Objective:To investigate the immunomodulatory effects of Chai Ge oral liquid on mice with bronchiolitis model. Methods:60 mice were divided into control group, model group, Chai Ge oral liquid low dose group (5.18 mg·kg-1·d-1), high dose group (23.1 mg·kg-1·d-1), ribavirin group (10 mg·kg-1·d-1), each group had 12 rats. Model establishment:after the mice were successfully anesthetized, 100 μl of RSV virus was instilled into the nasal cavity of the mice. After the nasal drops, the heads of the mice were kept back for 1 minute to allow the RSV virus fluid to flow into the bronchus and trachea of the mice once a day for 2 days.The lung tissue virus titer and lung index were detected.The expression of Helper T cells 17 (Th17) and Regulatory T (Treg) cells were detected by flow cytometry. The interleukin-4 (IL-4), interleukin-10 (IL-10),interleukin-17 (IL-17) and transforming growth factor-beta (TGF-β) were measured by enzyme-linked immunosorbent assay (ELISA). Results:The lung index, lung pathology score, Th17 cells, IL-4 and IL-17 levels in the low dose group, the high dose group and the ribavirin group were higher than those in the control group (P<0.05); the Treg cells, IL-10 and TGF-β levels were lower than those in the control group (P<0.05).The virus titer, lung index, lung pathology score, Th17 cell, IL-4 and IL-17 levels in the low dose group, the high dose group and the ribavirin group were lower than those in the model group (P<0.05); the Treg cells, IL-10 and TGF-β levels were higher than those in the model group (P<0.05).The virus titer, lung index, lung pathology score, Th17 cell, IL-4 and IL-17 levels in the high dose group were significantly lower than those in the low dose group and the ribavirin group (P<0.05); the Treg cells, IL-10 and TGF-β levels were higher than those in the low dose group and the ribavirin group (P<0.05). There was no significant difference in each indicators between the low dose group and the ribavirin group (P>0.05). Conclusion:Chai Ge oral solution may play a therapeutic role in mice with bronchiolitis model by immunoregulatory mechanism. |
[1] NAPIERKOWSKI D B.Diagnosing and treating respiratory syncytial virus bronchiolitis[J].Nurse Pract,2016,41(9):1-4.
[2] ZHOU Y,BACHARIER L B,ISAACSON-SCHMID M,et al.Azithromycin therapy during respiratory syncytial virus bronchiolitis:Upper airway microbiome alterations and subsequent recurrent wheeze[J].J Allergy Clin Immunol,2016,138(4):1215-1219.e5.
[3] 赵金玉,郝瑞芳.柴葛解肌汤合银翘散加减治疗小儿流感发热60例[J].江西中医药,2015,46(7):34-35.
[4] LU S,HARTERT T V,EVERARD M L,et al.Predictors of asthma following severe respiratory syncytial virus(RSV) bronchiolitis in early childhood[J].Pediatr Pulmonol,2016,51(12):1382-1392.
[5] MANSBACH J M,HASEGAWA K,HENKE D M,et al.Respiratory syncytial virus and rhinovirus severe bronchiolitis are associated with distinct nasopharyngeal microbiota[J].J Allergy Clin Immunol,2016,137(6):1909-1913.e4.
[6] 马子风,尹磊淼,冉君,等.小鼠过敏性哮喘模型制备的特点分析[J].东南大学学报(医学版),2014,33(5):650-655.
[7] 吕红娇,张亚丽,王虹,等.小儿胸闷、气短相关原因分析[J].东南大学学报(医学版)2016,35(4):518-522.
[8] 汪秀梅.柴葛银翘散治疗小儿外感发热初期的体会[J].中医儿科杂志,2012,8(3):27-28.
[9] 王刚,谷容,刘彬,等.柴葛口服液制剂工艺研究[J].儿科药学杂志,2003(6):21-24.
[10] WU X,ZHOU X,HU Y,et al.Neutralization of nerve growth factor (NGF) inhibits the Th2 response and protects against the respiratory syncytial virus (RSV) infection[J].Immunol Res,2017,65(3):721-728.
[11] CHKHAIDZE I,ZIRAKISHVILI D,SHAVSHVISHVILI N,et al.Prognostic value of TH1/TH2 cytokines in infants with wheezing in a three year follow-up study[J].Pneumonol Alergol Pol,2016,84(3):144-150.
[12] PANCHAM K,PEREZ G F,HUSENI S,et al.Premature infants have impaired airway antiviral IFNγ responses to human metapneumovirus compared to respiratory syncytial virus[J].Pediatr Res,2015,78(4):389-394.
[13] ZHANG Y,QIAO L,HU X,et al.Baculovirus vectors expressing F proteins in combination with virus-induced signaling adaptor (VISA) molecules confer protection against respiratory syncytial virus infection[J].Vaccine,2016,34(2):252-260.
[14] AZIZI-JALILIAN F,YUSOFF K,SUHAIMI S,et al.Development of two salmonella-based oral vaccines against human respiratory syncytial virus[J].J Biol Regul Homeost Agents,2015,29(1):7-18.
[15] WANG J,KONG L,LUO Q,et al.Dual effects of respiratory syncytial virus infections on airway inflammation by regulation of Th17/Treg responses in ovalbumin-challenged mice[J].Inflammation,2014,37(6):1984-2005.
[16] TING H A,SCHALLER M A,de ALMEIDA-NAGATA D E,et al.Notch ligand Delta-like 4 promotes regulatory T cell identity in pulmonary viral infection[J].J Immunol,2017,198(4):1492-1502.
[17] MANGODT T C,van HERCK M A,NULLENS S,et al.The role of Th17 and Treg responses in the pathogenesis of RSV infection[J].Pediatr Res,2015,78(5):483-491. |