Evidence map›Paper›PMID 29360423›Full record

ArticleHuman vaccines & immunotherapeutics2018

Efficacy for lung metastasis induced by the allogeneic bEnd3 vaccine in mice.

Jun Zhao, Jing Lu, Lurong Zhou, Jimin Zhao, Ziming Dong

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

5 authors at 2 institutions in 1 country.

Jun Zhaoa Medical Oncology, Changzhi people's Hospital Affiliated to Shanxi Medical University , Changzhi , Shanxi Province , China.
Jing Lub Department of Pathophysiology , Medical School of Zhengzhou University , Zhengzhou , Henan Province , China.
Lurong Zhouc Quality Control Department , Changzhi people's Hospital Affiliated to Shanxi Medical University , Changzhi , Shanxi Province , China.
Jimin Zhaob Department of Pathophysiology , Medical School of Zhengzhou University , Zhengzhou , Henan Province , China.
Ziming Dongb Department of Pathophysiology , Medical School of Zhengzhou University , Zhengzhou , Henan Province , China.
Shanxi Medical University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mouse brain microvascular endothelial cell line bEnd.3 was used to develop a vaccine and its anti-tumor effect on lung metastases was observed in immunized mice.

methodsMouse bEnd.3 cells cultured in-vitro and then fixed with glutaraldehyde was used to immunize mice; mice were challenged with the metastatic cancer cell line U14, and changes in metastatic cancer tissues were observed through hematoxylin and eosin staining. Carboxyfluorescein succinimidyl amino ester (CSFE) and propidium iodide (PI) were used to detect cytotoxic activity of spleen T lymphocytes; the ratio of CD3

resultsThe number of metastatic nodules in bEnd.3 and human umbilical vein endothelial cell (HUVEC) vaccine groups was less than NIH3T3 vaccine group and phosphate buffered saline (PBS) control group. The bEnd.3-induced and HUVEC-induced cytotoxic T-lymphocytes (CTLs) showed significant lytic activity against bEnd.3 and HUVEC target cells, while the antisera of mice in bEnd.3 and HUVEC vaccine groups showed specific immune responses to membrane proteins and inhibited target cell proliferation in-vitro. Immunoblot results showed specific bands at 180KD and 220KD in bEnd.3 and at 130 kD and 220 kD in HUVEC lysates.

conclusionsAllogeneic bEnd.3 vaccine induced an active and specific immune response to tumor vascular endothelial cells that resulted in production of antibodies against the proliferation antigens VEGF-R II, integrin, Endog etc. Immunization with this vaccine inhibited lung metastasis of cervical cancer U14 cells and prolonged the survival of these mice.

Indexed as

Allogeneic CellsAnimalsCancer VaccinesCell Line, TumorEndothelial CellsFemaleHumansHuman Umbilical Vein Endothelial CellsImmunogenicity, VaccineLung NeoplasmsMiceMice, Inbred BALB CNIH 3T3 CellsSpecific Pathogen-Free OrganismsT-Lymphocytes, CytotoxicUterine Cervical NeoplasmsCancer VaccinesAllogeneic bEnd.3 vaccineImmune responselung metastatic cancermouse cervical cancer U14

Identifiers

PMID29360423
PMCPMC5989886
OpenAlexW2791639698

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Registered trials

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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.