Author

Michael J. Hogan

Children's Hospital of Philadelphia

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:mouse· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Assay:CITE-seq· 1 Research Focus:clustering· 1

Frequent Co-Authors

Laurence Crane EisenlohriD· 2 shared Stephen D. CarroiD· 2 shared Coral M. KasdeniD· 1 shared Emma J. HedgepethiD· 1 shared Hansell H. StedmaniD· 1 shared Hiromi MuramatsuiD· 1 shared James Heyes· 1 shared Julia E. RoodiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersImmunology

Laurence Crane EisenlohrORCID

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2 papers

Recent·Most cited

Cutting Edge: An mRNA Platform to Create Isolated, Monospecific Th1 Responses

Kathleen S Krauss, Stephen D. Carro, Michael J. Hogan, Laurence Crane Eisenlohr

This paper develops an mRNA platform to generate monospecific Th1 responses in mice by encoding epitopes linked to MHCII, demonstrating efficacy against Salmonella infection.

bioRxiv · Jul 23, 2025 · PreprintImmunology

Endogenous antigen processing promotes mRNA vaccine CD4+ T cell responses

Julia E. Rood, Suh Kyung Yoon, Mary K. Heard, Stephen D. Carro, Emma J. Hedgepeth, Mary E. O'Mara, Michael J. Hogan, Nhu Le, Hiromi Muramatsu, Kieu Lam, Petra Schreiner, Coral M. Kasden, Hansell H. Stedman, Ryan Andrew Langlois, James Heyes, , Laurence Crane Eisenlohr

This study shows that endogenous antigen processing via MHC II is critical for mRNA-LNP vaccine-induced CD4+ T cell responses, challenging the traditional view of exogenous antigen processing.

bioRxiv · Mar 11, 2025 · PreprintImmunology