Evidence map›Paper›PMID 38943249›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

NKG2A genetic deletion promotes human primary NK cell anti-tumor responses better than an anti-NKG2A monoclonal antibody.

Ying Gong, Wilfred T V Germeraad, Xulin Zhang, Nisha Wu, Bo Li, Lynn Janssen, Zongzhong He, Marion J J Gijbels, Bodeng Wu, Birgit L M G Gijsbers and 4 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
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  7. The CD94/NKG2A-HLA-E Axis as a Target in Cancer Immunotherapy: A Critical Perspective.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  8. [cGAS-STING agonist cGAMP enhances natural killer cell-mediated cytotoxicity against gastric cancer cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
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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.

Ying GongDepartment of Laboratory Medicine, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P.R. China; Department of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, 6227 HX Maastricht, the Netherlands; GROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands.
Wilfred T V GermeraadDepartment of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, 6227 HX Maastricht, the Netherlands; GROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands; CiMaas BV, 6202 AZ Maastricht, the Netherlands.
Xulin ZhangState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Vision Science, Guangzhou 510000, China.
Nisha WuDepartment of Breast and Thyroid Surgery, Southwest Hospital, Army Medical University, Chongqing 400038, P.R. China.
Bo LiDepartment of Laboratory Medicine, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P.R. China.
Lynn JanssenDepartment of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, 6227 HX Maastricht, the Netherlands; GROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands.
Zongzhong HeDepartment of Transfusion Medicine of General Hospital of Southern Theatre Command, Guangzhou 510515, P.R. China.
Marion J J GijbelsGROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands; Department of Pathology, Maastricht University Medical Center+, Maastricht, the Netherlands; Department of Medical Biochemistry, Experimental Vascular Biology, Amsterdam Cardiovascular Sciences, Amsterdam Infection and Immunity, Amsterdam UMC, 1081 HV Amsterdam, the Netherlands.
Bodeng WuDepartment of Laboratory Medicine, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P.R. China.
Birgit L M G GijsbersDepartment of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, 6227 HX Maastricht, the Netherlands; GROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands.
Timo I OlieslagersGROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands; Department of Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Center+, 6202 AZ Maastricht, the Netherlands.
Gerard M J BosDepartment of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, 6227 HX Maastricht, the Netherlands; GROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands; CiMaas BV, 6202 AZ Maastricht, the Netherlands.
Lei ZhengDepartment of Laboratory Medicine, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P.R. China. Electronic address: nfyyzhenglei@smu.edu.cn.
Roel G J Klein WolterinkDepartment of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, 6227 HX Maastricht, the Netherlands; GROW - Research Institute for Oncology & Reproduction, Maastricht University, 6202 AZ Maastricht, the Netherlands. Electronic address: roel.kleinwolterink@mumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells eliminate infected or cancer cells via their cytotoxic capacity. NKG2A is an inhibitory receptor on NK cells and cancer cells often overexpress its ligand HLA-E to evade NK cell surveillance. Given the successes of immune checkpoint blockade in cancer therapy, NKG2A is an interesting novel target. However, anti-NKG2A antibodies have shown limited clinical response. In the pursuit of enhancing NK cell-mediated anti-tumor responses, we devised a Cas9-based strategy to delete KLRC1, encoding NKG2A, in human primary NK cells. Our approach involved electroporation of KLRC1-targeting Cas9 ribonucleoprotein resulting in effective ablation of NKG2A expression. Compared with anti-NKG2A antibody blockade, NKG2A

Indexed as

Killer Cells, NaturalNK Cell Lectin-Like Receptor Subfamily CXenograft Model Antitumor AssaysAnimalsAntibodies, MonoclonalCell Line, TumorCRISPR-Cas SystemsCytotoxicity, ImmunologicGene DeletionHistocompatibility Antigens Class IHLA-E AntigensHumansMiceNeoplasmsAntibodies, MonoclonalHistocompatibility Antigens Class IHLA-E AntigensKLRC1 protein, humanNK Cell Lectin-Like Receptor Subfamily Cantibody-dependent cellular cytotoxicitycheckpoint inhibitor immunotherapyCRISPR-Cas9HLA-Emultiple immunofluorescence stainingnatural killer cellsNKG2Atumor microenvironment

Identifiers

PMID38943249
PMCPMC11405175

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.