Publications by authors named "Hiroshi Ishimoto"

Sargramostim, a recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) inhalation therapy, was recently approved for pharmaceutical use in Japan and shows promise as a treatment for autoimmune pulmonary alveolar proteinosis (APAP). For APAP patients with severe respiratory failure due to advanced lung fibrosis, lung transplantation is also a treatment option; however, APAP may recur after the procedure. Here, we report a case of successful sargramostim inhalation therapy for post-transplant APAP relapse in a patient who underwent living lung transplantation owing to severe fibrosis.

View Article and Find Full Text PDF

Objectives: Little is known about how various treatments impact the progression of interstitial lung disease (ILD) in rheumatoid arthritis (RA) patients. Here, we compared ILD progression in RA patients treated with Janus kinase inhibitors (JAKi) or biological disease-modifying anti-rheumatic drugs (bDMARDs). experiments were also performed to evaluate the potential effects of the drugs on epithelial-mesenchymal transition (EMT), a key event in pulmonary fibrosis.

View Article and Find Full Text PDF

Exophiala dermatitidis is an emerging black fungus that causes pulmonary infections that may be underestimated by conventional culture methods. We encountered one case that initially appeared to be yeast and was misidentified as Rhodotorula spp. using a commercial identification kit.

View Article and Find Full Text PDF

Background: Azithromycin has favorable effects on critical respiratory diseases owing to its antimicrobial and anti-inflammatory properties. During the early stages of the coronavirus disease 2019 (COVID-19) pandemic, azithromycin was frequently administered before specific treatments were developed. However, the efficacy of this treatment has not been verified.

View Article and Find Full Text PDF
Article Synopsis
  • Cryobiopsy is expected to be increasingly used for diagnosing lung diseases, but traditional methods pose challenges during tracheal intubation with endotracheal tubes.
  • A new method was developed, using a softer endotracheal tube with an externally attached suction tube for safer and simpler Fogarty catheter insertion.
  • The study found that this novel approach resulted in shorter bronchoscopy times without significantly increasing complications, demonstrating its practicality compared to conventional methods.
View Article and Find Full Text PDF
Article Synopsis
  • * In a case involving a 78-year-old man, TBLC combined with endobronchial ultrasonography (EBUS) successfully diagnosed adult T-cell lymphoma (ATL), marking it as the first such diagnosis using this method.
  • * A review of literature found 19 total cases of pulmonary lymphomas diagnosed via TBLC, primarily B-cell lymphomas (84.2%), and highlighted the effectiveness and safety of this technique, suggesting more research is needed to refine diagnostic guidelines.
View Article and Find Full Text PDF

A 63-year-old Japanese woman with multiple cysts in both lungs on chest computed tomography (CT) was referred to our hospital after a thorough examination, including a transbronchial lung biopsy (TBLB), failed to provide a diagnosis. Based on the findings on chest CT and pathological examination of the bronchoalveolar lavage fluid and transbronchial lung cryobiopsy (TBLC) specimen, the patient was diagnosed with pulmonary Langerhans cell histiocytosis (PLCH). TBLC may replace TBLB as the main diagnostic technique for PLCH, although further studies are required to determine the usefulness of TBLC for the diagnosis of PLCH.

View Article and Find Full Text PDF

Sarcoidosis is a systemic inflammatory disease characterized by noncaseating epithelioid cell granulomas. However, certain infections can exhibit similar histological findings. We present a case of a 69-year-old man who was initially diagnosed with sarcoidosis and later was confirmed, through 16S rRNA sequencing, to have disseminated infection.

View Article and Find Full Text PDF
Article Synopsis
  • Idiopathic pulmonary fibrosis (IPF) is a serious lung condition that leads to worsening lung function and overall poor health outcomes, primarily caused by the buildup of extracellular matrix (ECM) by myofibroblasts.
  • Type I collagen is a key component in the development of IPF, making it a potential target for new drug treatments aimed at combating fibrosis.
  • Heat shock protein 47 (HSP47) is a crucial protein that aids in collagen formation and has shown increased levels in IPF models, suggesting that exploring its role could help advance therapeutic options for the disease.
View Article and Find Full Text PDF

Studies indicated potential harm from empirical broad-spectrum therapy. A recent study of hospitalizations for community-acquired pneumonia suggested that empirical anti-methicillin-resistant (MRSA) therapy was associated with an increased risk of death and other complications. However, limited evidence supports empirical anti-MRSA therapy for older patients with aspiration pneumonia.

View Article and Find Full Text PDF
Article Synopsis
  • Olaparib, a PARP inhibitor effective for certain cancers, has been linked to a rare but severe side effect known as drug-induced interstitial lung disease (DIILD), highlighting the need for awareness and early detection.
  • This report details three cases of Japanese women with ovarian cancer who developed DIILD after taking olaparib, with symptoms ranging from fever to severe respiratory issues.
  • All patients discontinued olaparib, and treatment varied based on the severity of their conditions, underscoring the importance of monitoring lung health in patients receiving this medication.
View Article and Find Full Text PDF

This study aimed to examine the validity of urinary N-terminal titin fragment/creatinine (urinary N-titin/Cr) reflecting muscle damage biomarker in patients with interstitial lung disease. This retrospective study enrolled patients with interstitial lung disease. We measured urinary N-titin/Cr.

View Article and Find Full Text PDF

The potential antimicrobial and anti-inflammatory effectiveness of azithromycin against severe influenza is yet unclear. We retrospectively investigated the effect of intravenous azithromycin administration within 7 days of hospitalization in patients with influenza virus pneumonia and respiratory failure. Using Japan's national administrative database, we enrolled and classified 5066 patients with influenza virus pneumonia into severe, moderate, and mild groups based on their respiratory status within 7 days of hospitalization.

View Article and Find Full Text PDF

Background: Idiopathic pulmonary fibrosis (IPF) is characterised by worsening dyspnoea and exercise intolerance.

Research Question: Does a long-term pulmonary rehabilitation improve exercise tolerance in patients with IPF treated with standard antifibrotic drugs, which are expected to reduce disease progression?

Methods: This open-label randomised controlled trial was performed at 19 institutions. Stable patients receiving nintedanib were randomised into pulmonary rehabilitation and control groups (1:1).

View Article and Find Full Text PDF

Commensal microbes influence various aspects of vertebrate and invertebrate brain function. We previously reported that Lactiplantibacillus plantarum SBT2227 promotes sleep in the fruit fly, Drosophila melanogaster. However, how widely the sleep-promoting effects are conserved in gut bacterial species remains unknown.

View Article and Find Full Text PDF
Article Synopsis
  • Primary ciliary dyskinesia (PCD) is a rare genetic condition affecting ciliary function and structure, diagnosed through genotyping, with an estimated incidence of 1 in 15,000-20,000 individuals.
  • A 39-year-old Japanese woman suffering from long-term respiratory issues was diagnosed with PCD after whole-exome analysis revealed novel genetic variants and confirmed lack of a key protein in her cilia.
  • The case highlights that patients with certain PCD variants may experience moderate ciliary dysfunction, a reduced number of moving cilia, and potentially severe respiratory conditions.
View Article and Find Full Text PDF

Pulmonary nodular lymphoid hyperplasia (PNLH) is a very rare disease, and it is difficult to diagnose PNLH and distinguish it from mucosa-associated lymphoid tissue (MALT) lymphoma. In addition, information on bronchoalveolar lavage fluid (BALF) analyses is lacking. We herein report a 36-year-old Japanese woman diagnosed with PLNH by a surgical biopsy and analysis of BALF.

View Article and Find Full Text PDF

Managing mild illness in COVID-19 and predicting progression to severe disease are concerning issues. Here, we investigated the outcomes of Japanese patients with mild COVID-19, and identified triage risk factors for further hospitalization and emergency department (ED) visits at a single tertiary hospital. A triage checklist with 30 factors was used.

View Article and Find Full Text PDF
Article Synopsis
  • Idiopathic pulmonary fibrosis is a severe lung disease that leads to death, and while current treatments can slow it down, they aren't cures.
  • This study found that human γδ T cells can significantly lower collagen type I levels in lung fibroblasts, which is important for fibrosis, but only when they are in direct contact with those cells.
  • The research also discovered that these T cells can produce soluble factors that independently reduce collagen levels, and that their effectiveness is influenced by specific immune signals like interferon-γ and interleukin-18, suggesting a potential new therapy using γδ T cell transfer.
View Article and Find Full Text PDF
Article Synopsis
  • - A 36-year-old Japanese man was diagnosed with multisystem Langerhans cell histiocytosis (LCH) after showing lung cavities and spine lesions, having previously experienced milder pulmonary LCH symptoms.
  • - Three years earlier, he had upper lung lesions that improved after quitting smoking, suggesting a possible link between smoking and his condition.
  • - The case highlights that even if pulmonary LCH improvements occur after smoking cessation, there's a risk of relapse or progression, making regular medical monitoring essential.
View Article and Find Full Text PDF

Lactic acid bacteria (LAB) influence multiple aspects of host brain function via the production of active metabolites in the gut, which is known as the pre/probiotic action. However, little is known about the biogenic effects of LAB on host brain function. Here, we reported that the SBT2227 promoted sleep in .

View Article and Find Full Text PDF
Article Synopsis
  • * Out of 288 IIP patients, 6.9% tested positive for anti-Ro52, with a notable overlap of 40% with another autoantibody, anti-ARS.
  • * Anti-Ro52-positive patients exhibited clinical features more aligned with interstitial pneumonia with autoimmune features (IPAF), indicating its potential role in identifying autoimmune traits in IIP cases.
View Article and Find Full Text PDF
Article Synopsis
  • - A 26-year-old Japanese woman with Hermansky-Pudlak syndrome experienced worsened pulmonary fibrosis, high fever, diarrhea, and dyspnea, prompting medical treatment.
  • - Imaging revealed new ground-glass opacities in her lungs, and a colon biopsy indicated significant inflammation linked to elevated myeloperoxidase (MPO) anti-neutrophil cytoplasmic antibodies.
  • - Treatment with steroid pulse therapy and intravenous cyclophosphamide led to improvement in her symptoms and chest CT results, suggesting the need for immunosuppressant therapy for the related systemic inflammation.
View Article and Find Full Text PDF

A 65-year-old Japanese man with interstitial pneumonia demonstrated honeycomb lung with thickened walls on chest high-resolution computed tomography (HRCT) and predominance of neutrophils in the cell fraction of the bronchoalveolar lavage fluid. Although there were no centrilobular nodular or branching shadows on chest HRCT suggestive of diffuse panbronchiolitis, he exhibited sinusitis and had the human leukocyte antigen (HLA)-B54 antigen. With long-term macrolide therapy, the cough and sputum production markedly improved, wall thickening of the honeycomb lung on chest HRCT decreased, and the forced vital capacity increased.

View Article and Find Full Text PDF
Article Synopsis
  • Anti-ARS antibodies are linked to a specific type of interstitial pneumonia that typically responds well to steroid and immunosuppressive treatment, but in some cases, such as the one described, treatment can worsen the condition.
  • A 66-year-old male patient with respiratory issues was initially diagnosed with anti-ARS antibody-positive interstitial pneumonia; however, his symptoms failed to improve and worsened after starting treatment.
  • Upon further investigation, the patient was found to have autoimmune pulmonary alveolar proteinosis instead, which can mimic interstitial pneumonia, highlighting the importance of accurate diagnosis in treatment decisions.
View Article and Find Full Text PDF