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流式细胞术在噬血细胞综合征诊断中的应用进展 被引量:1

Advances in the application of flow cytometry in the diagnosis of hemophagocytic syndrome
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摘要 噬血细胞性淋巴组织细胞增多症(Hemophagocytic lymphohistiocytosis,HLH)是一种以免疫系统过度激活,导致炎性细胞因子分泌过多为特征的综合征。患者通常表现为高热、细胞减少、高铁蛋白血症和肝脾肿大。其疾病过程从轻度到致命的多器官衰竭不等,该病进展迅速,且容易误诊,病死率高。对该疾病的早期认识和及时诊治有助于预防致命的后果。现行的HLH诊治中国专家共识中,对于最后2个标准[即sIL-2受体和自然杀伤(natural killer,NK)细胞活性]的测定,流式细胞术发挥着重要作用。近年来,利用流式细胞术检测潜在生物标志物为HLH的诊断开辟了新的途径。本综述将围绕流式细胞术在其中的应用展开对该疾病的一些思考。 Hemophagocytic lymphohistiocytosis(HLH)is a syndrome characterized by excessive secretion of inflammatory cytokines due to excessive activation of the immune system.Patients usually present hyperpyrexia,cell loss,methemoglobinemia and hepatosplenomegaly.The course of the disease ranges from mild to fatal multiple organ failure.With high mortality,the disease progresses rapidly and is easily misdiagnosed.Early recognition and timely diagnosis and treatment of the disease are helpful to prevent fatal consequences.In the current consensus of Chinese experts on HLH diagnosis and treatment,flow cytometry plays an important role in the determination of the last two criteria[sIL-2 receptor and natural killer(NK)cell activity].In recent years,the detection of potential biomarkers by flow cytometry has opened up a new way for the diagnosis of HLH.This review will focus on the application of flow cytometry to the disease.
作者 杨雨宇 杨金荣(综述) 曾云 武坤(审校) YANG Yuyu;YANG Jinrong;ZENG Yun;WU Kun(Department of Hematology,First Affiliated Hospital of Kunming Medical University/Yunnan Blood Disease Research Center,Kunming 650032,China)
出处 《临床与病理杂志》 CAS 2021年第4期942-947,共6页 Journal of Clinical and Pathological Research
基金 云南省教育厅科学研究基金(2020J0172)。
关键词 噬血细胞性淋巴组织细胞增多症 流式细胞术 可溶性白细胞介素-2受体 自然杀伤细胞活性 生物标志物 hemophagocytic lymphohistiocytosis flow cytometry soluble interleukin-2 receptor natural killer cell activity biomarkers
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  • 1Henter JI, Elinder G, Soder O, et al. Hypercytokinemia in familial hemophagocytic lymphohistiocytosis. Blood, 1991,78 : 2918-2922.
  • 2Osugi Y, Hara J, Tagawa S, et al. Cytokine production regulating Thl and Th2 cytokines in hemophagocytic lymphohistiocytosis. Blood, 1997,89:4100-4103.
  • 3Tang Y, Xu X, Song H, et al. Early diagnostic and prognostic significance of a specific Thl/Th2 cytokine pattern in children with haemophagocytic syndrome. Br J Haematol, 2008,143:84-91.
  • 4Henter JI,Elinder G,Ost A. Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society. Semin Oncol, 1991,18:29-33.
  • 5Henter JI, Horne A, Arico M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer, 2007,48 : 124-131.
  • 6Henter JI, Arico M, Egeler RM, et al. HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society. Med Pediatr Oncol, 1997,28:342-347.
  • 7Palazzi DL, McClain KL, Kaplan SL. Hemophagocytic syndrome in children: an important diagnostic consideration in fever of unknown origin. Clin Infect Dis, 2003,36:306-312.
  • 8Castillo L, Carcillo J. Secondary hemophagocytic lymphohistiocytosis and severe sepsis/ systemic inflammatory response syndrome/ multiorgan dysfunction syndrome/macrophage activation syndrome share common intermediate phenotypes on a spectrum of inflammation. Pediatr Crit Care Med, 2009,10:387-392.
  • 9Tang Y, Xu X. Advances in hemophagocytic lymphohistiocytosis: pathogenesis, early diagnosis/differential diagnosis, and treatment. Scientific World J, 2011, 11 : 697-708.
  • 10Paehlopnik SJ, Ho CH, Chretien F, et al. Neutralization of IFNgamma defeats haemophagocytosis in LCMV-infected perforin- and Rab27a-deficient mice. EMBO Mol Med, 2009,1 : 112-124.

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