[1] |
Polaris Observatory Collaborators. Global prevalence, treatment, and prevention of hepatitis B virus infection in 2016: a modelling study[J]. Lancet Gastroenterol Hepatoly, 2018, 3(6): 383-403.
|
[2] |
张敏, 李静, 王福生. 儿童慢性乙型肝炎抗病毒治疗与临床治愈: 进展与挑战[J]. 中华肝脏病杂志, 2021, 29(12): 1218-1223.
|
[3] |
Bertoletti A, Ferrari C. Innate and adaptive immune responses in chronic hepatitis B virus infections: towards restoration of immune control of viral infection[J]. Gut, 2012, 61(12): 1754-1764.
doi: 10.1136/gutjnl-2011-301073
pmid: 22157327
|
[4] |
中华医学会感染病学分会, 中华医学会肝病学分会. 慢性乙型肝炎防治指南(2019年版)[J]. 中华传染病杂志, 2019, 37(12): 711-736.
|
[5] |
Tan HY, Yong YK, Ng CS, et al. Mucosal-associated invariant T cells: diplomatic front-runners in the fight against hepatitis B virus infection[J]. Crit Rev Immunol, 2021, 41(5): 1-16.
|
[6] |
Jahreis S, Boettcher S, von Lilienfeld-Toal M, et al. MAIT cell activation by fungal pathogens[J]. Methods Mol Biol, 2020, 2098: 167-177.
doi: 10.1007/978-1-0716-0207-2_11
pmid: 31792822
|
[7] |
Preeyaa SU, Murugesan A, Sopnajothi S, et al. Peripheral follicular T helper cells and mucosal-associated invariant T cells represent activated phenotypes during the febrile phase of acute dengue virus infection[J]. Viral Immunol, 2020, 33(9): 610-615.
|
[8] |
Boeijen LL, Montanari NR, Groen RA, et al. Mucosal-associated invariant T cells are more activated in chronic hepatitis B, but not depleted in blood: reversal by antiviral therapy[J]. J Infect Dis, 2017, 216(8): 969-976.
doi: 10.1093/infdis/jix425
pmid: 28968772
|
[9] |
Huang W, He W, Shi X, et al. Mucosal-associated invariant T-cells are severely reduced and exhausted in humans with chronic HBV infection[J]. J Viral Hepat, 2020, 27(11): 1096-1107.
|
[10] |
Yong YK, Saeidi A, Tan HY, et al. Hyper-expression of PD-1 is associated with the levels of exhausted and dysfunctional phenotypes of circulating CD161++ TCR iVα7.2+ mucosal-associated invariant T cells in chronic hepatitis B virus infection[J]. Front Immunol, 2018, 9: 472.
|
[11] |
Healy K, Pavesi A, Parrot T, et al. Human MAIT cells endowed with HBV specificity are cytotoxic and migrate towards HBV-HCC while retaining antimicrobial functions[J]. JHEP Rep, 2021, 3(4): 100318.
|
[12] |
Shao L, Zhao H, Guo RF, et al. Biopsy-based single-cell transcriptomics reveals MAIT cells as potential targets for controlling fibrosis-related liver inflammation due to chronic hepatitis-B infection[J]. Clin Transl Med, 2022, 12(10): e1073.
doi: 10.1002/ctm2.1073
pmid: 36263680
|
[13] |
Yong YK, Tan HY, Saeidi A, et al. Decrease of CD69 levels on TCR Va7.2+ CD4+ innate-like lymphocytes is associated with impaired cytotoxic functions in chronic hepatitis B virus-infected patients[J]. Innate Immun, 2017, 23(5): 459-467.
|
[14] |
Dias J, Boulouis C, Gorin JB, et al. The CD4- CD8-MAIT cell subpopulation is a functionally distinct subset developmentally related to the main CD8+ MAIT cell pool[J]. Proc Natl Acad Sci U S A, 2018, 115(49): E11513-E11522.
|
[15] |
Huang W, He W, Shi X, et al. The role of CD1d and MR1 restricted T cells in the liver[J]. Front Immunol, 2018, 9: 2424.
doi: 10.3389/fimmu.2018.02424
pmid: 30425710
|
[16] |
Khanam A, Chua JV, Kottilil S. Immunopathology of chronic hepatitis B infection: Role of innate and adaptive immune response in disease progression[J]. Int J Mol Sci, 2021, 22(11): 5497.
|