Author

M. E. Raeber

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· 5

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Organism:human· 4 Research Focus:host-pathogen & immune response· 3 Assay:proteomics· 3 Research Focus:cell type annotation· 2 Assay:flow cytometry· 2 Research Focus:clustering· 1 Organism:mouse· 1

Frequent Co-Authors

O. Boyman· 5 shared C. Cervia· 4 shared J. Nilsson· 4 shared S. Adamo· 4 shared Y. Zurbuchen· 4 shared A. Rudiger· 2 shared D. J. Schaer· 2 shared J. Michler· 2 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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5 shared papersImmunology

O. Boyman

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5 papers

Recent·Most cited

IL-2 immunotherapy rescues irradiation-induced T cell exhaustion in vivo

C. S. M. Yong, I. Telarovic, L. Gregor, M. E. Raeber, M. Pruschy, O. Boyman

This study shows that timed CD25-biased IL-2 immunotherapy after RT enhances anti-tumor effects by promoting CD8+ T cell expansion and reducing exhaustion.

bioRxiv · Jan 29, 2024 · PreprintImmunology

Fate and plasticity of SARS-CoV-2-specific B cells during memory and recall response in humans

Y. Zurbuchen, J. Michler, P. Taeschler, S. Adamo, C. Cervia, M. E. Raeber, I. E. Acar, J. Nilsson, M. B. Soyka, A. E. Moor, O. Boyman

The paper tracks SARS-CoV-2-specific memory B cell fate transitions in humans, showing single clones can adopt distinct functional trajectories during memory and recall responses.

bioRxiv · Oct 7, 2022 · PreprintImmunology

CD8+ T cell signature in acute SARS-CoV-2 infection identifies memory precursors

S. Adamo, J. Michler, Y. Zurbuchen, C. Cervia, P. Taeschler, M. E. Raeber, S. Baghai Sain, J. Nilsson, A. Moor, O. Boyman

The paper identifies a transcriptional signature in SARS-CoV-2-specific CD8+ T cells that distinguishes short-lived from long-lived memory cells one year post-infection.

bioRxiv · Jul 22, 2021Immunology

A distinct innate immune signature marks progression from mild to severe COVID-19

S. Chevrier, Y. Zurbuchen, C. Cervia, S. Adamo, M. E. Raeber, N. de Souza, S. Sivapatham, A. Jacobs, E. Bächli, A. Rudiger, M. Stüssi-Helbling, L. C. Huber, D. J. Schaer, J. Nilsson, O. Boyman, B. Bodenmiller

The paper identifies an innate immune signature associated with progression from mild to severe COVID-19 using mass cytometry and proteomics.

bioRxiv · Aug 4, 2020Immunology

Systemic and mucosal antibody secretion specific to SARS-CoV-2 during mild versus severe COVID-19

C. Cervia, J. Nilsson, Y. Zurbuchen, A. Valaperti, J. Schreiner, A. Wolfensberger, M. E. Raeber, S. Adamo, M. Emmenegger, S. Hasler, P. P. Bosshard, E. De Cecco, E. Baechli, A. Rudiger, M. Stuessi-Helbling, , O. Boyman

This study compares SARS-CoV-2-specific antibody responses in mild and severe COVID-19 patients and healthcare workers, finding higher systemic IgA and IgG in severe cases and mucosal IgA in asymptomatic exposed individuals.

bioRxiv · May 21, 2020Immunology