英夫利昔单抗预防小鼠自身免疫性肝炎的机制

Mengyu Sun, C. Wan, Mengnan Lyu, Yan Song, R. Ma, Wen-tian Liu
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The level of cytokine interleukin (IL)-6, IL-1β, interferon gamma (IFN-γ), IL-4, IL-17A, IL-10 and chemokine C-X-C motif ligand 10 (CXCL10) was measured by enzyme-linked immunosorbent assay (ELISA). Liver samples were taken 12 h after Con-A/PBS injection for hematoxylin-eosin staining. Liver infiltrated lymphocytes were assessed by flow cytometry. The expression of T-box transcription factor 21 (TBX21), GATA binding protein 3 (GATA3), RAR related orphan receptor C (RORC) and CXCL10 at mRNA level was evaluated by quantitative real-time polymerase chain reaction (qRT-PCR). The expression of CXCL10 in liver was detected by Western blotting. Paired t test and one-way analysis of variance were used for statistic analysis. \n \n \nResults \nAt 8, 12, and 24 h after Con-A injection, the serum ALT level, AST level, IL-1β and IFN-γ of prevention group were all lower than those of control group ((545.8±190.3) U/L vs. (865.8±237.7) U/L, (947.6±267.9) U/L vs. (1 448.0±403.5) U/L, (508.6±131.1) U/L vs. (976.6±207.6) U/L; (620.7±132.0) U/L vs. (952.9±106.8) U/L, (801.6±212.0) U/L vs. (1 424.8±236.0) U/L, (632.1±117.8) U/L vs. (1 008.3±187.5) U/L; (31.38±10.12) ng/L vs. (48.12±11.53) ng/L, (39.34±11.40) ng/L vs. (60.00±14.17) ng/L, (29.49±8.22) ng/L vs. (46.89±5.50) ng/L; and (432.93±66.82) ng/L vs. (674.66±97.88) ng/L, (655.09±169.17) ng/L vs. (937.90±166.36) ng/L, (263.40±54.97) ng/L vs. (410.74±86.64) ng/L), and the differences were statistically significant (t = 2.350, 2.308, 4.263, 4.374, 4.860, 3.806, 2.440, 2.541, 3.939, 4.560, 2.660 and 3.210; all P 0.05). \n \n \nConclusions \nInfliximab has certain preventive effects in mice AIH model, which may be achieved by antagonizing TNF-α and decreasing the expression of CXCL10 in liver, reducing the infiltration of T-helper 1 cells and CD8+ T cells into liver, and by reducing T lymphocyte activation induced by inflammatory cytokines thus alleviating the damage of T lymphocytes to hepatocytes. \n \n \nKey words: \nHepatitis, autoimmune; Infliximab; C-X-C motif chemokine ligand 10; Mice","PeriodicalId":10009,"journal":{"name":"中华消化杂志","volume":"25 1","pages":"192-198"},"PeriodicalIF":0.0000,"publicationDate":"2020-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanism of infliximab in preventing autoimmune hepatitis in mice model\",\"authors\":\"Mengyu Sun, C. 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引用次数: 0

摘要

目的观察英夫利昔单抗对自身免疫性肝炎(AIH)的预防作用,并探讨其作用机制。方法采用尾静脉注射刀豆蛋白A (cona)建立小鼠AIH模型。将40只小鼠分为预防组和对照组,每组20只。预防组小鼠在注射Con-A前1 h静脉注射英夫利昔单抗(20 mg/kg),对照组小鼠灌胃200 μL磷酸缓冲盐水(PBS)。注射Con-A/PBS后3、8、12、24 h采集血清。采用比色法检测血清谷草转氨酶(AST)和丙氨酸转氨酶(ALT)水平。采用酶联免疫吸附法(ELISA)检测细胞因子白介素(IL)-6、IL-1β、干扰素γ (IFN-γ)、IL-4、IL- 17a、IL-10和趋化因子C-X-C基序配体10 (CXCL10)的水平。注射Con-A/PBS后12 h取肝脏标本进行苏木精-伊红染色。流式细胞术检测肝脏浸润淋巴细胞。采用实时荧光定量聚合酶链式反应(qRT-PCR)检测T-box转录因子21 (TBX21)、GATA结合蛋白3 (GATA3)、RAR相关孤儿受体C (RORC)和CXCL10 mRNA水平的表达。Western blotting检测CXCL10在肝脏中的表达。采用配对t检验和单因素方差分析进行统计分析。结果Con-A注射后8、12、24 h,预防组血清ALT水平、AST水平、IL-1β、IFN-γ均低于对照组((545.8±190.3)U/L比(865.8±237.7)U/L,(947.6±267.9)U/L比(1 448.0±403.5)U/L,(508.6±131.1)U/L比(976.6±207.6)U/L;(620.7±132.0)U / L和(952.9±106.8)/ L, U / L(801.6±212.0)和(424.8±236.0)U / L, U / L(632.1±117.8)和(008.3±187.5)U / L;(31.38±10.12)ng / L和(48.12±11.53)ng / L ng / L(39.34±11.40)和(60.00±14.17)ng / L ng / L(29.49±8.22)和(46.89±5.50)ng / L;(432.93±66.82)ng/L vs(674.66±97.88)ng/L,(655.09±169.17)ng/L vs(937.90±166.36)ng/L,(263.40±54.97)ng/L vs(410.74±86.64)ng/L),差异均有统计学意义(t = 2.350、2.308、4.263、4.374、4.860、3.806、2.440、2.541、3.939、4.560、2.660、3.210;P < 0.05)。结论英夫利昔单抗对小鼠AIH模型具有一定的预防作用,其机制可能是拮抗TNF-α,降低肝脏中CXCL10的表达,减少T-辅助性1细胞和CD8+ T细胞向肝脏的浸润,减少炎症因子诱导的T淋巴细胞活化,从而减轻T淋巴细胞对肝细胞的损伤。关键词:肝炎;自身免疫;英夫利昔单抗;C-X-C基序趋化因子配体;老鼠
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Mechanism of infliximab in preventing autoimmune hepatitis in mice model
Objective To observe the preventive effects of infliximab in autoimmune hepatitis (AIH) and to explore its mechanism. Methods The mice AIH model was established by injecting concanavalin A (Con-A) into the caudal vein. Forty mice were divided into prevention group and control group, with 20 mice in each group. The mice of prevention group were injected intravenously with infliximab (20 mg/kg) one hour before Con-A injection and the mice of control group were administrated with 200 μL phosphate buffered saline (PBS). Serum was collected 3, 8, 12 and 24 h after Con-A/PBS injection. The serum level of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) was detected by colorimetry. The level of cytokine interleukin (IL)-6, IL-1β, interferon gamma (IFN-γ), IL-4, IL-17A, IL-10 and chemokine C-X-C motif ligand 10 (CXCL10) was measured by enzyme-linked immunosorbent assay (ELISA). Liver samples were taken 12 h after Con-A/PBS injection for hematoxylin-eosin staining. Liver infiltrated lymphocytes were assessed by flow cytometry. The expression of T-box transcription factor 21 (TBX21), GATA binding protein 3 (GATA3), RAR related orphan receptor C (RORC) and CXCL10 at mRNA level was evaluated by quantitative real-time polymerase chain reaction (qRT-PCR). The expression of CXCL10 in liver was detected by Western blotting. Paired t test and one-way analysis of variance were used for statistic analysis. Results At 8, 12, and 24 h after Con-A injection, the serum ALT level, AST level, IL-1β and IFN-γ of prevention group were all lower than those of control group ((545.8±190.3) U/L vs. (865.8±237.7) U/L, (947.6±267.9) U/L vs. (1 448.0±403.5) U/L, (508.6±131.1) U/L vs. (976.6±207.6) U/L; (620.7±132.0) U/L vs. (952.9±106.8) U/L, (801.6±212.0) U/L vs. (1 424.8±236.0) U/L, (632.1±117.8) U/L vs. (1 008.3±187.5) U/L; (31.38±10.12) ng/L vs. (48.12±11.53) ng/L, (39.34±11.40) ng/L vs. (60.00±14.17) ng/L, (29.49±8.22) ng/L vs. (46.89±5.50) ng/L; and (432.93±66.82) ng/L vs. (674.66±97.88) ng/L, (655.09±169.17) ng/L vs. (937.90±166.36) ng/L, (263.40±54.97) ng/L vs. (410.74±86.64) ng/L), and the differences were statistically significant (t = 2.350, 2.308, 4.263, 4.374, 4.860, 3.806, 2.440, 2.541, 3.939, 4.560, 2.660 and 3.210; all P 0.05). Conclusions Infliximab has certain preventive effects in mice AIH model, which may be achieved by antagonizing TNF-α and decreasing the expression of CXCL10 in liver, reducing the infiltration of T-helper 1 cells and CD8+ T cells into liver, and by reducing T lymphocyte activation induced by inflammatory cytokines thus alleviating the damage of T lymphocytes to hepatocytes. Key words: Hepatitis, autoimmune; Infliximab; C-X-C motif chemokine ligand 10; Mice
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