Author

B. Davenport

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 Physiology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 8 Research Focus:cell type annotation· 3 Research Focus:host-pathogen & immune response· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:differential expression· 2 Assay:flow cytometry· 2 Organism:human· 2 Organism:mouse· 2

Frequent Co-Authors

D. Homann· 4 shared K. Jhun· 4 shared V. van der Heide· 4 shared F. Victorino· 3 shared H. Jones· 3 shared J. Eberlein· 3 shared R. Wilson· 3 shared T. Nguyen· 3 shared

Activity by Year

2017-2024 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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4 shared papersImmunology

D. Homann

Mutual co-authors in cluster

Author profile →

8 papers

Recent·Most cited

Nanoparticle-mediated delivery of placental gene therapy via uterine artery catheterization in a pregnant rhesus macaque

J. Schmidt, R. Wilson, B. Davenport, T. Hacker, C. Fitz, H. A. Simmons, M. L. Schotzko, T. Golos, H. Jones

This study delivers hIGF1-loaded nanoparticles to the placenta of a pregnant rhesus macaque via uterine artery catheterization, showing successful placental uptake and expression of hIGF1.

bioRxiv · Apr 10, 2024Physiology

Placental Nanoparticle-mediated IGF1 Gene Therapy Corrects Fetal Growth Restriction in a Guinea Pig Model

B. Davenport, R. Wilson, A. Williams, H. Jones

This paper demonstrates that placental nanoparticle-mediated IGF1 gene therapy corrects fetal growth restriction in a guinea pig model by improving fetal weight, blood glucose, and reducing cortisol levels.

bioRxiv · Apr 5, 2024Physiology

Functional impairment of "helpless" CD8+ memory T cells is transient and driven by prolonged but finite cognate antigen presentation

V. van der Heide, B. Davenport, B. Cubitt, V. Roudko, D. Choo, E. Humblin, K. Jhun, K. Angeliadis, T. Dawson, G. Furtado, A. O. Kamphorst, R. Ahmed, J. C. de la Torre, D. Homann

This study shows that helpless CD8+ memory T cells, which form without CD4+ help, have transient functional impairments due to prolonged antigen exposure, which resolve over time.

bioRxiv · Jan 22, 2024Immunology

Chikungunya virus infection disrupts lymph node lymphatic endothelial cell composition and function via MARCO

C. Lucas, R. Sheridan, G. Reynoso, B. Davenport, M. McCarthy, A. Martin, J. Hesselberth, H. Hickman, B. Tamburini, T. Morrison

This study shows CHIKV infection disrupts lymph node lymphatic endothelial cell composition and function through MARCO interactions, leading to impaired antigen acquisition and increased inflammation.

JCI Insight · Jan 9, 2024Peer-reviewedImmunology

Placental treatment with insulin-like growth factor 1 via nanoparticle differentially impacts vascular remodeling factors in guinea pig sub-placenta/decidua

B. Davenport, H. Jones, R. Wilson

This study shows that hIGF-1 nanoparticle treatment differentially affects vascular remodeling factors in guinea pig sub-placenta/decidua under FGR and normal conditions.

bioRxiv · Sep 26, 2022Physiology

Chemokine Signatures Of Pathogen-Specific T Cells I: Effector T Cells

J. Eberlein, B. Davenport, T. Nguyen, F. Victorino, K. Jhun, V. van der Heide, M. Kuleshov, A. Maayan, R. Kedl, D. Homann

This study defines the chemokine profiles of pathogen-specific effector T cells and identifies their temporospatial organization and regulatory mechanisms.

bioRxiv · Feb 5, 2020Immunology

Aging Boosts Antiviral CD8+T Cell Memory Through Improved Engagement Of Diversified Recall Response Determinants

B. Davenport, J. Eberlein, T. Nguyen, F. Victorino, K. Jhun, H. Abuirqeba, V. van der Heide, P. Heeger, D. Homann

This study shows that aging enhances CD8+ memory T cell recall responses by utilizing diverse molecular mechanisms, supporting the rebound model of immune memory.

bioRxiv · Oct 22, 2018Immunology

Aging Of Antiviral CD8+ Memory T Cells Fosters Increased Survival, Metabolic Adaptations And Lymphoid Tissue Homing

B. Davenport, J. Eberlein, V. van der Heide, K. Jhun, T. Nguyen, F. Victorino, A. Trotta, J. Chipuk, Z. Yi, W. Zhang, E. Clambey, D. K. Scott, D. Homann

This study shows that aging of antiviral CD8+ memory T cells leads to increased survival, metabolic adaptations, and lymphoid tissue homing, enhancing their recall response capabilities.

bioRxiv · Sep 22, 2017Immunology