Author

Jun Liu

University of TorontoORCID 0000-0002-0522-6733Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Jun Liu17 papers · Baylor College of Medicine

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Jacqueline WattiD· 3 shared Dustin SokolowskiiD· 2 shared Blair R. G. GordoniD· 1 shared David G. BrooksiD· 1 shared Jason Galutira· 1 shared Kyle BurrowsiD· 1 shared Wenxi Xu· 1 shared Ying Quan· 1 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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3 shared papersImmunology

Jacqueline WattORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

In-Depth Immune Profiling Reveals Cell-Type, Sex and Infection-Stage Dependent Differences for Tuberculosis Control

Jacqueline Watt, Dustin Sokolowski, Jun Liu

This study profiles the immune environment in male and female mice following TB infection and vaccination, identifying sex-specific immune markers and known protective responses.

bioRxiv · Oct 7, 2026 · PreprintImmunology

Mycobacterium tuberculosis Δlsr2 Vaccine Enhances Protection Against Tuberculosis

Jacqueline Watt, Jun Liu

This study evaluates a modified Mycobacterium tuberculosis vaccine, Δlsr2, showing stronger immune responses and better protection against tuberculosis in mice and guinea pigs compared to BCG.

bioRxiv · Jul 11, 2026 · PreprintImmunology

High Dimensional Immune Profiling Reveals CD39 as a Correlate of Tuberculosis Disease Severity

Jacqueline Watt, Dustin Sokolowski, Wenxi Xu, Ying Quan, Kyle Burrows, Jason Galutira, Blair R. G. Gordon, David G. Brooks, Jun Liu

This study uses high-dimensional immune profiling to identify CD39 as a correlate of tuberculosis disease severity and shows its potential as a therapeutic target.

bioRxiv · Jul 7, 2026 · PreprintImmunology