Author

M. R. Witt

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:cell signaling & trafficking· 1 Assay:flow cytometry· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

B. G. Seman· 2 shared C. M. Robinson· 2 shared J. K. Vance· 2 shared A. B. Huckaby· 1 shared J. M. Povroznik· 1 shared M. Barbier· 1 shared S. D. Bradford· 1 shared T. W. Rawson· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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2 shared papersImmunology

B. G. Seman

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Neonatal granulocytic MDSCs possess phagocytic properties during bacterial infection.

B. G. Seman, J. K. Vance, M. R. Witt, C. M. Robinson

This study shows human granulocytic MDSCs can phagocytose bacteria but are less efficient than monocytes, releasing DNA that affects bacterial viability but not monocyte function.

bioRxiv · Dec 30, 2019 · PreprintImmunology

Elevated levels of interleukin-27 in early life compromise protective immunity during neonatal sepsis

B. G. Seman, J. K. Vance, T. W. Rawson, M. R. Witt, A. B. Huckaby, J. M. Povroznik, S. D. Bradford, M. Barbier, C. M. Robinson

This study shows elevated IL-27 in neonates worsens sepsis outcomes by impairing bacterial control and promoting inflammation.

bioRxiv · Sep 20, 2019Immunology