A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Ann Surg. 2013 May;257(5):961-7. doi: 10.1097/SLA.0b013e31826ed043.
Our objective was to define the optimal growth factor treatment to be used in combination with lymph node transfer to normalize lymphatic vascular anatomy.
In the lymph node transfer method, lymphatic anastomoses are expected to form spontaneously. However, lymphangiogenic growth factor therapies have shown promising results in preclinical models of lymphedema.
The inguinal lymphatic vasculature of pigs was surgically destroyed around the inguinal lymph node. To enhance the regrowth of the lymphatic network in the defected area, adenoviral vascular endothelial growth factor C (VEGF-C) was administered intranodally or perinodally. Control animals received injections of saline or control vector. The lymphangiogenic effect of the growth factor therapy and any potential adverse effects associated with the 2 alternative delivery routes were examined 2 months postoperatively.
Both routes of growth factor administration induced robust growth of lymphatic vessels and helped to preserve the structure of the transferred lymph nodes in comparison with the controls. The lymph nodes of the control treated animals regressed in size and their nodal structure was partly replaced by fibro-fatty scar tissue. Intranodally injected adenoviral VEGF-C and adenoviral vector encoding control gene LacZ induced macrophage accumulation inside the node, whereas perinodal administration of VEGF-C did not have this adverse effect.
Lymphangiogenic growth factors improve lymphatic vessel regeneration and lymph node function after lymph node transfer. The perinodal route of delivery provides a basis for future clinical trials in lymphedema patients.
我们的目的是确定与淋巴结转移相结合以正常化淋巴管解剖结构的最佳生长因子治疗方法。
在淋巴结转移方法中,预期会自发形成淋巴管吻合。然而,淋巴生成生长因子疗法在淋巴水肿的临床前模型中显示出有希望的结果。
猪的腹股沟淋巴管在腹股沟淋巴结周围通过手术被破坏。为了增强缺陷区域中淋巴管网络的再生,将腺病毒血管内皮生长因子 C(VEGF-C)经淋巴结内或周围注射。对照动物接受盐水或对照载体注射。术后 2 个月检查生长因子治疗的淋巴管生成效果和两种替代传递途径的任何潜在不良反应。
与对照组相比,两种生长因子给药途径都诱导了淋巴管的强烈生长,并有助于保留转移淋巴结的结构。接受对照处理的动物的淋巴结缩小,其淋巴结结构部分被纤维脂肪瘢痕组织取代。腺病毒 VEGF-C 经淋巴结内注射和编码对照基因 LacZ 的腺病毒载体诱导了节点内巨噬细胞的积聚,而 VEGF-C 经淋巴结周围给药则没有这种不良反应。
淋巴管生成生长因子可改善淋巴结转移后淋巴管的再生和淋巴结功能。递药途径为淋巴水肿患者的未来临床试验提供了基础。