Author

C. P. Arevalo

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 Microbiology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

S. E. Hensley· 3 shared A. E. Baxter· 2 shared A. Pattekar· 2 shared A. R. Greenplate· 2 shared A. R. Weisman· 2 shared C. A. G. Ittner· 2 shared D. Mathew· 2 shared E. C. Goodwin· 2 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersImmunology

S. E. Hensley

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3 papers

Recent·Most cited

MicrobiologybioRxivSep 27, 2022

IgG3 subclass antibodies recognize antigenically drifted influenza viruses and SARS-CoV-2 variants through efficient bivalent binding

M. Bolton, C. P. Arevalo, T. Griesman…·S. E. Hensley

This study shows that IgG3 subclass antibodies neutralize antigenically drifted influenza and SARS-CoV-2 variants more effectively than other subclasses.

DOI 10.1073/pnas.2216521120

humanproteomics

𝕏 PostBluesky

ImmunologybioRxivMay 20, 2020

Deep immune profiling of COVID-19 patients reveals patient heterogeneity and distinct immunotypes with implications for therapeutic interventions

D. Mathew, J. R. Giles, A. E. Baxter…·E. J. Wherry

The paper identifies distinct immunotypes in COVID-19 patients through high-dimensional cytometry, linking them to disease severity and potential therapeutic implications.

DOI 10.1126/science.abc8511

humanflow cytometry

𝕏 PostBluesky

ImmunologybioRxivPreprintMay 18, 2020

Immunologic perturbations in severe COVID-19/SARS-CoV-2 infection

L. Kuri-Cervantes, M. B. Pampena, W. Meng…·M. R. Betts

The paper identifies broad immune perturbations in severe COVID-19, including innate and adaptive immune cell changes and heterogeneity in B cell responses and antibody production.

DOI 10.1101/2020.05.18.101717

humanflow cytometry

𝕏 PostBluesky