Evidence map›Paper›PMID 34007176›Full record

ArticleInternational journal of nanomedicine2021

Nanobubbles Containing sPD-1 and Ce6 Mediate Combination Immunotherapy and Suppress Hepatocellular Carcinoma in Mice.

Yandi Tan, Shiqi Yang, Yao Ma, Jinlin Li, Qian Xie, Chaoqi Liu, Yun Zhao

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

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  17. Recent advances in sonodynamic immunotherapy.Journal of cancer research and clinical oncology · 2023
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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

7 authors at 2 institutions in 1 country.

Yandi Tan *Medical College of China Three Gorges University, Yichang, Hubei, People's Republic of China.ORCID 0000-0002-6176-1351
Shiqi Yang *Medical College of China Three Gorges University, Yichang, Hubei, People's Republic of China.ORCID 0000-0002-3076-0567
Yao MaDepartment of Ultrasonography, Yichang Central People's Hospital, Yichang, People's Republic of China.
Jinlin LiMedical College of China Three Gorges University, Yichang, Hubei, People's Republic of China.
Qian XieMedical College of China Three Gorges University, Yichang, Hubei, People's Republic of China.
Chaoqi LiuMedical College of China Three Gorges University, Yichang, Hubei, People's Republic of China.
Yun ZhaoMedical College of China Three Gorges University, Yichang, Hubei, People's Republic of China.ORCID 0000-0003-4090-172X
China Three Gorges University · CNYichang Central People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmune checkpoint inhibitors (ICIs) and sonodynamic therapy (SDT) are types of immunotherapy. In order to combine soluble programmed cell death protein 1 (sPD-1)-mediated immune checkpoint therapy and chlorin e6 (Ce6)-assisted SDT, nanobubbles (NBs) were generated to simultaneously load sPD-1 and Ce6. MATERIALS AND

methodsThe sPD-1/Ce6-NBs, which were prepared by thin-film hydration and mechanical oscillation, had a stable physical condition, and delivered sPD-1 and Ce6 in a targeted manner. NBs could strengthen tumor suppression by increasing tumor-targeting accumulation of Ce6 and sPD-1, and by inducing ultrasound-targeted NB destruction. A mouse H22 cell hepatoma xenograft model was used to evaluate the synergetic immunotherapeutic effect and mechanism of sPD-1/Ce6-NBs.

resultsBy observing the tumor inhibition rate, tissue and cell apoptosis, apoptosis-related genes and protein expression, the best immunotherapeutic effect was exhibited by the sPD-1/Ce6-NBs group. The immunotherapeutic mechanism initially demonstrated that when tumor cells were transfected by sPD-1 delivered by NBs, which downregulated the expression of programmed death-ligand 1 (PD-L1) in tumor cells, and blocked the PD-1/PD-L1 signaling pathway, which improved T-cell-mediated tumor inhibition. Furthermore, ICIs combined with SDT induced immunogenic cell death by translocating calreticulin to the cell surface and then synergistically enhancing antitumor immune responses.

conclusionIn conclusion, sPD-1/Ce6-NBs were successfully designed. Ultrasound-mediated sPD-1/Ce6-NBs are potentially effective delivery systems for combination immunotherapy of hepatocellular carcinoma.

Indexed as

ImmunotherapyAnimalsApoptosisCarcinoma, HepatocellularChlorophyllidesHumansLiver NeoplasmsMaleMiceMice, Inbred BALB CNanoparticlesPorphyrinsProgrammed Cell Death 1 ReceptorRNA, MessengerT-LymphocytesTumor BurdenChlorophyllidesphytochlorinPorphyrinsProgrammed Cell Death 1 ReceptorRNA, Messengerdrug deliveryimmune checkpoint inhibitorsnanomaterialstumor therapyultrasonics

Identifiers

PMID34007176
PMCPMC8121678
OpenAlexW3161212189

What OpenQuestion holds

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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.