (1995)
Control of Regulatory T Cell Development by the Transcription Factor Foxp3
Shohei Hori;Takashi Nomura;Shimon Sakaguchi.
Science (2003)
Naturally Arising CD4+ Regulatory T Cells for Immunologic Self-Tolerance and Negative Control of Immune Responses
Shimon Sakaguchi.
Annual Review of Immunology (2004)
Regulatory T Cells and Immune Tolerance
Shimon Sakaguchi;Shimon Sakaguchi;Tomoyuki Yamaguchi;Takashi Nomura;Masahiro Ono.
Cell (2008)
Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in immunological tolerance to self and non-self.
Shimon Sakaguchi.
Nature Immunology (2005)
CTLA-4 Control over Foxp3+ Regulatory T Cell Function
Kajsa Wing;Yasushi Onishi;Yasushi Onishi;Paz Prieto-Martin;Tomoyuki Yamaguchi.
Science (2008)
Immunologic Self-Tolerance Maintained by Cd25+Cd4+Regulatory T Cells Constitutively Expressing Cytotoxic T Lymphocyte–Associated Antigen 4
Takeshi Takahashi;Tomoyuki Tagami;Sayuri Yamazaki;Toshimitsu Uede.
Journal of Experimental Medicine (2000)
Regulatory T cells: key controllers of immunologic self-tolerance.
Shimon Sakaguchi.
Cell (2000)
Stimulation of CD25 + CD4 + regulatory T cells through GITR breaks immunological self-tolerance
Jun Shimizu;Sayuri Yamazaki;Takeshi Takahashi;Yasumasa Ishida.
Nature Immunology (2002)
Immunologic tolerance maintained by CD25+ CD4+ regulatory T cells: their common role in controlling autoimmunity, tumor immunity, and transplantation tolerance.
Shimon Sakaguchi;Noriko Sakaguchi;Jun Shimizu;Sayuri Yamazaki.
Immunological Reviews (2001)
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