Evidence map›Paper›PMID 36159778›Full record

ArticleMolecular therapy oncolytics2022

A novel anti-B7-H3 chimeric antigen receptor from a single-chain antibody library for immunotherapy of solid cancers.

Kathleen Birley, Clara Leboreiro-Babe, Enrique Miranda Rota, Magdalena Buschhaus, Artemis Gavriil, Alice Vitali, Maria Alonso-Ferrero, Lee Hopwood, Lara Parienti, Gabrielle Ferry and 4 more

Abstract read
In one paragraph

Article in Molecular therapy oncolytics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  12. Blocking MIF secretion enhances CAR T-cell efficacy against neuroblastoma.European journal of cancer (Oxford, England : 1990) · 2025
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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

14 authors.

Kathleen BirleyZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Clara Leboreiro-BabeZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Enrique Miranda RotaThe Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Magdalena BuschhausThe Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Artemis GavriilZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Alice VitaliZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Maria Alonso-FerreroZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Lee HopwoodZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Lara ParientiZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Gabrielle FerryZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Barry FlutterZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Nourredine HimoudiZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.
Kerry ChesterThe Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
John AndersonZayed Centre for Research, University College London, 20c Guildford Street, London WC1N 1DZ, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B7-H3 (CD276) has emerged as a target for cancer immunotherapy by virtue of consistent expression in many malignancies, relative absence from healthy tissues, and an emerging role as a driver of tumor immune inhibition. Recent studies have reported B7-H3 to be a suitable target for chimeric antigen receptor-modified T cell (CAR-T) therapy using CARs constructed from established anti-B7-H3 antibodies converted into single-chain Fv format (scFv). We constructed and screened binders in an scFv library to generate a new anti-B7-H3 CAR-T with favorable properties. This allowed access to numerous specificities ready formatted for CAR evaluation. Selected anti-human B7-H3 scFvs were readily cloned into CAR-T and evaluated for anti-tumor reactivity in cytotoxicity, cytokine, and proliferation assays. Two binders with divergent complementarity determining regions were found to show optimal antigen-specific cytotoxicity and cytokine secretion. One binder in second-generation CD28-CD3ζ CAR format induced sustained

Indexed as

B7-H3CAR-T cellneuroblastomapediatric cancerphage displaysolid tumor

Identifiers

PMID36159778
PMCPMC9467911

What OpenQuestion holds

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Registered trials

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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.