Author

S. Howland

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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Cell Biology· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 3 Organism:human· 2 Organism:mouse· 2 Assay:proteomics· 2 Approach:wet-lab / biochemical assay· 2 Research Focus:benchmarking· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

A. Singhal· 2 shared D. Kumar· 2 shared M. Das· 2 shared P. Sharma· 2 shared R. D. Sharma· 2 shared V. Nandicoori· 2 shared A. Baeza Garcia· 1 shared A. Lee· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 34 mutual co-author links

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2 shared papersCell Biology

A. Singhal

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A mitochondrial quality control mechanism reverses the phagosome maturation arrest caused by Mycobacterium tuberculosis

S. Verma, S. Thakur, M. Das, R. D. Sharma, V. Yadav, P. Sharma, M. Marzuki, S. Foo, G. M. Piperno, M. Z. Khan, B. Mathew, M. Bajpai, J. S. Maras, S. Howland, S. Sarkar, , D. Kumar

This study identifies a mitochondrial quality control mechanism that reverses phagosome maturation arrest caused by Mycobacterium tuberculosis through RAB7 recruitment and lysosomal targeting.

bioRxiv · Dec 1, 2023 · PreprintCell Biology

Ly6G+Granulocytes-derived IL-17 limits protective host responses and promotes tuberculosis pathogenesis

P. Sharma, R. D. Sharma, B. Sarkar, V. Panwar, M. Das, L. Singh, N. Jain, S. Chaturvedi, L. Mehra, A. Rathee, S. Sharma, F. Shihui, A. Lee, P. N. Kumar, P. Das, , D. Kumar

This study identifies IL-17 and COX2 as negative regulators of protective immunity in tuberculosis, showing that Ly6G+ granulocytes are a major source of IL-17 and their inhibition reduces bacterial burden and pathology.

bioRxiv · Oct 5, 2023Immunology

Suppression of Plasmodium MIF-CD74 Signaling Protects Against Severe Malaria

A. Baeza Garcia, E. Siu, X. Du, L. Leng, B. Franke-Fayard, C. J. Janse, S. Howland, L. Renia, E. Lolis, R. Bucala

This study shows that blocking Plasmodium MIF-CD74 signaling protects against experimental cerebral malaria by preventing antigen presentation to CD8+ T cells.

bioRxiv · Feb 14, 2021Microbiology