Evidence map›Paper›PMID 31429073›Full record

ArticleClinical and experimental immunology2019

Functional analysis of a novel G87V TNFRSF1A mutation in patients with TNF receptor-associated periodic syndrome.

S Tsuji, H Matsuzaki, M Iseki, A Nagasu, H Hirano, K Ishihara, N Ueda, Y Honda, T Horiuchi, R Nishikomori and 2 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Clinical and experimental immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Cellular models in autoinflammatory disease research.Clinical & translational immunology · 2024
    Review
  2. Review
  3. Article
  4. TRAPS mutations inFrontiers in immunology · 2022
    Article
  5. Article
  6. 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

12 authors at 6 institutions in 1 country.

S TsujiDepartment of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.ORCID 0000-0001-9798-1287
H MatsuzakiDepartment of Life Sciences, Faculty of Life and Environmental Sciences, Prefectural University of Hiroshima, Shobara, Hiroshima, Japan.
M IsekiDepartment of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki, Okayama, Japan.
A NagasuDepartment of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
H HiranoDepartment of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.
K IshiharaDepartment of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki, Okayama, Japan.
N UedaDepartment of Internal Medicine, Miyazaki Prefectural Miyazaki Hospital, Miyazaki, Japan.
Y HondaDepartment of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
T HoriuchiDepartment of Internal Medicine, Kyushu University Beppu Hospital, Beppu, Oita, Japan.
R NishikomoriDepartment of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Y MoritaDepartment of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.ORCID 0000-0002-8000-0881
T MukaiDepartment of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan.ORCID 0000-0002-0103-1621
Kawasaki Medical School · JPKurume University · JPKyoto University · JPKyushu University Beppu Hospital · JPMiyazaki Prefectural Hospital · JPPrefectural University of Hiroshima · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) is an autoinflammatory disease that is caused by heterozygous mutations in the TNFRSF1A gene. Although more than 150 TNFRSF1A mutations have been reported to be associated with TRAPS phenotypes only a few, such as p.Thr79Met (T79M) and cysteine mutations, have been functionally analyzed. We identified two TRAPS patients in one family harboring a novel p.Gly87Val (G87V) mutation in addition to a p.Thr90Ile (T90I) mutation in TNFRSF1A. In this study, we examined the functional features of this novel G87V mutation. In-vitro analyses using mutant TNF receptor 1 (TNF-R1)-over-expressing cells demonstrated that this mutation alters the expression and function of TNF-R1 similar to that with the previously identified pathogenic T79M mutation. Specifically, cell surface expression of the mutant TNF-R1 in transfected cells was inhibited with both G87V and T79M mutations, whereas the T90I mutation did not affect this. Moreover, peripheral blood mononuclear cells (PBMCs) from TRAPS patients harboring the G87V and T90I mutations showed increased mitochondrial reactive oxygen species (ROS). Furthermore, the effect of various Toll-like receptor (TLR) ligands on inflammatory responses was explored, revealing that PBMCs from TRAPS patients are hyper-responsive to TLR-2 and TLR-4 ligands and that interleukin (IL)-8 and granulocyte-macrophage colony-stimulating factor (GM-CSF) are likely to be involved in the pathogenesis of TRAPS. These findings suggest that the newly identified G87V mutation is one of the causative mutations of TRAPS. Our findings based on unique TRAPS-associated mutations provide novel insight for clearer understanding of inflammatory responses, which would be basic findings of developing a new therapeutic and prophylactic approach to TRAPS.

Indexed as

Mutation, MissenseAdultAgedAmino Acid SequenceBase SequenceDNA Mutational AnalysisFemaleFeverGenetic Predisposition to DiseaseHereditary Autoinflammatory DiseasesHumansMalePedigreeReceptors, Tumor Necrosis Factor, Type ISequence Homology, Amino AcidReceptors, Tumor Necrosis Factor, Type ITNFRSF1A protein, humanautoinflammatory diseaseTNF-R1TNF receptor-associated periodic syndromeTNFRSF1A

Identifiers

PMID31429073
PMCPMC6857086
OpenAlexW2969938689

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.