Updated on 2025/06/09

Information

 

写真a

 
IKEGAME SATOSHI
 
Organization
Kyushu University Hospital Respiratory medicine Lecturer
School of Medicine Department of Medicine(Concurrent)
Title
Lecturer
Profile
臨床:呼吸器感染症の外来診療、他科コンサルト等 教育:医学部学生の講義(呼吸器感染症)、医学部学生の臨床実習指導、初期臨床研修医への指導、大学院生の研究指導 研究:新型コロナウイルス新規変異株を予測する系の開発等
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Degree

  • M.D. Ph.D

Research Interests・Research Keywords

  • Research theme: Research related to novel therapy against COVID-19 and vaccine developement

    Keyword: SARS-CoV-2

    Research period: 2022.4

Papers

  • Resected Pulmonary Achromobacter xylosoxidans Mimicking Aspergillosis Fungus Ball.

    Nakamura S, Akamine T, Ikegame S, Hashisako M, Nakagawa T, Kinoshita F, Kohno M, Ozono K, Takenaka T, Yoshizumi T

    Annals of thoracic surgery short reports   3 ( 1 )   171 - 174   2025.3

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    Language:English  

    DOI: 10.1016/j.atssr.2024.09.005

    PubMed

  • Immunophenotyping of T Cells in Lung Malignancies and Cryptogenic Organizing Pneumonia

    Yanagihara, T; Hata, K; Matsubara, K; Kunimura, K; Suzuki, K; Tsubouchi, K; Ikegame, S; Fukui, Y; Okamoto, I

    JOURNAL OF CLINICAL MEDICINE   14 ( 2 )   2025.1   ISSN:2077-0383 eISSN:2077-0383

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    Language:English   Publisher:Journal of Clinical Medicine  

    Background: Lung malignancies, including cancerous lymphangitis and lymphomas, can mimic interstitial lung diseases like cryptogenic organizing pneumonia (COP) on imaging, leading to diagnostic delays. We aimed to identify potential biomarkers to distinguish between these conditions. Methods: We analyzed bronchoalveolar lavage fluid from 8 patients (4 COP, mean age 59.8 ± 13.5 years; 4 lung malignancies including 2 cancerous lymphangitis, 1 MALT lymphoma, and 1 diffuse large B cell lymphoma, mean age 67.8 ± 4.5 years) using mass cytometry with 35 T cell markers. Data were analyzed using principal component analysis (PCA) and unsupervised Citrus clustering. Results: PCA of T cell marker intensities effectively separated the two groups, with IL-2Rα, PD-L2, CD45RA, CD44, and OX40 being the top discriminating markers. Citrus analysis showed a significant increase in the CD16+ CD4+ and CD16+ CD8+ T cell populations in the COP group compared to lung malignancies. Conclusions: Our findings reveal distinct T cell immunophenotypes in COP versus lung malignancies, particularly increased CD16+ T cells in COP, which could serve as potential diagnostic biomarkers.

    DOI: 10.3390/jcm14020316

    Web of Science

    Scopus

    PubMed

  • 喘息フェノタイプによって異なる呼気中揮発性有機化合物の同定 J-VOCSA試験(Identification of exhaled volatile organic compounds that characterize asthma phenotypes: A J-VOCSA study)

    Suzukawa Maho, Ohta Ken, Sugimoto Masahiro, Ohshima Nobuharu, Kobayashi Nobuyuki, Tashimo Hiroyuki, Tanimoto Yasushi, Itano Junko, Kimura Goro, Takata Shohei, Nakano Takako, Yamashita Takafumi, Ikegame Satoshi, Hyodo Kentaro, Abe Masahiro, Chibana Kenji, Kamide Yosuke, Sasaki Kazunori, Hashimoto Hiroya

    Allergology International   73 ( 4 )   524 - 531   2024.10   ISSN:1323-8930

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    Language:English   Publisher:(一社)日本アレルギー学会  

    重症喘息のフェノタイプによって異なる呼気中揮発性有機化合物(VOC)を同定するため、多施設共同前向き観察コホート研究を行った。参加した七つの医療機関でGINA step4または5の治療を受けている20歳以上の患者245例と健常対照50例を登録した。被験者の呼気を採取し、加熱脱着装置付GC/MSでVOCを測定した。以前に記述した、臨床的変数に基づく決定木に従って喘息患者を喘息フェノタイプ(1~5)に割り付けた。GC/MSにより検出された呼気中の243VOCのうち、頻度が高い142VOCを統計解析に用いた。クラスター分析を用いて、類似VOCプロファイルパターンを持つグループを隣同士に割り付けた。早期発症型フェノタイプ3と4は高い類似度を示した。対照的に、フェノタイプ5は最も際立つVOCプロファイルパターンを示した。ボルケーノプロット図上では健常対照と比べて、フェノタイプ1~5の6VOC強度は有意に高く、13VOCは有意に低かった。これら19VOCの中でメタンスルホン酸無水物のみがQ値<0.05を示したが、FDR調整後有意差は認められなかった。病因が未解明で、最も重症度が高いフェノタイプ5ではウンデカナールが亢進していることが判明したが、有意差は認められなかった。本研究の新規性は、GC/MSにより同定された呼気中のVOCプロファイルと臨床的フェノタイプが一致したことであった。

  • Identification of exhaled volatile organic compounds that characterize asthma phenotypes: A J-VOCSA study

    Suzukawa M., Ohta K., Sugimoto M., Ohshima N., Kobayashi N., Tashimo H., Tanimoto Y., Itano J., Kimura G., Takata S., Nakano T., Yamashita T., Ikegame S., Hyodo K., Abe M., Chibana K., Kamide Y., Sasaki K., Hashimoto H.

    Allergology International   73 ( 4 )   524 - 531   2024.10   ISSN:13238930

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    Publisher:Allergology International  

    Background: Asthma is characterized by phenotypes of different clinical, demographic, and pathological characteristics. Identifying the profile of exhaled volatile organic compounds (VOCs) in asthma phenotypes may facilitate establishing biomarkers and understanding asthma background pathogenesis. This study aimed to identify exhaled VOCs that characterize severe asthma phenotypes among patients with asthma. Methods: This was a multicenter cross-sectional study of patients with severe asthma in Japan. Clinical data were obtained from medical records, and questionnaires were collected. Exhaled breath was sampled and subjected to thermal desorption gas chromatography-mass spectrometry (GC/MS). Results: Using the decision tree established in the previous nationwide asthma cohort study, 245 patients with asthma were divided into five phenotypes and subjected to exhaled VOC analysis with 50 healthy controls (HCs). GC/MS detected 243 VOCs in exhaled breath samples, and 142 frequently detected VOCs (50% of all samples) were used for statistical analyses. Cluster analysis assigning the groups with similar VOC profile patterns showed the highest similarities between phenotypes 3 and 4 (early-onset asthma phenotypes), followed by the similarities between phenotypes 1 and 2 (late-onset asthma phenotypes). Comparisons between phenotypes 1–5 and HC revealed 19 VOCs, in which only methanesulfonic anhydride showed p < 0.05 adjusted by false discovery rate (FDR). Comparison of these phenotypes yielded several VOCs showing different trends (p < 0.05); however, no VOCs showed p < 0.05 adjusted by FDR. Conclusions: Exhaled VOC profiles may be useful for distinguishing asthma and asthma phenotypes; however, these findings need to be validated, and their pathological roles should be clarified.

    DOI: 10.1016/j.alit.2024.04.003

    Scopus

  • Immunological landscape of human lymphoid explants during measles virus infection

    Acklin J.A., Patel A.R., Kurland A.P., Horiuchi S., Moss A.S., DeGrace E.J., Ikegame S., Carmichael J., Kowdle S., Thibault P.A., Imai N., Ueno H., Tweel B., Johnson J.R., Rosenberg B.R., Lee B., Lim J.K.

    JCI Insight   9 ( 17 )   2024.9

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    Publisher:JCI Insight  

    In humans, lymph nodes are the primary site of measles virus (MeV) replication. To understand the immunological events that occur at this site, we infected human lymphoid tissue explants using a pathogenic strain of MeV that expresses GFP. We found that MeV infected 5%–15% of cells across donors. Using single-cell RNA-Seq and flow cytometry, we found that while most of the 29 cell populations identified in the lymphoid culture were susceptible to MeV, there was a broad preferential infection of B cells and reduced infection of T cells. Further subsetting of T cells revealed that this reduction may be driven by the decreased infection of naive T cells. Transcriptional changes in infected B cells were dominated by an interferon-stimulated gene (ISG) signature. To determine which of these ISGs were most substantial, we evaluated the proteome of MeV-infected Raji cells by mass spectrometry. We found that IFIT1, IFIT2, IFIT3, ISG15, CXCL10, MX2, and XAF1 proteins were the most highly induced and positively correlated with their expression in the transcriptome. These data provide insight into the immunological events that occur in lymph nodes during infection and may lead to the development of therapeutic interventions.

    DOI: 10.1172/jci.insight.172261

    Scopus

  • The Utility and Limitations of Universal Polymerase Chain Reaction Screening for SARS-CoV-2 During Hospital Admission Reviewed

    Naruhiko Ogo, Satoshi Ikegame, Taeko Hotta, Keiko Kan-O, Yasuto Yoneshima, Yoshimasa Shiraishi, Kazuya Tsubouchi, Kentaro Tanaka, Isamu Okamoto

    Cureus   16 ( 5 )   e61470   2024.5   ISSN:2168-8184 eISSN:2168-8184

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    Authorship:Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.7759/cureus.61470

    Web of Science

    PubMed

  • Exploratory mass cytometry analysis reveals immunophenotypes of cancer treatment-related pneumonitis

    Yanagihara, T; Hata, K; Matsubara, K; Kunimura, K; Suzuki, K; Tsubouchi, K; Ikegame, S; Baba, Y; Fukui, Y; Okamoto, I

    ELIFE   12   2024.4   ISSN:2050-084X

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  • A Case of Obstructing Bronchial Aspergillosis in a Patient Receiving Cytotoxic Chemotherapy and Inhaled Corticoid Therapy

    Tsuneoka Yuki, Tanaka Kentaro, Shimauchi Atsushi, Inoue Shigesato, Yoneshima Yasuto, Ikegame Satoshi, Harada Eiji, Okamoto Isamu

    Respiratory Endoscopy   1 ( 2 )   105 - 108   2023.11   eISSN:27583813

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    Language:English   Publisher:The Japan Society for Respiratory Endoscopy  

    <p>Among various types of aspergillosis, the clinical features of patients with obstructive bronchial aspergillosis remain unclear. Originally, it was reported to occur only in severely immunocompromised patients, such as acquired immunodeficiency syndrome (AIDS) or post-organ transplantation; however, recent reports have suggested that this disease could also affect patients seen in daily practice of pulmonary medicine. We describe a case of a 76-year-old woman with obstructing bronchial aspergillosis. This patient presented to the hospital with a productive cough during asthma and advanced lung cancer treatment. Chest CT showed stenosis of the bronchial lumen. Bronchoscopy showed no recurrence of lung cancer, and aspergillus was found in the granulation tissue. The cough improved with debridement of the lesion by bronchoscopy and oral antifungal medication treatment. Our review of previous case reports, including this case, revealed that obstructing bronchial aspergillosis might occur when patients have several factors inducing immunosuppression, such as solid tumors under anticancer treatment, inhaled corticosteroids, and aging. Since patients may be at risk of progressing to invasive aspergillosis, physicians must properly diagnose obstructing bronchial aspergillosis to deliver appropriate treatment.</p>

    DOI: 10.58585/respend.2023-0020

    CiNii Research

  • Successful Treatment against Mediastinal Methicillin-resistant <i>Staphylococcus aureus</i> Infection after an Endobronchial Ultrasound-guided Transbronchial Needle Aspiration Procedure

    Jo Akihiro, Ikegame Satoshi, Kiyozawa Daisuke, Yoneshima Yasuto, Oda Yoshinao, Okamoto Isamu

    Respiratory Endoscopy   1 ( 2 )   78 - 82   2023.11   eISSN:27583813

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    Language:English   Publisher:The Japan Society for Respiratory Endoscopy  

    <p>The case involves a 57-year-old man with a history of laryngeal and lung cancers. He underwent a laryngectomy and right upper lobectomy and developed tracheal methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) colonization. He also underwent endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) to diagnose right mediastinal lymph node adenopathy. His recovery was complicated by a mediastinal infection caused by MRSA five days post-procedure. Combining triple antibiotics comprising MEPM, DAP, and VCM for three weeks gradually improved the mediastinal infection. To our knowledge, this is the first report of mediastinal infection caused by MRSA after EBUS-TBNA. Our successful treatment of EBUS-TBNA-related infectious complications gives us information regarding rare complications management caused by EBUS-TBNA.</p>

    DOI: 10.58585/respend.2023-0007

    CiNii Research

  • Unraveling the immunophenotypes of pneumonitis in cancer treatment through mass cytometry exploration

    Yanagihara, T; Hata, K; Matsubara, K; Kunimura, K; Suzuki, K; Tsubouchi, K; Ikegame, S; Baba, Y; Fukui, Y; Okamoto, I

    RESPIROLOGY   28   94 - 95   2023.11   ISSN:1323-7799 eISSN:1440-1843

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  • 超音波気管支鏡ガイド下経気管支吸引針生検の処置後に縦隔のメチシリン耐性黄色ブドウ球菌感染を発症したが、その治療に成功した1例(Successful Treatment against Mediastinal Methicillin-resistant Staphylococcus aureus Infection after an Endobronchial Ultrasound-guided Transbronchial Needle Aspiration Procedure)

    Jo Akihiro, Ikegame Satoshi, Kiyozawa Daisuke, Yoneshima Yasuto, Oda Yoshinao, Okamoto Isamu

    Respiratory Endoscopy   1 ( 2 )   78 - 82   2023.11

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    Language:English   Publisher:(一社)日本呼吸器内視鏡学会  

    症例は57歳男性。11年前に右喉頭癌を放射線療法と化学療法で治療されていた。4年前には右肺腺癌に対し切除術と地固め化学療法を受けていた。さらに1年前には左喉頭癌と診断され喉頭全摘出術と永久気管切開術が行われたが、その術後10日目にメチシリン耐性黄色ブドウ球菌(MRSA)による手術部位感染が発生し、洗浄とデブリードマンで治癒していた。喉頭全摘出術から1年が経過した今回の経過観察受診時に縦隔リンパ節が1個腫大していることが判明した。そのリンパ節は16mm大で右傍気管領域に位置しており、FDG-PET所見でも陽性(SUVmax 3.97)が示されたことから癌の再発が疑われた。FDG-PET画像上、他の領域には癌再発を疑わせる所見は示されなかった。気管瘻孔を利用して超音波気管支鏡ガイド下経気管支吸引針生検(EBUS-TBNA)を行い、合併症なく、また予防的抗生物質投与も行われずに同日退院していた。その5日後に高熱を訴え当院を受診した。白血球数とC反応性蛋白の高値が示され、造影CTでは縦隔感染を示唆する所見が示された。EBUS-TBNA処置に関連した縦隔リンパ節および縦隔の感染症と診断し、抗生物質3剤併用療法(MEPM、VCM、DAP)を3週間行ったところ同感染症は徐々に改善していった。生検結果からは右喉頭癌の再発と最終診断し、ペムブロリズマブの投与を開始した。

  • 細胞傷害性化学療法と吸入コルチコイド療法を受けており閉塞性気管支アスペルギルス症を発症した1例(A Case of Obstructing Bronchial Aspergillosis in a Patient Receiving Cytotoxic Chemotherapy and Inhaled Corticoid Therapy)

    Tsuneoka Yuki, Tanaka Kentaro, Shimauchi Atsushi, Inoue Shigesato, Yoneshima Yasuto, Ikegame Satoshi, Harada Eiji, Okamoto Isamu

    Respiratory Endoscopy   1 ( 2 )   105 - 108   2023.11

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    Language:English   Publisher:(一社)日本呼吸器内視鏡学会  

    症例は77歳女性。喘息の持病があった。約5年前、慢性咳嗽の症状で当院を受診し、左肺下葉の肺腺癌(cT2aN1M0、病期IIA)と診断された。根治的放射線療法を受けたが、約2年前には肺癌が再発したため標準的な免疫化学療法(シスプラチン、ペメトレキセド、ペムブロリズマブ)と維持化学療法(ペメトレキセド+ペムブロリズマブ)が1年間行われた。本年になってから咳嗽が悪化しており、聴診所見から気管支喘息の増悪を疑って吸入皮質ステロイド療法を強化したが症状はさらに悪化した。血液検査ではアスペルギルスの抗原と特異的IgEはいずれも陰性所見であった。胸部CT画像では気管支腔の狭窄が示され、肺癌の気管支内への進行が疑われた。しかし、気管支鏡検査では肺癌の再発は認められず、代わりに左気管支の上葉支の内部に1個の白色病変が発見された。その病変の検体を採取したが、その際には抵抗を感じることなく採取することができた。その病理学的診断は閉塞性気管支アスペルギルス症とされた。白色病変のデブリードマン処置を行い、経口ボリコナゾールを開始したところ咳嗽は徐々に改善し、上昇していた白血球数とC反応性蛋白値も正常化した。6ヵ月後の気管支鏡評価では左上葉支にわずかな白色苔癬が観察されたが、生検ではアスペルギルスの菌糸は発見されなかった。そのためボリコナゾールを終了する判断をした。

  • Mass cytometry analysis of B-cell populations in extranodal marginal-zone lymphoma of mucosa-associated lymphoid tissue of the lung

    Yanagihara, T; Hata, K; Matsubara, K; Kunimura, K; Suzuki, K; Tsubouchi, K; Ikegame, S; Baba, Y; Fukui, Y; Okamoto, I

    ANNALS OF HEMATOLOGY   102 ( 10 )   2959 - 2961   2023.10   ISSN:0939-5555 eISSN:1432-0584

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    Language:English   Publisher:Annals of Hematology  

    DOI: 10.1007/s00277-023-05391-3

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  • Altered macrophage phenotypes in a case of autoimmune pulmonary alveolar proteinosis

    Hata, K; Yanagihara, T; Matsubara, K; Kunimura, K; Eto, D; Suzuki, K; Tsubouchi, K; Ikegame, S; Fukui, Y; Okamoto, I

    ERJ OPEN RESEARCH   9 ( 5 )   2023.9   ISSN:2312-0541 eISSN:2312-0541

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    Language:English   Publisher:ERJ Open Research  

    DOI: 10.1183/23120541.00500-2023

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  • Metagenomics-enabled reverse-genetics assembly and characterization of myotis bat morbillivirus

    Ikegame S., Carmichael J.C., Wells H., Furler O’Brien R.L., Acklin J.A., Chiu H.P., Oguntuyo K.Y., Cox R.M., Patel A.R., Kowdle S., Stevens C.S., Eckley M., Zhan S., Lim J.K., Veit E.C., Evans M.J., Hashiguchi T., Durigon E., Schountz T., Epstein J.H., Plemper R.K., Daszak P., Anthony S.J., Lee B.

    Nature Microbiology   8 ( 6 )   1108 - 1122   2023.6

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    Publisher:Nature Microbiology  

    Morbilliviruses are among the most contagious viral pathogens of mammals. Although previous metagenomic surveys have identified morbillivirus sequences in bats, full-length morbilliviruses from bats are limited. Here we characterize the myotis bat morbillivirus (MBaMV) from a bat surveillance programme in Brazil, whose full genome was recently published. We demonstrate that the fusion and receptor binding protein of MBaMV utilize bat CD150 and not human CD150, as an entry receptor in a mammalian cell line. Using reverse genetics, we produced a clone of MBaMV that infected Vero cells expressing bat CD150. Electron microscopy of MBaMV-infected cells revealed budding of pleomorphic virions, a characteristic morbillivirus feature. MBaMV replication reached 103–105 plaque-forming units ml−1 in human epithelial cell lines and was dependent on nectin-4. Infection of human macrophages also occurred, albeit 2–10-fold less efficiently than measles virus. Importantly, MBaMV is restricted by cross-neutralizing human sera elicited by measles, mumps and rubella vaccination and is inhibited by orally bioavailable polymerase inhibitors in vitro. MBaMV-encoded P/V genes did not antagonize human interferon induction. Finally, we show that MBaMV does not cause disease in Jamaican fruit bats. We conclude that, while zoonotic spillover into humans may theoretically be plausible, MBaMV replication would probably be controlled by the human immune system.

    DOI: 10.1038/s41564-023-01380-4

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  • Expansion of ST2-expressing macrophages in a patient with bronchiolitis obliterans syndrome

    Yanagihara, T; Hata, K; Suzuki, K; Matsubara, K; Kunimura, K; Tsubouchi, K; Eto, D; Ando, H; Uehara, M; Ikegame, S; Fukui, Y; Okamoto, I

    ERJ OPEN RESEARCH   9 ( 3 )   2023.5   ISSN:2312-0541 eISSN:2312-0541

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    Language:English   Publisher:ERJ Open Research  

    DOI: 10.1183/23120541.00033-2023

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  • Respiratory Virus Infections during the COVID-19 Pandemic Revealed by Multiplex PCR Testing in Japan

    Yamashita, S; Ikegame, S; Nakatomi, K; Sakurai, Y; Shuto, H; Sato, N; Mizoguchi, Y; Uehara, M; Nakashima, N; Okamoto, I; Koto, H

    MICROBIOLOGY SPECTRUM   11 ( 2 )   e0416222   2023.4   eISSN:2165-0497

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    Language:English   Publisher:Microbiology Spectrum  

    Under the strict quarantine policy imposed to combat the COVID-19 (coronavirus disease 2019) pandemic in Japan, the prevalence of respiratory infections by viruses other than SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) has been largely unknown. However, such information on viral circulation is important in order to develop better management policies that are based on scientific data. Here, we retrospectively investigated respiratory virus infections in individuals who visited a community hospital with respiratory symptoms between June of 2020 and September of 2021 with the use of the BioFire FilmArray Respiratory Panel 2.1. Virus was detected in 65 out of a total of 328 subjects, with SARS-CoV-2 (67.7%), rhino/enterovirus (18.5%), and parainfluenza virus 3 (7.7%) accounting for most of the infections. No influenza virus or respiratory syncytial virus (RSV) infections were detected. The monthly cases of rhino/enterovirus infection were highest from winter to spring, with this temporal pattern differing from that of SARS-CoV-2. SARS-CoV-2 was detected more frequently (P , 0.001) in subjects with cough (31/104 cases, 29.8%) than in those without cough (13/ 224 cases, 5.8%), suggesting that cough might contribute to the prediction of COVID-19. Our findings also suggest that testing for rhino/enterovirus and parainfluenza virus 3, in addition to SARS-CoV-2, may be important for the rigorous diagnosis of respiratory virus infections. IMPORTANCE Influenza virus, RSV, adenovirus, and rhino/enterovirus were the major respiratory viruses before COVID-19 pandemic. Circulating respiratory viruses may have been affected by our strong quarantine policy during the COVID-19 pandemic. We checked the circulating respiratory viruses from our outpatients by using a multiplex PCR kit that had recently been released. SARS-CoV-2 was the most frequently detected virus, and it was followed by rhino/enterovirus and parainfluenza virus 3. No influenza virus or RSV infections were detected during our study period, suggesting that influenza virus and RSV became almost extinct. COVID-19 cases frequently experienced cough, and this frequency was statistically significantly higher than that observed in the cases without SARS-CoV-2 detection. The cough can be an indicator of COVID-19.

    DOI: 10.1128/spectrum.04162-22

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  • Mass cytometry identifies characteristic immune cell subsets in bronchoalveolar lavage fluid from interstitial lung diseases

    Hata, K; Yanagihara, T; Matsubara, K; Kunimura, K; Suzuki, K; Tsubouchi, K; Eto, D; Ando, H; Uehara, M; Ikegame, S; Baba, Y; Fukui, Y; Okamoto, I

    FRONTIERS IN IMMUNOLOGY   14   1145814   2023.3   ISSN:1664-3224

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    Language:English   Publisher:Frontiers in Immunology  

    Immune cells have been implicated in interstitial lung diseases (ILDs), although their phenotypes and effector mechanisms remain poorly understood. To better understand these cells, we conducted an exploratory mass cytometry analysis of immune cell subsets in bronchoalveolar lavage fluid (BALF) from patients with idiopathic pulmonary fibrosis (IPF), connective-tissue disease (CTD)-related ILD, and sarcoidosis, using two panels including 64 markers. Among myeloid cells, we observed the expansion of CD14+ CD36hi CD84hiCCR2– monocyte populations in IPF. These CD14+ CD36hi CD84hi CCR2– subsets were also increased in ILDs with a progressive phenotype, particularly in a case of acute exacerbation (AEx) of IPF. Analysis of B cells revealed the presence of cells at various stages of differentiation in BALF, with a higher percentage of IgG memory B cells in CTD-ILDs and a trend toward more FCRL5+ B cells. These FCRL5+ B cells were also present in the patient with AEx-IPF and sarcoidosis with advanced lung lesions. Among T cells, we found increased levels of IL-2R+ TIGIT+ LAG3+ CD4+ T cells in IPF, increased levels of CXCR3+ CD226+ CD4+ T cells in sarcoidosis, and increased levels of PD1+ TIGIT+ CD57+ CD8+ T cells in CTD-ILDs. Together, these findings underscore the diverse immunopathogenesis of ILDs.

    DOI: 10.3389/fimmu.2023.1145814

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  • Respiratory Virus Infections during the COVID-19 Pandemic Revealed by Multiplex PCR Testing in Japan Reviewed International journal

    #Sho Yamashita,@Satoshi Ikegame,@Keita Nakatomi,@Yuko Sakurai,@Hiroe Shuto,@Noriko Sato,@Yoshihiro Mizoguchi,@Maki Uehara,@Nobutaka Nakashima,@Isamu Okamoto,@Hiroshi Koto

    Microbiology spectrum   2023.2

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    Language:English   Publishing type:Research paper (scientific journal)  

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Presentations

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Professional Memberships

  • 日本呼吸器学会

  • 日本内科学会

  • 日本感染症学会

  • 日本呼吸器内視鏡学会

  • 日本ウイルス学会

Research Projects

  • 新型コロナウイルスのワクチン感受性などに関する研究

    2024

    Grants-in-Aid for Scientific Research  キョーリン製薬 医薬に関する研究活動サポート

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    Authorship:Principal investigator  Grant type:Competitive funding other than Grants-in-Aid for Scientific Research

  • SARS-CoV-2感染症治療のための高親和性ACE2の開発

    2023.4

    九州大学病院 呼吸器内科 

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    Authorship:Principal investigator 

    ●研究背景
    ウイルス感染症の予防・治療において、ワクチン接種による中和抗体誘導や抗体製剤投与の有効性は多くのウイルス感染症で証明されているが、新型コロナウイルス感染症においては初期に開発されたワクチン、抗体製剤は変異株の出現により治療効果が大きく減弱した。変異に影響されない治療法を探索する中で、ACE2の細胞外領域をウイルス粒子表面のスパイクタンパク質に吸着させウイルスを中和する系が注目されている。新型コロナウイルスは宿主細胞侵入のためACE2と必ず結合するため、この系ではウイルス変異の影響を受けないとされる。スパイクとの親和性を高めた変異ACE2ではより治療効果が高いとされ、新しい変異ACE2の発見が新規治療開発につながることが期待される。

    ●研究方法
    変異ACE2を効率的に発見するため、ウイルスゲノムにACE2を導入した組換えウイルスを作成する。
    このウイルスはACE2遺伝子がスパイクンパク質との結合を強化する方向に変異誘導され、ウイルスを特定の条件下で継代培養することで高親和性のACE2を取得できることが期待できる。
    実際に発見された変異ACE2の精製蛋白を作成し、新型コロナウイルスをどの程度中和できるかを調べることで新規治療薬として利用可能かを評価する予定である。

    ●期待される成果
    スパイク蛋白質との親和性が大きく向上したACE2変異が発見されれば、ウイルスの変異に影響されない新規治療として利用できることが期待される。

  • SARS-CoV-2新規変異株を予測同定するmutagenesis screening

    2023 - 2027

    Grants-in-Aid for Scientific Research  公益財団法人武田科学振興財団 2023年度ハイリスク新興感染症研究助成

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    Authorship:Principal investigator  Grant type:Competitive funding other than Grants-in-Aid for Scientific Research

  • オミクロン株を中心とした新型コロナウイルス変異株のワクチン耐性の分子学的機序の解明

    2023 - 2024

    Grants-in-Aid for Scientific Research  新日本先進医療研究財団 令和4年度研究助成事業

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    Authorship:Principal investigator  Grant type:Competitive funding other than Grants-in-Aid for Scientific Research

  • SARS-CoV-2のワクチン感受性低下と関連する新規変異株を安全に予測する系の確立

    2022.4

    九州大学病院 呼吸器内科 

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    Authorship:Principal investigator 

    ●研究背景
    2021年に新型コロナウイルスのワクチンが開発され、良好な予防効果が報告されていたが、開発当初のワクチンは発生直後の起源株から設計されたワクチンであり、オミクロン株などのスパイク変異株の出現によりワクチンの予防効果が大きく減弱した。オミクロン株の大流行に合わせ新規変異株用のワクチンも開発されたもののさらなる変異株の出現が懸念されている。
    どのような新規変異株を出現しうるかを事前に予測できる技術の開発が待望される。
    本物の新型コロナウイルスを用いて新規変異の誘導を行うような研究もあるが、本物のコロナウイルス変異株を扱う研究の危険性もあり、より安全な実験系の開発が必要とされる。

    ●研究方法
    水疱性口内炎ウイルス(vesicular stomatitis virus: VSV)というヒトには病原性がほとんどないウイルスを元に新型コロナウイルスのスパイクタンパク質を発現するように改変を試みる。具体的にはVSVの表面蛋白質部分をコロナウイルスのスパイクと組換え、また、安全性をさらに高めるためウイルスの増殖に必須のタンパク質をウイルスから除去し、外部供給という形で補充することで特定の環境下でのみ増殖する限定増殖型のウイルスとする。
    作り出したウイルスを利用して、ワクチン後血清からの逃避変異株の取得を試みることでどのような変異がワクチン後免疫で抑制しにくいかを解析するよていである。

    ●期待される成果
    ワクチン耐性の変異株を先回りで予測することが期待でき、サーベイランスの改善や新規ワクチン株の効果的な選定に繋がることが期待できる。

  • Prediction of the vaccine escape SARS-CoV2 mutants

    Grant number:2 2 K 2 0 7 7 3  2022 - 2023

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Research Activity start-up

    ikegame satoshi

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    Authorship:Principal investigator  Grant type:Scientific research funding

    I modified vesicular stomatitis virus (VSV) so that VSV express spike of SARS-CoV-2. I made modification in VSV so that VSV can only grow in special cell lines to make virus safe. I generated the cells which can allow replication of VSV expressing spike. I checked the neutralization activity of serum after vaccination and trying to acquire vaccine escape mutants.
    I was unable to introduce mutation at first attempt, so I am now trying to change the condition of culture and serum dilution. I will try to start mutant selection using new culture condition and serum dilution.

    CiNii Research

  • SARS-CoV-2 Spikeタンパク質研究のための限定増殖型組換えウイルスの開発

    2022 - 2023

    Grants-in-Aid for Scientific Research  科学技術研究助成 (柿原科学技術研究財団)

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    Authorship:Principal investigator  Grant type:Competitive funding other than Grants-in-Aid for Scientific Research

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Educational Activities

  • 医学部学生の講義(呼吸器感染症、胸部診察手技)、医学部学生の臨床実習指導、初期臨床研修医への指導、大学院生の研究指導等に従事しております。

Class subject

  • 3学年系統医学Ⅱ・呼吸器

    2024.8 - 2024.10  

  • 臨床医学Ⅲ-②

    2024.4 - 2024.9   First semester

  • 3学年系統医学Ⅱ・呼吸器

    2023.10 - 2024.3   Second semester

  • 臨床医学Ⅲ-②

    2023.4 - 2023.9   First semester

  • 3学年系統医学Ⅱ・呼吸器

    2022.10 - 2023.3   Second semester

  • 臨床医学Ⅲ-②

    2022.4 - 2022.9   First semester

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Specialized clinical area

  • Biology / Medicine, Dentistry and Pharmacy / Internal Medicine / Respiratory Medicine

Clinician qualification

  • Specialist

    The Japanese Respiratory Society

  • Preceptor

    The Japanese Respiratory Society

  • Specialist

    The Japanese Society of Internal Medicine(JSIM)

  • Preceptor

    The Japanese Society of Internal Medicine(JSIM)

  • Specialist

    The Japan Society for Respiratory Endoscopy(JSRE)

  • Preceptor

    The Japan Society for Respiratory Endoscopy(JSRE)

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Year of medical license acquisition

  • 2002