Evidence map›Paper›PMID 27695122›Full record

ArticlePloS one2016

Involvement of Macrophages in the Pathogenesis of Familial Amyloid Polyneuropathy and Efficacy of Human iPS Cell-Derived Macrophages in Its Treatment.

Genki Suenaga, Tokunori Ikeda, Yoshihiro Komohara, Koutaro Takamatsu, Tatsuyuki Kakuma, Masayoshi Tasaki, Yohei Misumi, Mitsuharu Ueda, Takaaki Ito, Satoru Senju and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-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

10 citing papers in PubMed, 18 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Genki SuenagaDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Tokunori IkedaDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Yoshihiro KomoharaDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Koutaro TakamatsuDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Tatsuyuki KakumaDepartment of Biostatistics Center, Kurume University, School of Medicine, Kurume, Japan.
Masayoshi TasakiDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Yohei MisumiDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Mitsuharu UedaDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Takaaki ItoDepartment of Pathology and Experimental Medicine, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Satoru SenjuDepartment of Immunogenetics, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Yukio AndoDepartment of Neurology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Kumamoto University · JPKurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We hypothesized that tissue-resident macrophages in familial amyloid polyneuropathy (FAP) patients will exhibit qualitative or quantitative abnormalities, that may accelerate transthyretin (TTR)-derived amyloid deposition. To evaluate this, we examined the number and subset of tissue-resident macrophages in heart tissue from amyloid-deposited FAP and control patients. In both FAP and control patients, tissue-resident macrophages in heart tissue were all Iba+/CD163+/CD206+ macrophages. However, the number of macrophages was significantly decreased in FAP patients compared with control patients. Furthermore, the proportion of intracellular TTR in CD14+ monocytes was reduced in peripheral blood compared with healthy donors. Based on these results, we next examined degradation and endocytosis of TTR in human induced pluripotent stem (iPS) cell-derived myeloid lineage cells (MLs), which function like macrophages. iPS-MLs express CD163 and CD206, and belong to the inhibitory macrophage category. In addition, iPS-MLs degrade both native and aggregated TTR in a cell-dependent manner in vitro. Further, iPS-MLs endocytose aggregated, and especially polymerized, TTR. These results suggest that decreased tissue-localized macrophages disrupt clearance of TTR-derived amyloid deposits, leading to progression of a pathological condition in FAP patients. To improve this situation, clinical application of pluripotent stem cell-derived MLs may be useful as an approach for FAP therapy.

Indexed as

AdultAgedAmyloidAmyloid Neuropathies, FamilialAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCase-Control StudiesCD163 AntigenCell DifferentiationCell Line, TumorCell SurvivalFemaleHumansInduced Pluripotent Stem CellsLectins, C-TypeAmyloidAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenLectins, C-TypeMannose-Binding LectinsMannose ReceptorPrealbuminReceptors, Cell Surface

Identifiers

PMID27695122
PMCPMC5047455
OpenAlexW2528243154

What OpenQuestion holds

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LicenceCC BY
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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.