Evidence map›Paper›PMID 32391011›Full record

ArticleFrontiers in immunology2020

Allergen-Specific Immunotherapy With Liposome Containing CpG-ODN in Murine Model of Asthma Relies on MyD88 Signaling in Dendritic Cells.

Ricardo Wesley Alberca-Custodio, Lucas D Faustino, Eliane Gomes, Fernanda Peixoto Barbosa Nunes, Mirian Krystel de Siqueira, Alexis Labrada, Rafael Ribeiro Almeida, Niels Olsen Saraiva Câmara, Denise Morais da Fonseca, Momtchilo Russo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Nanomaterials for antigen-specific immune tolerance therapy.Drug delivery and translational research · 2023
    Review
  10. Frequent IgE recognition ofFrontiers in immunology · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Harnessing the Antiinflammatory Power of MyD88 to Reduce Allergic Fungal Inflammation?American journal of respiratory cell and molecular biology · 2021
    Article
  15. 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 3 countries.

Ricardo Wesley Alberca-CustodioInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Lucas D FaustinoCenter for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Eliane GomesInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Fernanda Peixoto Barbosa NunesInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Mirian Krystel de SiqueiraInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Alexis LabradaDepartment of Allergens, National Center of Bioproducts (BIOCEN), Havana, Cuba.
Rafael Ribeiro AlmeidaInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Niels Olsen Saraiva CâmaraInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Denise Morais da FonsecaInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Momtchilo RussoInstitute of Biomedical Sciences, Department of Immunology, University of São Paulo, São Paulo, Brazil.
Universidade de São Paulo · BRCentro Nacional de Biopreparados (Cuba) · CUHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changing the immune responses to allergens is the cornerstone of allergen immunotherapy. Allergen-specific immunotherapy that consists of repeated administration of increasing doses of allergen extract is potentially curative. The major inconveniences of allergen-specific immunotherapy include failure to modify immune responses, long-term treatment leading to non-compliance and the potential for developing life-threating anaphylaxis. Here we investigated the effect of a novel liposomal formulation carrying low dose of allergen combined with CpG-ODN, a synthetic TLR9 agonist, on established allergic lung inflammation. We found that challenge with allergen (OVA) encapsulated in cationic liposome induced significantly less severe cutaneous anaphylactic reaction. Notably, short-term treatment (three doses) with a liposomal formulation containing co-encapsulated allergen plus CpG-ODN, but not allergen or CpG-ODN alone, reversed an established allergic lung inflammation and provided long-term protection. This liposomal formulation was also effective against allergens derived from

Indexed as

Adjuvants, ImmunologicAllergensAnaphylaxisAnimalsAsthmaDendritic CellsDesensitization, ImmunologicDisease Models, AnimalDrug Delivery SystemsFemaleGene Knockout TechniquesLiposomesMiceMice, Inbred C57BLMice, KnockoutMyeloid Differentiation Factor 88Adjuvants, ImmunologicAllergensCPG-oligonucleotideLiposomesMyd88 protein, mouseMyeloid Differentiation Factor 88Oligodeoxyribonucleotidesallergenasthmadendritic cellimmunotherapyMyD88

Identifiers

PMID32391011
PMCPMC7191058
OpenAlexW3019994113

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.