Evidence map›Paper›PMID 41516373›Full record

ArticleInternational journal of molecular sciences2026

A Novel MICB-Targeting CAR-NK Cells for the Treatment of Pancreatic Cancer.

Weiyang Jin, Mengying Wang, Jingwei Wang, Jinyi Fan, Jie Fang, Guanghua Yang

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. 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.

Weiyang JinInternational Research Center for Biological Sciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
Mengying WangInternational Research Center for Biological Sciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
Jingwei WangMedical Research Center, Academy of Chinese Medical Sciences, Zhejiang Chinese Medical University, Hangzhou 310050, China.
Jinyi FanInternational Research Center for Biological Sciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
Jie FangZhejiang Provincial Laboratory of Experimental Animal's & Nonclinical Laboratory Studies, Hangzhou Medical College, Hangzhou 310013, China.
Guanghua YangInternational Research Center for Biological Sciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China.

Funding

Nuclear (Shanghai) Pharmaceutical Technology Co., Ltd. NO
6 · The paper itself

Abstract

MICB-targeting CAR-NK (chimeric antigen receptor-modified natural killer cells) therapy may serve as off-the-shelf immunotherapy. We designed soluble Anti-MICB-scFv blocks tumor immune evasion targeting the MICB antigen, thereby enhancing CAR-NK cytotoxicity while reactivating endogenous immune attacks against malignancies. The Anti-MICB-CAR includes two Anti-MICB-scFv connected by an F2A linker, the CD8 hinge and transmembrane domain, the 4-1BB co-stimulatory domain, the CD3ζ activation domain, and IL-15. The expression efficiency of Anti-MICB-CAR in NK cells was investigated by flow cytometry; ELISA demonstrated that Anti-MICB-CAR-NK secreted free Anti-MICB-scFv and detected IL-15 secretion. Flow cytometry and CCK8 were utilized to study Anti-MICB-CAR-NK on tumor cell viability. The PANC-1 xenograft model was established in order to elucidate the anti-tumor effects of Anti-MICB-CAR-NK in vivo. In vitro investigations have demonstrated that the treatment of tumor cells with Anti-MICB-CAR-NK supernatant + NK cells or Anti-MICB-CAR-NK cells not only significantly increased the cytotoxic activity of tumor cells, but also secreted and produced higher levels of IL-15, IFN-γ, TNF-α, perforin, and granzyme B compared with NK cells. Anti-MICB-CAR-NK cells exhibit strong cytotoxic activity against tumor cells with high MICB expression. In vivo, Anti-MICB-CAR-NK cells exhibited a substantial inhibitory effect on tumor growth. The IHC results reveal that Anti-MICB-CAR-NK cells show a more pronounced ability to infiltrate the tumor. We demonstrated the successful expression of Anti-MICB-CAR in NK cells, which enhances the anti-tumor activity of NK cells both in vitro and in vivo. This stress ligand-targeting approach provides a promising strategy for solid tumors.

Indexed as

Immunotherapy, AdoptiveKiller Cells, NaturalPancreatic NeoplasmsReceptors, Chimeric AntigenAnimalsCell Line, TumorCytotoxicity, ImmunologicFemaleHistocompatibility Antigens Class IHumansInterleukin-15MiceXenograft Model Antitumor AssaysHistocompatibility Antigens Class IInterleukin-15MICB antigenReceptors, Chimeric AntigenCAR-NKIL-15immunotherapyMICBPANC-1

Identifiers

PMID41516373
PMCPMC12786817

What Socratic 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 Socratic graph.