Evidence map›Paper›PMID 42903486›Full record

ReviewhLife2024

Boosting CAR-T cell therapy with CRISPR technology.

Liyanran Yan, Shanzi Gao, Xinhui Wang, Xintao Zhou, Praopim Limsakul, Yiqian Wu

Abstract readReview
In one paragraph

Review in hLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Liyanran YanAcademy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Shanzi GaoCollege of Biological Sciences & Biotechnology, Beijing Forestry University, Beijing, China.
Xinhui WangSDU-ANU Joint Science College, Shandong University, Shandong, China.
Xintao ZhouCollege of Chemistry, South China Normal University, Guangdong, China.
Praopim LimsakulDivision of Physical Science, Faculty of Science, and Center of Excellence for Trace Analysis and Biosensor, Prince of Songkla University, Songkhla, Thailand.
Yiqian WuNational Biomedical Imaging Center, Peking University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-T cell therapy has made remarkable breakthroughs in treating cancers, especially hematologic malignancies, yet its broader application in cancer treatment is hindered by multiple challenges. Meanwhile, the development of clustered regularly interspaced short palindromic repeats (CRISPR) and its derived technologies has provided unprecedentedly efficient tools for genomic and cellular reprogramming, offering potential advantages for developing CAR-T cell therapy. There is hence a rapidly increasing interest in applying CRISPR to engineer CAR-T cells. Here, we present a review of recent research utilizing CRISPR to boost CAR-T cell therapy by enhancing its safety or effectiveness. We first provide an overview of CAR-T cell therapy and CRISPR technology, followed by discussions on how CRISPR and its related technologies can be adopted to tackle various issues associated with CAR-T cell therapy, either

Indexed as

chimeric antigen receptor (CAR)-T cell therapyclustered regularly interspaced short palindromic repeats (CRISPR)immunotherapy

Identifiers

PMID42903486
PMCPMC13681519

What OpenQuestion holds

Textmetadata
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.