Evidence map›Paper›PMID 31317199›Full record

ArticleSingapore medical journal2020

Generation of IgE-specific cytotoxic T lymphocytes as a novel immunotherapeutic approach for the treatment of allergic asthma.

Kangle Cui, Yanna Chen, Li Zhou, Chunxia Yang, Yao Du, Weixing Shi, Zeling Cai, Jian Chen

Open access · diamondAbstract read
In one paragraph

Article in Singapore medical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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 3 institutions in 2 countries.

Kangle CuiCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Yanna ChenCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Li ZhouCollege Hospital, Zhejiang Sci-Tech University, Hangzhou, China.
Chunxia YangShanghai Yuyan Cell Research Company, Shanghai, China.
Yao DuCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Weixing ShiCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Zeling CaiJohnson and Johnson Pharmaceutical Research and Development LLC, San Diego, CA, USA.
Jian ChenCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Zhejiang Sci-Tech University · CNJohnson & Johnson (United States) · USShanghai Cell Therapy Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOverproduction of immunoglobulin E (IgE) by a subset of B cells plays a key role in the pathogenesis of allergic asthma. Anti-IgE monoclonal antibodies have been successfully used to treat the disease, but long-term application is required.

methodsFor this study, cytotoxic T lymphocytes (CTLs) against IgE-producing B cells were generated ex vivo by stimulating naive CD8 T cells with IgE-derived peptides presented by Drosophila-derived artificial antigen-presenting cells. Based on the treatment of allergic asthma in mice, the inhibitive effect of this CTL on IgE responses and airway inflammation was determined with the enzyme-linked immunosorbent assay and histochemical method.

resultsThe IgE-specific CTLs effectively lysed target cells in vitro, while the adoptively transferred CTLs specifically inhibited IgE responses and airway inflammation in an asthmatic mouse model. The effect of IgE-specific CTLs is MHC (major histocompatibility complex) Class I-restricted and requires the expression of perforin.

conclusionIgE-specific CTLs generated ex vivo may provide a novel treatment for allergic asthma and lead to a new therapy for other immunological disorders.

Indexed as

AnimalsAsthmaDisease Models, AnimalHypersensitivityImmunoglobulin EImmunotherapyIn Vitro TechniquesMiceMice, Inbred BALB CMice, Inbred C57BLT-Lymphocytes, CytotoxicImmunoglobulin Eartificial antigen-presenting cellscytotoxic T lymphocytesimmunoglobulin Eperforin

Identifiers

PMID31317199
PMCPMC7905137
OpenAlexW2961470326

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.