Harrington D S
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha.
Am J Clin Pathol. 1990 Apr;93(4 Suppl 1):S38-43.
The advent of monoclonal antibody technology revolutionized the understanding of lymphoid and myeloid differentiation and greatly enhanced the ability to make a more accurate diagnosis. However, certain limitations became evident as monoclonal antibodies were increasingly applied to diagnostic hematologic problems. The T-cell antigens identified by monoclonal antibodies are not true clonal markers. B-cell immunoglobulin light chain restriction is a true clonal marker, but immunoglobulin is not expressed by many B-cell malignancies, diminishing its usefulness as a clonal marker. The development of molecular biologic techniques to augment diagnosis of hematologic neoplasms has revolutionized the understanding of neoplasia. Gene rearrangement analysis yields information concerning clonality and lineage. Gene rearrangement analysis can also identify chromosome breakpoints and translocations that correlate with specific diseases or prognoses. The purpose of this review is to familiarize the reader with the current applications of molecular biology to hematologic processes and to chart future directions of the application of these powerful techniques to diagnostic hematopathology.
单克隆抗体技术的出现彻底改变了对淋巴样和髓样分化的认识,并极大地提高了做出更准确诊断的能力。然而,随着单克隆抗体越来越多地应用于血液学诊断问题,某些局限性变得明显起来。单克隆抗体识别的T细胞抗原并非真正的克隆标志物。B细胞免疫球蛋白轻链限制是一种真正的克隆标志物,但许多B细胞恶性肿瘤并不表达免疫球蛋白,从而降低了其作为克隆标志物的实用性。增强血液肿瘤诊断的分子生物学技术的发展彻底改变了对肿瘤形成的认识。基因重排分析可产生有关克隆性和谱系的信息。基因重排分析还可以识别与特定疾病或预后相关的染色体断点和易位。本综述的目的是使读者熟悉分子生物学在血液学过程中的当前应用,并规划这些强大技术在诊断血液病理学中的未来应用方向。