Evidence map›Paper›PMID 34267335›Full record

ReviewCellular & molecular immunology2021

Chimeric antigen receptor- and natural killer cell receptor-engineered innate killer cells in cancer immunotherapy.

Cai Zhang, Yuan Hu, Weihua Xiao, Zhigang Tian

Open access · bronzeAbstract readReview
In one paragraph

Review in Cellular & molecular immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.9field-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

52 citing papers in PubMed, 80 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

4 authors at 2 institutions in 1 country.

Cai ZhangNK CellTech Co., Ltd., Shanghai International Medical Park, Shanghai, China. cai.zhang@nk-celltech.com.ORCID http://orcid.org/0000-0002-3849-6676
Yuan HuNK CellTech Co., Ltd., Shanghai International Medical Park, Shanghai, China.
Weihua XiaoNK CellTech Co., Ltd., Shanghai International Medical Park, Shanghai, China.
Zhigang TianNK CellTech Co., Ltd., Shanghai International Medical Park, Shanghai, China. tzg@ustc.edu.cn.
Shanghai International Medical Center · CNUniversity of Science and Technology of China · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81788101
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-engineered T-cell (CAR-T) therapy has demonstrated impressive therapeutic efficacy against hematological malignancies, but multiple challenges have hindered its application, particularly for the eradication of solid tumors. Innate killer cells (IKCs), particularly NK cells, NKT cells, and γδ T cells, employ specific antigen-independent innate tumor recognition and cytotoxic mechanisms that simultaneously display high antitumor efficacy and prevent tumor escape caused by antigen loss or modulation. IKCs are associated with a low risk of developing GVHD, thus offering new opportunities for allogeneic "off-the-shelf" cellular therapeutic products. The unique innate features, wide tumor recognition range, and potent antitumor functions of IKCs make them potentially excellent candidates for cancer immunotherapy, particularly serving as platforms for CAR development. In this review, we first provide a brief summary of the challenges hampering CAR-T-cell therapy applications and then discuss the latest CAR-NK-cell research, covering the advantages, applications, and clinical translation of CAR- and NK-cell receptor (NKR)-engineered IKCs. Advances in synthetic biology and the development of novel genetic engineering techniques, such as gene-editing and cellular reprogramming, will enable the further optimization of IKC-based anticancer therapies.

Indexed as

NeoplasmsReceptors, Chimeric AntigenHumansImmunotherapyImmunotherapy, AdoptiveReceptors, Natural Killer CellReceptors, Chimeric AntigenReceptors, Natural Killer CellAdoptive cell therapyChimeric antigen receptorGenetic engineeringInnate killer cellsNatural killer cell receptorTumor microenvironment

Identifiers

PMID34267335
PMCPMC8429625
OpenAlexW3179945349

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.