Evidence map›Paper›PMID 36156442›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Intraparticle Double-Scattering-Decoded Sonogenetics for Augmenting Immune Checkpoint Blockade and CAR-T Therapy.

Duo Wang, Mengqi Zhang, Yan Zhang, Guanhua Qiu, Jie Chen, Xiaoqi Zhu, Cunqing Kong, Xiuxin Lu, Xiayi Liang, Lixia Duan and 4 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 71 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

14 authors at 2 institutions in 2 countries.

Duo WangDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Mengqi ZhangDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Yan ZhangCentral Laboratory and Ultrasound Research and Education Institute, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-chang-zhong Road, Shanghai, 200072, P. R. China.
Guanhua QiuDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Jie ChenCentral Laboratory and Ultrasound Research and Education Institute, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-chang-zhong Road, Shanghai, 200072, P. R. China.
Xiaoqi ZhuDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Cunqing KongDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Xiuxin LuDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Xiayi LiangCentral Laboratory and Ultrasound Research and Education Institute, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-chang-zhong Road, Shanghai, 200072, P. R. China.
Lixia DuanCentral Laboratory and Ultrasound Research and Education Institute, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-chang-zhong Road, Shanghai, 200072, P. R. China.
Chao FangCentral Laboratory and Ultrasound Research and Education Institute, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-chang-zhong Road, Shanghai, 200072, P. R. China.
Junjie LiuDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Kun ZhangCentral Laboratory and Ultrasound Research and Education Institute, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-chang-zhong Road, Shanghai, 200072, P. R. China.ORCID 0000-0002-6971-1164
Tao LuoDepartment of Medical Ultrasound, Department of Interventional Therapy and Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, P. R. China.
Guangxi Medical University · CNTongji University · CN

Funding

Fundamental Research Funds for the Central Universities 22120210561Guangxi Key Research & Development Program 19QA1406800Guangxi Key Research & Development Program AB18221089National Natural Science Foundation of China 81960477National Natural Science Foundation of China 82022033National Natural Science Foundation of China 82160341Shanghai Talent Development Fund 2019040
6 · The paper itself

Abstract

Genetically arming new chimeric antigen receptors (CARs) on T cells is a prevalent method to fulfill CAR-T immunotherapy. However, this approach fails to completely address the poor infiltration, complex immunosuppressive tumor microenvironment (ITM), and insufficient immune cells, which are recognized as the three dominant hurdles to discouraging the trafficking and persistence of CAR-T and immune checkpoint blockade (ICB) immunotherapies against solid tumors. To address the three hurdles, a sonoimmunity-engineered nanoplatform is designed in which a rattle-type-structured carrier enables intraparticle-double-scattering to generate massive reactive oxygen species (ROS) during the sonodynamic process. Abundant ROS accumulation can directly kill tumor cells, release antigens, and activate systematic immune responses for expanding effector T or CAR-T cells, while alleviating ITM via immunosuppressive macrophage polarization and reduction in pro-tumorigenic cytokine secretion. Furthermore, the co-loaded phosphodiesterase-5 inhibitors release nitric oxide (NO) to impel vascular normalization and open the infiltration barrier (IB) for allowing more T cells to enter into the tumor. Systematic experiments demonstrate the feasibility of such intraparticle-double-scattering-decoded sonogenetics in the sonoimmunity-engineered nanoplatforms for expanding effector T or CAR-T cells, thereby promoting their infiltration into tumors and alleviating ITM. These compelling actions lead to excellent CAR-T and ICB immunotherapies against solid tumors with repressed tumor metastasis.

Indexed as

NeoplasmsReceptors, Chimeric AntigenHumansImmune Checkpoint InhibitorsImmunotherapy, AdoptiveReactive Oxygen SpeciesReceptors, Antigen, T-CellTumor MicroenvironmentImmune Checkpoint InhibitorsReactive Oxygen SpeciesReceptors, Antigen, T-CellReceptors, Chimeric Antigenchimeric antigen receptor-T replicationchimeric antigen receptor-T trafficking and persistenceimmunosuppressive tumor microenvironmentintraparticle double-scatteringsonogeneticsvascular normalization

Identifiers

PMID36156442
PMCPMC9661857
OpenAlexW4297192898

What OpenQuestion holds

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LicenceCC BY
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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.