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转化生长因子-β浓度和活性在新生血管性年龄相关性黄斑变性患者的房水中下调。

TGF-β concentrations and activity are down-regulated in the aqueous humor of patients with neovascular age-related macular degeneration.

机构信息

University of Siena, Ophthalmology Unit of the Department of Medicine, Surgery and Neuroscience, Siena, 53100, Italy.

University of Siena, Department of Biotechnology, Chemistry and Pharmacy, Siena, 53100, Italy.

出版信息

Sci Rep. 2018 May 23;8(1):8053. doi: 10.1038/s41598-018-26442-0.

DOI:10.1038/s41598-018-26442-0
PMID:29795291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5966430/
Abstract

Controversy still exists regarding the role of the TGF-β in neovascular age-related macular degeneration (nAMD), a major cause of severe visual loss in the elderly in developed countries. Here, we measured the concentrations of active TGF-β1, TGF-β2, and TGF-β3 by ELISA in the aqueous humor of 20 patients affected by nAMD, who received 3 consecutive monthly intravitreal injections of anti-VEGF-A antibody. Samples were collected at baseline (before the first injection), month 1 (before the second injection), and month 2 (before the third injection). The same samples were used in a luciferase-based reporter assay to test the TGF-β pathway activation. Active TGF-β1 concentrations in the aqueous humor were below the minimum detectable dose. Active TGF-β2 concentrations were significantly lower at baseline and at month 1, compared to controls. No significant differences in active TGF-β3 concentration were found among the sample groups. Moreover, TGF-β pathway activation was significantly lower at baseline compared to controls. Our data corroborate an anti-angiogenic role for TGF-β2 in nAMD. This should be considered from the perspective of a therapy using TGF-β inhibitors.

摘要

关于转化生长因子-β(TGF-β)在新生血管性年龄相关性黄斑变性(nAMD)中的作用仍存在争议,nAMD 是发达国家老年人严重视力丧失的主要原因。在这里,我们通过 ELISA 法测量了 20 名接受抗 VEGF-A 抗体连续 3 个月玻璃体内注射的 nAMD 患者房水中的活性 TGF-β1、TGF-β2 和 TGF-β3 浓度。这些样本在基线(第一次注射前)、第 1 个月(第二次注射前)和第 2 个月(第三次注射前)采集。相同的样本用于基于荧光素酶的报告基因检测,以测试 TGF-β 通路的激活情况。房水中活性 TGF-β1 浓度低于最低检测剂量。与对照组相比,基线和第 1 个月时房水中的活性 TGF-β2 浓度显著降低。在各组样本中,活性 TGF-β3 浓度无显著差异。此外,与对照组相比,基线时 TGF-β 通路的激活明显降低。我们的数据证实了 TGF-β2 在 nAMD 中的抗血管生成作用。这应该从使用 TGF-β 抑制剂治疗的角度来考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/05ac8d341a27/41598_2018_26442_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/fdfde1eb5779/41598_2018_26442_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/253f1d0a1e07/41598_2018_26442_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/fe7d76fb15d0/41598_2018_26442_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/ccca1fdfa2bb/41598_2018_26442_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/5a1b4ac1dea4/41598_2018_26442_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/f63bfd00fe63/41598_2018_26442_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/05ac8d341a27/41598_2018_26442_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/fdfde1eb5779/41598_2018_26442_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/253f1d0a1e07/41598_2018_26442_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/fe7d76fb15d0/41598_2018_26442_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/ccca1fdfa2bb/41598_2018_26442_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/5a1b4ac1dea4/41598_2018_26442_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/f63bfd00fe63/41598_2018_26442_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2924/5966430/05ac8d341a27/41598_2018_26442_Fig7_HTML.jpg

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