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结膜下注射贝伐单抗后泪液中补偿性生长因子和细胞因子反应。

Compensatory growth factor and cytokine response in tears after subconjunctival bevacizumab injection.

机构信息

Department of Ophthalmology, Chung-Ang University College of Medicine, Seoul, Republic of Korea.

出版信息

Cornea. 2011 Oct;30(10):1071-7. doi: 10.1097/ICO.0b013e31820cd3f4.

Abstract

PURPOSE

Recent studies support the use of bevacizumab to treat ocular neovascularization (NV). In this study, we aimed to investigate changes in growth factors and cytokines in human tears after a subconjunctival bevacizumab injection and to evaluate the clinical effects and safety of the drug in ocular surface NV.

METHODS

Bevacizumab (5 mg/0.2 mL) was injected into the subconjunctival space of 15 patients with corneal NV. Tear samples were collected before and at 1 day, 1 week, and 1 month after the injection. Using a multiarray immunobead assay, we measured vascular endothelial growth factor, epidermal growth factor, basic fibroblast growth factor, interleukin-1β, tumor necrosis factor-α, and matrix metalloproteinase-9 levels. We evaluated the changes in the extent of NV using anterior segment photographs.

RESULTS

Ten eyes (67%) showed significant improvement in the NV lesions, and the effect was especially prominent in patients with immune-mediated disease. Six eyes (40%) showed localized complications, but these improved spontaneously. The quantitative analysis showed a decrease in vascular endothelial growth factor and increases in epidermal growth factor, basic fibroblast growth factor, interleukin-1β, and tumor necrosis factor-α in tear samples.

CONCLUSIONS

These findings suggest that bevacizumab stabilizes angiogenesis at the ocular surface primarily by vascular endothelial growth factor suppression, but that compensatory changes in other growth factors and cytokines may contribute as well. Associated complications seem to be rare and not severe. Bevacizumab therefore may provide an effective and a safe new treatment option for corneal NV.

摘要

目的

近期的研究支持使用贝伐单抗治疗眼部新生血管(NV)。本研究旨在探讨玻璃体内注射贝伐单抗后人类泪液中生长因子和细胞因子的变化,并评估该药在眼表 NV 中的临床疗效和安全性。

方法

15 例角膜 NV 患者的结膜下空间注射 5mg/0.2mL 贝伐单抗。在注射前和注射后 1 天、1 周和 1 个月采集泪液样本。采用多阵列免疫珠测定法检测血管内皮生长因子(VEGF)、表皮生长因子(EGF)、碱性成纤维细胞生长因子(bFGF)、白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)和基质金属蛋白酶-9(MMP-9)水平。使用眼前节照相评估 NV 病变范围的变化。

结果

10 只眼(67%)的 NV 病变有明显改善,免疫介导性疾病患者的疗效更为显著。6 只眼(40%)出现局部并发症,但这些并发症会自行改善。定量分析显示泪液样本中 VEGF 减少,EGF、bFGF、IL-1β和 TNF-α增加。

结论

这些发现表明,贝伐单抗通过抑制 VEGF 稳定眼表面的血管生成,但其他生长因子和细胞因子的代偿性变化可能也有贡献。相关并发症似乎很少且不严重。因此,贝伐单抗可能为角膜 NV 提供一种有效且安全的新治疗选择。

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