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中华危重症医学杂志(电子版) ›› 2018, Vol. 11 ›› Issue (01) : 35 -40. doi: 10.3877/cma.j.issn.1674-6880.2018.01.006

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论著

急性髓样白血病干细胞CD200的表达及与疗效的相关分析
郑晓燕1, 贺超奇2, 陈芳建1, 黄卉1, 吴芬芝3, 詹碧翠4,()   
  1. 1. 324000 浙江衢州,衢州市人民医院检验科
    2. 311200 杭州,杭州市萧山区第一人民医院检验科
    3. 324000 浙江衢州,衢州市人民医院血液科
    4. 310014 杭州,杭州市中医院检验科
  • 收稿日期:2017-06-20 出版日期:2018-02-01
  • 通信作者: 詹碧翠
  • 基金资助:
    浙江省科技厅公益技术研究社会发展项目(2013C33SA100139); 杭州市科技局项目(20140633B50); 衢州市科技局项目(2015064)

Expression of CD200 in acute myeloid leukemia stem cells and its correlation with clinical efficacy

Xiaoyan Zheng1, Chaoqi He2, Fangjian Chen1, Hui Huang1, Fenzhi Wu3, Bicui Zhan4,()   

  1. 1. Department of Clinical Laboratory, Quzhou People's Hospital, Quzhou 324000, China
    2. Department of Clinical Laboratory, the First People's Hospital of Xiaoshan District, Hangzhou 311200, China
    3. Department of Hematology, Quzhou People's Hospital, Quzhou 324000, China
    4. Department of Clinical Laboratory, Hangzhou Chinese Medicine Hospital, Hangzhou 310014, China
  • Received:2017-06-20 Published:2018-02-01
  • Corresponding author: Bicui Zhan
  • About author:
    Corresponding author: Zhan Bicui, Email:
引用本文:

郑晓燕, 贺超奇, 陈芳建, 黄卉, 吴芬芝, 詹碧翠. 急性髓样白血病干细胞CD200的表达及与疗效的相关分析[J]. 中华危重症医学杂志(电子版), 2018, 11(01): 35-40.

Xiaoyan Zheng, Chaoqi He, Fangjian Chen, Hui Huang, Fenzhi Wu, Bicui Zhan. Expression of CD200 in acute myeloid leukemia stem cells and its correlation with clinical efficacy[J]. Chinese Journal of Critical Care Medicine(Electronic Edition), 2018, 11(01): 35-40.

目的

探究急性髓样白血病(AML)患者白血病干细胞(LSCs)中CD200的表达以及其与临床疗效的相关性。

方法

收集2014年4月至2017年4月衢州市人民医院收治的137例AML患者,进行AML分型,分为M1~M5型。并对患者临床疗效进行统计,分为三组:完全缓解(CR)组(59例)、部分缓解(PR)组(47例)和未缓解(NR)组(31例)。通过流式细胞仪分离患者治疗前后的骨髓LSCs,检测LSCs表达、CD200在LSCs中的表达水平。

结果

24.82%(34/137)AML患者的LSCs中表达CD200,且CD200在AML各亚型中表达的阳性占比的比较,差异有统计学意义(5/11、13/26、4/35、3/22、9/43,χ2=16.533,P=0.002)。AML-LSCs在AML各亚型中都存在高表达,且差异无统计学意义(F=0.980,P=0.421);除CD200在M3组的LSCs中呈现更低表达外[(10.1 ± 2.7)%],其在AML其他各亚型中表达差异均无统计学意义[(16.5 ± 2.8)%、(19.7 ± 4.0)%、(16.4 ± 2.4)%、(17.0 ± 3.1)%,P均> 0.05]。而在治疗疗效观察中,治疗前CD200在LSCs中的表达水平在CR、PR、NR三组间比较,差异均无统计学意义(P均> 0.05);治疗后随着症状的缓解程度提高,各组CD200在LSCs中表达水平也随之降低[(16.4 ± 3.6)%、(10.8 ± 2.6)%、(5.0 ± 1.8)%,P均< 0.05]。治疗后,CR与NR两组CD200阳性表达占比的比较,差异有统计学意义(5/59 vs. 14/31,P < 0.017);同时AML亚型分组中M3组内的CR、PR、NR三组CD200+/CD200-分布情况的比较,差异有统计学意义(0/22、1/11、1/0,χ2=17.786,P < 0.001)。

结论

AML患者LSCs中高表达CD200与不良预后有一定关系,可影响临床疗效。

Objective

To investigate the expression of CD200 in leukemia stem cells (LSCs) from the patients with acute myeloid leukemia (AML) and its correlation with clinical efficacy.

Methods

A total of 137 AML patients admitted to Quzhou People's Hospital from April 2014 to April 2017 were collected and divided into M1-M5 types, according to AML classification. Based on the clinical efficacy, AML patients were also statistically divided into three groups: complete remission (CR) group (n=59), partial remission (PR) group (n=47) and non-remission (NR) group (n=31). The flow cytometry was used for separating bone marrow LSCs and detecting the expressions of LSCs and CD200 in LSCs before and after treatment.

Results

24.82% (34/137) AML patients had CD200 expression in LSCs, while the positive proportions of CD200 expression in each subtype of AML were significantly different (5/11, 13/26, 4/35, 3/22, 9/43; χ2=16.533, P=0.002). AML-LSCs had high expressions in all AML subtypes, which showed no significant difference (F=0.980, P=0.421); except that the expression of CD200 in the LSCs was obviously lower in the M3 group [(10.1 + 2.7)%], the CD200 expressions were no difference in the other AML subtypes [(16.5 ± 2.8)%, (19.7 ± 4.0)%, (16.4 ± 2.4)%, (17.0 ± 3.1)%, all P > 0.05]. The treatment effect observation showed that the expressions of CD200 in the LSCs were not statistically significantly different among CR, PR and NR groups before treatment (all P > 0.05); the expression of CD200 in the LSCs decreased with the improvement of symptoms after treatment [(16.4 ± 3.6)%, (10.8 ± 2.6)%, (5.0 ± 1.8)%, all P < 0.05]. There was a significant difference of CD200 positive expression between CR and NR groups after treatment (5/59 vs. 14/31, P < 0.017); in addition, the comparison of CD200+/CD200- in CR, PR, NR subgroups of AML M3 group was significantly different (0/22, 1/11, 1/0; χ2=17.786, P < 0.001).

Conclusion

The high expression of CD200 in LSCs of AML patients has a certain relationship with poor prognosis, which can affect the clinical efficacy.

表1 AML初诊患者治疗前LSCs及CD200表达水平的比较(±s
表2 三组疗效分组患者治疗前后CD200在LSCs中表达水平的比较(±s
表3 AML初诊患者治疗后各亚型中CD200+/CD200-在CR、PR、NR组中分布情况(例)
[1]
Jentzsch M, Bill M, Nicolet D, et al. Prognostic im-pact of the CD34+/CD38- cell burden in patients with acute myeloid leukemia receiving allogeneic stem cell transplantation[J]. Am J Hematol, 2017, 92 (4): 388-396.
[2]
饶若,王述文,姚红霞,等. CD133两种亚型分子在急性白血病中的表达及意义[J].免疫学杂志,2017,33(3):273-276.
[3]
Jiang Y, Xu P, Yao D, et al. CD33, CD96 and death associated protein kinase (DAPK) expression are associated with the survival rate and/or response to the chemotherapy in the patients with acute myeloid leukemia (AML) [J]. Med Sci Monit, 2017 (23): 1725-1732.
[4]
Blum W, Sanford BL, Klisovic R, et al. Maintenance therapy with decitabine in younger adults with acute myeloid leukemia in first remission: a phase 2 Cancer and Leukemia Group B Study (CALGB 10503) [J]. Leukemia, 2017, 31 (1): 34-39.
[5]
Koller E. Acute myeloid leukemia: highlights from the 54th ASH meeting held in Atlanta, Georgia[J]. Memo, 2013, 6 (3): 185-188.
[6]
Blair A, Hogge DE, Sutherland HJ. Most acute mye-loid leukemia progenitor cells with long-term proliferative ability in vitro and in vivo have the phenotype CD34(+)/CD71(-)/HLA-DR-[J]. Blood, 1998, 92 (11): 4325-4335.
[7]
Blair A, Hogge DE, Ailles LE, et al. Lack of expre-ssion of Thy-1 (CD90) on acute myeloid leukemia cells with long-term proliferative ability in vitro and in vivo[J]. Blood, 1997, 89 (9): 3104-3112.
[8]
Blair A, Sutherland HJ. Primitive acute myeloid leuk-emia cells with long-term proliferative ability in vitro and in vivo lack surface expression of c-kit (CD117)[J]. Exp Hematol, 2000, 28 (28): 660-671.
[9]
Jordan CT, Upchurch D, Szilvassy SJ, et al. The in-terleukin-3 receptor alpha chain is a unique marker for human acute myelogenous leukemia stem cells[J]. Leukemia, 2000, 14 (10): 1777-1784.
[10]
Lapidot T, Sirard C, Vormoor J, et al. A cell initiating human acute myeloid leukaemia after transplantation into SCID mice[J]. Nature, 1994, 367 (6464): 645-648.
[11]
Bonnet D, Dick JE. Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell[J]. Nat Med, 1997, 3 (7): 730-737.
[12]
Jordan CT. Unique molecular and cellular features of acute myelogenous leukemia stem cells[J]. Leukemia, 2002, 16 (4): 559-562.
[13]
Guzman ML, Neering SJ, Upchurch D, et al. Nuclear factor-kappaB is constitutively activated in primitive human acute myelogenous leukemia cells[J]. Blood,2001, 98 (8): 2301-2307.
[14]
Kawasaki BT, Farrar WL. Cancer stem cells, CD200 and immunoevasion[J]. Trends Immunol, 2008, 29 (10): 464-468.
[15]
Gorczynski R, Chen Z, Kai Y, et al. CD200 is a ligand for all members of the CD200R family of immunoregulatory molecules[J]. J Immunol, 2004, 172 (12): 7744-7749.
[16]
Lauzon-Joset JF, Langlois A, Lai LJ, et al. Lung CD200 receptor activation abrogates airway hyperresponsiveness in experimental asthma[J]. Am J Respir Cell Mol Biol, 2015, 53 (2): 276-284.
[17]
Alapat D, Coviello-Malle J, Owens R, et al. Dia-gnostic usefulness and prognostic impact of CD200 expression in lymphoid malignancies and plasma cell myeloma[J]. Am J Clin Pathol, 2012, 137 (1): 93-100.
[18]
Tonks A, Hills R, White P, et al. CD200 as a prognostic factor in acute myeloid leukaemia[J]. Leukemia, 2007, 21 (3): 566-568.
[19]
Moreaux J, Hose D, Reme T, et al. CD200 is a new prognostic factor in multiple myeloma[J]. Blood, 2006, 108 (13): 4194-4197.
[20]
顾宝罗,赵洪灿,范剑,等. CD47在急性髓细胞白血病干细胞中表达的临床意义[J/CD].中华危重症医学杂志(电子版),2013,6(4):16-19.
[21]
胡蓓莉,张隽瑜,贺超奇,等.急性髓样白血病患者骨髓干细胞CD200的表达及与临床疗效的关系[J/CD].中华危重症医学杂志(电子版),2017,10(3):165-171.
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