Author

Hengxiang Yu

Peking University

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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Immunology· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Jun ZhangiD· 2 shared Lan Zhang· 2 shared Rong-Chun Tang· 2 shared Shijin Geng· 2 shared Yunxuan Zhou· 2 shared A R ZhangiD· 1 shared Ao ZhangiD· 1 shared Shuang‐Shuang YuiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

9 top collaborators · 32 mutual co-author links

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2 shared papersImmunology

Jun ZhangORCID

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Author profile →

2 papers

Recent·Most cited

IGF2BP3 amplifies antiviral innate immunity with implications for autoimmune diseases

Ao Zhang, Shijin Geng, Rong-Chun Tang, Hengxiang Yu, Yunxuan Zhou, Lan Zhang, Xiuyuan Sun, Jun Zhang

This paper identifies IGF2BP3 as a critical amplifier of antiviral innate immunity, showing it enhances viral RNA sensing and IFN-I production, and reveals its role in autoimmune diseases.

bioRxiv · Aug 6, 2026 · PreprintImmunology

The gut microbiota metabolite Urolithin A mitigates JAK signaling to suppress cytokine-mediated autoimmune diseases

Shijin Geng, Rong-Chun Tang, Hengxiang Yu, A R Zhang, Shuang‐Shuang Yu, Yunxuan Zhou, Lan Zhang, Jun Zhang

This study identifies Urolithin A as a gut microbiota metabolite that inhibits JAK signaling to reduce cytokine-driven autoimmune disease pathology.

bioRxiv · May 12, 2026 · PreprintImmunology