4.5 Article

Comparison of the immune responses to the CIA06-adjuvanted human papillomavirus L1 VLP vaccine with those against the licensed HPV vaccine Cervarix™ in mice

期刊

VACCINE
卷 30, 期 28, 页码 4127-4134

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2012.04.079

关键词

Human papillomavirus vaccine; Virus-like particle; CIA06; Adjuvant system

资金

  1. Korea Healthcare Technology R&D Project, Ministry for Health, Welfare Family Affairs [A085139]
  2. TEPIK [A103001]
  3. Basic Science Research Program through the National Research Foundation of Korea (NRF)
  4. Ministry of Education, Science and Technology, Republic of Korea [20090236]
  5. EyeGene
  6. Korea Health Promotion Institute [A085139] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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CIA05 is a toll-like receptor (TLR) 4 agonist derived from an Escherichia coli lipopolysaccharide (LPS) mutant and has been shown to have potential as a vaccine adjuvant. In this study, we investigated the immunopotentiating activity of the adjuvant system CIA06, which is comprised of CIA05 and aluminum hydroxide (alum), when used with the human papillomavirus (HPV)L1 virus-like particles (VLPs) vaccine. BALB/c mice were immunized intramuscularly three times at 2-week intervals with HPV16 L1 VLPs alone or in the presence of various combinations of CIA05 and alum, and the immune responses were assessed. We found that the combination of CIA05 and alum at a ratio of 1:50 (designated CIA06B) yielded the highest immune response in terms of serum anti-HPV L1 VLP IgG antibody titers, splenocyte interferon (IFN)-gamma secretion, and antigen-specific memory B cell responses. The immunogenicity of the CIA06B-adjuvanted HPV16/18 L1 VLP vaccine was compared with that of the currently licensed HPV vaccine Cervarix (TM). The CIA06B-adjuvanted vaccine was similar to Cervarix (TM) with regard to eliciting serum antigen-specific IgG antibodies and virus-neutralizing antibodies but more effective at inducing splenic cytokine production and memory B cells. We also observed that the antigen-specific IgG antibody titers, splenic IFN-gamma secretion and memory B cells induced by the CIA06B-adjuvanted HPV vaccine remained high up to 24 weeks post-immunization. Based on these data, we concluded that CIA06B may have potential as an adjuvant in a potent prophylactic vaccine against HPV infection. (C) 2012 Elsevier Ltd. All rights reserved.

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