Department Internal Medicine, Kalafong Hospital, University of Pretoria.
Mediterr J Hematol Infect Dis. 2010;2(3):e2010032. doi: 10.4084/MJHID.2010.032. Epub 2010 Nov 15.
HIV-1 infection is associated with various quantitative and qualitative changes in haemopoietic cells. Clear distinction between primary myelodysplastic syndrome (MDS) and secondary dysplasia may not always be possible. Adjunctive analyses used in the diagnosis of MDS include cytogenetics and flow cytometry (FCM). Much focus has been placed on establishing FCM guidelines aiding in the diagnosis of MDS, and to distinguish this condition from secondary dysplastic changes. One of the parameters often cited is the CD10 expression on the granulocyte population, as this marker denotes granulocytic maturation.
To determine the expression level of CD10 on granulocytes in HIV positive patients.
In total, 117 HIV-1 positive and 29 HIV-1 negative patients were included in this study. Bone marrow aspirate samples were evaluated in terms of morphological abnormality as well as CD10 expression on the granulocytic population.
The average CD10 expression among the HIV-1 positive patients were markedly reduced, at 18.4%, and 113 patients (96.6%) of these patients had expression levels below 50%.
Disease conditions causing secondary dysplasia, especially HIV-1 infection, is associated with a marked reduction in CD10 expression on the granulocyte population independent from the presence of myelodysplastic features. This marker is therefore of doubtful significance as a diagnostic tool in distinguishing between primary and secondary dysplasia.
HIV-1 感染与造血细胞的各种定量和定性变化有关。原发性骨髓增生异常综合征(MDS)和继发性发育不良之间的明确区分并不总是可能的。辅助分析用于 MDS 的诊断,包括细胞遗传学和流式细胞术(FCM)。人们非常关注建立有助于 MDS 诊断的 FCM 指南,并将这种情况与继发性发育不良变化区分开来。经常提到的参数之一是粒细胞群上的 CD10 表达,因为该标志物表示粒细胞成熟。
确定 HIV 阳性患者中性粒细胞上 CD10 的表达水平。
本研究共纳入 117 例 HIV-1 阳性和 29 例 HIV-1 阴性患者。评估骨髓抽吸样本的形态异常以及粒细胞群上的 CD10 表达。
HIV-1 阳性患者的平均 CD10 表达明显降低,为 18.4%,其中 113 例(96.6%)患者的表达水平低于 50%。
导致继发性发育不良的疾病状况,特别是 HIV-1 感染,与粒细胞群上 CD10 表达的明显降低有关,与是否存在骨髓增生异常特征无关。因此,该标志物作为区分原发性和继发性发育不良的诊断工具意义不大。