Change and significance of HBcAg-specific Th22 cells in patients with hepatitis B virus infection
-
摘要:
目的观察HBV感染者中辅助性T淋巴细胞(Th) 22、IL-22和转录因子芳香烃受体(AhR)的变化及与临床指标的相关性。方法选择2018年3月-2019年3月在西安市第八医院就诊的急性乙型肝炎(AHB)患者11例、慢性乙型肝炎(CHB)患者38例和健康对照者(HC) 16例,CHB患者使用替诺福韦酯(TDF)抗病毒治疗,收集AHB患者基线和出院6个月后的外周血,收集CHB患者基线、治疗6个月和治疗12个月的外周血,分离外周血单个核细胞(PBMC)和血浆,分别使用佛波酯+伊乌诺霉素和重组HBcAg刺激PBMC,流式细胞术检测非特异性CD3+CD4+IL-22+的Th22和HBcAg特异性Th22。ELISA检测血浆IL-22水平。实时定量PCR检测PBMC中AhR mRNA水平。符合正态分布的计量资料两组间比较采用t检验、配对t检验,多组间比较采用单因素方差分析,进一步两两比较采用LSD-t检验;非正态分布的计量资料多组间比较采用Kruskal-Wallis H检验。计数资料采用χ2检验。采用Spearman相关性分析进行相关性检验。结果 AHB患者非特异性Th2...
Abstract:Objective To investigate the changes of Th22 cells,interleukin-22( IL-22),and transcription factor aryl hydrocarbon receptor( AhR) in patients with hepatitis B virus( HBV) infection and their correlation with clinical indices. Methods A total of 11 patients with acute hepatitis B( AHB) and 38 patients with chronic hepatitis B( CHB) who attended Eighth Hospital of Xi'an from March 2018 to March 2019 were enrolled as AHB group and CHB group,respectively,and 16 healthy controls were enrolled as HC group. The patients with CHB received tenofovir disoproxil fumarate( TDF) antiviral therapy. Peripheral blood samples were collected for AHB patients at baseline and 6 months after discharge,and peripheral blood samples were collected for CHB patients at baseline and at months 6 and 12 of treatment;peripheral blood mononuclear cells( PBMCs) and plasma were isolated,then PBMCs were stimulated with phorbol ester + ionomycin or recombinant HBcAg,and flow cytometry was used to measure nonspecific CD3+CD4+IL-22+Th22 cells and HBcAg-specific Th22 cells.ELISA was used to measure the plasma level of IL-22,and quantitative real-time PCR was used to measure the mRNA expression of AhR in PBMCs. The t-test and the paired t-test were used for comparison of normally distributed continuous data between two groups; a one-way analysis of variance was used for comparison of normally distributed continuous data between multiple groups,and the least significant difference t-test was used for further comparison between two groups; the Kruskal-Wallis H test was used for comparison of non-normally distributed continuous data between multiple groups. The chi-square test was used for comparison of categorical data between groups. A Spearman correlation analysis was used to investigate correlation. Results The AHB group had a significantly higher percentage of nonspecific Th22 cells than the CHB group( 2. 86% ± 0. 45% vs 1. 39% ± 0. 33%,t = 11. 80,P < 0. 001) and the HC group( 2. 86% ± 0. 45%vs 0. 80% ± 0. 13%,t = 17. 30,P < 0. 001),and the CHB group also had a significantly higher percentage of nonspecific Th22 cells than the HC group( t = 6. 825,P < 0. 001). The AHB group had a significantly higher percentage of HBc Ag-specific Th22 cells than the CHB group( 2. 97% ± 0. 52% vs 1. 22% ± 0. 22%,t = 16. 58,P < 0. 001). The AHB group had a significantly higher plasma level of IL-22 than the CHB group( 130. 7 ± 39. 97 pg/ml vs 66. 59 ± 20. 83 pg/ml,t = 7. 176,P < 0. 001) and the HC group( 130. 7 ± 39. 97 pg/ml vs50. 63 ± 11. 07 pg/ml,t = 7. 662,P < 0. 001),and the CHB group also had a significantly higher plasma level of IL-22 than the HC group( t = 2. 887,P = 0. 006). The AHB group had significantly higher mRNA expression of AhR than the CHB group( 11. 45 ± 3. 03 vs 4. 81 ±1. 25,t = 10. 85,P < 0. 0001) and the HC group( 11. 45 ± 3. 03 vs 1. 10 ± 0. 17,t = 13. 75,P < 0. 001),and the CHB group also had significantly higher mRNA expression of AhR than the HC group( t = 11. 77,P < 0. 001). In both AHB and CHB patients,the percentage of HBc Ag-specific Th22 cells was positively correlated with alanine aminotransferase( ALT) level( r = 0. 638 and 0. 830,P = 0. 035 and0. 002),and the plasma level of IL-22 was also positively correlated with ALT level( r = 0. 552 and 0. 431,P = 0. 001 and 0. 007). The AHB patients were followed up at 6 months after discharge,and there were significant reductions in the percentage of HBc Ag-specific Th22 cells( 2. 79% ± 0. 56%,t = 3. 055,P = 0. 012) and the plasma level of IL-22( 105. 8 ± 25. 23 pg/ml,t = 2. 362,P = 0. 040) from baseline. All CHB patients received TDF antiviral therapy and were followed up at months 6 and 12 of treatment,and there were significant reductions in the percentage of HBc Ag-specific Th22 cells( t = 4. 353 and 3. 927,all P < 0. 001) and the plasma level of IL-22( t =4. 426 and 4. 810,both P < 0. 0001) from baseline to months 6 and 12 of treatment. Conclusion HBc Ag-specific Th22 cells and IL-22 are closely associated with inflammatory response to HBV infection.
-
Key words:
- hepatitis B virus /
- hepatitis B core antigens /
- interleukins /
- Th22 cells
-
[1] EZZIKOURI S,KAYESH M,BENJELLOUN S,et al. Targeting host innate and adaptive immunity to achieve the functional cure of chronic hepatitis B[J]. Vaccines(Basel),2020,8(2):e216. [2] WU J,HAN M,LI J,et al. Immunopathogenesis of HBV Infection[J]. Adv Exp Med Biol,2020,1179:71-107. [3] JIA L,WU C. The biology and functions of Th22 cells[J]. Adv Exp Med Biol,2014,841:209-230. [4] Chinese Society of Hepatology and Chinese Society of Infectious Diseases,Chinese Medical Association. The guideline of prevention and treatment for chronic hepatitis B:A 2015 update[J]. J Clin Hepatol,2015,31(12):1941-1960.(in Chinese)中华医学会肝病学分会,中华医学会感染病学分会.慢性乙型肝炎防治指南(2015年更新版)[J].临床肝胆病杂志,2015,31(12):1941-1960. [5] WEI X,WANG JP,HAO CQ,et al. Notch signaling contributes to liver inflammation by regulation of interleukin-22-producing cells in hepatitis B virus infection[J]. Front Cell Infect Microbiol,2016,6:132. [6] ZENEWICZ LA. IL-22:There is a gap in our knowledge[J].Immunohorizons,2018,2(6):198-207. [7] WANG W,ZHAO RR,YANG XF,et al. Influence of Notch signaling pathway on interleukin-22 secreted by CD4+T cells in patients with hepatitis B[J]. J Chin Hepatol,2016,32(7):1315-1318.(in Chinese)王伟,赵荣荣,杨晓飞,等.Notch信号通路对乙型肝炎患者CD4+T淋巴细胞分泌白细胞介素22的影响[J].临床肝胆病杂志,2016,32(7):1315-1318. [8] WANG B,ZHAO XP,FAN YC,et al. IL-17A but not IL-22suppresses the replication of hepatitis B virus mediated by over-expression of Mx A and OAS mRNA in the HepG2. 2. 15cell line[J]. Antiviral Res,2013,97(3):285-292. [9] ZHANG Y,COBLEIGH MA,LIAN JQ,et al. A proinflammatory role for interleukin-22 in the immune response to hepatitis B virus[J]. Gastroenterology,2011,141(5):1897-1906. [10] ZHAO J,ZHANG Z,LUAN Y,et al. Pathological functions of interleukin-22 in chronic liver inflammation and fibrosis with hepatitis B virus infection by promoting T helper 17 cell recruitment[J]. Hepatology,2014,59(4):1331-1342. [11] FENG D,KONG X,WENG H,et al. Interleukin-22 promotes proliferation of liver stem/progenitor cells in mice and patients with chronic hepatitis B virus infection[J]. Gastroenterology,2012,143(1):188-198. e7. [12] MO R,WANG P,LAI R,et al. Persistently elevated circulating Th22 reversely correlates with prognosis in HBV-related acuteon-chronic liver failure[J]. J Gastroenterol Hepatol,2017,32(3):677-686. [13] JIANG BC,LIU X,LIU XH,et al. Notch signaling regulates circulating T helper 22 cells in patients with chronic hepatitis C[J]. Viral Immunol,2017,30(7):522-532. [14] COBLEIGH MA,ROBEK MD. Protective and pathological properties of IL-22 in liver disease:Implications for viral hepatitis[J].Am J Pathol,2013,182(1):21-28. [15] GAO W,FAN YC,ZHANG JY,et al. Emerging role of interleukin 22 in hepatitis B virus infection:A double-edged sword[J]. J Clin Transl Hepatol,2013,1(2):103-108. [16] REHERMANN B,THIMME R. Insights from antiviral therapy into immune responses to hepatitis B and C virus infection[J].Gastroenterology,2019,156(2):369-383. [17] HAO C,WANG J,KANG W,et al. Kinetics of Th17 cytokines during telbivudine therapy in patients with chronic hepatitis B[J]. Viral Immunol,2013,26(5):336-342.
计量
- 文章访问数: 4845
- HTML全文浏览量: 40
- PDF下载量: 78
- 被引次数: 0