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外周耐受诱导:来自免疫豁免部位和组织的经验教训。

Peripheral tolerance induction: lessons from immune privileged sites and tissues.

作者信息

Streilein J W

机构信息

Schepens Eye Research Institute, Harvard Medical School, Boston, Massachusetts 02114, USA.

出版信息

Transplant Proc. 1996 Aug;28(4):2066-70.

PMID:8769158
Abstract

Immune privilege is finally emerging from the curiosity shop into the mainstream of immunology. Immune privileged tissues and sites play a critical role in creating the privileged status, in part by creating peripheral tolerance among antigen-specific T and B cells. While the old idea of "antigen sequestration behind blood: tissue barriers and at sites without efferent lymphatics" seems effete, it appears that a novel view of antigen sequestration is emerging that requires that both immunologic ignorance and peripheral tolerance be considered as relevant to the privileged state. We have argued that immune privilege is an evolutionary adaptation that enables "vulnerable" tissues to arrange for immune protection without suffering the consequences of immunopathogenic damage. In the case of the eye (our organ of interest), privilege enables the eye to avoid immunogenic inflammation. For this specialized organ of sense, inflammation is an unavoidable cause of blindness because inflammation disrupts microanatomic arrangements, and maintenance of the microanatomy of the visual axis is essential for sight. Because immune privilege requires active participation of the immune system for its induction and its maintenance, and since this participation involves the systemic immune apparatus, the tolerance achieved by antigens placed in privileged sites is actually systemic. Therefore, the strategies that are used by privileged sites and tissues to create tolerance parochially, may actually have relevance for creating tolerance of antigenic materials placed at nonprivileged sites of the body.

摘要

免疫赦免终于从稀奇事物变成了免疫学的主流。免疫赦免组织和部位在建立赦免状态中发挥着关键作用,部分原因是通过在外周抗原特异性T细胞和B细胞中建立外周耐受。虽然“血液屏障和无输出淋巴管部位背后的抗原隔离”这一旧观念似乎已过时,但一种新的抗原隔离观点正在出现,这种观点认为免疫忽视和外周耐受都与赦免状态相关。我们认为免疫赦免是一种进化适应,它使“脆弱”组织能够在不遭受免疫致病损伤后果的情况下获得免疫保护。就眼睛(我们感兴趣的器官)而言,赦免使眼睛能够避免免疫原性炎症。对于这个特殊的感觉器官来说,炎症是导致失明的一个不可避免的原因,因为炎症会破坏微观解剖结构,而视觉轴微观解剖结构的维持对视力至关重要。由于免疫赦免需要免疫系统的积极参与来诱导和维持,而且这种参与涉及全身免疫系统,因此置于赦免部位的抗原所实现的耐受实际上是全身性的。所以,赦免部位和组织局部建立耐受所采用的策略,实际上可能与在身体非赦免部位建立抗原物质的耐受有关。

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Peripheral tolerance induction: lessons from immune privileged sites and tissues.外周耐受诱导:来自免疫豁免部位和组织的经验教训。
Transplant Proc. 1996 Aug;28(4):2066-70.
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引用本文的文献

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Failed central nervous system regeneration: a downside of immune privilege?中枢神经系统再生失败:免疫豁免的一个负面影响?
Neuromolecular Med. 2005;7(3):217-28. doi: 10.1385/NMM:7:3:217.
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Ocular toxoplasmosis: the role of retinal pigment epithelium migration in infection.眼部弓形虫病:视网膜色素上皮迁移在感染中的作用
Parasitol Res. 2004 Apr;92(6):467-72. doi: 10.1007/s00436-003-1031-2. Epub 2004 Feb 20.
3
Retinal pigment epithelial cells phagocytosis of T lymphocytes: possible implication in the immune privilege of the eye.
视网膜色素上皮细胞对T淋巴细胞的吞噬作用:可能与眼的免疫赦免有关。
Br J Ophthalmol. 2002 Dec;86(12):1417-21. doi: 10.1136/bjo.86.12.1417.
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Mycophenolate mofetil versus cyclosporin A in high risk keratoplasty patients: a prospectively randomised clinical trial.霉酚酸酯与环孢素A用于高危角膜移植患者的前瞻性随机临床试验
Br J Ophthalmol. 1999 Nov;83(11):1268-71. doi: 10.1136/bjo.83.11.1268.
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Effect of mycophenolate mofetil, cyclosporin A, and both in combination in a murine corneal graft rejection model.霉酚酸酯、环孢素A及其联合用药在小鼠角膜移植排斥模型中的作用
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A variety of cytokines and immunologically relevant surface molecules are expressed by normal human skeletal muscle cells under proinflammatory stimuli.在促炎刺激下,正常人骨骼肌细胞会表达多种细胞因子和免疫相关表面分子。
Clin Exp Immunol. 1998 Sep;113(3):407-14. doi: 10.1046/j.1365-2249.1998.00664.x.
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Astrocytic factors deactivate antigen presenting cells that invade the central nervous system.星形胶质细胞因子可使侵入中枢神经系统的抗原呈递细胞失活。
Brain Pathol. 1998 Jul;8(3):459-74. doi: 10.1111/j.1750-3639.1998.tb00168.x.