Evidence map›Paper›PMID 41225393›Full record

ArticleBMC infectious diseases2025

Serum cytokine analysis in cavitary and non-cavitary pulmonary Mycobacterium avium complex disease: a cross-sectional study.

Keita Takeda, Maho Suzukawa, Yuko Matsumoto, Yume Nakamura, Eri Nakano, Masato Watanabe, Yasuhiro Morimoto, Takafumi Kato, Osamu Narumoto, Masahiro Kawashima and 6 more

Abstract read
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Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Keita TakedaCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan. takeda.keita.ax@mail.hosp.go.jp.
Maho SuzukawaClinical Research Center, National Hospital Organization Tokyo National Hospital, Tokyo, Japan.
Yuko MatsumotoCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Yume NakamuraCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Eri NakanoCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Masato WatanabeCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Yasuhiro MorimotoCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Takafumi KatoCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Osamu NarumotoCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Masahiro KawashimaCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Junko SuzukiCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Atsuhisa TamuraCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Hideaki NagaiCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Yoshiteru MorioCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Hirotoshi MatsuiCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.
Yuka SasakiCenter for Pulmonary Diseases, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose, Tokyo, 204-8585, Japan.

Funding

the Grant-in-Aid for Clinical Research of the National Hospital Organization R5-NHO(PI)-01the SHIONOGI Infectious Disease Research Promotion Foundation 2023N018
6 · The paper itself

Abstract

backgroundIn pulmonary Mycobacterium avium complex (MAC) disease, serum cytokine profiles may offer insights into the immune responses underlying cavitary lesion development. We aimed to compare serum cytokine profiles between patients with cavitary and those with non-cavitary nodular bronchiectasis (NB) and to identify cytokines potentially associated with cavitary lung lesions.

methodsThis single-center, cross-sectional study included patients with pulmonary MAC disease presenting with NB, categorized into the cavitary and non-cavitary groups. The serum levels of 34 exploratory cytokines were measured using the MAGPIX system and enzyme-linked immunosorbent assays. Intergroup comparisons were subsequently performed.

resultsNine and 45 patients with cavitary and non-cavitary NB MAC, respectively, were included. Significantly higher levels of interleukin (IL)-6 and IL-8/C-X-C motif chemokine ligand 8 (inflammatory markers), matrix metalloproteinase-8 and chitinase-3-like protein 1 (tissue remodeling factors), and IL-17E/IL-25 and suppression of tumorigenicity 2/IL-33R (T-helper type 2-related cytokines) were observed in the cavitary group. No significant differences were identified for the remaining cytokines.

conclusionsCavitary lung lesions in pulmonary MAC disease are associated with elevated levels of inflammatory markers, tissue remodeling factors, and T-helper type 2 related cytokines. Future research should investigate whether these cytokine differences contribute to cavity formation or occur as a consequence, and explore their potential as therapeutic targets.

Indexed as

CytokinesMycobacterium avium ComplexMycobacterium avium-intracellulare InfectionAgedAged, 80 and overBronchiectasisCross-Sectional StudiesFemaleHumansLungMaleMiddle AgedCytokinesCytokine profileInflammationLung cavityMycobacterium intracellulareNon-tuberculous mycobacteria

Identifiers

PMID41225393
PMCPMC12613673

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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.