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Phase 1 trial of first Ebola vaccine based on 2014 virus strain shows vaccine is safe and provokes an immune response

Date:
March 25, 2015
Source:
The Lancet
Summary:
Medical researchers now have the results from the first phase 1 trial of an Ebola vaccine based on the current (2014) strain of the virus.  Until now, all tested Ebola virus vaccines have been based on the virus strain from the Zaire outbreak in 1976.  The results suggest that the new vaccine is safe, and provokes an immune response in recipients, although further long-term testing will be needed to establish whether it can protect against the Ebola virus.
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Hypodermic needle (stock image).
Credit: © Nicola De Mitri / Fotolia

Results from the first phase 1 trial of an Ebola vaccine based on the current (2014) strain of the virus are today published in The Lancet. Until now, all tested Ebola virus vaccines have been based on the virus strain from the Zaire outbreak in 1976. The results suggest that the new vaccine is safe, and provokes an immune response in recipients, although further long-term testing will be needed to establish whether it can protect against the Ebola virus.

A team of researchers, led by Professor Fengcai Zhu, from the Jiangsu provincial center for disease prevention and control in China, tested the safety and immunogenicity of a novel Ebola vaccine, based on the 2014 Zaire Guinea Ebola strain, and delivered by a virus-like structure (known as a recombinant adenovirus type-5 vaccine). The experimental vaccine was developed by Beijing Institute of Biotechnology in Beijing, China, and Tianjin CanSino Biotechnology in Tianjin, China.

120 healthy Chinese adults were randomly assigned in equal numbers to receive placebo, a low dose, or high dose of the vaccine. The randomised, double-blind, placebo-controlled, phase 1 clinical trial took place at one site in Taizhou County, Jiangsu Province, China.

28 days after vaccination, 38 out of 40 participants in the low-dose group and all 40 of those in the high-dose group had a positive immune response to the vaccine, with participants in the high-dose group producing higher quantities of antibodies than those in the low-dose group. No specific immune response was recorded in the placebo group.

The study does not show whether the level of immune response observed might ultimately be able to offer protection against Ebola virus, and previous trials of this type of vaccine have suggested that pre-existing immunity to the virus vector used to deliver the vaccine may affect its ability to protect against the virus. However, the high dose of vaccine used in the study appeared to partly circumvent pre-existing immunity to the vector, because participants in the high-dose group had a 100% response rate, with no resultant increase in adverse events.

Nonetheless, it will only be possible to assess the vaccine's protective ability with further trials in Africa, say the authors. Moreover, previous research has indicated that this type of vaccine may increase the risk of HIV acquisition, so future trials will need to take this into account.

According to Professor Zhu, "On the basis of our findings, we believe that the Ebola vaccine we assessed has some potential, and a significant advantage of this type of vaccine is that stable and much easier to store or transport in tropical areas with inadequate cold-chain capacity, such as Africa. However, whether this candidate vaccine could become a final vaccine for widespread use against Ebola outbreaks is still uncertain, because of the issues of HIV-1 acquisition rates and the pre-existing immunity, especially in west Africa. More evidence from clinical trials is needed about these concerns. Furthermore, these results only assess immune response up to 28 days, so we plan to assess the persistence of the specific immune response by following up the vaccine recipients of this study."

No serious adverse events were recorded during the 28 days of follow-up, although participants in the high dose group were more likely to report pain and redness at the injection site, with a smaller number reporting mild fever and vomiting. The incidence of adverse reactions was in line with findings from previous studies of other viral-vectored Ebola vaccines.

Writing in a linked Comment, Andrea Marzi from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, USA, and Darryl Falzarano from the University of Saskatchewan, Saskatoon, Canada, say, "This adenovirus type-5 Ebola vaccine vector is an example of how quickly existing vaccine platforms can be modified to incorporate a new virus strain, and moved, with minimum testing in animals, into trials in humans during a crisis situation. However…ultimately, the effectiveness of all these vaccines will only become clear when they proceed to phase 2 efficacy trials in outbreak regions."

The study was funded by China National Science and Technology, Beijing Institute of Biotechnology, and Tianjin CanSino Biotechnology.


Story Source:

Materials provided by The Lancet. Note: Content may be edited for style and length.


Journal Reference:

  1. Feng-Cai Zhu, Li-Hua Hou, Jing-Xin Li, Shi-Po Wu, Pei Liu, Gui-Rong Zhang, Yue-Mei Hu, Fan-Yue Meng, Jun-Jie Xu, Rong Tang, Jin-Long Zhang, Wen-Juan Wang, Lei Duan, Kai Chu, Qi Liang, Jia-Lei Hu, Li Luo, Tao Zhu, Jun-Zhi Wang, Wei Chen. Safety and immunogenicity of a novel recombinant adenovirus type-5 vector-based Ebola vaccine in healthy adults in China: preliminary report of a randomised, double-blind, placebo-controlled, phase 1 trial. The Lancet, March 25, 2015 DOI: 10.1016/S0140-6736(15)60553-0

Cite This Page:

The Lancet. "Phase 1 trial of first Ebola vaccine based on 2014 virus strain shows vaccine is safe and provokes an immune response." ScienceDaily. ScienceDaily, 25 March 2015. <www.sciencedaily.com/releases/2015/03/150325110731.htm>.
The Lancet. (2015, March 25). Phase 1 trial of first Ebola vaccine based on 2014 virus strain shows vaccine is safe and provokes an immune response. ScienceDaily. Retrieved May 23, 2017 from www.sciencedaily.com/releases/2015/03/150325110731.htm
The Lancet. "Phase 1 trial of first Ebola vaccine based on 2014 virus strain shows vaccine is safe and provokes an immune response." ScienceDaily. www.sciencedaily.com/releases/2015/03/150325110731.htm (accessed May 23, 2017).

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