Maini, MK;
(2023)
Tissue T cells in prophylactic and therapeutic vaccination responses.
Seminars in Arthritis and Rheumatism
, 63
, Article 152287. 10.1016/j.semarthrit.2023.152287.
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Abstract
In this conference report, I highlight the potential to target tissue-resident T cells to enhance prophylactic and therapeutic vaccine immunity. I describe our recent findings on exploiting frontline sentinal immunosurveillance by liver-resident immunity for functional cure of hepatitis B. We showed that therapeutic vaccine-induced HBV-specific T cells are constrained by liver-resident NK cells; cytokine-activation and PD-L1 blockade of NK cells converted them into helpers able to instead boost HBV-specific T cells. Turning to tissue-resident T cells in the lung, we found this pool can include T cells able to recognise SARS-CoV-2, including cross-reactive responses present prior to the pandemic. The importance of inducing T cells with future prophylactic vaccines was underscored by their selective expansion in a subset of donors aborting SARS-CoV-2 infection without detectable antibodies.
Type: | Article |
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Title: | Tissue T cells in prophylactic and therapeutic vaccination responses |
Location: | United States |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1016/j.semarthrit.2023.152287 |
Publisher version: | https://doi.org/10.1016/j.semarthrit.2023.152287 |
Language: | English |
Additional information: | © 2023 The Author(s). Published by Elsevier Inc. under a Creative Commons license (http://creativecommons.org/licenses/by/4.0/). |
Keywords: | Hepatitis B functional cure, SARS-CoV-2 vaccination, T cells, Therapeutic vaccination, Tissue-resident immunity |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity |
URI: | https://discovery.ucl.ac.uk/id/eprint/10181338 |
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