Evidence map›Paper›PMID 41131535›Full record

Observational studyBMC infectious diseases2025

Association between immunity and antimicrobial treatment resistance in patients with Mycobacterium avium complex pulmonary disease: a multicenter observational study.

Akinobu Matsuura, Yuichiro Shindo, Daisuke Sugiyama, Taku Nakagawa, Yuta Hayashi, Masahiro Sano, Yosuke Goto, Saki Kato, Hiroyoshi Nishikawa, Kenji Ogawa and 1 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study 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.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Akinobu Matsuura *Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya, 466-8550, Japan.
Yuichiro Shindo *Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya, 466-8550, Japan. shindo.yuichiro.y7@f.mail.nagoya-u.ac.jp.
Daisuke SugiyamaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Taku NakagawaDepartment of Respiratory Medicine, NHO Higashinagoya National Hospital, Nagoya, Japan.
Yuta HayashiDepartment of Respiratory Medicine, NHO Higashinagoya National Hospital, Nagoya, Japan.
Masahiro SanoDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya, 466-8550, Japan.
Yosuke GotoDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya, 466-8550, Japan.
Saki KatoDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya, 466-8550, Japan.
Hiroyoshi NishikawaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kenji OgawaDepartment of Respiratory Medicine, NHO Higashinagoya National Hospital, Nagoya, Japan.
Makoto IshiiDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya, 466-8550, Japan.

Funding

Japan Society for the Promotion of Science 24K11362
6 · The paper itself

Abstract

backgroundMycobacterium avium complex pulmonary disease (MAC-PD) is a refractory infectious disease, with a low success rate of the antimicrobial therapy. T cells and macrophages play a critical role in regulating the mechanism of immunity against mycobacterial infections. Although T cell dysfunction may be associated with treatment failure in MAC-PD, supporting evidence is scarce. This study aimed to elucidate the immunological characteristics of patients with refractory MAC-PD, focusing on immunosuppression and T cell exhaustion.

methodsPatients with MAC-PD who received standard antimicrobial therapy for at least 12 months were enrolled and classified into treatment success or failure groups. Flow cytometry was used to investigate CD4

resultsThis study involved 41 patients, including 21 and 20 in the treatment success and failure groups, respectively. Patients with MAC-PD had higher expression of co-inhibitory molecules, including PD-1 and TIM-3, as well as CD160, LAG-3, and 2B4, on CD4

conclusionsThe effector functions of CD4

trial registrationThis study was registered with the University Hospital Medical Information Network of Japan (registration number: UMIN000043426, registration date: March 1, 2021).

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialLung DiseasesMycobacterium avium ComplexMycobacterium avium-intracellulare InfectionAdultAgedCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleHumansMaleMiddle AgedAnti-Bacterial AgentsDisease durationHost-directed therapyRefractory MAC-PDT cell exhaustionTreatment failure

Identifiers

PMID41131535
PMCPMC12548183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.