Author

P. Uchil

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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Microbiology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:host-pathogen & immune response· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:flow cytometry· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

W. Mothes· 2 shared A. Finzi· 1 shared A. K. Barczak· 1 shared A. Laumaea· 1 shared A. Marsh· 1 shared A. T. McGuire· 1 shared A. Tauzin· 1 shared C. Bourassa· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

W. Mothes

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Vps18 contributes to phagosome membrane integrity in Mycobacterium tuberculosis-infected macrophages.

C. Jani, A. Marsh, P. Uchil, N. Jain, Z. R. Baskir, O. Glover, D. E. Root, J. G. Doench, A. K. Barczak

This study identifies Vps18 as a host factor critical for maintaining phagosomal membrane integrity in Mtb-infected macrophages, showing increased phagosomal damage and reduced antibiotic efficacy in its absence.

bioRxiv · Oct 1, 2023 · PreprintMicrobiology

A single BNT162b2 mRNA dose elicits antibodies with Fc-mediated effector functions and boost pre-existing humoral and T cell responses

A. Tauzin, M. Nayrac, M. Benlarbi, S. Y. Gong, R. Gasser, G. Beaudoin-Bussieres, N. Brassard, A. Laumaea, D. Vezina, J. Prevost, S. P. Anand, C. Bourassa, G. Gendron-Lepage, H. Medjahed, G. Goyette, , A. Finzi

This study shows a single dose of the BNT162b2 mRNA vaccine elicits strong antibody and T cell responses, including Fc-mediated effector functions, and boosts pre-existing immunity in previously infected individuals.

bioRxiv · Mar 18, 2021 · PreprintImmunology

Longitudinal bioluminescent imaging of HIV-1 infection during antiretroviral therapy and treatment interruption in humanized mice

J. D. Ventura, J. Beloor, E. J. Allen, T. Zhang, K. Haugh, P. Uchil, C. Ochsenbauer, C. Kieffer, P. Kumar, T. J. Hope, W. Mothes

This study uses bioluminescent imaging to monitor HIV-1 infection dynamics in humanized mice during and after antiretroviral therapy, showing rebound in previously infected lymphoid tissues.

bioRxiv · Aug 24, 2019Microbiology