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角膜新生血管化眼中免疫赦免的丧失与恢复

Loss and restoration of immune privilege in eyes with corneal neovascularization.

作者信息

Dana M R, Streilein J W

机构信息

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

出版信息

Invest Ophthalmol Vis Sci. 1996 Nov;37(12):2485-94.

PMID:8933765
Abstract

PURPOSE

To delineate the time course for loss of immune privilege after induction of corneal neovascularization (NV), and to test whether treatment with angiostatic agents can restore the eye's capacity to induce anterior chamber-associated immune deviation (ACAID).

METHODS

Corneal NV in murine eyes was induced by placement of intrastromal sutures. At different time points after NV induction, study eyes were initiated on a 10-day regimen of one of a variety of anti-inflammatory or angiostatic agents. After the completion of their treatment regimen, eyes were tested as to whether they could support ACAID. To test whether any observed effect on the delayed-type hypersensitivity response was because of a systemic absorption of the topically applied medication, certain animals had only their fellow eyes treated.

RESULTS

Inflammatory corneal NV leads to the loss of immune privilege during the first week of the NV induction. Left untreated, these eyes remain incapable of supporting ACAID, even weeks after the initial corneal insult. However, when treatment with an anti-inflammatory agent is initiated during the first 2 weeks after the NV induction, these eyes show a restored capacity for ACAID induction, and this appears to be unrelated to any systemic effect of the treatment regimen. Treatment started at later time points is not capable of restoring the eye's normal capacity for inducing deviant immunity.

CONCLUSIONS

Corneal neovascularization leads to loss of immune privilege in the anterior segment manifested as the inability to sustain ACAID. Moreover, topical angiostatic strategies can lead to restoration of immune privilege when instituted sufficiently early in the course of the neovascular response.

摘要

目的

描绘诱导角膜新生血管化(NV)后免疫赦免丧失的时间进程,并测试使用血管生成抑制药物治疗是否能恢复眼睛诱导前房相关免疫偏离(ACAID)的能力。

方法

通过基质内缝线植入诱导小鼠眼睛角膜NV。在NV诱导后的不同时间点,研究眼开始接受为期10天的多种抗炎或血管生成抑制药物之一的治疗方案。在完成治疗方案后,测试眼睛是否能支持ACAID。为了测试对迟发型超敏反应的任何观察到的影响是否是由于局部应用药物的全身吸收,某些动物仅对其对侧眼进行治疗。

结果

炎症性角膜NV在NV诱导的第一周导致免疫赦免丧失。如果不进行治疗,即使在最初的角膜损伤数周后,这些眼睛仍无法支持ACAID。然而,当在NV诱导后的前2周内开始用抗炎药物治疗时,这些眼睛显示出恢复的ACAID诱导能力,这似乎与治疗方案的任何全身作用无关。在较晚时间点开始治疗不能恢复眼睛诱导异常免疫的正常能力。

结论

角膜新生血管化导致眼前节免疫赦免丧失,表现为无法维持ACAID。此外,局部血管生成抑制策略在新生血管反应过程中足够早地实施时可导致免疫赦免的恢复。

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