Evidence map›Paper›PMID 33747727›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

Avidity-Based Selection of Tissue-Specific CAR-T Cells from a Combinatorial Cellular Library of CARs.

Peixiang Ma, Ping Ren, Chuyue Zhang, Jiaxing Tang, Zheng Yu, Xuekai Zhu, Kun Fan, Guanglei Li, Wei Zhu, Wei Sang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 17 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

15 authors at 5 institutions in 2 countries.

Peixiang MaShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.ORCID https://orcid.org/0000-0001-6794-1663
Ping RenShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Chuyue ZhangShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Jiaxing TangShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Zheng YuShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Xuekai ZhuShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Kun FanShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Guanglei LiSchool of Life Science and Technology ShanghaiTech University Shanghai 201210 China.
Wei ZhuShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Wei SangDepartment of Hematology The Affiliated Hospital of Xuzhou Medical University Institute of Hematology Xuzhou Medical University Xuzhou 221000 China.
Chenyu MinVelox Pharmaceuticals Changzhou 213000 China.
Wenzhang ChenShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Xingxu HuangSchool of Life Science and Technology ShanghaiTech University Shanghai 201210 China.
Guang YangShanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 China.
Richard A LernerDepartment of Chemistry Scripps Research Institute La Jolla CA 92037 USA.ORCID https://orcid.org/0000-0003-4399-874X
ShanghaiTech University · CNChinese Academy of Sciences · CNEloxx Pharmaceuticals (United States) · USScripps Research Institute · USXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using T-cell chimeric antigen receptors (CAR-T) to activate and redirect T cells to tumors expressing the cognate antigen represents a powerful approach in cancer therapy. However, normal tissues with low expression of tumor-associated antigens (TAAs) can be mistargeted, resulting in severe side effects. An approach using a collection of T cells expressing a diverse, 10

Indexed as

CD38chimeric antigen receptorcombinatorial antibody librarytumor‐associated antigen

Identifiers

PMID33747727
PMCPMC7967050
OpenAlexW3128340189

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.