Molero T, Lemes A, DE LA Iglesia S, Scott C S
Servicio de Hematologia y Hemoterapia, Hospital Universitario de Gran Canaria Dr Negrín, Las Palmas de Gran Canaria, Spain.
Int J Lab Hematol. 2007 Dec;29(6):446-53. doi: 10.1111/j.1751-553X.2007.00934.x.
Using previously described procedures, this study quantified T-cell, T-cell subset, B-cell and NK-cell populations with the CD-Sapphire haematology analyser in a series of patients with mild to moderate lymphocytosis. Lymphocyte counts ranged from 6.0 to 14.9 x 10(9)/l, with 86/97 being <10.0 x 10(9)/l. Immunophenotyping (CD3/CD19/HLA-DR, CD4/CD8 and CD16/CD56 combinations) was performed using EDTA-anticoagulated blood, automated CD-Sapphire analysis and subsequent software processing. Of 35 samples from younger (<12 years) patients, 22 (63%) had nonspecific lymphocyte changes, 4 (11%) showed specific increases in nonreactive T-Helper or T-Suppressor cells, and five showed a reactive T-cell lymphocytosis. The remaining four were classified as 'Transient/Persistent NK-associated (NKa) Expansion' (n = 3) and specific B-cell lymphocytosis (n = 1). For older patients (n = 59), 15 (25%) had an increase (>1.5 x 10(9)/l) in B-cells, and seven investigated for surface immunoglobulin expression were all found to be clonal. The remaining samples were categorized as 'Transient/Persistent NK-associated (NKa) Expansion' (13/59), Reactive Lymphocytosis (5/59), 'Reactive Lymphocytosis or Transient/Persistent NKa Expansion' (8/59), specific T-Helper cell (n = 8) or T-Suppressor cell (n = 3) lymphocytosis, and 'Lymphocytosis of Undetermined Significance' (n = 7). This study has demonstrated the feasibility of applying limited immunophenotyping protocols to the investigation of patients with abnormal lymphocyte counts in routine haematology. By using commercially purchased liquid monoclonal reagents to determine lymphocyte subpopulation profiles, haematology laboratories can provide more definitive information of potential clinical importance.
本研究采用先前描述的方法,使用CD - 蓝宝石血液分析仪对一系列轻至中度淋巴细胞增多症患者的T细胞、T细胞亚群、B细胞和NK细胞群体进行了定量分析。淋巴细胞计数范围为6.0至14.9×10⁹/L,其中86/97例低于10.0×10⁹/L。免疫表型分析(CD3/CD19/HLA - DR、CD4/CD8和CD16/CD56组合)采用乙二胺四乙酸(EDTA)抗凝血液,通过CD - 蓝宝石自动分析及后续软件处理完成。在35例年龄小于12岁患者的样本中,22例(63%)有非特异性淋巴细胞变化,4例(11%)显示非反应性辅助性T细胞或抑制性T细胞特异性增加,5例显示反应性T细胞淋巴细胞增多。其余4例分别归类为“短暂性/持续性NK相关(NKa)扩增”(3例)和特异性B细胞淋巴细胞增多(1例)。对于年龄较大的患者(n = 59),15例(25%)B细胞增多(>1.5×10⁹/L),对7例进行表面免疫球蛋白表达检测的患者均发现为克隆性。其余样本分类为“短暂性/持续性NK相关(NKa)扩增”(13/59)、反应性淋巴细胞增多(5/59)、“反应性淋巴细胞增多或短暂性/持续性NKa扩增”(8/59)、特异性辅助性T细胞(n = 8)或抑制性T细胞(n = 3)淋巴细胞增多以及“意义未明的淋巴细胞增多”(n = 7)。本研究证明了在常规血液学中应用有限免疫表型分析方案来调查淋巴细胞计数异常患者的可行性。通过使用商业购买的液体单克隆试剂来确定淋巴细胞亚群谱,血液学实验室能够提供更具潜在临床重要性的明确信息。