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Influenza Vaccination Induces NK-Cell-Mediated Type-II IFN Response that Regulates Humoral Immunity in an IL-6-Dependent Manner.流感疫苗接种诱导 NK 细胞介导的 II 型 IFN 反应,以 IL-6 依赖的方式调节体液免疫。
Cell Rep. 2019 Feb 26;26(9):2307-2315.e5. doi: 10.1016/j.celrep.2019.01.104.
2
NK Cells Activated through Antibody-Dependent Cell Cytotoxicity and Armed with Degranulation/IFN-γ Production Suppress Antibody-dependent Enhancement of Dengue Viral Infection.自然杀伤细胞通过抗体依赖性细胞毒性被激活,并具有脱颗粒/IFN-γ产生能力,可抑制登革热病毒感染的抗体依赖性增强作用。
Sci Rep. 2019 Feb 1;9(1):1109. doi: 10.1038/s41598-018-36972-2.
3
Influenza Virus Infection Enhances Antibody-Mediated NK Cell Functions via Type I Interferon-Dependent Pathways.流感病毒感染通过 I 型干扰素依赖途径增强抗体介导的 NK 细胞功能。
J Virol. 2019 Feb 19;93(5). doi: 10.1128/JVI.02090-18. Print 2019 Mar 1.
4
Anti-NKG2A mAb Is a Checkpoint Inhibitor that Promotes Anti-tumor Immunity by Unleashing Both T and NK Cells.抗 NKG2A mAb 是一种检查点抑制剂,通过释放 T 细胞和 NK 细胞来促进抗肿瘤免疫。
Cell. 2018 Dec 13;175(7):1731-1743.e13. doi: 10.1016/j.cell.2018.10.014. Epub 2018 Nov 29.
5
RAB11FIP5 Expression and Altered Natural Killer Cell Function Are Associated with Induction of HIV Broadly Neutralizing Antibody Responses.RAB11FIP5 的表达和自然杀伤细胞功能的改变与 HIV 广谱中和抗体反应的诱导有关。
Cell. 2018 Oct 4;175(2):387-399.e17. doi: 10.1016/j.cell.2018.08.064. Epub 2018 Sep 27.
6
Affinity Maturation Is Impaired by Natural Killer Cell Suppression of Germinal Centers.自然杀伤细胞抑制生发中心导致亲和力成熟受损。
Cell Rep. 2018 Sep 25;24(13):3367-3373.e4. doi: 10.1016/j.celrep.2018.08.075.
7
Natural killer cells and other innate lymphoid cells in cancer.自然杀伤细胞和癌症中的其他固有淋巴细胞。
Nat Rev Immunol. 2018 Nov;18(11):671-688. doi: 10.1038/s41577-018-0061-z.
8
Human iPSC-Derived Natural Killer Cells Engineered with Chimeric Antigen Receptors Enhance Anti-tumor Activity.人诱导多能干细胞来源的嵌合抗原受体修饰自然杀伤细胞增强抗肿瘤活性。
Cell Stem Cell. 2018 Aug 2;23(2):181-192.e5. doi: 10.1016/j.stem.2018.06.002. Epub 2018 Jun 28.
9
Immune Correlate-Guided HIV Vaccine Design.免疫相关性指导的 HIV 疫苗设计。
Cell Host Microbe. 2018 Jul 11;24(1):25-33. doi: 10.1016/j.chom.2018.06.012.
10
Blockade of the checkpoint receptor TIGIT prevents NK cell exhaustion and elicits potent anti-tumor immunity.阻断检查点受体 TIGIT 可防止 NK 细胞耗竭并引发强大的抗肿瘤免疫。
Nat Immunol. 2018 Jul;19(7):723-732. doi: 10.1038/s41590-018-0132-0. Epub 2018 Jun 18.

自然杀伤细胞在病毒感染中的 B 细胞反应调节。

Natural Killer Cell Regulation of B Cell Responses in the Context of Viral Infection.

机构信息

Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

Pathobiology and Molecular Medicine Graduate Program, University of Cincinnati, Cincinnati, Ohio, USA.

出版信息

Viral Immunol. 2020 May;33(4):334-341. doi: 10.1089/vim.2019.0129. Epub 2019 Dec 3.

DOI:10.1089/vim.2019.0129
PMID:31800366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7247022/
Abstract

Secretion of both neutralizing and nonneutralizing virus-specific antibodies by B cells is a key component of immune control of many virus infections and a critical benchmark of successful preventative vaccines. Natural killer (NK) cells also play a vital role in antiviral immune defense via cytolytic elimination of infected cells and production of proinflammatory antiviral cytokines. Accumulating evidence points to multifaceted crosstalk between NK cells and antiviral B cell responses that can determine virus elimination, pathogenesis of infection, and efficacy of vaccine-elicited protection. These outcomes are a result of both positive and negative influences of NK cells on the B cell responses, as well as canonical antiviral killing of infected B cells. On one hand, NK cell-derived cytokines such as interferon-gamma (IFN-) may promote B cell activation and enhance immunoglobulin production. In contrast, NK cell immunoregulatory killing of CD4 T cells can limit affinity maturation in germinal centers resulting in weak infection or vaccine induction of antiviral neutralizing antibodies. In this review, we will discuss these and other dueling contributions of NK cells to B cell responses during virus infection or vaccination.

摘要

B 细胞分泌中和性和非中和性病毒特异性抗体是许多病毒感染免疫控制的关键组成部分,也是成功预防疫苗的关键基准。自然杀伤 (NK) 细胞也通过溶细胞消除感染细胞和产生促炎抗病毒细胞因子在抗病毒免疫防御中发挥重要作用。越来越多的证据表明,NK 细胞与抗病毒 B 细胞反应之间存在多方面的相互作用,这可以决定病毒的清除、感染的发病机制和疫苗引发的保护效果。这些结果是 NK 细胞对 B 细胞反应的正、负影响的结果,以及感染的 B 细胞的经典抗病毒杀伤的结果。一方面,NK 细胞衍生的细胞因子,如干扰素-γ (IFN-),可能促进 B 细胞的激活并增强免疫球蛋白的产生。相比之下,NK 细胞的免疫调节性杀伤 CD4 T 细胞会限制生发中心中的亲和力成熟,导致对感染或疫苗诱导的抗病毒中和抗体的反应较弱。在这篇综述中,我们将讨论这些以及 NK 细胞在病毒感染或接种疫苗期间对 B 细胞反应的其他相互竞争的贡献。