Evidence map›Paper›PMID 37078788›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

BiTE-Secreting CAR-γδT as a Dual Targeting Strategy for the Treatment of Solid Tumors.

Shi-Wei Huang, Chih-Ming Pan, Yu-Chuan Lin, Mei-Chih Chen, Yeh Chen, Chia-Ing Jan, Chung-Chun Wu, Fang-Yu Lin, Sin-Ting Wang, Chen-Yu Lin and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06150885 (A Single Arm, Open Label, Dose-escalation Phase I and Dose-expansion Phase IIa Clinical Study to Evaluate the Feasibility, Safety, and Efficacy of Allogeneic Chimeric Antigen Receptor), which is not on this map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
10.4field-weighted citation impact, top 1% 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.

NCT06150885 phase1 / phase2recruitingnot on this mapstarted 2024, after this paper: background citation

A Single Arm, Open Label, Dose-escalation Phase I and Dose-expansion Phase IIa Clinical Study to Evaluate the Feasibility, Safety, and Efficacy of Allogeneic Chimeric Antigen Receptor (CAR) Gamma-Delta T Cells CAR001 in Subjects with Relapsed/refractory Solid Tumors

TypeinterventionalSponsorEver Supreme Bio Technology Co., Ltd.Ran2024 to 2027Enrolled60ConditionsSolid TumorArmsHLA-G-CAR.BiTE allogeneic γδ T cells
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 45 citations in OpenAlex.

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  8. Immune cell engagers in lung cancer.Frontiers in immunology · 2026
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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

18 authors at 3 institutions in 1 country.

Shi-Wei HuangTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.ORCID 0000-0002-0050-0959
Chih-Ming PanTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Yu-Chuan LinTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Mei-Chih ChenTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Yeh ChenInstitute of New Drug Development, China Medical University, Taichung, 40447, Taiwan.
Chia-Ing JanDepartment of Pathology, Kaohsiung Veterans General Hospital, Kaohsiung, 813414, Taiwan.
Chung-Chun WuTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Fang-Yu LinTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Sin-Ting WangDepartment of Dermatology, Taichung Veterans General Hospital, Taichung, 40447, Taiwan.
Chen-Yu LinTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Pei-Ying LinTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Wei-Hsaing HuangTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Yu-Ting ChiangTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Wan-Chen TsaiTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Ya-Hsu ChiuTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Ting-Hsun LinTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Shao-Chih ChiuTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.
Der-Yang ChoTranslational Cell Therapy Center, Department of Medical Research, China Medical University Hospital, Taichung, 40447, Taiwan.ORCID 0000-0002-6429-3565
China Medical University · TWKaohsiung Veterans General Hospital · TWTaichung Veterans General Hospital · TW

Funding

China Medical University Hospital DMR-CARGDT-01China Medical University Hospital DMR-CELL-2104China Medical University Hospital Cancer Research Center of Excellence MOHW108-TDU-B-212-124024Ministry of Education MOHW108-TDU-B-212-124024Ministry of Education (Higher Education Sprout Project)Ministry of Science and Technology 109-2314-B-039 -047-MY3Ministry of Science and Technology 111-2321-B-039 -006Ministry of Science and Technology MOST 110-2314-B-039 -052Ministry of Science and Technology MOST 110-2314-B-039 -053Ministry of Science and Technology, Taiwan 111-2321-B-039 -006 -
6 · The paper itself

Abstract

HLA-G is considered as an immune checkpoint protein and a tumor-associated antigen. In the previous work, it is reported that CAR-NK targeting of HLA-G can be used to treat certain solid tumors. However, the frequent co-expression of PD-L1 and HLA-G) and up-regulation of PD-L1 after adoptive immunotherapy may decrease the effectiveness of HLA-G-CAR. Therefore, simultaneous targeting of HLA-G and PD-L1 by multi-specific CAR could represent an appropriate solution. Furthermore, gamma-delta T (γδT) cells exhibit MHC-independent cytotoxicity against tumor cells and possess allogeneic potential. The utilization of nanobodies offers flexibility for CAR engineering and the ability to recognize novel epitopes. In this study, Vδ2 γδT cells are used as effector cells and electroporated with an mRNA-driven, nanobody-based HLA-G-CAR with a secreted PD-L1/CD3ε Bispecific T-cell engager (BiTE) construct (Nb-CAR.BiTE). Both in vivo and in vitro experiments reveal that the Nb-CAR.BiTE-γδT cells could effectively eliminate PD-L1 and/or HLA-G-positive solid tumors. The secreted PD-L1/CD3ε Nb-BiTE can not only redirect Nb-CAR-γδT but also recruit un-transduced bystander T cells against tumor cells expressing PD-L1, thereby enhancing the activity of Nb-CAR-γδT therapy. Furthermore, evidence is provided that Nb-CAR.BiTE redirectes γδT into tumor-implanted tissues and that the secreted Nb-BiTE is restricted to the tumor site without apparent toxicity.

Indexed as

NeoplasmsReceptors, Chimeric AntigenB7-H1 AntigenHLA-G AntigensHumansT-LymphocytesB7-H1 AntigenHLA-G AntigensReceptors, Chimeric Antigenantigen heterogenicitybispecific T-cell engagerchimeric antigen receptorgamma-delta TmRNAnanobody

Identifiers

PMID37078788
PMCPMC10265101
OpenAlexW4366463570

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.