噬血细胞性淋巴组织细胞增生症诊断和治疗的进展

吴聪, 郭涛. 噬血细胞性淋巴组织细胞增生症诊断和治疗的进展[J]. 临床血液学杂志, 2025, 38(1): 41-46. doi: 10.13201/j.issn.1004-2806.2025.01.008
引用本文: 吴聪, 郭涛. 噬血细胞性淋巴组织细胞增生症诊断和治疗的进展[J]. 临床血液学杂志, 2025, 38(1): 41-46. doi: 10.13201/j.issn.1004-2806.2025.01.008
WU Cong, GUO Tao. Progress in diagnosis and treatment of hemophagocytic lymphohistiocytosis[J]. J Clin Hematol, 2025, 38(1): 41-46. doi: 10.13201/j.issn.1004-2806.2025.01.008
Citation: WU Cong, GUO Tao. Progress in diagnosis and treatment of hemophagocytic lymphohistiocytosis[J]. J Clin Hematol, 2025, 38(1): 41-46. doi: 10.13201/j.issn.1004-2806.2025.01.008

噬血细胞性淋巴组织细胞增生症诊断和治疗的进展

详细信息
    作者简介:

    郭涛,华中科技大学同济医学院附属协和医院血液科主任医师、博士生导师。担任中国医师协会血液科医师分会委员,海峡两岸医药卫生交流协会血液病学专业委员会副主任委员,武汉血液学会主任委员,中国研究型医院协会生物治疗学组常务委员。《临床血液学杂志》《血栓与止血学》《国际输血及血液学杂志》及《临床急诊杂志》编委。湖北省噬血细胞综合征专家联盟理事长。

    通讯作者: 郭涛,E-mail:guotao1968@163.com
  • 中图分类号: R55

Progress in diagnosis and treatment of hemophagocytic lymphohistiocytosis

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  • 噬血细胞性淋巴组织细胞增生症(hemophagocytic lymphohistiocytosis,HLH),又称噬血细胞综合征(hemophagocytic syndrome,HPS),是一种以免疫系统过度激活为特征的免疫失调综合征,由于T淋巴细胞、巨噬细胞和自然杀伤(NK)细胞无法控制的过度激活从而产生大量的细胞因子,进而引发多器官功能损伤、衰竭甚至死亡。目前,多部国内外指南或共识对HLH的诊断治疗和监测提出了原则性和针对性的指导意见。本文将结合目前国内外的指南、专家共识及现有的研究证据,对HLH诊断和治疗及其进展作一总结。
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  • [1]

    Grom AA, Horne A, De Benedetti F. Macrophage activation syndrome in the era of biologic therapy[J]. Nat Rev Rheumatol, 2016, 12(5): 259-268. doi: 10.1038/nrrheum.2015.179

    [2]

    Al-Samkari H, Berliner N. Hemophagocytic Lymphohistiocytosis[J]. Annu Rev Pathol, 2018, 13: 27-49. doi: 10.1146/annurev-pathol-020117-043625

    [3]

    Sandler RD, Tattersall RS, Schoemans H, et al. Diagnosis and Management of Secondary HLH/MAS Following HSCT and CAR-T Cell Therapy in Adults; A Review of the Literature and a Survey of Practice Within EBMT Centres on Behalf of the Autoimmune Diseases Working Party(ADWP)and Transplant Complications Working Party(TCWP)[J]. Front Immunol, 2020, 11: 524. doi: 10.3389/fimmu.2020.00524

    [4]

    中国医师协会血液科医师分会, 中华医学会儿科学分会血液学组, 噬血细胞综合征中国专家联盟. 中国噬血细胞综合征诊断与治疗指南(2022年版)[J]. 中华医学杂志, 2022, 102(20): 1492-1499. doi: 10.3760/cma.j.cn112137-20220310-00488

    [5]

    Henter JI, Elinder G, Ost A. Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society[J]. Semin Oncol, 1991, 18(1): 29-33.

    [6]

    Henter JI, Aricò M, Egeler RM, et al. HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society[J]. Med Pediatr Oncol, 1997, 28(5): 342-347. doi: 10.1002/(SICI)1096-911X(199705)28:5<342::AID-MPO3>3.0.CO;2-H

    [7]

    Henter JI, Horne A, Aricó M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis[J]. Pediatr Blood Cancer, 2007, 48(2): 124-131. doi: 10.1002/pbc.21039

    [8]

    Janka GE. Hemophagocytic syndromes[J]. Blood Rev, 2007, 21(5): 245-253. doi: 10.1016/j.blre.2007.05.001

    [9]

    Trottestam H, Horne A, Aricò M, et al. Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol[J]. Blood, 2011, 118(17): 4577-4584. doi: 10.1182/blood-2011-06-356261

    [10]

    Bergsten E, Horne A, Aricó M, et al. Confirmed efficacy of etoposide and dexamethasone in HLH treatment: long-term results of the cooperative HLH-2004 study[J]. Blood, 2017, 130(25): 2728-2738. doi: 10.1182/blood-2017-06-788349

    [11]

    La Rosée P, Horne A, Hines M, et al. Recommendations for the management of hemophagocytic lymphohistiocytosis in adults[J]. Blood, 2019, 133(23): 2465-2477. doi: 10.1182/blood.2018894618

    [12]

    吴小艳, 王琳, 陈鸿博. 噬血细胞综合征研究进展[J]. 中华实用儿科临床杂志, 2020, 35(15): 1125-1129. doi: 10.3760/cma.j.cn101070-20200715-01182

    [13]

    Lee JC, Logan AC. Diagnosis and Management of Adult Malignancy-Associated Hemophagocytic Lymphohistiocytosis[J]. Cancers(Basel), 2023, 15(6): 1839.

    [14]

    Rosado FG, Gopal P. Laboratory Features and Pathology of Cytokine Storm Syndromes[J]. Adv Exp Med Biol, 2024, 1448: 43-58.

    [15]

    Fatma A, Raida BS, Mourad C, et al. Performances of the H-score and the HLH-2004 score in the positive diagnosis of secondary hemophagocytic lymphohistiocytosis[J]. Curr Res Transl Med, 2024, 72(2): 103430. doi: 10.1016/j.retram.2023.103430

    [16]

    Fardet L, Galicier L, Lambotte O, et al. Development and validation of the HScore, a score for the diagnosis of reactive hemophagocytic syndrome[J]. Arthritis Rheumatol, 2014, 66(9): 2613-2620. doi: 10.1002/art.38690

    [17]

    Debaugnies F, Mahadeb B, Ferster A, et al. Performances of the H-Score for Diagnosis of Hemophagocytic Lymphohistiocytosis in Adult and Pediatric Patients[J]. Am J Clin Pathol, 2016, 145(6): 862-870. doi: 10.1093/ajcp/aqw076

    [18]

    王昭, 王晶石. 成人噬血细胞综合征诊断与治疗进展[J]. 临床血液学杂志, 2022, 35(1): 1-5. https://lcxy.whuhzzs.com/article/doi/10.13201/j.issn.1004-2806.2022.01.001

    [19]

    Zoref-Lorenz A, Murakami J, Hofstetter L, et al. An improved index for diagnosis and mortality prediction in malignancy-associated hemophagocytic lymphohistiocytosis[J]. Blood, 2022, 139(7): 1098-1110. doi: 10.1182/blood.2021012764

    [20]

    La Rosée P. Detecting HLH in hematologic malignancies[J]. Blood, 2022, 139(7): 961-963. doi: 10.1182/blood.2021014675

    [21]

    王迁, 王旖旎, 王嫱, 等. 风湿性疾病相关噬血细胞综合征诊疗规范[J]. 中华内科杂志, 2023, 62(1): 23-30. doi: 10.3760/cma.j.cn112138-20221010-00749

    [22]

    Ravelli A, Minoia F, Davì S, et al. 2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative[J]. Arthritis Rheumatol, 2016, 68(3): 566-576. doi: 10.1002/art.39332

    [23]

    Rubin TS, Zhang K, Gifford C, et al. Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH[J]. Blood, 2017, 129(22): 2993-2999. doi: 10.1182/blood-2016-12-753830

    [24]

    Xu XJ, Tang YM. Dilemmas in diagnosis and management of hemophagocytic lymphohistiocytosis in children[J]. World J Pediatr, 2020, 16(4): 333-340. doi: 10.1007/s12519-019-00299-3

    [25]

    Xu XJ, Luo ZB, Song H, et al. Simple Evaluation of Clinical Situation and Subtypes of Pediatric Hemophagocytic Lymphohistiocytosis by Cytokine Patterns[J]. Front Immunol, 2022, 13: 850443. doi: 10.3389/fimmu.2022.850443

    [26]

    Yuan S, Wang Y, Luo H, et al. Serum soluble VSIG4 as a surrogate marker for the diagnosis of lymphoma-associated hemophagocytic lymphohistiocytosis[J]. Br J Haematol, 2020, 189(1): 72-83. doi: 10.1111/bjh.16299

    [27]

    Sadaat M, Jang S. Hemophagocytic lymphohistiocytosis with immunotherapy: brief review and case report[J]. J Immunother Cancer, 2018, 6(1): 49. doi: 10.1186/s40425-018-0365-3

    [28]

    Wang Y, Huang W, Hu L, et al. Multicenter study of combination DEP regimen as a salvage therapy for adult refractory hemophagocytic lymphohistiocytosis[J]. Blood, 2015, 126(19): 2186-2192. doi: 10.1182/blood-2015-05-644914

    [29]

    Wang J, Wang Y, Wu L, et al. PEG-aspargase and DEP regimen combination therapy for refractory Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis[J]. J Hematol Oncol, 2016, 9(1): 84. doi: 10.1186/s13045-016-0317-7

    [30]

    Marsh RA. Salvage Therapy and Allogeneic Hematopoietic Cell Transplantation for the Severe Cytokine Storm Syndrome of Hemophagocytic Lymphohistiocytosis[J]. Adv Exp Med Biol, 2024, 1448: 611-622.

    [31]

    Horne A, Wickström R, Jordan MB, et al. How to Treat Involvement of the Central Nervous System in Hemophagocytic Lymphohistiocytosis?[J]. Curr Treat Options Neurol, 2017, 19(1): 3. doi: 10.1007/s11940-017-0439-4

    [32]

    Lounder DT, Khandelwal P, Chandra S, et al. Incidence and Outcomes of Central Nervous System Hemophagocytic Lymphohistiocytosis Relapse after Reduced-Intensity Conditioning Hematopoietic Stem Cell Transplantation[J]. Biol Blood Marrow Transplant, 2017, 23(5): 857-860. doi: 10.1016/j.bbmt.2017.02.011

    [33]

    Ehl S, Astigarraga I, von Bahr Greenwood T, et al. Recommendations for the Use of Etoposide-Based Therapy and Bone Marrow Transplantation for the Treatment of HLH: Consensus Statements by the HLH Steering Committee of the Histiocyte Society[J]. J Allergy Clin Immunol Pract, 2018, 6(5): 1508-1517. doi: 10.1016/j.jaip.2018.05.031

    [34]

    Jesudas R, Nichols KE. Recent advances in the treatment of hemophagocytic lymphohistiocytosis and macrophage activation syndrome[J]. Curr Opin Allergy Clin Immunol, 2022, 22(6): 364-370. doi: 10.1097/ACI.0000000000000865

    [35]

    Locatelli F, Jordan MB, Allen C, et al. Emapalumab in Children with Primary Hemophagocytic Lymphohistiocytosis[J]. N Engl J Med, 2020, 382(19): 1811-1822. doi: 10.1056/NEJMoa1911326

    [36]

    Albeituni S, Verbist KC, Tedrick PE, et al. Mechanisms of action of ruxolitinib in murine models of hemophagocytic lymphohistiocytosis[J]. Blood, 2019, 134(2): 147-159. doi: 10.1182/blood.2019000761

    [37]

    Keenan C, Nichols KE, Albeituni S. Use of the JAK Inhibitor Ruxolitinib in the Treatment of Hemophagocytic Lymphohistiocytosis[J]. Front Immunol, 2021, 12: 614704. doi: 10.3389/fimmu.2021.614704

    [38]

    Charlesworth JEG, Kavirayani A. Intravenous anakinra for the treatment of haemophagocytic lymphohistiocytosis/macrophage activation syndrome: A systematic review[J]. Eur J Haematol, 2023, 111(3): 458-476. doi: 10.1111/ejh.14029

    [39]

    Mehta P, Cron RQ, Hartwell J, et al. Silencing the cytokine storm: the use of intravenous anakinra in haemophagocytic lymphohistiocytosis or macrophage activation syndrome[J]. Lancet Rheumatol, 2020, 2(6): e358-e367. doi: 10.1016/S2665-9913(20)30096-5

    [40]

    Ghuman A, Kumar K, Singh A. The use of intravenous anakinra in the treatment of secondary haemophagocytic lymphohistiocytosis(HLH): a case series[J]. Rheumatology, 2019, 58(Supplement_3): kez110.046. doi: 10.1093/rheumatology/kez110.046

    [41]

    Eloseily EM, Weiser P, Crayne CB, et al. Benefit of Anakinra in Treating Pediatric Secondary Hemophagocytic Lymphohistiocytosis[J]. Arthritis Rheumatol, 2020, 72(2): 326-334. doi: 10.1002/art.41103

    [42]

    Dufranc E, Del Bello A, Belliere J, et al. IL6-R blocking with tocilizumab in critically ill patients with hemophagocytic syndrome[J]. Crit Care, 2020, 24(1): 166. doi: 10.1186/s13054-020-02878-7

    [43]

    Kim JY, Kim M, Park JK, et al. Limited efficacy of tocilizumab in adult patients with secondary hemophagocytic lymphohistiocytosis: a retrospective cohort study[J]. Orphanet J Rare Dis, 2022, 17(1): 363. doi: 10.1186/s13023-022-02516-1

    [44]

    Geerlinks AV, Dvorak AM. A Case of XIAP Deficiency Successfully Managed with Tadekinig Alfa(rhIL-18BP)[J]. J Clin Immunol, 2022, 42(4): 901-903. doi: 10.1007/s10875-022-01236-2

    [45]

    Liu P, Pan X, Chen C, et al. Nivolumab treatment of relapsed/refractory Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in adults[J]. Blood, 2020, 135(11): 826-833. doi: 10.1182/blood.2019003886

    [46]

    Rajapakse P, Andanamala H. Hemophagocytic Lymphohistiocytosis Secondary to Immune Checkpoint Inhibitor Therapy[J]. World J Oncol, 2022, 13(2): 49-52. doi: 10.14740/wjon1464

    [47]

    Marsh RA, Allen CE, McClain KL, et al. Salvage therapy of refractory hemophagocytic lymphohistiocytosis with alemtuzumab[J]. Pediatr Blood Cancer, 2013, 60(1): 101-109. doi: 10.1002/pbc.24188

    [48]

    Dettmer-Monaco V, Weißert K, Ammann S, et al. Gene editing of hematopoietic stem cells restores T-cell response in familial hemophagocytic lymphohistiocytosis[J]. J Allergy Clin Immunol, 2024, 153(1): 243-255. e14. doi: 10.1016/j.jaci.2023.08.003

    [49]

    Weißert K, Ammann S, Kögl T, et al. Adoptive T cell therapy cures mice from active hemophagocytic lymphohistiocytosis(HLH)[J]. EMBO Mol Med, 2022, 14(12): e16085. doi: 10.15252/emmm.202216085

    [50]

    Li X, Wirtz T, Weber T, et al. Precise CRISPR-Cas9 gene repair in autologous memory T cells to treat familial hemophagocytic lymphohistiocytosis[J]. Sci Immunol, 2024, 9(92): eadi0042. doi: 10.1126/sciimmunol.adi0042

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出版历程
收稿日期:  2024-11-30
刊出日期:  2025-01-01

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