Evidence map›Paper›PMID 36702861›Full record

ArticleCommunications biology2023

The HDAC inhibitor zabadinostat is a systemic regulator of adaptive immunity.

Geng Liu, Wojciech Barczak, Lian Ni Lee, Amit Shrestha, Nicholas M Provine, Gulsah Albayrak, Hong Zhu, Claire Hutchings, Paul Klenerman, Nicholas B La Thangue

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Geng Liu *Laboratory of Cancer Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK.
Wojciech Barczak *Laboratory of Cancer Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK.ORCID 0000-0002-9603-2028
Lian Ni LeePeter Medawar Building for Pathogen Research, University of Oxford, Oxford, OX1 3SY, UK.ORCID 0000-0003-3915-3015
Amit ShresthaLaboratory of Cancer Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK.
Nicholas M ProvineTranslational Gastroenterology Unit, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 9DU, UK.
Gulsah AlbayrakLaboratory of Cancer Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK.
Hong ZhuLaboratory of Cancer Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK.
Claire HutchingsPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, OX1 3SY, UK.ORCID 0000-0002-7858-6924
Paul KlenermanPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, OX1 3SY, UK.
Nicholas B La ThangueLaboratory of Cancer Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK. nick.lathangue@oncology.ox.ac.uk.ORCID 0000-0003-2568-3736
University of Oxford · GBCancer Research UK · GBSichuan University · CN

Funding

Cancer Research UK (CRUK) A20776
6 · The paper itself

Abstract

Protein acetylation plays a key role in regulating cellular processes and is subject to aberrant control in diverse pathologies. Although histone deacetylase (HDAC) inhibitors are approved drugs for certain cancers, it is not known whether they can be deployed in other therapeutic contexts. We have explored the clinical HDAC inhibitor, zabadinostat/CXD101, and found that it is a stand-alone regulator of the adaptive immune response. Zabadinostat treatment increased expression of MHC class I and II genes in a variety of cells, including dendritic cells (DCs) and healthy tissue. Remarkably, zabadinostat enhanced the activity of DCs, and CD4 and CD8 T lymphocytes. Using an antigenic peptide presented to the immune system by MHC class I, zabadinostat caused an increase in antigen-specific CD8 T lymphocytes. Further, mice immunised with covid19 spike protein and treated with zabadinostat exhibit enhanced covid19 neutralising antibodies and an increased level of T lymphocytes. The enhanced humoral response reflected increased activity of T follicular helper (Tfh) cells and germinal centre (GC) B cells. Our results argue strongly that zabadinostat has potential to augment diverse therapeutic agents that act through the immune system.

Indexed as

COVID-19Immunity, HumoralAdaptive ImmunityAnimalsAntigensHistone Deacetylase InhibitorsMiceT-Lymphocytes, Helper-InducerAntigensHistone Deacetylase Inhibitors

Identifiers

PMID36702861
PMCPMC9878486
OpenAlexW4318067203

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.