Miao Yi, Fan Lei, Wu Yu-Jie, Xia Yi, Qiao Chun, Wang Yan, Wang Li, Hong Min, Zhu Hua-Yuan, Xu Wei, Li Jian-Yong
Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing 210029, China.
Collaborative Innovation Center for Cancer Personalized Medicine, Nanjing Medical University, Nanjing 210029, China.
Oncotarget. 2016 Mar 22;7(12):13551-62. doi: 10.18632/oncotarget.6948.
CD200, formerly known as OX-2, is a type I glycoprotein that is expressed on a variety of cell types. CD200 has been shown to be overexpressed in chronic lymphocytic leukemia (CLL). Although previous studies have confirmed the diagnostic value of CD200 in differentiating CLL from to other B-cell chronic lymphoproliferative disorders especially mantle cell lymphoma, whether CD200 has prognostic significance in CLL remains to be determined. We evaluated the mean fluorescence intensity (MFI) of CD200 in 307 consecutive, untreated patients with CLL in our center using flow cytometry. Using a CD200 MFI cutoff of 189.5, these cases could be divided into two groups. Patients with lower CD200 MFI (< 189.5) had a significantly shorter time-to-treatment (TTT) than those with higher CD200 MFI (≥ 189.5) (median TTT: 2 months vs 28 months, p = 0.0008). However, the effect of CD200 MFI on overall survival was not significant (CD200 MFI < 189.5: undefined vs CD200 MFI ≥ 189.5: undefined, P = 0.2379). In subgroup analysis, CD200 MFI retained its prognostic value in patients with favourable characteristics such as Binet stage A disease, mutated IGHV status, normal TP53 or negative CD38 expression. In conclusion, our study identified CD200 MFI as a potential prognostic factor in CLL.
CD200,以前称为OX-2,是一种I型糖蛋白,在多种细胞类型上表达。已证明CD200在慢性淋巴细胞白血病(CLL)中过表达。尽管先前的研究已证实CD200在鉴别CLL与其他B细胞慢性淋巴细胞增殖性疾病尤其是套细胞淋巴瘤方面具有诊断价值,但CD200在CLL中是否具有预后意义仍有待确定。我们使用流式细胞术评估了本中心307例连续未经治疗的CLL患者中CD200的平均荧光强度(MFI)。使用CD200 MFI临界值189.5,这些病例可分为两组。CD200 MFI较低(<189.5)的患者治疗时间(TTT)明显短于CD200 MFI较高(≥189.5)的患者(中位TTT:2个月对28个月,p = 0.0008)。然而,CD200 MFI对总生存期的影响不显著(CD200 MFI <189.5:未定义对CD200 MFI≥189.5:未定义,P = 0.2379)。在亚组分析中,CD200 MFI在具有有利特征的患者中保留其预后价值,如Binet分期A期疾病、IGHV突变状态、TP53正常或CD38表达阴性。总之,我们的研究确定CD200 MFI是CLL的一个潜在预后因素。