Evidence map›Paper›PMID 36012691›Full record

ArticleInternational journal of molecular sciences2022

Selective Expansion of NKG2C+ Adaptive NK Cells Using K562 Cells Expressing HLA-E.

Minh-Trang Thi Phan, Jinho Kim, Seung Kwon Koh, Yuree Lim, Hongbi Yu, Mijeong Lee, Jong-Min Lee, Eun-Suk Kang, Hyun-Young Kim, Sang-Ki Kim and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. HLA-E-Directed Accumulation of KIRInternational journal of molecular sciences · 2026
    Article
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  3. Review
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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

12 authors at 5 institutions in 1 country.

Minh-Trang Thi PhanCell and Gene Therapy Institute (CGTI), Samsung Medical Center, Seoul 06351, Korea.
Jinho KimDepartment of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul 06355, Korea.
Seung Kwon KohDepartment of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul 06355, Korea.
Yuree LimDepartment of Biopharmaceutical Convergence, Sungkyunkwan University, Suwon 16419, Korea.
Hongbi YuDepartment of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul 06355, Korea.
Mijeong LeeDepartment of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul 06355, Korea.
Jong-Min LeeBio Research Center, Lugensci Co., Ltd., Bucheon 14556, Korea.
Eun-Suk KangDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Hyun-Young KimDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.ORCID 0000-0003-0553-7096
Sang-Ki KimDepartment of Companion and Laboratory Animal Science, Kongju National University, Yesan 32439, Korea.ORCID 0000-0003-0292-8200
Ilwoong HwangDepartment of Emergency Medicine, Soonchunhyang University Gumi Hospital, Gumi 39371, Korea.
Duck ChoCell and Gene Therapy Institute (CGTI), Samsung Medical Center, Seoul 06351, Korea.
Samsung (South Korea) · KRSamsung Medical Center · KRKongju National University · KRSoonchunhyang University Hospital Seoul · KRSungkyunkwan University · KR

Funding

BK21 FOUR Project 00000Korea Health Industry Development Institute HI22C1363Ministry of Education 2021R1A2B5B0100214911
6 · The paper itself

Abstract

Adaptive natural killer (NK) cells expressing self-specific inhibitory killer-cell immunoglobulin-like receptors (KIRs) can be expanded in vivo in response to human cytomegalovirus (HCMV) infection. Developing a method to preferentially expand this subset is essential for effective targeting of allogeneic cancer cells. A previous study developed an in vitro method to generate single KIR+ NK cells for enhanced targeting of the primary acute lymphoblastic leukemia cells; however, the expansion rate was quite low. Here, we present an effective expansion method using genetically modified K562-HLA-E feeder cells for long-term proliferation of adaptive NK cells displaying highly differentiated phenotype and comparable cytotoxicity, CD107a, and interferon-γ (IFN-γ) production. More importantly, our expansion method achieved more than a 10,000-fold expansion of adaptive NK cells after 6 weeks of culture, providing a high yield of alloreactive NK cells for cell therapy against cancer.

Indexed as

Cytomegalovirus InfectionsNK Cell Lectin-Like Receptor Subfamily CCytomegalovirusHistocompatibility Antigens Class IHLA-E AntigensHumansK562 CellsKiller Cells, NaturalReceptors, KIRHistocompatibility Antigens Class IHLA-E AntigensNK Cell Lectin-Like Receptor Subfamily CReceptors, KIRadaptive NK cellseffective expansionK562-HLA-E feeder cellslong-term persistencesingle KIR NKG2C

Identifiers

PMID36012691
PMCPMC9409060
OpenAlexW4293030285

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.