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自然杀伤细胞成熟的最后步骤:1型-2型分化模型?

Final steps of natural killer cell maturation: a model for type 1-type 2 differentiation?

作者信息

Loza M J, Perussia B

机构信息

Kimmel Cancer Center, Jefferson Medical College, Department of Microbiology and Immunology, Philadelphia, PA, USA.

出版信息

Nat Immunol. 2001 Oct;2(10):917-24. doi: 10.1038/ni1001-917.

Abstract

Analysis of cytokine and differentiation antigen expression in human natural killer (NK) cells revealed that interleukin 13 (IL-13) and interferon gamma (IFN-gamma) are produced at sequential stages during irreversible IL-12-induced differentiation. In human NK cell clones, polyclonal CD3-CD161+CD56- cells and peripheral lymphocytes, IL-4 induced the proliferation of both IL-13+ NK and T cells, whereas IL-12 allowed a proliferation-independent accumulation of IFN-gamma+ cells. These data disproved the NK1-NK2 hypothesis and challenge the current T helper 1 (TH1)-TH2 paradigm. We propose that the cytokine environment regulates a type 2-->0-->1 developmental progression, with IL-12 needed for terminal differentiation and IL-4 delaying this process, rather than a type 1 versus type 2 decision of a type 0 cell.

摘要

对人类自然杀伤(NK)细胞中细胞因子和分化抗原表达的分析表明,白细胞介素13(IL-13)和干扰素γ(IFN-γ)是在白细胞介素12诱导的不可逆分化过程中的连续阶段产生的。在人类NK细胞克隆、多克隆CD3-CD161+CD56-细胞和外周淋巴细胞中,IL-4诱导IL-13+NK细胞和T细胞增殖,而IL-12则使IFN-γ+细胞在不依赖增殖的情况下积累。这些数据反驳了NK1-NK2假说,并对当前的辅助性T细胞1(TH1)-辅助性T细胞2(TH2)范式提出了挑战。我们提出,细胞因子环境调节2型→0型→1型的发育进程,终末分化需要IL-12,而IL-4会延迟这一过程,而不是0型细胞在1型和2型之间做出选择。

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