Takashi Imai

Assistant Professor

Saitama Medical University

Japan

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Takashi Imai is an Assistant Professor at Saitama Medical University in Japan. His research focuses on malaria, immunology, and vaccine development, as evidenced by his recent articles on malaria-infected erythroblasts, immunization-based models for visual detection of parasites, and next-generation vaccines. He also explores the immunogenicity of tumor cells and the effects of social stress on behavior through extracellular vesicle alterations.

Articles (13)

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2025

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2025

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2023

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2022

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2022

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2021

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2021

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2020

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2020

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2020

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2020

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2020

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2020

Collaborators (5)

Shinichi Kano

Associate Professor

The University of Alabama

UNITED STATES

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Wataru Kagaya

Assistant professor

Nagasaki University

JAPAN

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Xiaolei Zhu

POSTDOC; INSTRUCTOR; ASSISTANT PROFESSOR

Johns Hopkins University

UNITED STATES

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atsushi Kamiya

Professor

Johns Hopkins University School of Medicine

UNITED STATES

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Yoshiaki Ohtsu

Assistant Professor

Gunma University Graduate School of Medicine

JAPAN

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Takashi Imai

Research Interests

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Articles (13)

Quantification and visualization of malaria-infected erythroblasts by imaging flow cytometry

Visual Detection of Malaria Parasite-Parasitized Erythroblasts in Peripheral Blood via Immunization-Based Model

Infection of tumor cells with Salmonella typhimurium mimics immunogenic cell death and elicits tumor-specific immune responses

Live Vaccination with Blood-Stage Plasmodium yoelii 17XNL Prevents the Development of Experimental Cerebral Malaria

Development of Next-Generation Vaccines

Alterations in circulating extracellular vesicles underlie social stress-induced behaviors in mice.

Single Amino Acid Deletion at N-Terminus of the Target Antigen in DNA Vaccine Induces Altered CD8+ T Cell Responses against Tumor Antigen

Blood-cerebrospinal fluid barrier: another site disrupted during experimental cerebral malaria caused by Plasmodium berghei ANKA.

Potential and Limitations of Cross-Protective Vaccine against Malaria by Blood-Stage Naturally Attenuated Parasite

CD8+ regulatory T cells are critical in prevention of autoimmune-mediated diabetes.

Chemotaxis Assay for Marsupenaeus japonicas Hemocytes and Application for the Development of an Oral Immunostimulant Against White Spot Syndrome Virus.

IL-33 is essential to prevent high fat diet-induced obesity in mice infected with an intestinal helminth.

Suppression of systemic lupus erythematosus in NZBWF1 mice infected with Hymenolepis microstoma.

Collaborators (5)

Shinichi Kano

Wataru Kagaya

Xiaolei Zhu

atsushi Kamiya

Yoshiaki Ohtsu

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