期刊文献+

CD58在成人B-ALL微小残留病监测中的应用 被引量:2

Expression of CD58 in Adult B-ALL and its significance for monitoring minimal residual diseases
暂未订购
导出
摘要 目的研究淋巴细胞功能相关抗原-3(LFA-3、CD58)在成人急性B淋巴细胞白血病(B-ALL)中的表达,并探讨联合CD19、CD34、CD20、CD10和CD45等免疫分子用于成人B-ALL微小残留病(MRD)监测的可行性,以及CD58对于成人B-ALL预后的意义。方法选取CD10/CD58/CD19/CD45和CD34/CD20/CD45抗体组合,应用多参数流式细胞术(FCM)检测36例缺铁性贫血治疗后(对照组)和39例BALL初诊及治疗后(实验组)患者的骨髓标本。根据抗体表达规律将对照组正常分化的B系前体细胞分成早期、中期和成熟3个阶段;实验组白血病细胞按CD58的平均荧光强度(MFI)分为高表达组与低表达组。分别比较CD58在对照组和实验组不同阶段或组别表达强度差异。结果正常分化的B系前体细胞CD58表达强度整体呈现低表达水平。高表达组异常细胞CD58表达强度显著高于对照组(P<0.05);同时低表达组异常细胞CD58表达强度与对照组比较,差异无统计学意义。治疗后共有32例患者定期监测骨髓MRD,监测12个月数据表明:高表达组8例MRD阳性,CD58 MFI为(25.19±3.57),15例MRD阴性,CD58 MFI为(5.25±1.23);低表达组7例MRD阳性,CD58 MFI为(6.96±0.94),2例MRD阴性,CD58 MFI为(6.80±1.27)。结论CD58在异常细胞的表达强度稳定,联合CD19、CD34、CD20、CD10和CD45抗体组合可以用于CD58高表达组BALL患者MRD的监测,其表达强度的高低对于治疗效果评估具有很好的提示作用,即CD58低表达提示化疗效果不理想,预后不良。 Objective To investigate the expression of CD58 in adult acute B-lymphocytic leukemia( B-ALL), and analyze the feasibility and significance of CD58 in monitoring of minimal residual disease(MRD) for adult B-ALL. Methods The combination of antibodies CD10/CD58/CD19/CD45 and CD34/CD20/CD45 were detected in bone marrow samples from 36 patients of iron deficient anemia after treatment ( Control Group) and 39 patients with newly diagnosed B-ALL (Experimental Group) by Multi-parameter flow cytometry (FCM). According to the antibody expression, Nonmalignant B cells were designated as early, mid, and mature. Experimental Group was divided into the CD58 higher expression group and the CD58 lower expression group. Combined with clinical outcomes, the differences of CD58 expression in the Control Group and Experimental Group to assess the prompt significance of CD58 high and low expression groups for the prognosis of B-ALL. Results The mean value of CD58 showed low expression levels as a whole. The mean value of CD58 of high expression group was significantly higher than that in control group (P 〈 0. 05 ) , while low expression group with no significant difference of B lineage precursor cells expression. A total of 32 patients monitored minimal residual diseases regularly after treatment. The data of 12 months indicated: 8 of high expression group showed MRD( + )MFI (25.19± 3.57),while 15 of the group showed MRD ( - ) MFI (5.25± 1.23). 7 of low expression group showed MRD ( + ) MFI (6.96 ± 0. 94), the 2 of the group showed MRD ( - ) MFI (6.80 ± 1.27 ). Conclusion The expression of CD58 of abnormal cells was strong and stable. The vast majority of patients with B-ALL leukemia cells were abnormally high expression of CD58 and the expression levels were significantly higher than nonmalignant B-cell populations at any maturational stage. It is concluded that CD58 combined with CD19/CD34/CD20/CD10/CD45 can be used as an indicator for detection of MRD in B-ALL patients. The expression of the intensity level is a good mark of treatment assessment.
出处 《安徽医科大学学报》 CAS 北大核心 2013年第12期1491-1494,共4页 Acta Universitatis Medicinalis Anhui
基金 国家自然科学基金(编号:81141104) 安徽省科技攻关类战略新兴产业项目(编号:11010402168)
关键词 CD58 急性B淋巴细胞白血病 微小残留病 流式细胞术 CD58 acute B-lymphoblastic leukemia minimal residual disease flow cytometry
  • 相关文献

参考文献14

  • 1Inaba H,Greaves M,Mullighan C G.Acute lymphoblastic leuke-mia in adults [J].Lancet,2013,381 (9881):1943-55.
  • 2戴海明,翟志敏,何晓东,等.113例白血病免疫分型特点分析[J].安黴医科大学学报,2001,36(3):207-10.
  • 3Patkar N,Alex.A A,Ahmed R,et al.Standardizing minimal re-sidual disease by flow cytometry for precursor B lineage acute lym-phoblastic leukemia in a developing country [J].Cytometry B ClinCytom,2012,82(4):252-8.
  • 4Lee R V,Braylan R C,Rimsza L M.CD58 expression decreasesas nonmalignant B cells mature inbone marrow and is frequentlyoverexpressed in adult and pediatric precursor B-cell acute lympho-blastic leukemia [J].Am J Clin Pathol,2005,123 (1):119-24.
  • 5Veltroni M,De Zen L,Sanzari MC,et al.Expression of CD58 innormal,regenerating and leukemic bone marrowBcells:implica-tions for the detection of minimal residual disease in acutelympho-cytic leukemia[J].Haematologica,2003,88 (11):1245-52.
  • 6McKenna R W,Washington L T,Aquino DB,et al.Immunophe-notypic analysis of hematogones( B-lymphocyte precursors) in 662consecutive bone marrow specimens by 4-color flow cytometry[J].Blood,2001,98(8):2498-507.
  • 7Comerci C J,Mace E M,Baneijee P P.CD2 promotes human nat-ural killer cell membrane nanotube formation [J].PLoS One,2012,7(10):e47664.
  • 8Webb D S,Shimizu Y,Van Seventer GA,et al.LFA-3,CD44,and CD45:physiologic triggers of human monocyte TNF and IL-1release [J].Science,1990,249(4974):1295-7.
  • 9Denys B,van der Sluijs-Gelling A J,Homburg C,et al.Improvedflowcytometric detection of minimal residual disease in childhoodacute lymphoblastic [J].Leukemia,2013,27(3):635-41.
  • 10Bartram C R,Schrauder A,Kohler R,et al.Acute lymphoblasticleukemia in children:treatment planning via minimal residual dis-ease assessment [J].Dtsch Arztebllnt,2012,109(40):652-8.

二级参考文献21

  • 1谢明,王香玲,纪玉强,李洁,孟照俊,史霖,袁育康.外周血单核细胞CD58和CD58mRNA表达与HBV感染关系的研究[J].微生物学免疫学进展,2005,33(2):36-40. 被引量:7
  • 2赖苇,杨晋辉,董树强,杨婧,唐映梅,张宏英,程思根.肝硬化患者红细胞CD_(58)、T细胞亚群表达与胆碱酯酶相关研究[J].中国现代医学杂志,2007,17(3):294-297. 被引量:5
  • 3窦永喜,景志忠,侯俊玲,骆学农,张强,刘齐,左志林,才学鹏.猪CD58分子基因克隆、表达及其结构功能预测[J].畜牧兽医学报,2007,38(4):388-394. 被引量:5
  • 4郭晓青,何玉林,王清峰,关慧敏.CD2和CD58在宫颈癌组织中的表达及临床意义[J].细胞与分子免疫学杂志,2007,23(5):445-446. 被引量:5
  • 5Philip L,Allan CB,Lisa M.The role of the CD58 locus in multiple sclerosis[J] .PNAS,2009,106( 13): 5264-5269.
  • 6Arulanandam AR,Withka JM,Wyss DF,et al.The CD58 (LFA-3) binding site is a localized and highly charged surface area on the AGFCC'C'' face of the human CD2 adhesion domain.Proc Natl Acad Sci USA,1993;90:11613-11617
  • 7Seed B.An LFA-3 cDNA encodes a phospholipid-linked membrane protein homologous to its receptor CD2.Nature,1987;329(6142):840-842
  • 8Carrera AC,Rincon M,Sanchez-Madrid F,et al.Triggering of co-mitogenic signals in T cell proliferation by anti-LFA-1(CD18,CD11a),LFA-3,and CD7 monoclonal antibodies.J Immunol,1988;141:1919-1924
  • 9Shaw S,Luce GE,Quinones R,et al.Two antigen-independent adhesion pathways used by human cytotoxic T-cell clones.Nature,1986;323(6085):262-264
  • 10Billaud M,Rousset F,Calender A,et al.Low expression of lymphocyte function-associated antigen (LFA)-1 and LFA-3 adhesion molecules is a common trait in Burkitt's lymphoma associated with and not associated with Epstein-Barr virus.Blood,1990;75:1827-1833

共引文献6

同被引文献9

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部