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Large granular lymphocyte disorders: new etiopathogenetic clues as a rationale for innovative therapeutic approaches.大颗粒淋巴细胞疾病:新的发病机制线索为创新治疗方法提供了依据。
Haematologica. 2009 Oct;94(10):1341-5. doi: 10.3324/haematol.2009.012161.
2
Clinical Features, Pathogenesis, and Treatment of Large Granular Lymphocyte Leukemias.大颗粒淋巴细胞白血病的临床特征、发病机制及治疗
Intern Med. 2017;56(14):1759-1769. doi: 10.2169/internalmedicine.56.8881. Epub 2017 Jul 15.
3
Mixed-phenotype large granular lymphocytic leukemia: a rare subtype in the large granular lymphocytic leukemia spectrum.混合表型大颗粒淋巴细胞白血病:大颗粒淋巴细胞白血病谱中的一种罕见亚型。
Hum Pathol. 2018 Nov;81:96-104. doi: 10.1016/j.humpath.2018.06.023. Epub 2018 Jun 24.
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The root of many evils: indolent large granular lymphocyte leukaemia and associated disorders.诸多恶疾之源:惰性大颗粒淋巴细胞白血病及相关疾病。
Hematol Oncol. 2010 Sep;28(3):105-17. doi: 10.1002/hon.917.
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Analysis of a French cohort of patients with large granular lymphocyte leukemia: a report on 229 cases.分析法国大颗粒淋巴细胞白血病患者队列:229 例报告。
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Pathophysiologic mechanisms and management of neutropenia associated with large granular lymphocytic leukemia.大颗粒淋巴细胞白血病相关中性粒细胞减少症的病理生理机制和治疗。
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T Cell Repertoire Analysis as a Molecular Signature of the Spectrum of T-LGL Lymphoproliferative Disorders: Tracing the Literature.T细胞受体谱分析作为T大颗粒淋巴细胞增殖性疾病谱的分子特征:文献追踪
Curr Issues Mol Biol. 2025 Apr 8;47(4):264. doi: 10.3390/cimb47040264.
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Defining TCRγδ lymphoproliferative disorders by combined immunophenotypic and molecular evaluation.通过联合免疫表型和分子评估来定义 TCRγδ 淋巴增殖性疾病。
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Comparison of hematologic abnormalities between hospitalized coronavirus disease 2019 positive and negative patients with correlation to disease severity and outcome.比较住院的 2019 冠状病毒病阳性和阴性患者的血液学异常与疾病严重程度和结局的相关性。
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Neutropenia and Large Granular Lymphocyte Leukemia: From Pathogenesis to Therapeutic Options.中性粒细胞减少症和大颗粒淋巴细胞白血病:从发病机制到治疗选择。
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Blood cell morphology and COVID-19 clinical course, severity, and outcome.血细胞形态与新型冠状病毒肺炎的临床病程、严重程度及预后
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Int J Mol Sci. 2021 Jan 12;22(2):705. doi: 10.3390/ijms22020705.
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Insights Into Genetic Landscape of Large Granular Lymphocyte Leukemia.对大颗粒淋巴细胞白血病基因图谱的见解
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本文引用的文献

1
Therapeutic implications of variable expression of CD52 on clonal cytotoxic T cells in CD8+ large granular lymphocyte leukemia.CD8+ 大颗粒淋巴细胞白血病中克隆性细胞毒性 T 细胞 CD52 可变表达的治疗意义。
Haematologica. 2009 Oct;94(10):1407-14. doi: 10.3324/haematol.2009.009191.
2
Interleukin-15 enhances proteasomal degradation of bid in normal lymphocytes: implications for large granular lymphocyte leukemias.白细胞介素-15增强正常淋巴细胞中Bid的蛋白酶体降解:对大颗粒淋巴细胞白血病的影响。
Cancer Res. 2009 May 1;69(9):3986-94. doi: 10.1158/0008-5472.CAN-08-3735. Epub 2009 Apr 14.
3
TSC-22 contributes to hematopoietic precursor cell proliferation and repopulation and is epigenetically silenced in large granular lymphocyte leukemia.TSC-22促进造血前体细胞增殖和再增殖,并在大颗粒淋巴细胞白血病中发生表观遗传沉默。
Blood. 2009 May 28;113(22):5558-67. doi: 10.1182/blood-2009-02-205732. Epub 2009 Mar 27.
4
Clonal expansion of T/NK-cells during tyrosine kinase inhibitor dasatinib therapy.酪氨酸激酶抑制剂达沙替尼治疗期间T/NK细胞的克隆性扩增。
Leukemia. 2009 Aug;23(8):1398-405. doi: 10.1038/leu.2009.46. Epub 2009 Mar 19.
5
T-cell large granular lymphocyte leukemia associated with myelodysplastic syndrome: a clinicopathologic study of nine cases.与骨髓增生异常综合征相关的T细胞大颗粒淋巴细胞白血病:9例临床病理研究
Am J Clin Pathol. 2009 Mar;131(3):347-56. doi: 10.1309/AJCP6YHI1JEXAWAP.
6
Natural killer or natural killer/T cell lineage large granular lymphocytosis associated with dasatinib therapy for Philadelphia chromosome positive leukemia.与达沙替尼治疗费城染色体阳性白血病相关的自然杀伤细胞或自然杀伤细胞/T细胞系大颗粒淋巴细胞增多症。
Haematologica. 2009 Jan;94(1):135-9. doi: 10.3324/haematol.13151. Epub 2008 Dec 9.
7
Network model of survival signaling in large granular lymphocyte leukemia.大颗粒淋巴细胞白血病生存信号的网络模型
Proc Natl Acad Sci U S A. 2008 Oct 21;105(42):16308-13. doi: 10.1073/pnas.0806447105. Epub 2008 Oct 13.
8
Clinical improvement by farnesyltransferase inhibition in NK large granular lymphocyte leukemia associated with imbalanced NK receptor signaling.法尼基转移酶抑制对与自然杀伤细胞受体信号失衡相关的自然杀伤大颗粒淋巴细胞白血病具有临床改善作用。
Blood. 2008 Dec 1;112(12):4694-8. doi: 10.1182/blood-2008-02-136382. Epub 2008 Sep 12.
9
Expanded cells in monoclonal TCR-alphabeta+/CD4+/NKa+/CD8-/+dim T-LGL lymphocytosis recognize hCMV antigens.单克隆TCR-αβ⁺/CD4⁺/NKa⁺/CD8⁻/⁺dim T-LGL淋巴细胞增多症中扩增的细胞识别hCMV抗原。
Blood. 2008 Dec 1;112(12):4609-16. doi: 10.1182/blood-2008-03-146241. Epub 2008 Sep 2.
10
Long-term responses and outcomes following immunosuppressive therapy in large granular lymphocyte leukemia-associated pure red cell aplasia: a Nationwide Cohort Study in Japan for the PRCA Collaborative Study Group.大颗粒淋巴细胞白血病相关纯红细胞再生障碍性贫血免疫抑制治疗后的长期反应和结局:日本全国性队列研究,PRCA协作研究组
Haematologica. 2008 Oct;93(10):1555-9. doi: 10.3324/haematol.12871. Epub 2008 Jul 18.

大颗粒淋巴细胞疾病:新的发病机制线索为创新治疗方法提供了依据。

Large granular lymphocyte disorders: new etiopathogenetic clues as a rationale for innovative therapeutic approaches.

出版信息

Haematologica. 2009 Oct;94(10):1341-5. doi: 10.3324/haematol.2009.012161.

DOI:10.3324/haematol.2009.012161
PMID:19794080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2754948/
Abstract

The pathogenesis of large granular lymphocytic disorders is now being unravelled. Knowledge of the various cells of origin and the (often viral) drivers of proliferation is emerging. Leukemic transformation involves acquisition of mechanisms to escape death and to continue to proliferate. In this perspective article, Drs. Zambello and Semenzato examine new etiopathogenetic clues as a rationale for innovative therapeutic approaches. See related article on page 1407.

摘要

大颗粒淋巴细胞疾病的发病机制正在被揭示。人们对各种起源细胞以及(通常是病毒)增殖驱动因素的认识正在不断涌现。白血病转化涉及获得逃避死亡和继续增殖的机制。在这篇观点文章中,Zambello 和 Semenzato 博士探讨了新的病因发病学线索,作为创新治疗方法的依据。详见 1407 页相关文章。