In the recurring, deadly Ebola outbreaks in parts of Africa, today’s health workers now have at least some tools to fight the disease: vaccines. Vaccines against Ebola have been administered to over 100,000 people to date, but they are barely out of the experimental stage. It is not known how well these vaccines will provide long-term protection across a broad population. Furthermore, on the basic scientific level, the effects of vaccination on the immune system and how the immune response of vaccinated individuals compares with that of individuals who have survived Ebola infections was not known. A Weizmann Institute of Science lab recently joined forces with a research team in Cologne, Germany, to uncover the details of the molecular response that occurs in the immune system after vaccination against Ebola. Their findings may help health organizations devise better strategies for containing and preventing the disease.
Dr. Ron Diskin of the Institute’s Department of Structural Biology explains: “These vaccines – made by recombinant methods that attach an Ebola protein to a harmless virus – are hard to produce, and thus there is not enough of them to vaccinate an entire population. In addition, the civil strife in some areas where Ebola is rampant today, the fact that it is often needed in villages that are hard to reach and because of its scarcity, the vaccine tends to be given only to those most closely connected to individuals who are already sick. Understanding exactly how the immune response is produced following vaccination will not only help refine the vaccine itself. It can help us understand whether it will work against different strains of the virus or whether the dose given today is the best one.”
The study began in the lab of Dr. Florian Klein of the University of Cologne. Dr. Klein, an immunologist, and his group looked for signs of the immune response in blood samples from six people who had received the vaccine a year or more earlier. The group singled out B cells – which produce the antibodies that make up our “immune memory” – and conducted deep sequencing, tracing the lineages of those cells and isolating individual antibodies that bound to viral proteins.
Cells from each of the six people produced a wide number of antibodies, and Dr. Diskin and his team ‒ including lab member Dr. Hadas Cohen-Dvashi and Dr. Nadav Elad of Chemical Research Support ‒ decided to focus on two promising ones they believed were strongly involved in the long-term immune response.
The first step was to understand exactly how and where the antibodies bind to the viral glycoprotein (part of a virus’s outer membrane) used in the vaccine, and just how such binding neutralizes the virus so effectively. To do so, the team used a new piece of equipment: a top-of-the-line, high-powered electron microscope. In fact, this study was the first conducted with the new microscope, recently installed in the Institute’s Electron Microscopy Unit. Advances in the preparation, detection, automation, and computational analysis (some of which garnered their developers a Nobel Prize in 2017) have made this latest version of the electron microscope able to reveal the 3D structure, practically down to the last atom, of an antibody bound to its target on the glycoprotein. “Until recently, the work of structural biology involved painstaking crystallization and X-ray diffraction – a process that could take at least half-a-year to a year,” says Dr. Elad. “We can now skip the crystallization altogether, and the entire process ‒ including extremely involved computational analysis ‒ is completed within a couple of weeks.”
Although many of the antibodies produced by the B cells did bind to the glycoproteins – some apparently more effectively than others – the research group was able to show why the two antibodies characterized by Dr. Diskin and his group were very efficient at stopping the virus. These bound to two sites on the viral glycoprotein known for their vulnerability, but they bound in a different way than other antibodies that had been studied.
Dr. Diskin and the group were able to distinguish the exact makeup of these antibodies – the way that one so-called “heavy chain” combined with a “light chain” – and to map the precise points at which these attached to the viral protein. “In fact,” says Dr. Diskin, “the antibodies we studied are much more effective at binding than those that are being tested today to treat Ebola.” Comparing the map of binding sites to those studied in Ebola survivors, which are known to be protective, showed a nearly identical pattern. Further research in the German lab, as well as others, tested the antibodies against the Ebola protein ‒ even against the live virus ‒ and these confirmed that the part of the immune response that was created by the vaccine, and which was studied by the group, is indeed effective, ultimately explaining the mechanism of protection.
Although there is still too little information to enable scientists to tell whether the vaccine can produce an immune response against other species of the Ebola virus, the study suggested that the antibodies did work against multiple isolates of a single species, and Dr. Diskin hopes that further research will show whether, as they hope, a single vaccine can fight the disease across the continent.
Another reason for hope, says Dr. Diskin, is that subjects who had received a lower-dose version of the vaccine had a similar number of effective antibodies to subjects who had received a higher dose, and this could lead to a reconsideration of protocols for administration and possibly afford more people protection.
Dr. Diskin and the German research team intend to continue this research. Based on an additional surprising observation from this study, that a particular group of effective antibodies sharing the same heavy-and-light-chain germline combination was elicited robustly in all the vaccinated individuals, they want to know precisely why and how these particular antibodies are produced, and how they manage to work so effectively against the virus. They also want to understand whether there are any serious limiting factors that could prevent the antibodies produced following this specific vaccination from targeting all the Ebola virus species, or if the breadth of this response might possibly be expanded by improving the vaccines.
Dr. Ron Diskin’s research is supported by the Moross Integrated Cancer Center; the Dr. Barry Sherman Institute for Medicinal Chemistry; the Jeanne and Joseph Nissim Center for Life Sciences Research; and the Estate of Emile Mimran.
