Evidence map›Paper›PMID 38038136›Full record

ArticleThe Journal of clinical investigation2023

Activation of the pentose phosphate pathway in macrophages is crucial for granuloma formation in sarcoidosis.

Satoshi Nakamizo, Yuki Sugiura, Yoshihiro Ishida, Yoko Ueki, Satoru Yonekura, Hideaki Tanizaki, Hiroshi Date, Akihiko Yoshizawa, Teruasa Murata, Kenji Minatoya and 8 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. 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
5.3field-weighted citation impact, top 3% 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, 30 citations in OpenAlex.

  1. Article
  2. New Therapies for Sarcoidosis: Molecular and Pathophysiological Basis.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Tissue Immunometabolism in Autoimmunity.European journal of immunology · 2026
    Review
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  8. Article
  9. Article
  10. Review
  11. Article
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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

18 authors at 6 institutions in 3 countries.

Satoshi NakamizoDepartment of Dermatology.
Yuki SugiuraCenter for Cancer Immunotherapy and Immunobiology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yoshihiro IshidaDepartment of Dermatology.
Yoko UekiDepartment of Dermatology, Kansai Medical University, Osaka, Japan.
Satoru YonekuraDepartment of Dermatology.
Hideaki TanizakiDepartment of Dermatology, Kansai Medical University, Osaka, Japan.
Hiroshi DateDepartment of Thoracic Surgery and.
Akihiko YoshizawaDepartment of Diagnostic Pathology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Teruasa MurataDepartment of Dermatology, Hyogo College of Medicine, Nishinomiya, Japan.
Kenji MinatoyaDepartment of Cardiovascular Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mikako KatagiriDepartment of Cardiovascular Medicine and.
Seitaro NomuraDepartment of Cardiovascular Medicine and.
Issei KomuroDepartment of Frontier Cardiovascular Science, Graduate School of Medicine, The University of Tokyo, Tokyo.
Seishi OgawaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Saeko NakajimaDepartment of Dermatology.
Naotomo KambeDepartment of Dermatology.
Gyohei EgawaDepartment of Dermatology.
Kenji KabashimaDepartment of Dermatology.
Kyoto University · JPKansai Medical University · JPThe University of Tokyo · JPAgency for Science, Technology and Research · SGHyogo Medical University · JPInstitute for Advanced Medical Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoidosis is a disease of unknown etiology in which granulomas form throughout the body and is typically treated with glucocorticoids, but there are no approved steroid-sparing alternatives. Here, we investigated the mechanism of granuloma formation using single-cell RNA-Seq in sarcoidosis patients. We observed that the percentages of triggering receptor expressed on myeloid cells 2-positive (TREM2-positive) macrophages expressing angiotensin-converting enzyme (ACE) and lysozyme, diagnostic makers of sarcoidosis, were increased in cutaneous sarcoidosis granulomas. Macrophages in the sarcoidosis lesion were hypermetabolic, especially in the pentose phosphate pathway (PPP). Expression of the PPP enzymes, such as fructose-1,6-bisphosphatase 1 (FBP1), was elevated in both systemic granuloma lesions and serum of sarcoidosis patients. Granuloma formation was attenuated by the PPP inhibitors in in vitro giant cell and in vivo murine granuloma models. These results suggest that the PPP may be a promising target for developing therapeutics for sarcoidosis.

Indexed as

Pentose Phosphate PathwaySarcoidosisAnimalsGlucocorticoidsGranulomaHumansMacrophagesMiceGlucocorticoidsAntigen-presenting cellsDermatologyImmunologyMacrophagesSkin

Identifiers

PMID38038136
PMCPMC10688990
OpenAlexW4389165679

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.