Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Am J Clin Pathol. 2010 Apr;133(4):592-601. doi: 10.1309/AJCPS1K0OHLJYWWV.
Little information exists regarding the detection of minimal residual disease (MRD) in adult T-cell leukemia/lymphoma (ATLL). We evaluated 75 peripheral blood samples from 17 ATLL cases using flow cytometry (FC); 50 of the samples were concurrently evaluated by polymerase chain reaction (PCR) for clonal T-cell receptor gamma chain (TRG) gene rearrangement and the presence of human T-cell lymphotropic virus-1 proviral sequences. Residual ATLL cells were identified using a multiparametric approach to identify aberrant T-cell immunophenotypes. Malignant T cells were CD4+, CD3 dim+, CD26-, CD25 bright, CD7+, and CD27+, with occasional dim expression of CD2 or CD5. FC exhibited a high sensitivity, detecting as few as 0.29% ATLL cells/WBC (4.9 cells/microL) in the peripheral blood. PCR for TRG gene rearrangement was slightly more sensitive, and FC and PCR complemented each other in detecting MRD. In 2 patients, there was complete remission; 4 patients had disease refractory to therapy, and 3 died; 11 others had persistent disease with variable numbers of ATLL cells in the peripheral blood. Higher levels of ATLL cells appeared to correlate with disease severity. FC detection of aberrant T cells permits sensitive and quantitative monitoring of MRD in ATLL.
成人 T 细胞白血病/淋巴瘤(ATLL)中微小残留病(MRD)的检测信息有限。我们使用流式细胞术(FC)评估了 17 例 ATLL 病例的 75 份外周血样本;其中 50 份样本同时通过聚合酶链反应(PCR)评估克隆 T 细胞受体γ链(TRG)基因重排和人类 T 细胞嗜淋巴细胞病毒-1 前病毒序列的存在。使用多参数方法识别异常 T 细胞免疫表型来识别残留的 ATLL 细胞。恶性 T 细胞呈 CD4+、CD3 弱表达、CD26-、CD25 高表达、CD7+和 CD27+,偶尔 CD2 或 CD5 弱表达。FC 具有很高的灵敏度,在外周血中可检测到低至 0.29%的 ATLL 细胞/WBC(4.9 个细胞/μL)。TRG 基因重排的 PCR 检测略敏感,FC 和 PCR 相互补充以检测 MRD。在 2 例患者中,完全缓解;4 例患者对治疗有抗药性,3 例死亡;其余 11 例患者有持续性疾病,外周血中有不同数量的 ATLL 细胞。较高水平的 ATLL 细胞似乎与疾病严重程度相关。FC 检测异常 T 细胞可敏感且定量监测 ATLL 的 MRD。