Evidence map›Paper›PMID 36591283›Full record

ArticleFrontiers in immunology2022

Increased CEACAM1 expression on peripheral blood neutrophils in patients with rheumatoid arthritis.

Haruki Matsumoto, Yuya Fujita, Michio Onizawa, Kenji Saito, Yuya Sumichika, Shuhei Yoshida, Jumpei Temmoku, Naoki Matsuoka, Makiko Yashiro-Furuya, Tomoyuki Asano and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. 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
1.0field-weighted citation impact, top 21% 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. The role of CEACAMs in neutrophil function.European journal of clinical investigation · 2024
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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

15 authors at 1 institution in 1 country.

Haruki MatsumotoDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Yuya FujitaDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Michio OnizawaDepartment of Gastroenterology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Kenji SaitoDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Yuya SumichikaDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Shuhei YoshidaDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Jumpei TemmokuDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Naoki MatsuokaDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Makiko Yashiro-FuruyaDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Tomoyuki AsanoDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Shuzo SatoDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Eiji SuzukiDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Takeshi MachidaDepartment of Immunology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Hiroshi WatanabeDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Kiyoshi MigitaDepartment of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
Fukushima Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Altered expression of adhesion molecules in immune cells has been demonstrated in rheumatoid arthritis (RA). Carcinoembryonic-antigen-related cell-adhesion molecule 1 (CEACAM1) is an adhesion molecule that acts as a coinhibitory receptor in the immune system. We investigated the role of CEACAM1 in immune cell subsets of patients with RA. Peripheral blood was obtained from 37 patients with RA and 20 healthy controls (HC). The expression of CEACAM1 and T-cell immunoglobulin mucin domain molecule (TIM) -3 on peripheral blood mononuclear cells and neutrophils was analyzed by flow cytometry. Intracellular TIM-3 expression was analyzed using cellular lysates by Western blot analysis. Serum levels of soluble CEACAM1 (sCEACAM1) were estimated by an enzyme-linked immunosorbent assay. CEACAM1 expression was not detected in peripheral blood mononuclear cells, including in CD14(+) monocytes and CD3(+) lymphocytes isolated from patients with RA or HC. However, substantial cell-surface expression of CEACAM1 was detected in peripheral blood neutrophils, and it was significantly elevated in samples from patients with RA without remission compared to those in remission. There was no significant difference in serum levels of sCEACAM1 between patients with RA and HC. Cell-surface expression of TIM-3 was not detected in peripheral blood neutrophils from patients with RA or HC but was seen in CD14(+) monocytes. However, there was no significant difference in TIM-3 expression on monocytes between patients with RA and HC. Our data indicate that cell-surface expression of CEACAM1 on peripheral blood neutrophils are higher in patients with RA and that it is associated with rheumatoid inflammation. Further studies are needed to explore the potential role of CEACAM1 in rheumatoid inflammatory pathways.

Indexed as

Antigens, CDArthritis, RheumatoidLeukocytes, MononuclearCell Adhesion MoleculesHumansInflammationNeutrophilsAntigens, CDCD66 antigensCell Adhesion MoleculesCEACAM1monocytesneutrophilsrheumatoid arthritisTIM–3

Identifiers

PMID36591283
PMCPMC9794574
OpenAlexW4311496567

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Registered trials

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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.