Author

E. Kroon

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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Approach:experimental assay· 3 Organism:human· 3 Research Focus:host-pathogen & immune response· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:proteomics· 1

Frequent Co-Authors

J. Ananworanich· 3 shared N. Phanuphak· 3 shared C. Sacdalan· 2 shared D. Hsu· 2 shared M. L. Robb· 2 shared N. Tulmethakaan· 2 shared S. Buranapraditkun· 2 shared S. Pinyakorn· 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

J. Ananworanich

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Author profile →

3 papers

Recent·Most cited

Productive and latent HIV infections originate in resting CD4+ T cells

S. Wietgrefe, J. Anderson, L. Duan, P. J. Southern, P. Zuck, G. Wu, B. Howell, C. Reilly, E. Kroon, S. Chottanapund, S. Buranapraditkun, C. Sacdalan, N. Tulmethakaan, D. J. Colby, N. Chomchey, , A. T. Haase

This study shows that resting CD4+ T cells are the initial source of both productive and latent HIV infections in the earliest stages of detectable infection.

bioRxiv · Aug 26, 2022 · PreprintImmunology

HIV rapidly targets a diverse pool of CD4+ T cells to establish productive and latent infections

P. Gantner, S. Buranapraditkun, A. Pagliuzza, C. Dufour, M. Pardons, J. L. Mitchell, E. Kroon, C. Sacdalan, N. Tulmethakaan, S. Pinyakorn, M. L. Robb, N. Phanuphak, J. Ananworanich, D. Hsu, S. Vasan, , N. Chomont

This study identifies that HIV initially infects diverse CD4+ T cells in blood and lymph nodes, establishing both productive infections and latent reservoirs simultaneously.

bioRxiv · May 10, 2022Microbiology

Dendritic cells focus CTL responses toward highly conserved and topologically important HIV epitopes

T. M. Garcia-Bates, M. L. Palma, D. C. HSU, J. Ananworanich, B. T. Korber, G. D. Gaiha, N. Phanuphak, R. Thomas, S. Tovanabutra, B. D. Walker, J. W. Mellors, P. A. Piazza, E. Kroon, S. A. Riddler, N. L. Michael, , R. B. Mailliard

This study uses dendritic cells to focus CD8+ T cell responses on conserved and topologically important HIV epitopes to prevent immune escape.

bioRxiv · Jul 13, 2020Immunology