Thilakaratne Dilini N, Mayer Monique N, MacDonald Valerie S, Jackson Marion L, Trask Brenda R, Kidney Beverly A
Department of Veterinary Pathology, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.
Can Vet J. 2010 Jan;51(1):79-84.
Polymerase chain reaction (PCR) assays for the immunoglobulin and T-cell receptor genes were utilized to determine phenotype and clonality from lymph node cytologic smears and peripheral blood lymphocytes from 10 dogs with lymphoma, before chemotherapy and during remission. Results were compared with those from 13 dogs with a cytologic diagnosis of lymph node hyperplasia. Clonality was identified in 7 of the lymphomas on the basis of either lymph node cytology or peripheral blood lymphocytes before treatment. No lymph node hyperplasia samples were clonal. In 6 of the dogs with lymphoma, clonality was demonstrated during clinical remission. Detection of PCR clonality during clinical remission is an effective means of identifying minimal residual disease in canine lymphoma and thus additional work is warranted to determine if molecular remission is prognostic or predictive for outcome in well-controlled and well-defined lymphoma subtypes.
利用聚合酶链反应(PCR)检测免疫球蛋白和T细胞受体基因,以确定10只淋巴瘤犬化疗前及缓解期淋巴结细胞涂片和外周血淋巴细胞的表型和克隆性。将结果与13只经细胞学诊断为淋巴结增生的犬的结果进行比较。根据治疗前淋巴结细胞学或外周血淋巴细胞,在7只淋巴瘤中鉴定出克隆性。无淋巴结增生样本为克隆性。6只淋巴瘤犬在临床缓解期表现出克隆性。临床缓解期PCR克隆性检测是识别犬淋巴瘤微小残留病的有效手段,因此有必要开展更多工作,以确定分子缓解对控制良好且定义明确的淋巴瘤亚型的预后或结局是否具有预测性。