Bowen D, Williams K, Phillips I, Cavill I
Department of Haematology, University of Wales College of Medicine, Cardiff, UK.
Clin Lab Haematol. 1996 Sep;18(3):155-60. doi: 10.1046/j.1365-2257.1996.00175.x.
Myelodysplasia is characterized by a hypoproliferative anaemia with ineffective intramedullary erythropoiesis. We have used the novel technology of the Bayer H3 analyser to characterize reticulocytes (RNA containing red cells) from 32 MDS patients and 10 elderly normal subjects. In comparison with reticulocytes from normal subjects, those from MDS patients were larger with a lower haemoglobin concentration. Reticulocytes from sideroblastic patients had a lower haemoglobin content and concentration than for refractory anaemia patients but no other differences between FAB subtypes were found. H3 reticulocyte RNA content parameters correlated poorly with those derived by the Sysmex R-1000, particularly in the MDS group. On reticulocyte maturation to red cells MDS patients concentrated haemoglobin more than normal subjects and this was most evident in the sideroblastic group. Platelet depletion of whole blood suggested that large platelets in the sideroblastic group may have partly contributed to this observation. Prospective evaluation of changes towards normal reticulocyte cytometric parameters may assist in assessment of early erythroid response to therapy in MDS patients.
骨髓发育异常的特征是增生低下性贫血伴骨髓内红细胞生成无效。我们使用了拜耳H3分析仪的新技术来对32例骨髓增生异常综合征(MDS)患者和10名老年正常受试者的网织红细胞(含RNA的红细胞)进行特征分析。与正常受试者的网织红细胞相比,MDS患者的网织红细胞更大,血红蛋白浓度更低。铁粒幼细胞性贫血患者的网织红细胞血红蛋白含量和浓度低于难治性贫血患者,但未发现FAB亚型之间的其他差异。H3网织红细胞RNA含量参数与Sysmex R-1000得出的参数相关性较差,尤其是在MDS组中。在网织红细胞成熟为红细胞的过程中,MDS患者比正常受试者更能浓缩血红蛋白,这在铁粒幼细胞性贫血组中最为明显。全血血小板减少提示铁粒幼细胞性贫血组中的大血小板可能部分促成了这一观察结果。对网织红细胞细胞计数参数向正常变化的前瞻性评估可能有助于评估MDS患者对治疗的早期红系反应。