Evidence map›Paper›PMID 36868236›Full record

ArticleCell reports. Medicine2023

A bispecific T cell engager recruits both type 1 NKT and Vγ9Vδ2-T cells for the treatment of CD1d-expressing hematological malignancies.

Roeland Lameris, Jurjen M Ruben, Victoria Iglesias-Guimarais, Milon de Jong, Myrthe Veth, Fleur S van de Bovenkamp, Iris de Weerdt, Arnon P Kater, Sonja Zweegman, Sjeng Horbach and 7 more

Open access · goldFull text read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 31 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

17 authors at 4 institutions in 2 countries.

Roeland LamerisAmsterdam UMC location Vrije University Amsterdam, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Jurjen M RubenLAVA Therapeutics, Utrecht, the Netherlands.
Victoria Iglesias-GuimaraisLAVA Therapeutics, Utrecht, the Netherlands.
Milon de JongAmsterdam UMC location Vrije University Amsterdam, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Myrthe VethAmsterdam UMC location Vrije University Amsterdam, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Fleur S van de BovenkampLAVA Therapeutics, Utrecht, the Netherlands.
Iris de WeerdtAmsterdam UMC location University of Amsterdam, Department of Hematology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Arnon P KaterAmsterdam UMC location University of Amsterdam, Department of Hematology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Sonja ZweegmanAmsterdam UMC location Vrije University Amsterdam, Department of Hematology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Sjeng HorbachJ&S Preclinical Solutions, Oss, the Netherlands.
Thilo RiedlLAVA Therapeutics, Utrecht, the Netherlands.
Benjamin WinogradLAVA Therapeutics, Utrecht, the Netherlands; LAVA Therapeutics, Philadelphia, PA, USA.
Rob C RooversLAVA Therapeutics, Utrecht, the Netherlands.
Anton E P AdangLAVA Therapeutics, Utrecht, the Netherlands.
Tanja D de GruijlAmsterdam UMC location Vrije University Amsterdam, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands.
Paul W H I ParrenLAVA Therapeutics, Utrecht, the Netherlands; Leiden University Medical Center, Department of Immunology, Leiden, the Netherlands.
Hans J van der VlietAmsterdam UMC location Vrije University Amsterdam, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands; LAVA Therapeutics, Utrecht, the Netherlands. Electronic address: h.vandervliet@lavatherapeutics.com.
Lava Therapeutics (Netherlands) · NLAmsterdam University Medical Centers · NLClinical Solutions · USLeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bispecific T cell engagers (bsTCEs) hold great promise for cancer treatment but face challenges due to the induction of cytokine release syndrome (CRS), on-target off-tumor toxicity, and the engagement of immunosuppressive regulatory T cells that limit efficacy. The development of Vγ9Vδ2-T cell engagers may overcome these challenges by combining high therapeutic efficacy with limited toxicity. By linking a CD1d-specific single-domain antibody (VHH) to a Vδ2-TCR-specific VHH, we create a bsTCE with trispecific properties, which engages not only Vγ9Vδ2-T cells but also type 1 NKT cells to CD1d

Indexed as

Hematologic NeoplasmsLeukemia, Lymphocytic, Chronic, B-CellLeukemia, Myeloid, AcuteAnimalsMiceT-Lymphocytes, Regulatoryacute myeloid leukemiabispecific T cell engagersCD1dchronic lymphocytic leukemiamultiple myelomanon-human primatepreclinicalsingle-domain antibodytype 1 NKT cellVγ9Vδ2-T cell

Identifiers

PMID36868236
PMCPMC10040383
OpenAlexW4322767176

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read86
identifiers read2
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.