Evidence map›Paper›PMID 30885291›Full record

ArticleBMB reports2019

Interleukin-2/antibody complex expanding Foxp3

Sung-Wook Hong, Eunju O, Jun Young Lee, Jaeu Yi, Kyungjin Cho, Juhee Kim, Daeun Kim, Charles D Surh, Kwang Soon Kim

Open access · goldAbstract read
In one paragraph

Article in BMB reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

9 authors at 2 institutions in 1 country.

Sung-Wook HongAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea.
Eunju OAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Jun Young LeeAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Jaeu YiAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Kyungjin ChoAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Juhee KimAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Daeun KimAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Charles D SurhAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Kwang Soon KimAcademy of Immunology and Microbiology, Institute for Basic Science (IBS), Pohang 37673, Korea; Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Pohang University of Science and Technology · KRInstitute for Basic Science · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foxp3+ regulatory CD4+ T (Treg) cells play an essential role in preventing overt immune responses against self and innocuous foreign antigens. Selective expansion of endogenous Treg cells in response to the administration of interleukin (IL)-2/antibody complex, such as the IL-2/JES6-1 complex (IL-2C) in mice, is considered an attractive therapeutic approach to various immune disorders. Here, we investigated the therapeutic potential of IL-2C in allergic airway inflammation models. IL-2C treatment ameliorated Th17-mediated airway inflammation; however, unexpectedly, IL-2C treatment exacerbated Th2-mediated allergic airway inflammation by inducing the selective expansion of Th2 cells and type-2 innate lymphoid cells. We also found that IL-2 signaling is required for the expansion of Th2 cells in lymphoproliferative disease caused by Treg cell depletion. Our data suggest that IL-2C is selectively applicable to the treatment of allergic airway diseases depending on the characteristics of airway inflammation. [BMB Reports 2019; 52(4): 283-288].

Indexed as

AnimalsAntibodies, MonoclonalAsthmaCytokinesForkhead Transcription FactorsHypersensitivityImmune ToleranceImmunity, InnateInterleukin-2MiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutRespiratory HypersensitivityTh17 CellsTh2 CellsAntibodies, MonoclonalCytokinesForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-2

Identifiers

PMID30885291
PMCPMC6507850
OpenAlexW2943103324

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.