与外周血相比,脐血单核细胞中T细胞抑制性受体水平较低。

Q1 Biochemistry, Genetics and Molecular Biology Stem cell investigation Pub Date : 2019-10-21 DOI:10.21037/sci.2019.09.01
Ying Lin, Jinrong Lin, Jingying Huang, Youchun Chen, Jiaxiong Tan, Yangqiu Li, Shaohua Chen
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引用次数: 3

摘要

T细胞抑制受体在维持T细胞稳态中起着重要作用。脐带血(CB) T细胞中这种负共刺激信号转导通路的特征尚不清楚。本研究检测了细胞程序性死亡-1 (PD-1)、细胞毒性T淋巴细胞抗原-4 (CTLA-4)、T细胞免疫球蛋白粘蛋白-3 (Tim-3)、淋巴细胞活化基因-3 (LAG-3)、B和T淋巴细胞衰减剂(BTLA)等T细胞抑制受体在CB中的表达水平,并与外周血(PB)进行了比较。CB中PD-1、CTLA-4、LAG-3和BTLA的表达量显著降低,而Tim-3在CB和PB中表达量相近。综上所述,该T细胞抑制受体在脐带血干细胞移植中的不同表达模式值得进一步探讨其在脐带血干细胞移植及异体嵌合抗原受体T细胞产生中的免疫应答作用。
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Lower T cell inhibitory receptor level in mononuclear cells from cord blood compared with peripheral blood.
T cell inhibitory receptors play important role in maintaining T cell homeostasis. The feature of such negative costimulator signal transduction pathway in cord blood (CB) T cells remains unclear. In this study, the expression levels of T cell inhibitory receptors including programmed death-1 (PD-1), cytotoxic T lymphocyte antigen-4 (CTLA-4), T cell immunoglobulin mucin-3 (Tim-3), lymphocyte activation gene-3 (LAG-3) and B and T lymphocyte attenuator (BTLA) were characterized in CB and compared with peripheral blood (PB). Significant lower expression of PD-1, CTLA-4, LAG-3 and BTLA was found in CB, while similar expression level of Tim-3 was showed between CB and PB. Together, different expression pattern of such T cell inhibitory receptor in CB is worthy to further discuss their role on immune response when CB is used in cord blood stem cell transplantation as well as allogeneic chimeric antigen receptor T-cell producing.
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来源期刊
Stem cell investigation
Stem cell investigation Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
5.80
自引率
0.00%
发文量
9
期刊介绍: The Stem Cell Investigation (SCI; Stem Cell Investig; Online ISSN: 2313-0792) is a free access, peer-reviewed online journal covering basic, translational, and clinical research on all aspects of stem cells. It publishes original research articles and reviews on embryonic stem cells, induced pluripotent stem cells, adult tissue-specific stem/progenitor cells, cancer stem like cells, stem cell niche, stem cell technology, stem cell based drug discovery, and regenerative medicine. Stem Cell Investigation is indexed in PubMed/PMC since April, 2016.
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