4.8 Article

Immunity and clinical efficacy of an inactivated enterovirus 71 vaccine in healthy Chinese children: a report of further observations

Journal

BMC MEDICINE
Volume 13, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12916-015-0448-7

Keywords

Cross-neutralization; Enterovirus 71; Hand; foot; and mouth disease; Inactivated vaccine; Long-term effect

Funding

  1. National Basic Research Programme [2011CB504903]
  2. National High-Tech RD Programme [2012AA02A404]
  3. State Project for Essential Drug Research and Development [2012ZX09101319, 2014ZX09102042]
  4. National Natural Science Foundation [81373142]
  5. Technology Development Research Institutes [2013EG150137]
  6. Yunnan Province Project [2013FA024, 2012ZA009, 2014HB066]
  7. University of Malaya Research Grant [RG480/12HTM]
  8. High Impact Research Grant from the Ministry of Education of the Malaysia Government [H20001-E00004]

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Background: To investigate the long-term effects on immunity of an inactivated enterovirus 71 (EV71) vaccine and its protective efficacy. Methods: A sub-cohort of 1,100 volunteers from Guangxi Province in China was eligible for enrolment and randomly administered either the EV71 vaccine or a placebo on days 0 and 28 in a phase III clinical trial and then observed for the following 2 years with approval by an independent ethics committee of Guangxi Zhuang Autonomous Region, China. Serum samples from the 350 participants who provided a full series of blood samples (at all the sampling points) within the 2-year period were collected. Vaccine-induced immune effects, including the neutralizing antibody titres and cross-protection against different genotypes of EV71, were examined. This study also evaluated the protective efficacy of this vaccine based upon clinical diagnosis. Results: This sub-cohort showed a >60% drop-out rate over 2 years. The seroconversion rates among the 161 immunized subjects remained >95 % at the end of study. The geometric mean titres of neutralizing antibodies (anti-genotype C4) 360 days after vaccination in 350 subjects were 81.0 (subjects aged 6-11 months), 98.4 (12-23 months), 95.0 (24-35 months), and 81.8 (36-71 months). These titres subsequently increased to 423.1, 659.0, 545.0, and 321.9, respectively, at 540 days post-immunization (d.p.i.), and similar levels were maintained at 720 d.p.i. Higher IFN-gamma/IL-4-specific responses to the C4 genotype of EV71 and cross-neutralization reactivity against major EV71 genotype strains were observed in the vaccine group compared to those in the placebo group. Five EV71-infected subjects were observed in the placebo-treated control group and none in the vaccine-immunized group in per-protocol analysis. Conclusion: These results are consistent with the induction of dynamic immune responses and protective efficacy of the vaccine against most circulating EV71 strains.

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