Evidence map›Paper›PMID 36316414›Full record

ArticleNPJ vaccines2022

TAFA4-IL-10 axis potentiate immunotherapy for airway allergy by induction of specific regulatory T cells.

Shuyao Qiu, Xiangqian Luo, Lihua Mo, Shuang Zhang, Yun Liao, Li Guan, Liteng Yang, Qinmiao Huang, Dabo Liu, Pingchang Yang

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Neuroimmune Circuits in Allergic Diseases.Annual review of immunology · 2025
    Review
  3. Article
  4. 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

10 authors at 3 institutions in 1 country.

Shuyao Qiu *Department of Pediatric Otolaryngology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Xiangqian Luo *Department of Pediatric Otolaryngology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Lihua MoDepartment of Pediatric Otolaryngology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Shuang ZhangGuangdong Provincial Regional Disease Key Laboratory, Shenzhen, China.
Yun LiaoGuangdong Provincial Regional Disease Key Laboratory, Shenzhen, China.
Li GuanDepartment of Allergy & Respirology, Third Affiliated Hospital of Shenzhen University, Shenzhen, China.
Liteng YangDepartment of Allergy & Respirology, Third Affiliated Hospital of Shenzhen University, Shenzhen, China.
Qinmiao HuangDepartment of Allergy & Respirology, Third Affiliated Hospital of Shenzhen University, Shenzhen, China.
Dabo LiuDepartment of Pediatric Otolaryngology, Shenzhen Hospital, Southern Medical University, Shenzhen, China. daboliu@mailnesia.com.
Pingchang YangGuangdong Provincial Regional Disease Key Laboratory, Shenzhen, China. pcy2356@szu.edu.cn.ORCID http://orcid.org/0000-0002-5421-0308
Shenzhen University · CNSouthern Medical University Shenzhen Hospital · CNThird Affiliated Hospital of Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergen-specific immunotherapy (AIT) is the main treatment for allergic diseases. The therapeutic efficacy of AIT has to be improved. Neuropeptides, such as TAFA4, have immune-regulating features. The objective of this study is to promote the efficacy of AIT in experimental allergic rhinitis (AR) by the concurrent use of TAFA chemokine as a family member 4 (TAFA4). In this study, an AR mouse model was developed using ovalbumin (OVA) as the specific antigen. The AR response was assessed in mice after treatment with AIT or/and TAFA4. We found that exposure to TAFA4 activated dendritic cells (DCs) in the airway tissues. Activation of DC by TAFA4 resulted in the expression of IL-10. TAFA4 also promoted the activities of c-Maf inducing protein. The FPR1-MyD88-AKT signal pathway was associated with the TAFA4-induced Il10 expression in the DCs. Co-administration of AIT/TAFA4 attenuated the AR response in mice by inducing antigen-specific Tr1 cells. In conclusion, TAFA4 induces the expression of IL-10 in DCs. Acting as an adjuvant, TAFA4 significantly improves AIT's therapeutic efficacy against AR by inducing antigen-specific Tr1 cells.

Identifiers

PMID36316414
PMCPMC9622679
OpenAlexW4307893919

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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.