David Price

Professor of Infection and Immunity

Cardiff University

United Kingdom

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David Price is a Professor of Infection and Immunity at Cardiff University, UK. His research focuses on T cell responses, the immune mechanisms involved in cancer vaccination, and the implications of aging and inflammation on immune efficacy, particularly in the context of SARS-CoV-2 and long COVID. Recent articles authored by Professor Price explore the proteolytic processes of immune molecules, the impact of dendritic cell vaccination on various cancers, and the characterization of immune responses in chronic infections.

David Price

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Articles (20)

TCR activation stimulates regulated intramembrane proteolysis of L-selectin by presenilin 1 and localized proteasomal degradation of the cytoplasmic tail

<i>WT1</i>-mRNA dendritic cell vaccination of patients with glioblastoma multiforme, malignant pleural mesothelioma, metastatic breast cancer, and other solid tumors: type 1 T-lymphocyte responses are associated with clinical outcome

<i>WT1</i>-mRNA dendritic cell vaccination of patients with glioblastoma multiforme, malignant pleural mesothelioma, metastatic breast cancer, and other solid tumors: type 1 T-lymphocyte responses are associated with clinical outcome (vol 18, 9, 2025)

Aging and inflammation limit the induction of SARS-CoV-2-specific CD8+T cell responses in severe COVID-19

Identification of soluble biomarkers that associate with distinct manifestations of long COVID

Repertoire-based mapping and time-tracking of T helper cell subsets in scRNA-Seq

Targeting the SARS-CoV-2 reservoir in long COVID

Inhibitory KIRs decrease HLA class II-mediated protection in Type 1 Diabetes

Attenuated effector T cells are linked to control of chronic HBV infection

Immunotoxin-mediated depletion of Gag-specific CD8+ T cells undermines natural control of SIV

Author Correction: Human circulating and tissue-resident memory CD8+ T cells

Human circulating and tissue-resident memory CD8+ T cells

The superantigens SpeC and TSST-1 specifically activate TRBV12-3/12-4+ memory T cells

The superantigens SpeC and TSST-1 specifically activate TRBV12-3/12-4(+) memory T cells

Ageing Curtails the Diversity and Functionality of Nascent CD8<sup>+</sup> T Cell Responses against SARS-CoV-2

Ageing Curtails the Diversity and Functionality of Nascent CD8(+) T Cell Responses against SARS-CoV-2

CD4+T cell-mediated recognition of a conserved cholesterol-dependent cytolysin epitope generates broad antibacterial immunity

Altered Basal Lipid Metabolism Underlies the Functional Impairment of Naive CD8(+) T Cells in Elderly Humans

Ancestral SARS-CoV-2-specific T cells cross-recognize the Omicron variant

Epitope length variants balance protective immune responses and viral escape in HIV-1 infection

Collaborators (7)

Marcus Buggert

James McLaren

Kristin Ladell

James Redman

Antonella Caputo

Francesco Nicoli

Laura Mackay

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