Author

C. Kontos

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:human· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Hoffmann· 2 shared A. Kapurniotu· 2 shared C. Weber· 2 shared J. Bernhagen· 2 shared L. Maegdefessel· 2 shared M. Brandhofer· 2 shared O. El Bounkari· 2 shared R. T. A. Megens· 2 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersImmunology

A. Hoffmann

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2 papers

Recent·Most cited

MIF-2/D-DT is an atypical atherogenic chemokine that promotes advanced atherosclerosis and hepatic lipogenesis

O. El Bounkari, C. Zan, J. Wagner, E. Bugar, P. Bourilhon, C. Kontos, M. Zarwel, D. Sinitski, J. Milic, Y. Jansen, W. Kempf, L. Maegdefessel, A. Hoffmann, M. Brandhofer, R. Bucala, , J. Bernhagen

This study identifies MIF-2 as an atherogenic chemokine that promotes atherosclerosis and hepatic lipogenesis by acting through CXCR4 and SREBP pathways.

bioRxiv · Dec 28, 2021 · PreprintImmunology

Heterocomplexes between the Atypical Chemokine MIF and the CXC-Motif Chemokine CXCL4L1 Regulate Inflammation and Thrombus Formation

M. Brandhofer, A. Hoffmann, X. Blanchet, E. Siminkovitch, A.-K. Rohlfing, O. El Bounkari, J. A. Nestele, A. Bild, C. Kontos, K. Hille, V. Rohde, A. Froehlich, J. Golemi, O. Goekce, C. M. Krammer, , J. Bernhagen

This study identifies a novel interaction between the atypical chemokine MIF and the CXC-motif chemokine CXCL4L1, showing that their heterocomplex formation modulates inflammation and thrombus formation.

bioRxiv · Nov 26, 2021Immunology