Evidence map›Paper›PMID 26131270›Full record

ArticleInternational journal of clinical and experimental medicine2015

Construction of the recombinant vaccine based on T-cell epitope encoding Der p1 and evaluation on its specific immunotherapy efficacy.

Jinhong Zhao, Chaopin Li, Beibei Zhao, Pengfei Xu, Haifeng Xu, Lianping He

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Homology modeling and epitope prediction of Der f 33.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2018
    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

6 authors at 2 institutions in 1 country.

Jinhong ZhaoDepartment of Medical Parasitology, School of Basic Medicine, Wannan Medical University Wuhu 241002, Anhui, China.
Chaopin LiDepartment of Medical Parasitology, School of Basic Medicine, Wannan Medical University Wuhu 241002, Anhui, China ; Laboratory of Environment and Health, School of Earth and Environment, Anhui University of Science & Technology Huainan 232001, Anhui, China.
Beibei ZhaoDepartment of Medical Parasitology, School of Basic Medicine, Wannan Medical University Wuhu 241002, Anhui, China.
Pengfei XuLaboratory of Environment and Health, School of Earth and Environment, Anhui University of Science & Technology Huainan 232001, Anhui, China.
Haifeng XuLaboratory of Environment and Health, School of Earth and Environment, Anhui University of Science & Technology Huainan 232001, Anhui, China.
Lianping HeDepartment of Medical Parasitology, School of Basic Medicine, Wannan Medical University Wuhu 241002, Anhui, China.
Anhui University of Science and Technology · CNWannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Specific immunotherapy (SIT) is currently recognized as the only etiological therapy to ameliorate asthmatic symptom. The current study was aimed at evaluating the immune effect of vaccine MAT3T designed on MHCII pathway, which includes T cell fusion peptide encoding Dermatophagoides pteronyssinus class 1 allergen (Der p1). We initially cloned the nucleotide sequences of TAT, IhC and 3 segments of T cell epitope coding for Der p1, and reassembled these sequences in linear manner to form fusion gene named MAT3T, which was applied to immunize the asthmatic models of mice induced by Der p1 allergen for tentative SIT. ELISA results showed that MAT3T was able to increase the level of IFN-γ in BALF and allergen specific antibody IgG2a in serum, while decrease the level of IL-13 in BALF and allergen specific antibody IgE and IgG1. Pathological confirmation further revealed that the inflammatory reactions and inflammatory cell infiltration were totally reduced in lung tissue of mice after MAT3T treatment. Our results show that the recombinant allergen MAT3T can effectively correct the imbalance of Th1/Th2, and MAT3T may be used as candidate vaccine against asthma on SIT basis.

Indexed as

allergic asthmachimeric allergensclass 1 allergenDermatophagoides pteronyssinus

Identifiers

PMID26131270
PMCPMC4483893
OpenAlexW1142366962

What OpenQuestion holds

Textmetadata
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.