脾边缘区淋巴瘤患者IGHV突变状态分析

目的研究脾边缘区淋巴瘤(SMZL)患者免疫球蛋白重链可变区(IGHV)基因突变状态及典型模式的分布情况,并与国外报道的数据进行对比,以探讨其差异。方法对40例SMZL患者资料进行回顾性分析。采用克隆测序法检测IGHV的VDJ序列并进行比对及聚类分析,明确是否存在B细胞受体的典型模式,分析IGHV突变患者与未突变患者的临床特征。结果40例患者中,IGHV突变者30例(75.0%),未突变者10例(25.0%),两者比例与国外报道相当。在V区基因,V2-70的使用频率高于同外报道(10.3%对0.8%,P=0.002),而V3-23明显减低(2.6%对18.0%,P=0.006)。在D区基因中,D...

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Published in中华血液学杂志 Vol. 37; no. 9; pp. 774 - 778
Main Author 杨文娟 于珍 吕瑞 李增军 李姮 熊文婕 易树华 刘薇 邱录贵
Format Journal Article
LanguageChinese
Published 中山大学孙逸仙纪念医院 510120%中国医学科学院、北京协和医学院血液学研究所、血液病医院, 天津,300020 2016
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ISSN0253-2727
DOI10.3760/cma.j.issn.0253-2727.2016.09.009

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Abstract 目的研究脾边缘区淋巴瘤(SMZL)患者免疫球蛋白重链可变区(IGHV)基因突变状态及典型模式的分布情况,并与国外报道的数据进行对比,以探讨其差异。方法对40例SMZL患者资料进行回顾性分析。采用克隆测序法检测IGHV的VDJ序列并进行比对及聚类分析,明确是否存在B细胞受体的典型模式,分析IGHV突变患者与未突变患者的临床特征。结果40例患者中,IGHV突变者30例(75.0%),未突变者10例(25.0%),两者比例与国外报道相当。在V区基因,V2-70的使用频率高于同外报道(10.3%对0.8%,P=0.002),而V3-23明显减低(2.6%对18.0%,P=0.006)。在D区基因中,D2-21和D6-13均高于国外报道(17.9%对2.3%,12.8%对3.8%,P值分别为0.000、0.046)。40例患者中发现1对新的典型模式,同时SMZL特异性的V1—2基因使用频率也最高(25.6%)。与IGHV突变组相比,未突变组患者的IgG、IgA表达水平显著增高[10.70(5.28~15.50)g/L对12.90(7.71~23.50)g/L,1.06(0.21~3.13)g/L对1.66(0.81~2.93)g/L,P值分别为0.038、0.040)],2例17p缺失患者的IGHV均呈未突变状态。与IGHV未突变组相比,突变组患者的无进展生存期显著延长(P=0.009),但总生存期差异无统计学意义(P=-0.430)。结论在SMZL患者中,IGHV突变与未突变患者比例与国外报道相当,但V区和D区基因的使用频率仍存在差异,而且VI-2基因的使用呈现疾病特异性,同时发现1例新的典型模式。IGHV突变可降低患者的IgG、IgA表达水平。
AbstractList 目的研究脾边缘区淋巴瘤(SMZL)患者免疫球蛋白重链可变区(IGHV)基因突变状态及典型模式的分布情况,并与国外报道的数据进行对比,以探讨其差异。方法对40例SMZL患者资料进行回顾性分析。采用克隆测序法检测IGHV的VDJ序列并进行比对及聚类分析,明确是否存在B细胞受体的典型模式,分析IGHV突变患者与未突变患者的临床特征。结果40例患者中,IGHV突变者30例(75.0%),未突变者10例(25.0%),两者比例与国外报道相当。在V区基因,V2-70的使用频率高于同外报道(10.3%对0.8%,P=0.002),而V3-23明显减低(2.6%对18.0%,P=0.006)。在D区基因中,D2-21和D6-13均高于国外报道(17.9%对2.3%,12.8%对3.8%,P值分别为0.000、0.046)。40例患者中发现1对新的典型模式,同时SMZL特异性的V1—2基因使用频率也最高(25.6%)。与IGHV突变组相比,未突变组患者的IgG、IgA表达水平显著增高[10.70(5.28~15.50)g/L对12.90(7.71~23.50)g/L,1.06(0.21~3.13)g/L对1.66(0.81~2.93)g/L,P值分别为0.038、0.040)],2例17p缺失患者的IGHV均呈未突变状态。与IGHV未突变组相比,突变组患者的无进展生存期显著延长(P=0.009),但总生存期差异无统计学意义(P=-0.430)。结论在SMZL患者中,IGHV突变与未突变患者比例与国外报道相当,但V区和D区基因的使用频率仍存在差异,而且VI-2基因的使用呈现疾病特异性,同时发现1例新的典型模式。IGHV突变可降低患者的IgG、IgA表达水平。
目的 研究脾边缘区淋巴瘤(SMZL)患者免疫球蛋白重链可变区(IGHV)基因突变状态及典型模式的分布情况,并与国外报道的数据进行对比,以探讨其差异.方法 对40例SMZL患者资料进行回顾性分析.采用克隆测序法检测IGHV的VDJ序列并进行比对及聚类分析,明确是否存在B细胞受体的典型模式,分析IGHV突变患者与未突变患者的临床特征.结果 40例患者中,IGHV突变者30例(75.0%),未突变者10例(25.0%),两者比例与国外报道相当.在V区基因,V2-70的使用频率高于国外报道(10.3%对0.8%,P=0.002),而V3-23明显减低(2.6%对18.0%,P=0.006).在D区基因中,D2-21和D6-13均高于国外报道(17.9%对2.3%,12.8%对3.8%,P值分别为0.000、0.046).40例患者中发现1对新的典型模式,同时SMZL特异性的V1-2基因使用频率也最高(25.6%).与IGHV突变组相比,未突变组患者的IgG、IgA表达水平显著增高[10.70(5.28~15.50)g/L对12.90(7.71~23.50)g/L,1.06(0.21~3.13)g/L对1.66(0.81~2.93)g/L,P值分别为0.038、0.040)],2例17p缺失患者的IGHV均呈未突变状态.与IGHV未突变组相比,突变组患者的无进展生存期显著延长(P=0.009),但总生存期差异无统计学意义(P=0.430).结论 在SMZL患者中,IGHV突变与未突变患者比例与国外报道相当,但V区和D区基因的使用频率仍存在差异,而且V1-2基因的使用呈现疾病特异性,同时发现1例新的典型模式.IGHV突变可降低患者的IgG、IgA表达水平.
Abstract_FL Objective To investigate the IGHV mutational status and its differences from Caucasian in splenic marginal zone lymphoma (SMZL).Methods A retrospective study on 40 SMZL cases were performed to detect the V-D-J sequence of IGHV by plasmid cloning sequencing,comparing the data with the most homologous germ line V sequence in database,identifying the stereotype of patients through cluster analysis and alignment.The clinical and laboratory characteristics were compared between the patients with IGHV mutation and without mutations.Results In SMZL patients,the proportion of IGHV mutations was 75%,consistent with data from Caucasian.In V region,the usage of V3-23 subtype was lower in Chinese patients compared with Caucasian (2.6% vs 18.0%,P=0.006),whereas the V2-70 subtype was used with high proportion (10.3% vs 0.8%,P=0.002).In D region,the D2-21 and D6-13 gene were used frequently (17.9% vs 2.3%,P<0.001;12.8% vs 3.8%,P=0.046).One new stereotype was found,and the SMZL-biased V1-2 gene was mostly used (25.6%).The levels of IgG and IgA were significantly increased in IGHV without mutations as compared with mutations [10.70 (5.28-15.50)g/L vs 12.90 (7.71-23.50) g/L,1.06 (0.21-3.13) g/L vs 1.66 (0.81-2.93) g/L,P=0.038,0.040].The only two 17p deletion patients were IGHV without mutaions.The progression free survival (PFS) was significantly prolonged in IGHV mutations (P=0.009),and there was no significant difference regarding to the overall survival between the two subgroups (P=0.430).Conclusion The proportion of IGHV mutaions was similar to the data in Caucasian.There was disparity in the usage of V and D regions between Chinese and Caucasian,and the SMZL-biased V1-2 gene were used more frequently in Chinese patients.One new stereotype was identified.In the IGHV without mutations group,the levels of IgG and IgA were significantly increased.
Author 杨文娟 于珍 吕瑞 李增军 李姮 熊文婕 易树华 刘薇 邱录贵
AuthorAffiliation 中国医学科学院、北京协和医学院血液学研究所、血液病医院,天津300020
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DocumentTitleAlternate IGHV mutational statue in patients with splenic marginal zone lymphoma
DocumentTitle_FL IGHV mutational statue in patients with splenic marginal zone lymphoma
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Keywords Receptors,antigen,B-cell
Lymphoma,B-cell,marginal zone
淋巴瘤,B细胞,边缘区
Immunoglobulin heavy chains
突变
受体,抗原,B细胞
免疫球蛋白重链
Mutation
Language Chinese
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Notes Yang Wenjuan, Yu Zhen, Lyu Rui, Li Zengjun, Li Heng, Xiong Wenjie, H Shuhua, Liu Wei, Qiu Lugui(State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin 300020, China)
Lymphoma, B-cell, marginal zone; Immunoglobulin heavy chains; Mutation;Receptors, antigen, B-cell
12-1090/R
Objective To investigate the IGHV mutational status and its differences from Caucasian in splenic marginal zone lymphoma (SMZL). Methods A retrospective study on 40 SMZL cases were performed to detect the V-D-J sequence of IGHV by plasmid cloning sequencing, comparing the data with the most homologous germ line V sequence in database, identifying the stereotype of patients through cluster analysis and alignment. The clinical and laboratory characteristics were compared between the patients with IGHV mutation and without mutations. Results In SMZL patients, the proportion of IGHV mutations was 75%, consistent with data fro
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Publisher 中山大学孙逸仙纪念医院 510120%中国医学科学院、北京协和医学院血液学研究所、血液病医院, 天津,300020
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目的 研究脾边缘区淋巴瘤(SMZL)患者免疫球蛋白重链可变区(IGHV)基因突变状态及典型模式的分布情况,并与国外报道的数据进行对比,以探讨其差异.方法...
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SubjectTerms B细胞
免疫球蛋白重链
受体
抗原
淋巴瘤
突变
边缘区
Title 脾边缘区淋巴瘤患者IGHV突变状态分析
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