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本文引用的文献

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A spread-deficient cytomegalovirus for assessment of first-target cells in vaccination.用于评估疫苗接种中第一靶细胞的缺陷型巨细胞病毒。
J Virol. 2010 Aug;84(15):7730-42. doi: 10.1128/JVI.02696-09. Epub 2010 May 12.
2
Cross-presentation of a spread-defective MCMV is sufficient to prime the majority of virus-specific CD8+ T cells.一种传播缺陷的 MCMV 的交叉呈递足以刺激大多数病毒特异性 CD8+T 细胞。
PLoS One. 2010 Mar 12;5(3):e9681. doi: 10.1371/journal.pone.0009681.
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Diversity in T cell memory: an embarrassment of riches.T 细胞记忆的多样性:丰富得令人尴尬。
Immunity. 2009 Dec 18;31(6):859-71. doi: 10.1016/j.immuni.2009.11.007.
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Homeostatic proliferation and survival of naïve and memory T cells.初始和记忆T细胞的稳态增殖与存活。
Eur J Immunol. 2009 Aug;39(8):2088-94. doi: 10.1002/eji.200939444.
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Stem cell-like plasticity of naïve and distinct memory CD8+ T cell subsets.初始及不同记忆性CD8 + T细胞亚群的干细胞样可塑性。
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Migration, maintenance and recall of memory T cells in peripheral tissues.外周组织中记忆性T细胞的迁移、维持与召回
Nat Rev Immunol. 2009 Mar;9(3):153-61. doi: 10.1038/nri2496.
7
Effector memory T cell responses are associated with protection of rhesus monkeys from mucosal simian immunodeficiency virus challenge.效应记忆T细胞反应与恒河猴免受黏膜猿猴免疫缺陷病毒攻击的保护作用相关。
Nat Med. 2009 Mar;15(3):293-9. doi: 10.1038/nm.1935. Epub 2009 Feb 15.
8
Homeostasis of naive and memory T cells.初始T细胞和记忆T细胞的稳态。
Immunity. 2008 Dec 19;29(6):848-62. doi: 10.1016/j.immuni.2008.11.002.
9
Memory inflation during chronic viral infection is maintained by continuous production of short-lived, functional T cells.慢性病毒感染期间的记忆性膨胀是由短命的功能性T细胞持续产生所维持的。
Immunity. 2008 Oct 17;29(4):650-9. doi: 10.1016/j.immuni.2008.07.017.
10
Cutting edge: local recall responses by memory T cells newly recruited to peripheral nonlymphoid tissues.前沿:新招募到外周非淋巴组织的记忆T细胞引发的局部回忆反应。
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剖析维持 CMV 特异性记忆 T 细胞库所需的条件。

Dissecting the requirements for maintenance of the CMV-specific memory T-cell pool.

机构信息

Division of Immune Regulation, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.

出版信息

Viral Immunol. 2011 Aug;24(4):351-5. doi: 10.1089/vim.2010.0140. Epub 2011 Jul 1.

DOI:10.1089/vim.2010.0140
PMID:21721929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3154399/
Abstract

Cytomegalovirus (CMV) infection promotes a broad T-cell response, with the resulting memory cells displaying diverse phenotypes. CMV establishes lifelong persistence/latency, and it is thought that viral antigens expressed during this period may regulate the expansion and/or maintenance of "inflationary" CD8 T-memory populations that display an effector memory phenotype. We show here that mouse CMV (MCMV)-specific inflationary memory T cells do not decrease in number after thymectomy, indicating that recent thymic emigrants are not strictly required for their maintenance. Furthermore, persistent MCMV replication in the salivary gland does not significantly impact the T-cell memory compartment, as surgical removal did not alter its composition. These results shed light upon the mechanisms required for maintenance of the large, MCMV-specific T-cell memory pool.

摘要

巨细胞病毒 (CMV) 感染可促进广泛的 T 细胞反应,由此产生的记忆细胞表现出不同的表型。CMV 建立终身持续性/潜伏性,据认为在此期间表达的病毒抗原可能调节“膨胀”的 CD8 T 记忆细胞群体的扩增和/或维持,这些细胞群体表现出效应记忆表型。我们在这里表明,鼠巨细胞病毒 (MCMV)-特异性膨胀性记忆 T 细胞在胸腺切除后数量不会减少,这表明近期胸腺迁出细胞并非其维持所必需的。此外,唾液腺中持续的 MCMV 复制对 T 细胞记忆区室没有显著影响,因为手术切除并没有改变其组成。这些结果揭示了维持大量 MCMV 特异性 T 细胞记忆库所需的机制。