Author

T. Jacobs

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 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Organism:Drosophila· 1 Assay:flow cytometry· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. Vanegas Ramirez· 1 shared B. Volkmer· 1 shared C. Camelo· 1 shared C. Lehmann· 1 shared D. Forster· 1 shared H. Fehling· 1 shared H. Lotter· 1 shared J. Barton· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperImmunology

A. Vanegas Ramirez

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Antimicrobial Activity of NK Cells to Trypanosoma cruzi Infected Human Primary Keratinocytes

K. Kroh, J. Barton, H. Fehling, H. Lotter, B. Volkmer, R. Greinert, M. Mhamdi-Ghodbani, A. Vanegas Ramirez, T. Jacobs, R. Galvez

This study investigates NK cell activation by T. cruzi-infected keratinocytes and finds that NK cells are strongly activated despite minimal ligand changes, with IFN-gamma enhancing ligand expression on keratinocytes.

bioRxiv · Aug 17, 2023 · PreprintImmunology

Acute manipulation and real-time visualization of membrane trafficking and exocytosis in Drosophila

J. Glashauser, C. Camelo, M. Hollmann, W. Backer, T. Jacobs, J. Isasti Sanchez, R. Schleutker, D. Forster, N. Berns, V. Riechmann, S. Luschnig

This study presents a system for acute manipulation and real-time visualization of membrane trafficking in Drosophila by adapting the RUSH approach to control protein trafficking in living organisms.

bioRxiv · Mar 25, 2022 · PreprintCell Biology

T cells expressing multiple co-inhibitory molecules in acute malaria are not exhausted but exert a suppressive function

J. Brandi, C. Lehmann, L.-C. Kaminski, J. Schulze zur Wiesch, M. Addo, M. Ramharter, M. Mackroth, T. Jacobs, M. Riehn

The paper identifies malaria-induced T cells expressing co-inhibitory molecules that are not exhausted but have suppressive function, resembling regulatory T cells.

bioRxiv · Apr 19, 2021Immunology