期刊文献+

PIKA Provides an Adjuvant Effect to Induce Strong Mucosal and Systemic Humoral Immunity Against SARS-CoV 被引量:5

PIKA Provides an Adjuvant Effect to Induce Strong Mucosal and Systemic Humoral Immunity Against SARS-CoV
下载PDF
导出
摘要 Severe Acute Respiratory Syndrome (SARS) is a deadly infectious disease caused by SARS Coronavirus (SARS-CoV). Inactivated SARS-CoV has been explored as a vaccine against SARS-CoV. However, safe and potent adjuvants, especially with more efficient and economical needle-free vaccination are alw needed more urgently in a pandemic. The development of a safe and effective mucosal adjuvant and vaccine ays for prevention of emergent infectious diseases such as SARS will be an important advancement. PIKA, a stabilized derivative of Poly (I:C), was previously reported to be safe and potent as adjuvant in mouse models. In the present study, we demonstrated that the intraperitoneal and intranasal co-administration of inactivated SARS-CoV vaccine together with this improved Poly (I:C) derivative induced strong anti-SARS-CoV mucosal and systemic humoral immune responses with neutralizing activity against pseudotyped virus. Although intraperitoneal immunization of inactivated SARS-CoV vaccine alone could induce a certain level of neutralizing activity in serum as well as in mucosal sites, co-administration of inactivated SARS-CoV vaccine with PIKA as adjuvant could induce a much higher neutralizing activity. When intranasal immunization was used, PIKA was obligatorily for inducing neutralizing activity in serum as well as in mucosal sites and was correlated with both mucosal IgA and mucosal IgG response. Overall, PIKA could be a good mucosal adjuvant candidate for inactivated SARS-CoV vaccine for use in possible future pandemic. Severe Acute Respiratory Syndrome(SARS) is a deadly infectious disease caused by SARS Coronavirus(SARS-CoV).Inactivated SARS-CoV has been explored as a vaccine against SARS-CoV.However,safe and potent adjuvants,especially with more efficient and economical needle-free vaccination are always needed more urgently in a pandemic.The development of a safe and effective mucosal adjuvant and vaccine for prevention of emergent infectious diseases such as SARS will be an important advancement.PIKA,a stabilized derivative of Poly(I:C),was previously reported to be safe and potent as adjuvant in mouse models.In the present study,we demonstrated that the intraperitoneal and intranasal co-administration of inactivated SARS-CoV vaccine together with this improved Poly(I:C) derivative induced strong anti-SARS-CoV mucosal and systemic humoral immune responses with neutralizing activity against pseudotyped virus.Although intraperitoneal immunization of inactivated SARS-CoV vaccine alone could induce a certain level of neutralizing activity in serum as well as in mucosal sites,co-administration of inactivated SARS-CoV vaccine with PIKA as adjuvant could induce a much higher neutralizing activity.When intranasal immunization was used,PIKA was obligatorily for inducing neutralizing activity in serum as well as in mucosal sites and was correlated with both mucosal IgA and mucosal IgG response.Overall,PIKA could be a good mucosal adjuvant candidate for inactivated SARS-CoV vaccine for use in possible future pandemic.
出处 《Virologica Sinica》 SCIE CAS CSCD 2011年第2期81-94,共14页 中国病毒学(英文版)
基金 supported by the National Natural Science Foundation of China (30670097) National Basic Research Program of China (973 Program) (2005CB522903) National Key R&D Program (2007BAI28B04) National S&T Major Project on Major Infectious Diseases (2008ZX10001-010)from the Ministry of Science and Technology of the People’s Republic of China
关键词 SARS Coronavirus (SARS-CoV) Immune responses ADJUVANT PIKA SARS病毒 佐剂效应 免疫系统 体液免疫 鼠兔 粘膜 诱导 SARS冠状病毒
  • 相关文献

参考文献2

二级参考文献11

  • 1梁晓峰,陈园生,王晓军,贺雄,陈丽娟,王骏,林长缨,白呼群,严俊,崔钢,于竞进.中国3岁以上人群乙型肝炎血清流行病学研究[J].中华流行病学杂志,2005,26(9):655-658. 被引量:967
  • 2Gupta R K.Aluminum compounds as vaccine adjuvants[J].Adv Drug Deliv Rev,1998;32:155-172.
  • 3Zinkernagel R M.Immunity,immunopathology and vaccines against HIV[J].Vaccine,2002;20(6):1913-1917.
  • 4Zinkernagel R M.Immunology taught by viruses[J].Science,1996;271:173-178.
  • 5Lindblad E B.Aluminium adjuvants--in retrospect and prospect[J].Vaccine,2004;22(27-28):3658-3668.
  • 6Lin H X,Gontier C,Saron M F et al.A new immunostimulatory complex(PICKCa) in experimental rabies:antiviral and adjuvant effects[J].Arch Virol,1993; 131(3-4):307-319.
  • 7Wille-Reece U,Chang-You W,Flynn B J et al.Immunization with HIV-1 gag protein conjugated to a TLR7/8 agonist results in the generation of HIV-1 gag-spesific Th1 and CD8+T cell responses[J].J Immunol,2005;174(12):7676-7683.
  • 8Janeway C A J,Medzhitov R.Introduction:the role of innate immunity in the adaptive immune response[J].Semin Immunol,1998;10(5):349-350.
  • 9林海祥,PerrinP.皮卡狂犬病疫苗的实验研究[J].中国生物制品学杂志,1998,11(3):137-140. 被引量:6
  • 10朱荣平,林海祥.激光光散射法表征人用皮卡狂犬病疫苗分子量与人体副反应关系的观察[J].现代计量测试,1999,7(6):57-58. 被引量:1

共引文献13

同被引文献37

引证文献5

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部