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在异基因造血干细胞移植后发生腺病毒相关呼吸衰竭的患儿中,于体外膜肺氧合(ECMO)期间采用抗原特异性 T 细胞过继免疫疗法。

Adoptive immunotherapy with antigen-specific T cells during extracorporeal membrane oxygenation (ECMO) for adenovirus-related respiratory failure in a child given haploidentical stem cell transplantation.

机构信息

Department of Pediatric Intensive Care, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.

出版信息

Pediatr Blood Cancer. 2014 Feb;61(2):376-9. doi: 10.1002/pbc.24753. Epub 2013 Aug 26.

DOI:10.1002/pbc.24753
PMID:24039155
Abstract

We report on the successful infusion of human adenovirus (HAdV)-specific T cells in a child with congenital amegakaryocytic thrombocytopenia, given T-cell-depleted hematopoietic stem cell transplantation (HSCT) from the HLA-haploidentical mother during extracorporeal membrane oxygenation (ECMO) for severe HAdV-related respiratory failure. Donor-derived, interferon (IFN)-γ-secreting HAdV-specific T cells were enriched using the cytokine capture assay, after in vitro stimulation with overlapping peptides from the immunodominant HAdV5 hexon protein. Two weeks after T-cell transfer, viral load decreased and ECMO was discontinued. T-cell responses to HAdV antigens were documented after four weeks and were associated with viral clearance, immune reconstitution and clinical amelioration.

摘要

我们报告了一例成功输注人腺病毒(HAdV)特异性 T 细胞的病例,该患者因严重 HAdV 相关呼吸衰竭在体外膜氧合(ECMO)期间接受了 HLA 单倍体相合母亲来源的 T 细胞耗竭的造血干细胞移植(HSCT)。在体外用免疫优势 HAdV5 六邻体蛋白的重叠肽刺激后,使用细胞因子捕获测定法对供体来源的 IFN-γ 分泌 HAdV 特异性 T 细胞进行了富集。T 细胞转移后两周,病毒载量下降,ECMO 停止。在四周后记录到针对 HAdV 抗原的 T 细胞反应,并与病毒清除、免疫重建和临床改善相关。

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Adoptive immunotherapy with antigen-specific T cells during extracorporeal membrane oxygenation (ECMO) for adenovirus-related respiratory failure in a child given haploidentical stem cell transplantation.在异基因造血干细胞移植后发生腺病毒相关呼吸衰竭的患儿中,于体外膜肺氧合(ECMO)期间采用抗原特异性 T 细胞过继免疫疗法。
Pediatr Blood Cancer. 2014 Feb;61(2):376-9. doi: 10.1002/pbc.24753. Epub 2013 Aug 26.
2
Clinical grade generation of hexon-specific T cells for adoptive T-cell transfer as a treatment of adenovirus infection after allogeneic stem cell transplantation.用于过继性T细胞转移的六邻体特异性T细胞的临床级生成,作为异基因干细胞移植后腺病毒感染的一种治疗方法。
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T-cell lines specific for peptides of adenovirus hexon protein and devoid of alloreactivity against recipient cells can be obtained from HLA-haploidentical donors.可从HLA单倍型相同的供体获得对腺病毒六邻体蛋白肽具有特异性且对受体细胞无同种异体反应性的T细胞系。
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