Author

H. Kamada

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

S. Nagata· 2 shared T. Ise· 2 shared H. Akiba· 1 shared H. Konishi· 1 shared H. Ohno· 1 shared J. Fujita· 1 shared K. Fukao· 1 shared K. Furukawa· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersMicrobiology

S. Nagata

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2 papers

Recent·Most cited

Discovery of anti-SARS-CoV-2 S2 protein antibody CV804 with broad-spectrum reactivity with various beta coronaviruses and analysis of its pharmacological properties in vitro and in vivo

Y. Tsugawa, K. Furukawa, T. Ise, M. Takayama, T. Ota, T. Kuroda, S. Shano, T. Hashimoto, H. Konishi, T. Ishihara, M. Sato, H. Kamada, K. Fukao, T. Shishido, T. Takahashi, S. Nagata

This study identifies an antibody, CV804, that targets the conserved S2 domain of coronaviruses and shows broad cross-reactivity and ADCC activity against SARS-CoV-2 and related viruses.

bioRxiv · Feb 28, 2024Microbiology

Development of a 1:1-binding biparatopic anti-TNFR2 antagonist by epitope selection

H. Akiba, J. Fujita, T. Ise, K. Nishiyama, T. Miyata, T. Kato, K. Namba, H. Ohno, H. Kamada, S. Nagata, K. Tsumoto

This study develops a biparatopic anti-TNFR2 antagonist that binds in a 1:1 ratio, preventing unwanted signal transduction and suppressing regulatory T cell proliferation.

bioRxiv · Dec 15, 2022Biochemistry