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在细粒棘球蚴清除过程中的 T 细胞耐受和耗竭:接种量在定量肝实验模型中的作用。

T-cell tolerance and exhaustion in the clearance of Echinococcus multilocularis: role of inoculum size in a quantitative hepatic experimental model.

机构信息

State Key Laboratory Incubation Base of Xinjiang Major Diseases Research, and WHO Collaborating Centre on Prevention and Case Management of Echinococcosis, Clinical Medicine Institute, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.

Department of Hepatic Hydatid and Hepatobiliary Surgery, Digestive and Vascular Surgery Centre, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.

出版信息

Sci Rep. 2017 Sep 11;7(1):11153. doi: 10.1038/s41598-017-11703-1.

DOI:10.1038/s41598-017-11703-1
PMID:28894272
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5593833/
Abstract

The local immune mechanisms responsible for either self-healing or sustained chronic infection are not clear, in the development of E. multilocularis larvae. Here, we developed a suitable experimental model that mimics naturally infected livers, according to the parasite load. We demonstrated that local cellular immunity and fibrogenesis are actually protective and fully able to limit metacestode growth in the liver of low or medium dose-infected mice (LDG or MDG), or even to clear it, while impairment of cellular immunity is followed by a more rapid and severe course of the disease in high dose-infected mice (HDG). And recruitment and/ or proliferation of memory T cells (including CD4 Tem, CD8 Tcm and CD8 Tem) and imbalance of T1/T2/T17/Treg-type T cells in liver were not only associated with clearance of the parasite infection in LDG, but also with increased hepatic injury in HDG; in particular the dual role of CD8 T cells depending on the parasite load and the various stages of metacestode growth. Besides, we first demonstrate the association between LAG3- or 2B4-expressing T cells exhaustion and HD inocula in late stages. Our quantitative experimental model appears fully appropriate to study immunomodulation as a therapeutic strategy for patients with Alveolar Echinococcosis.

摘要

局部免疫机制负责自我修复或持续慢性感染尚不清楚,在多房棘球蚴幼虫的发展。在这里,我们根据寄生虫负荷开发了一种合适的实验模型,模拟自然感染的肝脏。我们证明,局部细胞免疫和纤维化实际上是保护性的,并完全能够限制低剂量或中剂量感染小鼠(LDG 或 MDG)肝脏中的包虫生长,甚至清除它,而细胞免疫的损害随后导致高剂量感染小鼠(HDG)疾病的更快和更严重的进程。记忆 T 细胞(包括 CD4 Tem、CD8 Tcm 和 CD8 Tem)的募集和/或增殖以及 T1/T2/T17/Treg 型 T 细胞的失衡不仅与 LDG 中的寄生虫感染清除有关,而且与 HDG 中的肝损伤增加有关;特别是 CD8 T 细胞的双重作用取决于寄生虫负荷和包虫生长的各个阶段。此外,我们首次证明了在晚期 LAG3 或 2B4 表达 T 细胞衰竭与 HD 接种之间的关联。我们的定量实验模型似乎完全适合研究免疫调节作为泡型包虫病患者的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/4459de92d8cc/41598_2017_11703_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/66c9dd8df6b7/41598_2017_11703_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/192aa736564a/41598_2017_11703_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/1afd558f5a87/41598_2017_11703_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/eb279190c593/41598_2017_11703_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/31458dcb3a72/41598_2017_11703_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/ff1faab6cd76/41598_2017_11703_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/b07de81538ed/41598_2017_11703_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/4459de92d8cc/41598_2017_11703_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/66c9dd8df6b7/41598_2017_11703_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/192aa736564a/41598_2017_11703_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/1afd558f5a87/41598_2017_11703_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/eb279190c593/41598_2017_11703_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/31458dcb3a72/41598_2017_11703_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/ff1faab6cd76/41598_2017_11703_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/b07de81538ed/41598_2017_11703_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5593833/4459de92d8cc/41598_2017_11703_Fig8_HTML.jpg

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