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Lancet. 2015 Feb 7;385(9967):517-528. doi: 10.1016/S0140-6736(14)61403-3. Epub 2014 Oct 13.
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Chimeric antigen receptor T cells for sustained remissions in leukemia.用于白血病持续缓解的嵌合抗原受体T细胞。
N Engl J Med. 2014 Oct 16;371(16):1507-17. doi: 10.1056/NEJMoa1407222.
3
TNF-receptor inhibitor therapy for the treatment of children with idiopathic pneumonia syndrome. A joint Pediatric Blood and Marrow Transplant Consortium and Children's Oncology Group Study (ASCT0521).肿瘤坏死因子受体抑制剂治疗儿童特发性肺炎综合征。儿科血液与骨髓移植联合会和儿童肿瘤学组联合研究(ASCT0521)。
Biol Blood Marrow Transplant. 2015 Jan;21(1):67-73. doi: 10.1016/j.bbmt.2014.09.019. Epub 2014 Sep 28.
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Current concepts in the diagnosis and management of cytokine release syndrome.细胞因子释放综合征的诊断和治疗的当前概念。
Blood. 2014 Jul 10;124(2):188-95. doi: 10.1182/blood-2014-05-552729. Epub 2014 May 29.
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Managing cytokine release syndrome associated with novel T cell-engaging therapies.管理与新型T细胞接合疗法相关的细胞因子释放综合征。
Cancer J. 2014 Mar-Apr;20(2):119-22. doi: 10.1097/PPO.0000000000000035.
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Randomized, double-blind, placebo-controlled trial of soluble tumor necrosis factor receptor: enbrel (etanercept) for the treatment of idiopathic pneumonia syndrome after allogeneic stem cell transplantation: blood and marrow transplant clinical trials network protocol.可溶性肿瘤坏死因子受体:恩利(依那西普)治疗异基因干细胞移植后特发性肺炎综合征的随机、双盲、安慰剂对照试验:血液和骨髓移植临床试验网络方案
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Blood. 2014 Apr 24;123(17):2625-35. doi: 10.1182/blood-2013-11-492231. Epub 2014 Feb 27.
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急性淋巴细胞白血病的T细胞疗法进展

Advances in T-cell therapy for ALL.

作者信息

Grupp Stephan A

机构信息

Perelman School of Medicine, University of Pennsylvania, USA; Center for Childhood Cancer Research, Children's Hospital of Philadelphia, USA.

出版信息

Best Pract Res Clin Haematol. 2014 Sep-Dec;27(3-4):222-8. doi: 10.1016/j.beha.2014.10.014. Epub 2014 Oct 27.

DOI:10.1016/j.beha.2014.10.014
PMID:25455270
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4277205/
Abstract

CD19-directed chimeric antigen receptor T cells (CART19 or CTL019) have been used with success in pediatric and adult acute lymphocytic leukemia (ALL) and chronic lymphocytic leukemia (CLL) patients. While this therapy has caused toxicities, including cytokine release syndrome and macrophage activation syndrome, these conditions are reversible with IL-6 blockade using the monoclonal antibody tocilizumab. Furthermore, 90% of the very high-risk patients who underwent infusion with CTL019 achieved a complete response, despite the fact that they previously failed multiple therapies and/or transplant. With improved cell persistence, this immunotherapy may one day prove to be more than a bridge to transplant and may in fact be a transplant alternative.

摘要

靶向CD19的嵌合抗原受体T细胞(CART19或CTL019)已成功用于儿科和成人急性淋巴细胞白血病(ALL)及慢性淋巴细胞白血病(CLL)患者。虽然这种疗法会引发毒性反应,包括细胞因子释放综合征和巨噬细胞活化综合征,但使用单克隆抗体托珠单抗进行IL-6阻断可使这些情况逆转。此外,尽管90%接受CTL019输注的极高危患者此前曾多次治疗和/或移植失败,但仍实现了完全缓解。随着细胞持久性的改善,这种免疫疗法有朝一日可能不仅仅是移植的桥梁,实际上可能成为移植的替代方案。