Evidence map›Paper›PMID 34588898›Full record

ArticleSaudi journal of biological sciences2021

Antitumor immunity enhancement through Newcastle viral oncolysate in mice model: A promising method to treat tumors.

Amir Sasan Mozaffari Nejad, Fatemeh Fotouhi, Parvaneh Mehrbod, Mohammad Yousef Alikhani

Open access · hybridAbstract read
In one paragraph

Article in Saudi journal of biological sciences, 2021. 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
1.2field-weighted citation impact, top 19% 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, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
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

4 authors at 2 institutions in 1 country.

Amir Sasan Mozaffari NejadResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Fatemeh FotouhiInfluenza and Respiratory Viruses Department, Pasteur Institute of Iran, Tehran, Iran.
Parvaneh MehrbodInfluenza and Respiratory Viruses Department, Pasteur Institute of Iran, Tehran, Iran.
Mohammad Yousef AlikhaniDepartment of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Hamedan University of Medical Sciences · IRPasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A Newcastle disease virus (NDV) oncolysate has been established as a unique and effective immune-stimulatory root for tumor treatment. Thus, the aim of the current study was to investigate the effects of intratumoral administration of NDV oncolysate on immune response and tumor regression of C57BL/6 mouse model of human papillomavirus (HPV) related transplanted with TC-1 syngeneic cancer cells. To further investigate the mechanism underlying the antitumor response, cytolytic and lymphocyte proliferation responses in splenocytes were measured using lactate dehydrogenase (LDH) release and MTT assays, respectively. In this regard, levels of IL-10, IFN-γ, and IL-4 were measured using ELISA after re-stimulation. The immune responses efficacy was evaluated by in vivo tumor regression assay. The results showed that immunization with the different titers of NDV lysate significantly reduced tumor volume in comparison with a combination of virus lysate and tumor cell lysate. Also, virus lysate could significantly enhance cytotoxic T lymphocyte production and lymphocyte proliferation rates versus tumor cell lysate. Also, our major findings are that the peritumorally injection of NDV oncolysate effectively induces antitumor immune responses through increased levels of IL-4, IFN-γ, and reduction of IL-10. These results indicate that this treatment is a specific, active immune mechanism stimulator, and may prove to be a useful therapeutic for a treatment against cervical cancers and merits further investigation.

Indexed as

DAMP, Danger-associated molecular patternELISA, Enzyme-Linked Immunosorbent AssayFBS, Fetal bovine serumFDA, Food and drug administrationHB1, Hitchner B1HPV, Human papillomavirusHuman papillomavirusLDH, Lactate dehydrogenaseMOI, Multiplicity of infectionNDV, Newcastle disease virusNewcastle disease virusOncolysateOncolyticOVs, Oncolytic virusesPBS, Phosphate-buffered salineRPMI, Roswell park memorial instituteTumor microenvironmentT-Vec, Talimogene laherparepvecUVB, Ultraviolet BVO, Viral oncolysate

Identifiers

PMID34588898
PMCPMC8459063
OpenAlexW3175107224

What OpenQuestion 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 OpenQuestion graph.