使用间充质干细胞成功治疗异体造血细胞移植后类固醇难治性晚发型特发性肺炎综合征。

IF 1.6 4区 医学 Q4 IMMUNOLOGY
Soichiro Nakako , Hideo Koh , Nobuhiro Sogabe , Masatomo Kuno , Yosuke Makuuchi , Teruhito Takakuwa , Hiroshi Okamura , Mitsutaka Nishimoto , Yasuhiro Nakashima , Masayuki Hino , Hirohisa Nakamae
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引用次数: 0

摘要

据报道,晚发性特发性肺炎综合征(IPS)的治疗效果不佳,因此需要新的治疗方法。一名 55 岁的男子一年前因骨髓增生异常综合征接受了异基因造血细胞移植(allo-HCT),在减量服用免疫抑制剂期间出现呼吸困难,并伴有急性皮肤移植物抗宿主病(GVHD)复发。他出现急性呼吸窘迫综合征,右上叶和左下叶出现磨玻璃不透明。所有感染性检查(包括鼻腔清洗液的多重聚合酶链反应)均为阴性,广谱抗生素治疗无效。患者被诊断为晚发性 IPS,甲基强的松龙脉冲疗法无效。随后,他对间质干细胞(MSC)输注产生了良好反应。经过八次间充质干细胞输注后,他在一年多的时间里没有再复发。最近,临床前研究报告了间充质干细胞输注治疗IPS的潜在疗效,我们的病例证实了间充质干细胞输注治疗晚发型IPS的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful treatment with mesenchymal stem cells for steroid-refractory late-onset idiopathic pneumonia syndrome following allogeneic hematopoietic cell transplantation

The reportedly poor outcome of late-onset idiopathic pneumonia syndrome (IPS) necessitates new approaches to its treatment. A 55-year-old man who had undergone allogeneic hematopoietic cell transplantation (allo-HCT) for myelodysplastic syndrome 1 year ago developed dyspnea with acute skin graft-versus-host disease (GVHD) flare-up while tapering immunosuppressive agents. He presented with acute respiratory distress syndrome with ground-glass opacities in the right upper and left lower lobes. All infectious tests, including multiplex polymerase chain reaction of nasal wash, were negative, and broad-spectrum antibiotic therapy was refractory. The patient was diagnosed with late-onset IPS and was refractory to methylprednisolone pulse therapy. He then showed a favorable response to mesenchymal stem cell (MSC) infusion. After eight infusions of MSCs, he had no IPS recurrence for over one year. Recently, preclinical studies have reported the potential therapeutic utility of MSC infusion for treating IPS, and our case supports its potential for treating late-onset IPS.

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来源期刊
Transplant immunology
Transplant immunology 医学-免疫学
CiteScore
2.10
自引率
13.30%
发文量
198
审稿时长
48 days
期刊介绍: Transplant Immunology will publish up-to-date information on all aspects of the broad field it encompasses. The journal will be directed at (basic) scientists, tissue typers, transplant physicians and surgeons, and research and data on all immunological aspects of organ-, tissue- and (haematopoietic) stem cell transplantation are of potential interest to the readers of Transplant Immunology. Original papers, Review articles and Hypotheses will be considered for publication and submitted manuscripts will be rapidly peer-reviewed and published. They will be judged on the basis of scientific merit, originality, timeliness and quality.
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