病態システム解析医学分野

Ito Hiroyasu

  (伊藤 弘康)

Profile Information

Affiliation
Fujita Health University
Degree
医学博士(岐阜大学)

Researcher number
80373075
J-GLOBAL ID
201601000738827795
researchmap Member ID
7000014447

近年、Toll用受容体のリガンドやNKT細胞の活性化分子などが同定され、宿主免疫系の修飾により様々な疾患に応用されつつある。また、免疫チェックポイント分子の同定も盛んに行われており、特に癌への治療応用が期待さえている。現在、このような免疫修飾技術を持ちいて、1)完全ウイルス排除を目指したHBV感染症治療法の開発、2)癌免疫療法の開発、3)臓器再生(肝再生・皮膚創傷治癒など)方法の確立に向けて基礎的実験を行っている。

Research History

 11

Education

 1

Papers

 229
  • Kouhei Sakurai, Tatsuya Ando, Yasuhiro Sakai, Yuichiro Mori, Satoru Nakamura, Taku Kato, Hiroyasu Ito
    Human cell, 37(5) 1559-1566, Sep, 2024  
    Lung neuroendocrine neoplasms (NENs) are a diverse group of tumors characterized by neuroendocrine (NE) differentiation. Among lung NENs, lung carcinoid (LC) is a rare tumor with unique characteristics. Recent research has highlighted the importance of transcription factors (TFs) in establishing gene expression programs in lung NENs such as small cell lung carcinoma. However, the TFs that control the gene expression of LC are largely unknown. In this study, we report the expression and potential function of a TF called Prospero homeobox protein1 (PROX1) in LC. Publicly available transcriptome data suggested that PROX1 was highly expressed in LC tissues, which was confirmed by immunohistochemical analysis on a tissue microarray. Knockdown of PROX1 did not impact the cellular viability of an LC-derived cell line, NCI-H727. Meanwhile, transcriptome analysis revealed that PROX1 knockdown altered the expression of genes involved in NE differentiation. ASCL1, CHGA, CALCA, and LINC00261 were suggested as downstream genes of PROX1. These findings indicate that PROX1 may play an important role in the NE identity of LC by regulating the expression of key target genes.
  • 東本 祐紀, 古川 源, 河村 吉紀, 小澤 慶, 三浦 浩樹, 井平 勝, 伊藤 弘康, 吉川 哲史
    日本臨床微生物学会雑誌, 34(Suppl.1) 293-293, Dec, 2023  
  • 中森 恵, 渡邉 恒夫, 中山 純里, 高田 彩永, 関根 綾子, 野久 謙, 池田 貴英, 森田 浩之, 伊藤 弘康
    日本臨床検査医学会誌, 71(10) 677-683, Oct, 2023  
    2018年2月~11月に当院生理検査室で滑膜炎評価目的に関節超音波検査を行ったRA患者31例を対象とし、血中IGF-1値とサルコペニア罹患率を調べ、コントロール群(RAや悪性腫瘍を患っていない65歳以上の患者27例)と比較検討した。結果、血中IGF-1値はコントロール群によりも有意に高く、サルコペニア罹患率もコントロール群に比べて有意に高かった。サルコペニア罹患の有無と血中IGF-1値との関係について検討した結果、両群ともサルコペニアに罹患しているグループの血中IGF-1は非罹患グループに比べて有意に低値であった。RA患者のみを対象とし、DAS28-CRPが2.3未満の群(13例)と2.3以上の群(18例)に分けてサルコペニア罹患率を比較したところ、2.3以上群が有意に高かった。
  • 中森 恵, 渡邉 恒夫, 中山 純里, 高田 彩永, 関根 綾子, 野久 謙, 池田 貴英, 森田 浩之, 伊藤 弘康
    日本臨床検査医学会誌, 71(10) 677-683, Oct, 2023  
  • Hiroya Menjo, Midori Hasegawa, Hidetsugu Fujigaki, Takuma Ishihara, Shun Minatoguchi, Shigehisa Koide, Hiroki Hayashi, Midori Saito, Kazuo Takahashi, Hiroyasu Ito, Yukio Yuzawa, Kuniaki Saito, Naotake Tsuboi
    Internal medicine (Tokyo, Japan), Sep 29, 2023  
    Objective The objective of this study was to estimate the humoral immune response evaluated by immunoglobulin G (IgG) against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike receptor-binding domain (RBD-IgG) following the third mRNA COVID-19 vaccination in patients with kidney disease who received immunosuppressive treatment. Methods The primary outcome was RBD-IgG levels after the third SARS-CoV-2 vaccination. The primary comparison was the RBD-IgG levels between patients with kidney disease who received immunosuppressive treatment (n=124) and those who did not (n=33). Results The RBD-IgG levels were significantly lower in the patients with kidney disease who received immunosuppressive treatment than in those who did not receive immunosuppressive treatment. The RBD-IgG levels were lower in patients treated with glucocorticoid monotherapy than in those who did not receive immunosuppressive treatment. Even in patients who received ≤ 5 mg prednisolone, the RBD-IgG levels were significantly lower. Nine of the 10 patients who received rituximab within one year before the first vaccination did not experience seroconversion after the third vaccination. Meanwhile, all nine patients who received rituximab only after the second vaccination experienced seroconversion, even if B cell recovery was insufficient. Patients treated with mycophenolate mofetil plus glucocorticoid plus belimumab had significantly lower RBD-IgG levels than those treated with mycophenolate mofetil plus glucocorticoid. Conclusions The RBD-IgG levels were lower in patients with kidney disease who received immunosuppressive treatment than in those who did not receive immunosuppressive treatment. Low-dose glucocorticoid monotherapy affected the humoral immune response following the third mRNA COVID-19 vaccination.

Misc.

 97

Teaching Experience

 1

Research Projects

 19

Social Activities

 1