Evidence map›Paper›PMID 31167966›Full record

ArticleJCI insight2019

Eosinophils downregulate lung alloimmunity by decreasing TCR signal transduction.

Oscar Okwudiri Onyema, Yizhan Guo, Bayan Mahgoub, Qing Wang, Amir Manafi, Zhongcheng Mei, Anirban Banerjee, Dongge Li, Mark H Stoler, Melissa T Zaidi and 5 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Activation of donor-derived eosinophils during static storage contributes to primary graft dysfunction after lung transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
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  8. IL-33: Friend or foe in transplantation?The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2024
    Review
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  15. Ischemia reperfusion injury facilitates lung allograft acceptance through IL-33-mediated activation of donor-derived IL-5 producing group 2 innate lymphoid cells.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  16. Article
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  19. Deciphering the role of eosinophils in solid organ transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Review
  20. 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 5 institutions in 1 country.

Oscar Okwudiri OnyemaDepartment of Surgery, Carter Center for Immunology, and.
Yizhan GuoDepartment of Surgery, Carter Center for Immunology, and.
Bayan MahgoubDepartment of Surgery, Carter Center for Immunology, and.
Qing WangDepartment of Surgery, Carter Center for Immunology, and.
Amir ManafiDepartment of Surgery, Carter Center for Immunology, and.
Zhongcheng MeiDepartment of Surgery, Carter Center for Immunology, and.
Anirban BanerjeeDepartment of Surgery, Carter Center for Immunology, and.
Dongge LiDepartment of Surgery, Carter Center for Immunology, and.
Mark H StolerDepartment of Pathology, University of Virginia, Charlottesville, Virginia, USA.
Melissa T ZaidiMolecular Microbiology and Immunology, Surgery, Bioengineering, University of Missouri, Columbia, Missouri, USA.
Adam G SchrumMolecular Microbiology and Immunology, Surgery, Bioengineering, University of Missouri, Columbia, Missouri, USA.
Daniel KreiselDepartment of Surgery, Washington University, St. Louis, Missouri, USA.
Andrew E GelmanDepartment of Surgery, Washington University, St. Louis, Missouri, USA.
Elizabeth A JacobsenDivision of Allergy, Asthma and Clinical Immunology, Mayo Clinic, Scottsdale, Arizona, USA.
Alexander Sasha KrupnickDepartment of Surgery, Carter Center for Immunology, and.
Carter Center · USUniversity of Missouri · USWashington University in St. Louis · USUniversity of Virginia · USWinnMed · US

Funding

The Role of Neutrophils in Regulating Lung Transplant ToleranceP01AI116501 · NIAID · WASHINGTON UNIVERSITY · PI ALEXANDER S. KRUPNICK · 2015 to 2026
$19.4M
EOSINOPHIL ACTIVITIES IN MURINE MODELS OF LUNG DISEASER01HL065228 · NHLBI · MAYO CLINIC COLL OF MED, MAYO CLINIC AZ · PI JACOBSEN, ELIZABETH A · 2000 to 2017
$6.7M
The Role of Eosinophils in the Lung AllograftR01AI145108 · NIAID · UNIVERSITY OF VIRGINIA · PI Elizabeth A Jacobsen, ALEXANDER S. KRUPNICK · 2019 to 2026
$4.1M
Measuring multiprotein assemblies that drive biological signalsR01GM103841 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI SCHRUM, ADAM G. · 2013 to 2023
$3.3M
Airway Sensory Nerves in AsthmaR01HL124165 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBSEN, ELIZABETH A, JACOBY, DAVID B · 2014 to 2017
$3.1M
Imaging Functionally Distinct Eosinophil Subtypes Within Tissue Biopsies Using Gene Expression Profiling and an In Situ Hybridization Approach based on a Concurrent Multiple RNA Targeting StrategyR21AI132840 · NIAID · MAYO CLINIC ARIZONA · PI JACOBSEN, ELIZABETH A · 2018 to 2019
$463k
Novel Immuno-oncology Strategy for Targeted Cytotoxic Lymphocyte ActivationR41CA224520 · NCI · COURIER THERAPEUTICS, INC. · PI KRUPNICK, ALEXANDER S. · 2018 to 2018
$288k
High-dose targeted and non-toxic IL-2 cytokine therapyI01BX004588 · VA · SALEM VA MEDICAL CENTER · PI KRUPNICK, ALEXANDER S. · 2019 to 2019
–
BLRD VA I01 BX004588NCI NIH HHS R41 CA224520NHLBI NIH HHS R01 HL065228NHLBI NIH HHS R01 HL124165NIAID NIH HHS P01 AI116501NIAID NIH HHS R01 AI145108NIAID NIH HHS R21 AI132840NIGMS NIH HHS R01 GM103841
6 · The paper itself

Abstract

Despite the accepted notion that granulocytes play a universally destructive role in organ and tissue grafts, it has been recently described that eosinophils can facilitate immunosuppression-mediated acceptance of murine lung allografts. The mechanism of eosinophil-mediated tolerance, or their role in regulating alloimmune responses in the absence of immunosuppression, remains unknown. Using lung transplants in a fully MHC-mismatched BALB/c (H2d) to C57BL/6 (H2b) strain combination, we demonstrate that eosinophils downregulate T cell-mediated immune responses and play a tolerogenic role even in the absence of immunosuppression. We further show that such downregulation depends on PD-L1/PD-1-mediated synapse formation between eosinophils and T cells. We also demonstrate that eosinophils suppress T lymphocyte responses through the inhibition of T cell receptor/CD3 (TCR/CD3) subunit association and signal transduction in an inducible NOS-dependent manner. Increasing local eosinophil concentration, through administration of intratracheal eotaxin and IL-5, can ameliorate alloimmune responses in the lung allograft. Thus, our data indicate that eosinophil mobilization may be utilized as a novel means of lung allograft-specific immunosuppression.

Indexed as

Lung TransplantationAllograftsAnimalsDown-RegulationEosinophilsFemaleImmune ToleranceLungMaleMiceMice, Inbred BALB CMice, Inbred C57BLReceptors, Antigen, T-CellSignal TransductionT-LymphocytesReceptors, Antigen, T-CellAdaptive immunityImmunologyT cellsToleranceTransplantation

Identifiers

PMID31167966
PMCPMC6629120
OpenAlexW2948036933

What OpenQuestion holds

Textmetadata
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.