Evidence map›Paper›PMID 33160971›Full record

ArticleThe Journal of allergy and clinical immunology2021

Combination blockade of OX40L and CD30L inhibits allergen-driven memory T

Donald T Gracias, Gurupreet S Sethi, Amit K Mehta, Haruka Miki, Rinkesh K Gupta, Hideo Yagita, Michael Croft

Open access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

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  13. The Opposite Functions of CD30 Ligand Isoforms.Current issues in molecular biology · 2024
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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

7 authors at 2 institutions in 2 countries.

Donald T GraciasCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, Calif.
Gurupreet S SethiCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, Calif.
Amit K MehtaCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, Calif.
Haruka MikiCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, Calif.
Rinkesh K GuptaCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, Calif.
Hideo YagitaDepartment of Immunology, Juntendo University School of Medicine, Tokyo, Japan.
Michael CroftCenter for Autoimmunity and Inflammation, La Jolla Institute for Immunology, La Jolla, Calif; Department of Medicine, University of California San Diego, La Jolla, Calif. Electronic address: mick@lji.org.
La Jolla Institute for Immunology · USJuntendo University · JP

Funding

TRM and airway inflammation and remodelingU19AI070535 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROIDE, DAVID H · 2006 to 2025
$34.2M
NIAID NIH HHS U19 AI070535
6 · The paper itself

Abstract

backgroundThe selective reduction of memory T

objectiveWe asked whether TNF family costimulatory molecules cooperated to promote accumulation and reactivity of effector memory CD4 T cells to inhaled complex allergen, and whether their neutralization could promote airway tolerance to subsequent reexposure to allergen.

methodsMice were sensitized intraperitoneally or intranasally with house dust mite and challenged with intranasal allergen after memory had developed. We assessed whether single or combined blockade of OX40L/CD252 and CD30L/CD153 inhibited memory T cells from driving acute asthmatic lung inflammation and protected mice following exposure to allergen at a later time.

resultsOX40- or CD30-deficient animals showed strong or partial protection against allergic airway inflammation; however, neutralizing either molecule alone during the secondary response to allergen had little effect on the frequency of effector memory CD4 T cells formed and acute lung inflammation. In contrast, a significant reduction in eosinophilic inflammation was observed when OX40L and CD30L were simultaneously neutralized, with dual blockade inhibiting effector memory T

conclusionMemory T-cell responses to complex allergens are controlled by several TNF costimulatory interactions, and their combination targeting might represent a strategy to reduce the severity of inflammatory reactions following reexposure to allergen.

Indexed as

Immunologic MemoryAllergensAnimalsAsthmaBiomarkersCD30 LigandDisease Models, AnimalDisease SusceptibilityHumansHypersensitivityMiceOX40 LigandPneumoniaTh2 CellsAllergensBiomarkersCD30 LigandOX40 LigandTNFSF4 protein, humanTNFSF8 protein, humanAllergenasthmaCD30LmemoryOX40LT(H)2 cellTNF family

Identifiers

PMID33160971
PMCPMC8096862
OpenAlexW3096326421

What OpenQuestion holds

Textmetadata
LicenceTDM
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.