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2
Reducing inflammation through delivery of lentivirus encoding for anti-inflammatory cytokines attenuates neuropathic pain after spinal cord injury.通过递送编码抗炎细胞因子的慢病毒减轻脊髓损伤后的神经病理性疼痛。
J Control Release. 2018 Nov 28;290:88-101. doi: 10.1016/j.jconrel.2018.10.003. Epub 2018 Oct 6.
3
Local Immunomodulation with Anti-inflammatory Cytokine-Encoding Lentivirus Enhances Functional Recovery after Spinal Cord Injury.局部免疫调节用抗炎细胞因子编码慢病毒增强脊髓损伤后的功能恢复。
Mol Ther. 2018 Jul 5;26(7):1756-1770. doi: 10.1016/j.ymthe.2018.04.022. Epub 2018 Apr 27.
4
Immunohistologic analysis of spontaneous recurrent laryngeal nerve reinnervation in a rat model.大鼠模型中喉返神经自发性再支配的免疫组织学分析
Laryngoscope. 2018 Mar;128(3):E117-E122. doi: 10.1002/lary.27004. Epub 2017 Dec 11.
5
The Involvement of the Myelin-Associated Inhibitors and Their Receptors in CNS Plasticity and Injury.髓鞘相关抑制剂及其受体在中枢神经系统可塑性和损伤中的作用。
Mol Neurobiol. 2018 Mar;55(3):1831-1846. doi: 10.1007/s12035-017-0433-6. Epub 2017 Feb 22.
6
Reducing neuroinflammation by delivery of IL-10 encoding lentivirus from multiple-channel bridges.通过多通道桥递送编码白细胞介素-10的慢病毒来减轻神经炎症。
Bioeng Transl Med. 2016 Jun;1(2):136-148. doi: 10.1002/btm2.10018. Epub 2016 Jul 19.
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Chondroitinase C Selectively Degrades Chondroitin Sulfate Glycosaminoglycans that Inhibit Axonal Growth within the Endoneurium of Peripheral Nerve.软骨素酶C选择性降解硫酸软骨素糖胺聚糖,这些糖胺聚糖会抑制周围神经神经内膜内的轴突生长。
PLoS One. 2016 Dec 14;11(12):e0167682. doi: 10.1371/journal.pone.0167682. eCollection 2016.
8
Interleukin-4 induced 1 (IL4I1) promotes central nervous system remyelination.白细胞介素4诱导因子1(IL4I1)促进中枢神经系统髓鞘再生。
Brain. 2016 Dec;139(Pt 12):3052-3054. doi: 10.1093/brain/aww266.
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IL4I1 augments CNS remyelination and axonal protection by modulating T cell driven inflammation.白细胞介素4诱导分子1(IL4I1)通过调节T细胞驱动的炎症反应增强中枢神经系统的髓鞘再生和轴突保护。
Brain. 2016 Dec;139(Pt 12):3121-3136. doi: 10.1093/brain/aww254. Epub 2016 Oct 25.
10
Carbon-nanotube-interfaced glass fiber scaffold for regeneration of transected sciatic nerve.用于横断坐骨神经再生的碳纳米管连接玻璃纤维支架
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采用多通道桥递送达白细胞介素 4 编码慢病毒可增强神经再生。

Delivery of Interleukin-4-Encoding Lentivirus Using Multiple-Channel Bridges Enhances Nerve Regeneration.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, Michigan.

Department of Biomedical Engineering, Michigan Medicine, Ann Arbor, Michigan.

出版信息

Laryngoscope. 2020 Dec;130(12):2802-2810. doi: 10.1002/lary.28629. Epub 2020 Mar 27.

DOI:10.1002/lary.28629
PMID:32220076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7893531/
Abstract

OBJECTIVES/HYPOTHESIS: Facial nerve injury is a source of major morbidity. This study investigated the neuroregenerative effects of inducing an anti-inflammatory environment when reconstructing a facial nerve defect with a multichannel bridge containing interleukin-4 (IL-4)-encoding lentivirus.

STUDY DESIGN

Animal study.

METHODS

Eighteen adult Sprague-Dawley rats were divided into three groups, all of which sustained a facial nerve gap defect. Group I had reconstruction performed via an IL-4 multichannel bridge, group II had a multichannel bridge with saline placed, and group III had no reconstruction.

RESULTS

Quantitative histomorphometric data were assessed 10 weeks after injury. On post hoc analysis, the IL-4 bridge group demonstrated superior regeneration compared to bridge alone on fiber density (mean = 2,380 ± 297 vs. 1,680 ± 441 fibers/mm , P = .05) and latency time (mean = 2.9 ms ± 0.6 ms vs. 3.6 ms ± 0.3 ms, P < .001). There was significantly greater regeneration in the IL-4 bridge group versus unreconstructed defect for total fiber and density measurements (P ≤ .05). Comparison of facial motor-evoked distal latencies between the IL-4 bridge group versus bridge alone revealed significant electrophysiological improvement at week 8 (P = .02).

CONCLUSIONS

Inflammation has been implicated in a variety of otolaryngologic disorders. This study demonstrates that placement of a multichannel bridge with lentivirus encoding IL-4 improves regenerative outcomes following facial nerve gap injury in rodents. This effect is likely mediated by promotion of an anti-inflammatory environment, and these findings may inform future therapeutic approaches to facial nerve injury.

LEVEL OF EVIDENCE

NA Laryngoscope, 2020.

摘要

目的/假设:面神经损伤是导致发病率高的主要原因。本研究通过使用含有白细胞介素 4(IL-4)编码慢病毒的多通道桥来重建面神经缺损,研究了诱导抗炎环境对面神经再生的影响。

研究设计

动物研究。

方法

将 18 只成年 Sprague-Dawley 大鼠分为三组,所有大鼠均发生面神经间隙缺损。组 I 通过 IL-4 多通道桥进行重建,组 II 放置多通道桥和盐水,组 III 不进行重建。

结果

在损伤后 10 周评估定量组织形态计量学数据。在事后分析中,与单独桥接相比,IL-4 桥组在纤维密度(平均值为 2380±297 与 1680±441 纤维/mm,P=0.05)和潜伏期(平均值为 2.9ms±0.6ms 与 3.6ms±0.3ms,P<.001)方面表现出更好的再生。与未修复的缺陷相比,IL-4 桥组的总纤维和密度测量值的再生明显增加(P≤0.05)。IL-4 桥组与单独桥组之间的面神经运动诱发远端潜伏期比较显示,在第 8 周时电生理有明显改善(P=0.02)。

结论

炎症已被牵连到多种耳鼻喉科疾病中。本研究表明,在啮齿动物面神经间隙损伤后,放置带有慢病毒编码白细胞介素 4 的多通道桥可改善再生结果。这种作用可能是通过促进抗炎环境介导的,这些发现可能为面神经损伤的未来治疗方法提供信息。

证据水平

无