Evidence map›Paper›PMID 25774686›Full record

ArticlePloS one2015

Concentrated protein body product derived from rice endosperm as an oral tolerogen for allergen-specific immunotherapy--a new mucosal vaccine formulation against Japanese cedar pollen allergy.

Yuhya Wakasa, Hidenori Takagi, Nobumasa Watanabe, Noriko Kitamura, Yoshihiro Fujiwara, Yuko Ogo, Shimpei Hayashi, Lijun Yang, Masaru Ohta, Wai Wai Thet Tin and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.3field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Plant Platforms for Efficient Heterologous Protein Production.Biotechnology and bioprocess engineering : BBE · 2021
    Review
  2. Review
  3. Article
  4. Article
  5. Next generation immunotherapy for tree pollen allergies.Human vaccines & immunotherapeutics · 2017
    Review
  6. Edible plants for oral delivery of biopharmaceuticals.British journal of clinical pharmacology · 2017
    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

15 authors at 2 institutions in 1 country.

Yuhya WakasaGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Hidenori TakagiGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Nobumasa WatanabeDepartment of Allergy and Immunology, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo, Japan.
Noriko KitamuraDepartment of Allergy and Immunology, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo, Japan.
Yoshihiro FujiwaraPrevenTec, Inc., Owashi, Tsukuba, Ibaraki, Japan.
Yuko OgoGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Shimpei HayashiGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Lijun YangGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Masaru OhtaGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Wai Wai Thet TinGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Kenji SekikawaPrevenTec, Inc., Owashi, Tsukuba, Ibaraki, Japan.
Makoto TakanoGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Kenjirou OzawaGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Takachika HiroiDepartment of Allergy and Immunology, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo, Japan.
Fumio TakaiwaGenetically Modified Organism Research Center, National Institute of Agrobiological Sciences, Kannondai, Tsukuba, Ibaraki, Japan.
Institute of Agrobiological Sciences · JPTokyo Metropolitan Institute of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endoplasmic reticulum-derived type-I protein body (PB-I) from rice endosperm cells is an ideal candidate formulation for the oral delivery of bioencapsulated peptides as tolerogens for allergen-specific immunotherapy. In the present study, PBs containing the deconstructed Japanese cedar pollen allergens Cryptomeria japonica 1 (Cry j 1) and Cry j 2 were concentrated by treatment with thermostable α-amylase at 90°C to remove the starch from milled rice powder, which resulted in a 12.5-fold reduction of dry weight compared to the starting material. The modified Cry j 1 and Cry j 2 antigens in this concentrated PB product were more resistant to enzymatic digestion than those in the milled seed powder despite the absence of intact cell wall and starch, and remained stable for at least 10 months at room temperature without detectable loss or degradation. The high resistance of these allergens could be attributed to changes in protein physicochemical properties induced by the high temperature concentration process, as suggested by the decreased solubility of the antigens and seed proteins in PBs in step-wise-extraction experiments. Confocal microscopy showed that the morphology of antigen-containing PB-Is was preserved in the concentrated PB product. The concentrated PB product induced specific immune tolerance against Cry j 1 and Cry j 2 in mice when orally administered, supporting its potential use as a novel oral tolerogen formulation.

Indexed as

AllergensAnimalsAntigens, PlantCryptomeriaDesensitization, ImmunologicDisease Models, AnimalEndospermImmunity, MucosalMaleMiceMucous MembraneOrganic ChemicalsOryzaPepsin APlants, Genetically ModifiedPollenAllergensAntigens, PlantOrganic ChemicalsPepsin ARecombinant ProteinsTolerogenVaccines

Identifiers

PMID25774686
PMCPMC4361645
OpenAlexW2032040437

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.