Department of Nephrology, Shenzhen Longhua District Central Hospital, Guangdong Medical University Affiliated Longhua District Central Hospital, Shenzhen, China.
Shenzhen Xenotransplantation Medical Engineering Research and Development Center, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen University School of Medicine, Shenzhen, China.
Xenotransplantation. 2019 May;26(3):e12502. doi: 10.1111/xen.12502. Epub 2019 Feb 16.
The major limitation of organ transplantation is the shortage of available organs from deceased human donors which leads to the deaths of thousands of patients each year. Xenotransplantation is considered to be an effective way to resolve the problem. Immune rejection and coagulation dysfunction are two major hurdles for the successful survival of pig xenografts in primate recipients. Pro-inflammatory cytokines, such as IL-6, TNF-α, and IL-17, play important roles in many diseases and in allotransplantation. However, the pathological roles of these pro-inflammatory cytokines in xenotransplantation remain unclear. Here, we briefly review the signaling transduction and expression regulation of IL-6, TNF-α, and IL-17 and evaluate their potential pathological roles in in vitro and in vivo models of xenotransplantation. We found that IL-6, TNF-α, and IL-17 were induced in most in vitro or in vivo xenotransplantation model. Blockade of these cytokines using gene modification, antibody, or inhibitor had different effects in xenotransplantation. Inhibition of IL-6 signaling with tocilizumab decreased CRP but did not increase xenograft survival. The one possible reason is that tocilizumab can not suppress IL-6 signaling in porcine cells or organs. Other drugs which inhibit IL-6 signaling need to be investigated in xenotransplantation model. Inhibition of TNF-α was beneficial for the survival of xenografts in pig-to-mouse, rat, or NHP models. Blockade of IL-17 using a neutralizing antibody also increased xenograft survival in several animal models. However, the role of IL-17 in the pig-to-NHP xenotransplantation model remains unclear and needs to be further investigated. Moreover, blockade of TNF-α and IL-6 together has got a better effect in pig-to-baboon kidney xenotransplantation. Blockade two or even more cytokines together might get better effect in suppressing xenograft rejection. Better understanding the role of these cytokines in xenotransplantation will be beneficial for choosing better immunosuppressive strategy or producing genetic modification pig.
器官移植的主要限制是可用的已故人类供体器官的短缺,这导致每年有数千名患者死亡。异种移植被认为是解决这一问题的有效方法。免疫排斥和凝血功能障碍是猪异种移植物在灵长类受体中成功存活的两个主要障碍。促炎细胞因子,如白细胞介素-6 (IL-6)、肿瘤坏死因子-α (TNF-α) 和白细胞介素-17 (IL-17),在许多疾病和同种异体移植中都发挥着重要作用。然而,这些促炎细胞因子在异种移植中的病理作用尚不清楚。在这里,我们简要回顾了 IL-6、TNF-α 和 IL-17 的信号转导和表达调控,并评估了它们在异种移植的体外和体内模型中的潜在病理作用。我们发现,IL-6、TNF-α 和 IL-17 在大多数体外或体内异种移植模型中都被诱导产生。使用基因修饰、抗体或抑制剂阻断这些细胞因子在异种移植中产生了不同的效果。用托珠单抗阻断 IL-6 信号降低了 CRP,但并没有增加异种移植物的存活率。一个可能的原因是托珠单抗不能抑制猪细胞或器官中的 IL-6 信号。需要在异种移植模型中研究其他抑制 IL-6 信号的药物。抑制 TNF-α有利于猪到鼠、大鼠或非人灵长类动物模型中异种移植物的存活。用中和抗体阻断 IL-17 也增加了几种动物模型中异种移植物的存活。然而,IL-17 在猪到非人灵长类动物异种移植模型中的作用尚不清楚,需要进一步研究。此外,在猪到狒狒肾脏异种移植中,同时阻断 TNF-α 和 IL-6 效果更好。同时阻断两种甚至更多的细胞因子可能会在抑制异种移植物排斥方面取得更好的效果。更好地了解这些细胞因子在异种移植中的作用将有助于选择更好的免疫抑制策略或产生基因修饰猪。