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肠道细菌对特定免疫细胞的影响是持续肝脏炎症的基础 [复制链接]

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发表于 2018-1-17 11:12 |只看该作者 |倒序浏览 |打印
Effect of gut bacteria on specific immune cells underlies persistent liver inflammation
January 16, 2018, Agency for Science, Technology and Research (A*STAR), Singapore

Persistent liver inflammation in sufferers of chronic viral hepatitis is likely caused by interactions between pro-inflammatory immune cells in the liver and products from gut bacteria, according to new work involving A*STAR researchers. The findings identify new therapeutic targets.

Chronic viral hepatitis is characterized by persistent inflammation of the liver, but the mechanism that maintains this inflammation has been poorly understood. The degree of inflammation does not correspond to the extent of viral activity in the liver, or to the activity of immune cells that specifically target the virus, as might be expected.

The new work, a collaboration between the laboratories of Antonio Bertoletti at the Duke-NUS Medical and Singapore Institute of Clinical Sciences, the laboratory of Qingfeng Chen at the A*STAR Institute of Molecular and Cell Biology and Charles-Antoine Dutertre in the laboratory of Florent Ginhoux from the A*STAR Singapore Immunology Network, aimed to determine the mechanisms underpinning the inflammation. The researchers focused on a different group of immune cells called macrophages, which are increasingly recognized as significant in liver disease.

They analyzed the molecular and functional profiles of macrophages in the livers of patients with chronic viral hepatitis and those of healthy people. In the livers of patients, there was an excess of macrophages with a specific profile that promotes inflammation. "Unlike macrophages found in a healthy liver, these macrophages have the capacity to continuously produce pro-inflammatory mediators when they encounter bacterial products," explains Dutertre.

The team studied this phenomenon further in mice engineered to have human liver cells and human immune cells. The mice were infected with hepatitis B virus, and consequently accumulated the same pro-inflammatory macrophage population in the liver as that seen in patients. Treatment of the mice with antibiotics to reduce the gut bacteria reversed the accumulation of these macrophages. "This demonstrated that bacterial products that leak from the gut into the liver are responsible for the accumulation of the pro-inflammatory macrophages," says Dutertre.

The results identify a novel mechanism that maintains inflammation in chronic viral hepatitis. Dutertre and colleagues say that their findings suggest new therapeutic approaches, in addition to targeting the virus, that involve modifying the intestinal bacteria or depleting the pro-inflammatory macrophages in the liver.

The researchers are now investigating the mechanism behind the effects of bacterial products on macrophages in the liver. So far they have identified certain soluble mediators that play a pivotal role. "Our hypothesis is that by inhibiting these soluble mediators, we could limit the accumulation of the pro-inflammatory macrophages and resolve liver inflammation in patients with chronic viral hepatitis," concludes Dutertre.


More information: Alfonso Tan-Garcia et al. Intrahepatic CD206 + macrophages contribute to inflammation in advanced viral-related liver disease, Journal of Hepatology (2017). DOI: 10.1016/j.jhep.2017.04.023

Provided by: Agency for Science, Technology and Research (A*STAR), Singapore search and more info

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发表于 2018-1-17 11:12 |只看该作者
肠道细菌对特定免疫细胞的影响是持续肝脏炎症的基础
2018年1月16日,新加坡科学技术研究局(A * STAR)

根据A * STAR研究人员的新工作,慢性病毒性肝炎患者持续性肝脏炎症很可能是由肝脏中的促炎性免疫细胞与肠道细菌产物之间的相互作用引起的。这些发现确定了新的治疗目标。

慢性病毒性肝炎的特征是持续的肝脏炎症,但是维持这种炎症的机制目前知之甚少。正如可以预料的那样,炎症的程度不对应于肝脏中病毒活性的程度,或不对应于特异性靶向病毒的免疫细胞的活性。

这项新工作是Duke-NUS医学院的Antonio Bertoletti实验室与新加坡临床科学研究所,A * STAR分子和细胞生物学研究所的Qingfeng Chen实验室以及Charles-Antoine Dutertre实验室之间的合作。来自A * STAR新加坡免疫学网络的Florent Ginhoux旨在确定支持炎症的机制。研究人员将重点放在一组称为巨噬细胞的免疫细胞上,这种细胞越来越被认为在肝脏疾病中显着。

他们分析了慢性病毒性肝炎患者和健康人群肝脏中巨噬细胞的分子和功能特征。在患者的肝脏中,具有促进炎症的特定分布的巨噬细胞过量。 Dutertre解释说:“与健康肝脏中发现的巨噬细胞不同,这些巨噬细胞有能力在遇到细菌产物时持续产生促炎介质。

研究小组进一步研究了这种现象,设计了具有人肝细胞和人免疫细胞的小鼠。这些小鼠感染了乙型肝炎病毒,并因此在患者肝脏中积累了相同的促炎巨噬细胞群。用抗生素治疗小鼠以减少肠道细菌逆转这些巨噬细胞的积累。 Dutertre说:“这表明从肠道泄漏到肝脏的细菌产物负责促炎巨噬细胞的积累。

结果确定了在慢性病毒性肝炎中维持炎症的新型机制。 Dutertre及其同事表示,他们的发现提示除了针对病毒之外,新的治疗方法还涉及修改肠道细菌或消耗肝脏中的促炎巨噬细胞。

研究人员正在研究细菌产物对肝脏巨噬细胞影响的机制。到目前为止,他们已经确定了一些可发挥关键作用的可溶性介质。 Dutertre总结说:“我们的假设是,通过抑制这些可溶性介质,我们可以限制促炎巨噬细胞的积累,并解决慢性病毒性肝炎患者的肝脏炎症。

进一步探索:锌可能是控制肝脏疾病的关键

更多信息:Alfonso Tan-Garcia et al。肝脏CD206 +巨噬细胞在晚期病毒相关的肝脏疾病中有助于炎症,“肝脏病学杂志”(2017)。 DOI:10.1016 / j.jhep.2017.04.023

由新加坡科学技术研究局(A * STAR)提供,搜索和更多信息

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发表于 2018-1-17 12:21 |只看该作者
我们的假设是,通过抑制这些可溶性介质,我们可以限制促炎巨噬细胞的积累,并解决慢性病毒性肝炎患者的肝脏炎症。
进一步探索:锌可能是控制肝脏疾病的关键

不错,补锌的文章已经在路上。。。

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