Evidence map›Paper›PMID 40931874›Full record

ArticleHaematologica2026

Distinct interleukin-6 production in IPL and TAFRO subtypes of idiopathic multicentric Castleman disease.

Asami Nishikori, Midori Filiz Nishimura, Yoshito Nishimura, Rio Yamada, Tomoka Haratake, Daisuke Ennishi, Ryota Chijimatsu, Toshihiro Ito, Tomohiro Koga, Sayaka Ochi and 8 more

Abstract read
In one paragraph

Article in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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.

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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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.

Asami NishikoriDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Midori Filiz NishimuraDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Yoshito NishimuraDivision of Hematology/Oncology, Mayo Clinic, Rochester, Minnesota,.
Rio YamadaDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Tomoka HaratakeDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Daisuke EnnishiCenter for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan; Department of Hematology and Oncology, Okayama University Hospital, Okayama.
Ryota ChijimatsuCenter for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama.
Toshihiro ItoDepartment of Immunology, Nara Medical University, Nara.
Tomohiro KogaDepartment of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki.
Sayaka OchiDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Yuri KawaharaDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Himawari UetaDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Yudai TakedaDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama.
Michael V GonzalezCenter for Cytokine Storm Treatment and Laboratory, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania,.
David C FajgenbaumCenter for Cytokine Storm Treatment and Laboratory, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA; Castleman Disease Collaborative Network, Philadelphia, Pennsylvania,.
Frits Van RheeUniversity of Arkansas for Medical Sciences, Little Rock, Arkansas,.
Shuji MomoseDepartment of Pathology, Saitama Medical Center, Saitama Medical University, Saitama.
Yasuharu SatoDepartment of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama. satou-y@okayama-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic multicentric Castleman disease (iMCD) is a rare lymphoproliferative disorder characterized by systemic inflammation and lymphadenopathy. Two major clinical subtypes, idiopathic plasmacytic lymphadenopathy (iMCD-IPL) and iMCD with thrombocytopenia, anasarca, fever, renal dysfunction/reticulin fibrosis, and organomegaly (iMCD-TAFRO), have distinct pathophysiological mechanisms. While interleukin-6 (IL-6) is known to be elevated in iMCD, differences in the sources of IL-6 production between subtypes remain unclear. We examined the source of IL-6 production and its transcriptional regulation across iMCD subtypes using immunohistochemistry, in situ hybridization, and gene expression profiling. Immunohistochemistry and in situ hybridization revealed that plasma cells were the predominant IL-6-expressing cells in iMCD-IPL, whereas vascular endothelial cells expressed IL-6 in iMCD-TAFRO. Plasma cells exhibited stronger IL-6 protein expression in iMCD-IPL than in iMCD-TAFRO. Gene expression analysis revealed upregulation of XBP1, MZB1, DERL3, SSR4, FKBP11, FKBP2, PIM2, RABAC1, and SDF2L1 in iMCD-IPL, implicating endoplasmic reticulum stress and plasma cell differentiation in IL-6 dysregulation. Our findings suggest that XBP1-mediated IL-6 production may contribute to the pathogenesis of iMCD-IPL, potentially explaining its favorable responses to IL-6 blockade therapy. In contrast, IL-6 production in iMCD-TAFRO may be predominantly from vascular endothelial cells, suggesting that elevated serum IL-6 is a secondary phenomenon of the cytokine storm in this subtype. Future studies should clarify how proteomics and gene expression profiling could inform subtype-specific therapeutic strategies in iMCD.

Indexed as

Castleman DiseaseInterleukin-6AdultFemaleGene Expression ProfilingGene Expression RegulationHumansMaleMiddle AgedPlasma CellsIL6 protein, humanInterleukin-6

Identifiers

PMID40931874
PMCPMC13136834

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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.