Evidence map›Paper›PMID 31564865›Full record

ArticleInternational journal of nanomedicine2019

Co-delivery of allergen epitope fragments and R848 inhibits food allergy by inducing tolerogenic dendritic cells and regulatory T cells.

Jingyi Hong, Xiaojun Xiao, Qichan Gao, Shanshan Li, Bei Jiang, Xizhuo Sun, Pixin Ran, Pingchang Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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  5. Nanomaterials for antigen-specific immune tolerance therapy.Drug delivery and translational research · 2023
    Review
  6. [Mechanism of Der f 1/IGF-1 nanoparticle promoting the production of regulatory T cell].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2023
    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

8 authors at 3 institutions in 1 country.

Jingyi Hong *Department of Allergy, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518020, People's Republic of China.
Xiaojun Xiao *Research Center of Allergy & Immunology, Department of Medicine, Shenzhen University, Shenzhen 518055, People's Republic of China.
Qichan Gao *Research Center of Allergy & Immunology, Department of Medicine, Shenzhen University, Shenzhen 518055, People's Republic of China.
Shanshan LiResearch Center of Allergy & Immunology, Department of Medicine, Shenzhen University, Shenzhen 518055, People's Republic of China.
Bei JiangResearch Center of Allergy & Immunology, Department of Medicine, Shenzhen University, Shenzhen 518055, People's Republic of China.
Xizhuo SunDepartment of Allergy, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518020, People's Republic of China.
Pixin RanState Key Laboratory of Respiratory Disease, Department of Allergy and Clinical Immunology, Guangzhou Medical University, Guangzhou 510006, People's Republic of China.
Pingchang YangResearch Center of Allergy & Immunology, Department of Medicine, Shenzhen University, Shenzhen 518055, People's Republic of China.
Shenzhen University · CNGuangzhou Medical University · CNShenzhen Third People’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFood allergy (FA) is a significant public health problem. The therapeutic efficacy for FA is unsatisfactory currently. The breakdown of intestinal immune tolerance is associated with the pathogenesis of FA. Therefore, it is of great significance to develop novel therapeutic methods to restore immune tolerance in treating FA.

methodsWe proposed an oral administration strategy to treat FA by co-delivering food allergen epitope fragment (peptide: IK) and adjuvant R848 (TLR7 ligand) in the mPEG-PDLLA nanoparticles (PPLA-IK/R848 NPs). The generation of tolerogenic dendritic cells (DCs) and regulatory T cells (Tregs) induced by PPLA-IK/R848 NPs were evaluated in vitro and in vivo. The therapeutic effects of PPLA-IK/R848 NPs were also assessed in an OVA-induced FA model.

resultsPPLA-IK/R848 NPs could efficiently deliver IK to DCs to drive DCs into the tolerogenic phenotypes and promote the differentiation of Tregs in vitro and in vivo, significantly inhibited FA responses through the recovery of intestinal immune tolerance.

conclusionOral administration of PPLA-IK/R848 NPs could efficiently deliver IK and R848 to intestinal DCs and stimulate DCs into allergen tolerogenic phenotype. These tolerogenic DCs could promote the differentiation of Tregs, which significantly protected mice from food allergic responses. This study provided an efficient formulation to alleviate FA through the recovery of immune tolerance.

Indexed as

Drug Delivery SystemsImmune ToleranceAllergensAmino Acid SequenceAnimalsCell DifferentiationDendritic CellsEpitopesFood HypersensitivityImidazolesMice, Inbred BALB CPeptidesPolyestersPolyethylene GlycolsT-Lymphocytes, RegulatoryAllergensEpitopesImidazolesmonomethoxypolyethylene glycolPeptidesPolyestersPolyethylene Glycolspoly(lactide)resiquimodallergen epitope fragmentco-deliverydendritic cellsfood allergyR848Tregs

Identifiers

PMID31564865
PMCPMC6722440
OpenAlexW2970851331

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.