Evidence map›Paper›PMID 32194859›Full record

ArticleTheranostics2020

LRR domain of NLRX1 protein delivery by dNP2 inhibits T cell functions and alleviates autoimmune encephalomyelitis.

Ja-Hyun Koo, Do-Hyun Kim, Donghun Cha, Min-Jong Kang, Je-Min Choi

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. The Application of Nanovaccines in Autoimmune Diseases.International journal of nanomedicine · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. CPP Applications in Immune Modulation and Disease Therapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Article
  12. NOD-like receptors in autoimmune diseases.Acta pharmacologica Sinica · 2021
    Review
  13. Review
  14. Focusing on the Cell Type Specific Regulatory Actions of NLRX1.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Behind the Scenes: Nod-Like Receptor X1 Controls Inflammation and Metabolism.Frontiers in cellular and infection microbiology · 2020
    Review
  17. 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

5 authors at 2 institutions in 2 countries.

Ja-Hyun KooDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Do-Hyun KimDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Donghun ChaDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Min-Jong KangSection of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Je-Min ChoiDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Hanyang University · KRYale University · US

Funding

The reduction of NLRX1 and its role in pulmonary agingR01AG053495 · NIA · YALE UNIVERSITY · PI KANG, MIN-JONG · 2016 to 2020
$1.7M
Role of NLRX1 in cigarette smoke-induced pulmonary inflammation and remodelingR01HL130283 · NHLBI · YALE UNIVERSITY · PI KANG, MIN-JONG · 2016 to 2019
$1.7M
NHLBI NIH HHS R01 HL130283NIA NIH HHS R01 AG053495
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a demyelinating inflammatory disease of the central nervous system (CNS), which is a chronic progressive disease and is caused by uncontrolled activation of myelin antigen specific T cells. It has high unmet medical needs due to the difficulty of efficient drug delivery into the CNS to control tissue inflammation. In this study, we demonstrate that a fusion protein of NOD-like receptor family member X1 (NLRX1) and blood brain barrier (BBB)-permeable peptide, dNP2 ameliorates experimental autoimmune encephalomyelitis (EAE).

Indexed as

Amino Acid SequenceAnimalsBlood-Brain BarrierCell-Penetrating PeptidesDrug CarriersDrug Evaluation, PreclinicalEncephalomyelitis, Autoimmune, ExperimentalFemaleHumansJurkat CellsLymphocyte ActivationLymphokinesMiceMice, Inbred C57BLMitochondrial ProteinsPeptide FragmentsCell-Penetrating PeptidesdNP2 peptideDrug CarriersLymphokinesMitochondrial ProteinsNLRX1 protein, mousePeptide FragmentsRecombinant ProteinsBBB-penetrating peptidedNP2experimental autoimmune encephalomyelitisNOD-like receptor family member X1T cell

Identifiers

PMID32194859
PMCPMC7053182
OpenAlexW3005543725

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.