Evidence map›Paper›PMID 38380329›Full record

ArticleFrontiers in immunology2024

Sustained silencing peanut allergy by xanthopurpurin is associated with suppression of peripheral and bone marrow IgE-producing B cell.

Nan Yang, Kamal Srivastava, Yujuan Chen, Hang Li, Anish Maskey, Patrick Yoo, Xiaohong Liu, Raj K Tiwari, Jan Geliebter, Anna Nowak-Wegrzyn and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

12 authors at 7 institutions in 2 countries.

Nan Yang *R & D Division, General Nutraceutical Technology, LLC, Elmsford, NY, United States.
Kamal Srivastava *R & D Division, General Nutraceutical Technology, LLC, Elmsford, NY, United States.
Yujuan ChenSchool of Life Science and Technology, Changchun University of Science and Technology, Changchun, Jilin, China.
Hang LiCentral Lab, Shenzhen Bao'an Chinese Medicine Hospital, Shenzhen, China.
Anish MaskeyDepartment of Pathology, Microbiology and Immunology, New York Medical College, Valhalla, NY, United States.
Patrick YooDepartment of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Xiaohong LiuDepartment of Respiratory, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Raj K TiwariDepartment of Pathology, Microbiology and Immunology, New York Medical College, Valhalla, NY, United States.
Jan GeliebterDepartment of Pathology, Microbiology and Immunology, New York Medical College, Valhalla, NY, United States.
Anna Nowak-WegrzynDepartment of Pediatrics, Hassenfeld Children's Hospital, NYU Grossman School of Medicine, New York, NY, United States.
Jixun ZhanDepartment of Biological Engineering, Utah State University, Logan, UT, United States.
Xiu-Min LiDepartment of Pathology, Microbiology and Immunology, New York Medical College, Valhalla, NY, United States.
New York Medical College · USChangchun University of Science and Technology · CNFirst Affiliated Hospital of Guangzhou University of Chinese Medicine · CNIcahn School of Medicine at Mount Sinai · USNew York University · USShenzhen Bao'an District People's Hospital · CNUtah State University · US

Funding

IgE-suppressing small molecule compound Xanthopurpurin analog for multiple food allergiesR41AI172572 · NIAID · GENERAL NUTRACEUTICAL TECHNOLOGY, LLC · PI LI, XIU-MIN, YANG, NAN · 2023 to 2023
$290k
NIAID NIH HHS R41 AI172572
6 · The paper itself

Abstract

Introduction: Peanut allergy is an immunoglobulin E (IgE) mediated food allergy. Methods: Compounds were isolated from Results: XPP significantly and dose-dependently suppressed the IgE production in U266 cells. XPP significantly reduced peanut-specific IgE (>80%, p <0.01), and plasma histamine levels and protected the mice against peanut-allergic reactions in both early and late treatment experiments (p < 0.05, n=9). XPP showed a strong protective effect even 5 weeks after discontinuing the treatment. XPP significantly reduced the IL-4 level without affecting IgG or IgA and IFN-γ production. Flow cytometry data showed that XPP reduced peripheral and bone marrow IgE Conclusions: XPP successfully protected peanut-allergic mice against peanut anaphylaxis by suppressing IgE production. XPP suppresses murine IgE-producing B cell numbers and inhibits IgE production and associated genes in human plasma cells. XPP may be a potential therapy for IgE-mediated food allergy.

Indexed as

AnaphylaxisFood HypersensitivityPeanut HypersensitivityAnimalsBone MarrowHistamineHumansImmunoglobulin EInterleukin-4MiceMice, Inbred C3HWaterHistamineImmunoglobulin EInterleukin-4Waterfood allergyIgERNA-SeqRubia cordifolia L.transcriptome

Identifiers

PMID38380329
PMCPMC10876879
OpenAlexW4391573147

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.