Koichi Araki

ORCID: 0000-0003-3478-6315
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • Viral Infections and Vectors
  • T-cell and B-cell Immunology
  • Immunotherapy and Immune Responses
  • Vector-Borne Animal Diseases
  • Viral Infections and Outbreaks Research
  • Carbohydrate Chemistry and Synthesis
  • Fire effects on ecosystems
  • T-cell and Retrovirus Studies
  • CAR-T cell therapy research
  • Cancer Immunotherapy and Biomarkers
  • Animal Disease Management and Epidemiology
  • Fluorine in Organic Chemistry
  • Glycosylation and Glycoproteins Research
  • Acute Myeloid Leukemia Research
  • Mosquito-borne diseases and control
  • Cytomegalovirus and herpesvirus research
  • Synthesis and Reactions of Organic Compounds
  • Synthesis of β-Lactam Compounds
  • Autophagy in Disease and Therapy
  • Amino Acid Enzymes and Metabolism
  • RNA Interference and Gene Delivery
  • PI3K/AKT/mTOR signaling in cancer
  • Polyamine Metabolism and Applications
  • Virus-based gene therapy research

Cincinnati Children's Hospital Medical Center
2022-2025

University of Cincinnati
2020-2025

University of Cincinnati Medical Center
2022-2025

Kyoto Sangyo University
2025

Emory University
2012-2023

Children’s Institute
2020-2023

Emory Healthcare
2010-2015

Emory and Henry College
2012

Oglethorpe University
2010-2011

Hokkaido University
1998-2009

Daniel J. Klionsky Kotb Abdelmohsen Akihisa Abe Md. Joynal Abedin Hagai Abeliovich and 95 more Abraham Acevedo‐Arozena Hiroaki Adachi Christopher M. Adams Peter D. Adams Khosrow Adeli Peter J. Adhihetty Sharon G. Adler Galila Agam Rajesh Agarwal Manish K. Aghi Maria Agnello Patrizia Agostinis Patricia V. Aguilar Julio A. Aguirre‐Ghiso Edoardo M Airoldi Slimane Ait‐Si‐Ali Takahiko Akematsu Emmanuel T. Akporiaye Mohamed Al‐Rubeai Guillermo M. Albaiceta Chris Albanese Diego Albani Matthew L. Albert Jesús Aldudo Hana Algül Mehrdad Alirezaei Iraide Alloza Alexandru Almasan Maylin Almonte-Beceril Emad S. Alnemri Covadonga Alonso Nihal Altan‐Bonnet Dario C. Altieri Silvia Álvarez Lydia Álvarez-Erviti Sandro Alves Giuseppina Amadoro Atsuo Amano Consuelo Amantini Santiago Ambrosio Ivano Amelio Amal O. Amer Mohamed Amessou Angelika Amon Zhenyi An Frank A. Anania Stig Uggerhøj Andersen Usha P. Andley Catherine Andreadi Nathalie Andrieu‐Abadie Alberto Anel David K. Ann Shailendra Anoopkumar‐Dukie Manuela Antonioli Hiroshi Aoki Nadezda Apostolova Saveria Aquila Katia Aquilano Koichi Araki Eli Arama Agustı́n Aranda Jun Araya Alexandre Arcaro Esperanza Arias Hirokazu Arimoto Aileen Ariosa Jane L. Armstrong Thierry Arnould Ivica Arsov Katsuhiko Asanuma Valerie Askanas Éric Asselin Ryuichiro Atarashi Sally S. Atherton Julie D. Atkin Laura D. Attardi Patrick Auberger Georg Auburger Laure Aurelian Riccardo Autelli Laura Avagliano Maria Laura Avantaggiati Limor Avrahami Suresh Awale Neelam Azad Tiziana Bachetti Jonathan Backer Dong-Hun Bae Jae‐sung Bae Ok‐Nam Bae Soo Han Bae Eric H. Baehrecke Seung‐Hoon Baek Stephen Baghdiguian Agnieszka Bagniewska‐Zadworna

In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, on this topic has continued to accelerate, and many new scientists have entered field. Our knowledge base relevant technologies also been expanding. Accordingly, it is important update these monitoring autophagy different organisms. Various reviews described range assays that used purpose. Nevertheless, there continues be confusion regarding acceptable methods measure autophagy, especially...

10.1080/15548627.2015.1100356 article EN cc-by-nc-sa Autophagy 2016-01-02

Inhibitory receptors play a crucial role in regulating CD8 T-cell function during chronic viral infection. Ig- and mucin-domain–containing molecule–3 (Tim-3) is well known to negatively regulate responses, but its exhaustion infection vivo remains unclear. In this study, we document coregulation of T cell by Tim-3 PD-1 lymphocytic choriomeningitis virus Whereas was only transiently expressed cells after acute infection, virus-specific retained high expression throughout The majority...

10.1073/pnas.1009731107 article EN Proceedings of the National Academy of Sciences 2010-08-02

PD-1 (programmed cell death-1) is the central inhibitory receptor regulating CD8 T exhaustion during chronic viral infection and cancer. Interestingly, also expressed transiently by activated cells acute infection, but role of in modulating effector differentiation function not well defined. To address this question, we examined expression kinetics lymphocytic choriomeningitis virus (LCMV) mice. was rapidly up-regulated vivo upon activation naive virus-specific within 24 h after LCMV less...

10.1073/pnas.1718217115 article EN Proceedings of the National Academy of Sciences 2018-04-13

T cell dysfunction is an important feature of many chronic viral infections. In particular, it was shown that programmed death-1 (PD-1) regulates during lymphocytic choriomeningitis virus infection in mice, and PD-1(hi) cells exhibit intense exhausted gene signature. These findings were extended to human infections such as HIV, hepatitis C virus, B virus. However, not known if healthy humans have the traits cells. this study, we provide a comprehensive description phenotype, function,...

10.4049/jimmunol.1001783 article EN The Journal of Immunology 2011-03-08

Regulatory T (T reg) cells are critical for preventing autoimmunity mediated by self-reactive cells, but their role in modulating immune responses during chronic viral infection is not well defined. To address this question and to investigate a reg exhaustion of virus-specific CD8 we depleted mice chronically infected with lymphocytic choriomeningitis virus (LCMV). cell ablation resulted 10–100-fold expansion functional LCMV-specific cells. Rescue exhausted was dependent on cognate antigen,...

10.1084/jem.20132577 article EN cc-by-nc-sa The Journal of Experimental Medicine 2014-08-11

This phase II trial was performed to evaluate the efficacy of a new granulocyte colony‐stimulating factor (G‐CSF)‐supported multi‐agent chemotherapy protocol, LSG15, for aggressive adult T‐cell leukaemia‐lymphoma (ATL). Ninety‐six previously untreated patients with ATL were enrolled and grouped as: acute type (58), lymphoma (28) unfavourable chronic (10). Therapy consisted seven cycles VCAP (vincristine, cyclophosphamide, doxorubicin prednisone), AMP (doxorubicin, ranimustine prednisone)...

10.1046/j.1365-2141.2001.02737.x article EN British Journal of Haematology 2001-05-01

MicroRNAs are important regulators of various developmental and physiological processes. However, their roles in the CD8 + T-cell response not well understood. Using an acute viral infection model, we show that microRNAs miR-17-92 cluster strongly induced after activation, down-regulated clonal expansion, further silenced during memory development. promotes cell-cycle progression effector T cells, its expression is critical to rapid expansion these cells. excessive enhances mammalian target...

10.1073/pnas.1207327109 article EN Proceedings of the National Academy of Sciences 2012-06-04

T cell exhaustion is a state of dysfunction associated with expression programmed death 1 (PD-1). Exhausted CD8+ cells are maintained by self-renewing stem-like that provide differentiated TIM3+ cells, part which possesses effector-like properties. PD-1-targeted therapies enhance response promoting differentiation toward but the role mTOR during remains elusive. Here, we showed inhibition has distinct outcomes beginning and after establishment chronic viral infection. Blocking expansion...

10.1172/jci160025 article EN cc-by Journal of Clinical Investigation 2022-11-15

PD-1 + TCF-1 stem-like CD8 T cells act as critical resource for maintaining cell immunity in chronic viral infections and cancer. In addition, they provide the proliferative burst of effector after programmed death protein 1 (PD-1)–directed immunotherapy. However, it is not known whether checkpoint blockade diminishes number these progenitor differentiation increases. To investigate this, we used mouse model lymphocytic choriomeningitis virus (LCMV) infection. Treatment chronically infected...

10.1126/sciimmunol.adg0539 article EN Science Immunology 2023-08-04

Abstract Recent evidence demonstrating that exposure to rapamycin during viral infection increased the quantity and quality of Ag-specific T cells poses an intriguing paradox, because is used in transplantation dampen, rather than enhance, donor-reactive cell responses. In this report, we compared effects on response a bacterial versus transplant. Using transgenic system which Ag responding population were identical both cases, observed treatment with augmented pathogen, whereas it failed do...

10.4049/jimmunol.1001176 article EN The Journal of Immunology 2010-07-14
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