Persephone Borrow

University of Oxford

United Kingdom

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Articles (14)

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2025

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2025

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2024

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2024

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2023

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2023

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2021

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2021

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (17)

Carolina Barra

Technical University of Denmark

DENMARK

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Simon Brackenridge

University of Oxford

UNITED KINGDOM

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Anna Schurich

King’s College London

UNITED KINGDOM

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Andreas Damianou

University of Oxford

UNITED KINGDOM

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Jamirah Nazziwa

Lund University

SWEDEN

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Sarah Rowland-Jones

University of Oxford

UNITED KINGDOM

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Andrew James McMichael

Emeritus Professor

University of Oxford

UNITED KINGDOM

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Jonathan Hare

Head of Immunology

UNITED KINGDOM

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Amin S Hassan

Lund University

SWEDEN

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Scott Sherrill-Mix

Assistant professor

Michigan State University

UNITED STATES

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Marco Fritzsche

University of Oxford

UNITED KINGDOM

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Edward Jenkins

University of Oxford

UNITED KINGDOM

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Sara Karlson

Lund University

SWEDEN

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Isabela Pedroza-Pacheco

University of Oxford

UNITED KINGDOM

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Mariolina Salio

University of Oxford

UNITED KINGDOM

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Angharad Fenton-May

University of Oxford

UNITED KINGDOM

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Adán Pinto-Fernández

University of Oxford

UNITED KINGDOM

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Persephone Borrow

Research Interests

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Articles (14)

Targeting MHC-E as a new strategy for vaccines and immunotherapeutics

In vivo enhancement of tumour-specific T cells via peptide–MHC-pseudotyped retroviral gene delivery

IL-15 reprogramming compensates for NK cell mitochondrial dysfunction in HIV-1 infection

MARS an improved de novo peptide candidate selection method for non-canonical antigen target discovery in cancer

Intracellular trafficking of HLA-E and its regulation

Human T follicular regulatory cells with helper and regulatory lineage origins

Deletion of the deISGylating enzyme USP18 enhances tumour cell antigenicity and radiosensitivity

Heightened resistance to host type 1 interferons characterizes HIV-1 at transmission and after antiretroviral therapy interruption

A Stronger Innate Immune Response During Hyperacute HIV-1 Infection is associated with ACUTE retroviral syndrome.

HLA-E–restricted, Gag-specific CD8+T cells can suppress HIV-1 infection, offering vaccine opportunities

Targeting autoantibodies in COVID-19.

Protein/AS01<sub>B</sub> vaccination elicits stronger, more Th2-skewed antigen-specific human T follicular helper cell responses than heterologous viral vectors.

<i>RAB11FIP5</i>-Deficient Mice Exhibit Cytokine-Related Transcriptomic Signatures.

Dynamics of Transforming Growth Factor (TGF)-β Superfamily Cytokine Induction During HIV-1 Infection Are Distinct From Other Innate Cytokines.

Collaborators (17)

Carolina Barra

Simon Brackenridge

Anna Schurich

Andreas Damianou

Jamirah Nazziwa

Sarah Rowland-Jones

Andrew James McMichael

Jonathan Hare

Amin S Hassan

Scott Sherrill-Mix

Marco Fritzsche

Edward Jenkins

Sara Karlson

Isabela Pedroza-Pacheco

Mariolina Salio

Angharad Fenton-May

Adán Pinto-Fernández

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