Evidence map›Paper›PMID 36389701›Full record

ReviewFrontiers in immunology2022

Chimeric antigen receptor T cells applied to solid tumors.

Zhongguo Zhou, Can Tao, Jianting Li, Johnny Cheuk-On Tang, Albert Sun-Chi Chan, Yuanyuan Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  7. The Tumor Immune Environment: Advances in the Cancer Immunotherapy Era.Methods in molecular biology (Clifton, N.J.) · 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

6 authors at 4 institutions in 3 countries.

Zhongguo ZhouSchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
Can TaoSchool of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
Jianting LiSchool of Biomedical Engineering, Sun Yat-sen University, Guangzhou, Guangdong, China.
Johnny Cheuk-On TangDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, Hong Kong SAR, China.
Albert Sun-Chi ChanSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yuanyuan ZhouSchool of Biomedical Engineering, Sun Yat-sen University, Guangzhou, Guangdong, China.
Sun Yat-sen University · CNAnhui Medical University · CNHong Kong Polytechnic University · HKUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T cell (CAR-T) therapy is novel tumor immunotherapy that enables autologous T to express synthetic receptors to specifically recognize the surface tumor-associated antigens for exerting subsequent antitumor effects, and eliminating the resistance, metastases and recurrence of cancer. Although CAR T cells have exhibited success in eradicating hematologic malignancies, their applications to solid tumors has not yet been achieved due to obstacles such as the immune-suppressor tumor microenvironment and lack of tumor specific target antigens. In this review, we presented advancements in the development of CAR T cell therapy in solid tumors, and offered a brief summary of the challenges, as well as novel engineering and pharmaceutical interventions to overcome these barriers. Looking forward, we discussed the latest studies which are expected to reach the clinicals in the next few years, including CRISPR screens-based CAR modification and CAR T cells driven from progenitor-like T cells. Collectively, this review may inspire researchers and clinicians to develop clinical available strategies of CAR T cell therapies in solid tumor.

Indexed as

NeoplasmsReceptors, Chimeric AntigenAntigens, NeoplasmHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellT-LymphocytesTumor MicroenvironmentAntigens, NeoplasmReceptors, Antigen, T-CellReceptors, Chimeric AntigenantigenheterogeneityCAR T cell therapycrispr screensneoantigenprogenitor-like T cellsolid tumortumor microenvironment

Identifiers

PMID36389701
PMCPMC9659902
OpenAlexW4307746764

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.