调节性T细胞在肝脏移植免疫耐受中的作用
Role of Regulatory T Cells in Immune Tolerance in Liver Transplantation
DOI: 10.12677/ACM.2021.114234, PDF,    国家自然科学基金支持
作者: 张 剑:重庆市璧山区妇幼保健院外科,重庆;刘 涛, 龚建平*:重庆医科大学附属第二医院肝胆外科,重庆
关键词: 调节性T细胞肝移植免疫耐受Regulatory T Cells Liver Transplantation Immune Tolerance
摘要: 肝移植是终末肝病唯一有效的治疗方式,但是肝移植术后建立免疫耐受的问题一直没有得到很好的解决。人的肝脏含有不同的效应性淋巴细胞亚群,它们由调节性T细胞(regulatory t cells, Treg)的细胞亚群来控制。免疫抑制是抗原特异性的,这需要Treg的激活来协调完成。因此,Treg在维持肝移植免疫耐受方面具有至关重要的作用,是诱导肝移植免疫耐受形成的关键细胞。本文将就Treg与肝移植免疫耐受的关系以及相关机制进行简要介绍。
Abstract: Liver transplantation is the only effective treatment for terminal liver disease, but the problem of establishing immune tolerance after liver transplantation has not been well solved. The human liver contains different subsets of effector lymphocytes that are kept in check by a subpopulation as Regulatory T cells (Treg). Treg plays an important role in immune regulation, so the balance between effector and regulatory lymphocytes usually determines the outcome of liver immunity. Therefore, Treg plays a crucial role in maintaining immune tolerance in liver transplantation and is a key cell for inducing the formation of immune tolerance in liver transplantation. This article will briefly introduce the relationship between Treg and immune tolerance in liver transplantation as well as the relevant mechanisms.
文章引用:张剑, 刘涛, 龚建平. 调节性T细胞在肝脏移植免疫耐受中的作用[J]. 临床医学进展, 2021, 11(4): 1630-1635. https://doi.org/10.12677/ACM.2021.114234

参考文献

[1] Trebicka, J., Sundaram, V., Moreau, R., et al. (2020) Liver Transplantation for Acute-on-Chronic Liver Failure: Science or Fiction? Liver Transplantation, 26, 906-915. [Google Scholar] [CrossRef] [PubMed]
[2] Yu, J., Liu, Z., Li, C., et al. (2020) Regulatory T Cell Therapy Following Liver Transplantation. Liver Transplantation, 27, 264-280. [Google Scholar] [CrossRef] [PubMed]
[3] Lee, J.C., Mehdizadeh, S., Smith, J., et al. (2020) Regulatory T Cell Control of Systemic Immunity and Immunotherapy Response in Liver Metastasis. Science Immunology, 5, eaba0759. [Google Scholar] [CrossRef] [PubMed]
[4] Huang, H., Lu, Y., Zhou, T., et al. (2018) Innate Immune Cells in Immune Tolerance after Liver Transplantation. Frontiers in Immunology, 9, 2401. [Google Scholar] [CrossRef] [PubMed]
[5] Jiang, Y., Que, W., Zhu, P., et al. (2020) The Role of Diverse Liver Cells in Liver Transplantation Tolerance. Frontiers in Immunology, 11, 1203. [Google Scholar] [CrossRef] [PubMed]
[6] Tedesco, D. and Grakoui, A. (2018) Environmental Peer Pressure: CD4(+) T Cell Help in Tolerance and Transplantation. Liver Transplantation, 24, 89-97. [Google Scholar] [CrossRef] [PubMed]
[7] Ni, X., Tao, J., Barbi, J., et al. (2018) YAP Is Essential for Treg-Mediated Suppression of Antitumor Immunity. Cancer Discovery, 8, 1026-1043. [Google Scholar] [CrossRef
[8] Tanaka, A. and Sakaguchi, S. (2017) Regulatory T Cells in Cancer Immunotherapy. Cell Research, 27, 109-118. [Google Scholar] [CrossRef] [PubMed]
[9] Śledzińska, A., Vila de Mucha, M., Bergerhoff, K., et al. (2020) Regulatory T Cells Restrain Interleukin-2- and Blimp-1-Dependent Acquisition of Cytotoxic Function by CD4(+) T Cells. Immunity, 52, 151-166.e6. [Google Scholar] [CrossRef] [PubMed]
[10] Jeffery, H.C., Braitch, M.K., Brown, S., et al. (2016) Clinical Potential of Regulatory T Cell Therapy in Liver Diseases: An Overview and Current Perspectives. Frontiers in Immunology, 7, 334. [Google Scholar] [CrossRef] [PubMed]
[11] Esensten, J.H., Muller, Y.D., Bluestone, J.A., et al. (2018) Regulatory T-Cell Therapy for Autoimmune and Autoinflammatory Diseases: The Next Frontier. The Journal of Allergy and Clinical Immunology, 142, 1710-1718. [Google Scholar] [CrossRef] [PubMed]
[12] von Knethen, A., Heinicke, U., Weigert, A., et al. (2020) Histone Deacetylation Inhibitors as Modulators of Regulatory T Cells. International Journal of Molecular Sciences, 21, 2356. [Google Scholar] [CrossRef] [PubMed]
[13] Shi, H. and Chi, H. (2019) Metabolic Control of Treg Cell Stability, Plasticity, and Tissue-Specific Heterogeneity. Frontiers in Immunology, 10, 2716. [Google Scholar] [CrossRef] [PubMed]
[14] Ohkura, N. and Sakaguchi, S. (2020) Transcriptional and Epigenetic Basis of Treg Cell Development and Function: Its Genetic Anomalies or Variations in Autoimmune Diseases. Cell Research, 30, 465-474. [Google Scholar] [CrossRef] [PubMed]
[15] Owen, D.L., Mahmud, S.A., Sjaastad, L.E., et al. (2019) Thymic Regulatory T Cells Arise via Two Distinct Developmental Programs. Nature Immunology, 20,195-205. [Google Scholar] [CrossRef] [PubMed]
[16] Boroughs, A.C., Larson, R.C., Choi, B.D., et al. (2019) Chimeric Antigen Receptor Costimulation Domains Modulate Human Regulatory T Cell Function. JCI Insight, 5, e126194. [Google Scholar] [CrossRef] [PubMed]
[17] Zhao, Y., Lee, C.K., Lin, C.H., et al. (2019) PD-L1:CD80 Cis-Heterodimer Triggers the Co-Stimulatory Receptor CD28 While Repressing the Inhibitory PD-1 and CTLA-4 Pathways. Immunity, 51, 1059-1073.e9. [Google Scholar] [CrossRef] [PubMed]
[18] Mitsuiki, N., Schwab, C. and Grimbacher, B. (2019) What Did We Learn from CTLA-4 Insufficiency on the Human Immune System? Immunological Reviews, 287, 33-49. [Google Scholar] [CrossRef] [PubMed]
[19] Fan, M.Y., Low, J.S., Tanimine, N., et al. (2018) Differential Roles of IL-2 Signaling in Developing versus Mature Tregs. Cell Reports, 25, 1204-1213.e4. [Google Scholar] [CrossRef] [PubMed]
[20] Rosenzwajg, M., Lorenzon, R., Cacoub, P., et al. (2019) Immunological and Clinical Effects of Low-Dose Interleukin-2 across 11 Autoimmune Diseases in a Single, Open Clinical Trial. Annals of the Rheumatic Diseases, 78, 209-217. [Google Scholar] [CrossRef] [PubMed]
[21] Flippe, L., Bezie, S., Anegon, I., et al. (2019) Future Prospects for CD8(+) Regulatory T Cells in Immune Tolerance. Immunological Reviews, 292, 209-224. [Google Scholar] [CrossRef] [PubMed]
[22] Bluestone, J.A. and Tang, Q. (2018) T(reg) Cells—The Next Frontier of Cell Therapy. Science (New York, NY), 362, 154-155. [Google Scholar] [CrossRef] [PubMed]
[23] Terry, L.V. and Oo, Y.H. (2020) The Next Frontier of Regulatory T Cells: Promising Immunotherapy for Autoimmune Diseases and Organ Transplantations. Frontiers in Immunology, 11, Article ID: 565518. [Google Scholar] [CrossRef] [PubMed]
[24] Fritsche, E., Volk, H.D., Reinke, P., et al. (2020) Toward an Optimized Process for Clinical Manufacturing of CAR-Treg Cell Therapy. Trends in Biotechnology, 38, 1099-1112. [Google Scholar] [CrossRef] [PubMed]