Evidence map›Paper›PMID 30609118›Full record

ArticleJournal of cellular biochemistry2019

Near-infrared fluorescence-labeled anti-PD-L1-mAb for tumor imaging in human colorectal cancer xenografted mice.

Mingyu Zhang, Huijie Jiang, Rongjun Zhang, Hao Jiang, Hailong Xu, Wenbin Pan, Xiaolin Gao, Zhongqi Sun

Open access · hybridAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Research square · 2023
    Article
  5. Article
  6. Article
  7. Radioimmunotherapy study ofEJNMMI research · 2022
    Article
  8. Development of Radiotracers for Imaging of the PD-1/PD-L1 Axis.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Frontiers in immunology · 2020
    Review
  14. Article
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

8 authors at 2 institutions in 1 country.

Mingyu ZhangDepartment of Radiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Huijie JiangDepartment of Radiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.ORCID 0000-0003-1927-2674
Rongjun ZhangJiangsu Institute of Nuclear Medicine, Wuxi, China.
Hao JiangDepartment of Radiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Hailong XuDepartment of Radiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Wenbin PanDepartment of Radiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Xiaolin GaoDepartment of Radiology, China-Japan Union Hospital, Jilin University, Changchun, China.
Zhongqi SunDepartment of Radiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Harbin Medical University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of programmed death ligand-1 (PD-L1) in tumor has been used as a biomarker to predict the anti-PD-L1 immunotherapy response. To develop a noninvasive imaging technique to monitor the dynamic changes in PD-L1 expression in colorectal cancer (CRC), we labeled an anti-PD-L1 monoclonal antibody with near-infrared (NIR) dye and tested the ability of the NIR-PD-L1-mAb probe to monitor the PD-L1 expression in CRC-xenografted mice by performing optical imaging. Consistent with the expression levels of PD-L1 protein in three CRC cell lines in vitro by flow cytometry and Western blot analyses, our in vivo imaging showed the highest fluorescence signal of the xenografted tumors in mice bearing SW620 CRC cells, followed by tumors derived from SW480 and HCT8 cell lines. We detected the highest fluorescent intensity of the tumor at 120 hours after injection of NIR-PD-L1-mAb. The highest fluorescence intensity was seen in the tumor, followed by the spleen and the liver in SW620 xenografted mice. In SW480 and HCT8 xenografted mice, however, the highest fluorescent signals were detected in the spleen, followed by the liver and the tumor. Our findings indicate that SW620 cells express a higher level of PD-L1, and the NIR-PD-L1-mAb binding to PD-L1 on the surface of CRC cells was specific. The technique was safe and could provide valuable information on PD-L1 expression of the tumor for development of a therapeutic strategy of personized targeted immunotherapies as well as treatment response of patients with CRC.

Indexed as

AnimalsAntibodies, MonoclonalB7-H1 AntigenCell Line, TumorColorectal NeoplasmsFeasibility StudiesFemaleHeterograftsHumansImmunoconjugatesMice, Inbred BALB CMice, NudeOptical ImagingReproducibility of ResultsAntibodies, MonoclonalB7-H1 AntigenCD274 protein, humanImmunoconjugatescolorectal cancerimmunotherapynoninvasive imagingoptical imagingprogrammed death ligand-1/programmed death ligand-1 checkpoint

Identifiers

PMID30609118
PMCPMC6590288
OpenAlexW2907714024

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.