M. Salem, M. Attia, S. Abdou, Abdel-Aziz A Zidan, Mona F Zidan
{"title":"A106:化疗后B-ALL患儿外周血中肿瘤干细胞数量增加","authors":"M. Salem, M. Attia, S. Abdou, Abdel-Aziz A Zidan, Mona F Zidan","doi":"10.1158/2326-6074.CRICIMTEATIAACR18-A106","DOIUrl":null,"url":null,"abstract":"Background: Acute lymphocytic leukemia (ALL) is biologically and clinically considered as a heterogeneous neoplasm of lymphoid progenitor cells in the bone marrow (BM). 15- 20 % of children with ALL who achieve an initial remission, will show relapse. One potential mechanism behind this relapse could be the emergence of cancer stem cells (CSCs), which are considered the driving force of tumorigenesis due to their ability of self-renewal as well as the emergence of immune regulatory cells including myeloid-derived suppressor cells (MDSCs) and regulatory T-cells (Treg). Aim: The main aim of this study was to analyze the numbers of CSCs and correlate these numbers with the numbers of blasT-cells, MDSCs and Treg cells in children with B-ALL before and after induction of chemotherapy. Materials and Methods: CSCs were defined as CD45dimCD19+CD10+CD34+CD38-, MDSCs were defined as Lin-HLA-DR-CD33+CD11b+ and Treg cells were defined as CD4+CD25+CD127-. The frequencies of these cells were analyzed in the peripheral blood of B-ALL patients before (n= 10) and after (n= 10) induction of chemotherapy using flow cytometry. Results: Significant increases in the numbers of CSCs were shown in B-ALL patients after induction of chemotherapy as compared to newly diagnosed patients (7.6± 8.3 vs. 2.7± 2.4, P Citation Format: Mohamed Labib Salem, Mohamed Attia, Said Abdou, Abdel-Aziz A. Zidan, Mona F. Zidan. Higher numbers of cancer stem cells in the peripheral blood of children with B-ALL after chemotherapy [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A106.","PeriodicalId":22141,"journal":{"name":"Tackling the Tumor Microenvironment: Beyond T-cells","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abstract A106: Higher numbers of cancer stem cells in the peripheral blood of children with B-ALL after chemotherapy\",\"authors\":\"M. Salem, M. Attia, S. Abdou, Abdel-Aziz A Zidan, Mona F Zidan\",\"doi\":\"10.1158/2326-6074.CRICIMTEATIAACR18-A106\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Acute lymphocytic leukemia (ALL) is biologically and clinically considered as a heterogeneous neoplasm of lymphoid progenitor cells in the bone marrow (BM). 15- 20 % of children with ALL who achieve an initial remission, will show relapse. 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引用次数: 0
摘要
背景:急性淋巴细胞白血病(Acute lymphocytic leukemia, ALL)在生物学和临床上被认为是一种骨髓淋巴样祖细胞(BM)的异质性肿瘤。15- 20%的ALL患儿在最初得到缓解后会复发。这种复发背后的一个潜在机制可能是癌症干细胞(CSCs)的出现,由于其自我更新的能力以及包括髓源性抑制细胞(MDSCs)和调节性t细胞(Treg)在内的免疫调节细胞的出现,CSCs被认为是肿瘤发生的驱动力。目的:本研究的主要目的是分析B-ALL患儿在诱导化疗前后CSCs的数量及其与blasT-cells、MDSCs和Treg细胞数量的关系。材料与方法:CSCs定义为CD45dimCD19+CD10+CD34+CD38-, MDSCs定义为Lin-HLA-DR-CD33+CD11b+, Treg细胞定义为CD4+CD25+CD127-。用流式细胞术分析B-ALL患者化疗前(n= 10)和诱导化疗后(n= 10)外周血中这些细胞的频率。结果:与新诊断的患者相比,B-ALL患者诱导化疗后的CSCs数量显著增加(7.6±8.3比2.7±2.4),P引用格式:Mohamed Labib Salem, Mohamed Attia, Said Abdou, Abdel-Aziz A. Zidan, Mona F. Zidan。化疗后B-ALL患儿外周血中肿瘤干细胞数量增加[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr A106。
Abstract A106: Higher numbers of cancer stem cells in the peripheral blood of children with B-ALL after chemotherapy
Background: Acute lymphocytic leukemia (ALL) is biologically and clinically considered as a heterogeneous neoplasm of lymphoid progenitor cells in the bone marrow (BM). 15- 20 % of children with ALL who achieve an initial remission, will show relapse. One potential mechanism behind this relapse could be the emergence of cancer stem cells (CSCs), which are considered the driving force of tumorigenesis due to their ability of self-renewal as well as the emergence of immune regulatory cells including myeloid-derived suppressor cells (MDSCs) and regulatory T-cells (Treg). Aim: The main aim of this study was to analyze the numbers of CSCs and correlate these numbers with the numbers of blasT-cells, MDSCs and Treg cells in children with B-ALL before and after induction of chemotherapy. Materials and Methods: CSCs were defined as CD45dimCD19+CD10+CD34+CD38-, MDSCs were defined as Lin-HLA-DR-CD33+CD11b+ and Treg cells were defined as CD4+CD25+CD127-. The frequencies of these cells were analyzed in the peripheral blood of B-ALL patients before (n= 10) and after (n= 10) induction of chemotherapy using flow cytometry. Results: Significant increases in the numbers of CSCs were shown in B-ALL patients after induction of chemotherapy as compared to newly diagnosed patients (7.6± 8.3 vs. 2.7± 2.4, P Citation Format: Mohamed Labib Salem, Mohamed Attia, Said Abdou, Abdel-Aziz A. Zidan, Mona F. Zidan. Higher numbers of cancer stem cells in the peripheral blood of children with B-ALL after chemotherapy [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A106.