Li Liang, Duan Mubing, Chen Weisan, Jiang An, Li Xiaoming, Yang Jun, Li Zongfang
National & Local Joint Engineering Research Center of Biodiagnosis and Biotherapy, The Second Affiliated Hospital, Xi'an Jiaotong University, No.157, Xiwu Road, Xi'an, 710004, Shaanxi, China.
Liver and Spleen Diseases Research Center, Shaanxi Province, No.157, Xiwu Road, Xi'an, 710004, Shaanxi, China.
J Transl Med. 2017 May 23;15(1):111. doi: 10.1186/s12967-017-1214-8.
The spleen is a secondary lymphoid organ which can influence the progression of multiple diseases, notably liver cirrhosis. In chronic liver diseases, splenomegaly and hypersplenism can manifest following the development of portal hypertension. These splenic abnormalities correlate with and have been postulated to facilitate the progression of liver fibrosis to cirrhosis, although precise mechanisms remain poorly understood. In this review, we summarize the literature to highlight the mechanistic contributions of splenomegaly and hypersplenism to the development of liver cirrhosis, focusing on three key aspects: hepatic fibrogenesis, hepatic immune microenvironment dysregulation and liver regeneration. We conclude with a discussion of the possible therapeutic strategies for modulating splenic abnormalities, including the novel potential usage of nanomedicine in non-surgically targetting splenic disorders for the treatment of liver cirrhosis.
脾脏是一个二级淋巴器官,可影响多种疾病的进展,尤其是肝硬化。在慢性肝病中,脾肿大和脾功能亢进可在门静脉高压形成后出现。这些脾脏异常与肝纤维化向肝硬化的进展相关,并被推测促进了这一进程,尽管确切机制仍知之甚少。在本综述中,我们总结文献以突出脾肿大和脾功能亢进对肝硬化发展的机制性作用,重点关注三个关键方面:肝纤维化形成、肝脏免疫微环境失调和肝再生。我们最后讨论了调节脾脏异常的可能治疗策略,包括纳米医学在非手术靶向脾脏疾病治疗肝硬化方面的新潜在用途。