Yerkes researchers have developed a COVID-19 vaccine that has proven safe and effective in mice and monkeys. The Emory MVA COVID-19 vaccine uses modified vaccinia Ankara (MVA), a harmless version of a poxvirus that is well-known for its use in HIV/AIDS vaccines. Like the Moderna and Pfizer COVID-19 vaccines, the Emory MVA COVID-19 vaccine induces strong neutralizing antibodies, which support the immune system’s ability to fight infections. However, the Emory MVA COVID-19 vaccine takes protection several steps further, starting with inducing killer CD8 T cells in addition to the neutralizing antibodies, providing a multi-pronged approach to halting SAR-COV-2. In addition, the Emory researchers say the vaccine is easily adaptable to address disease variants, can be used in combination with existing vaccines to improve their ability to combat variants, and has the potential to be equally effective with a single dose.
Lead researcher Rama Amara built the Emory MVA COVID-19 vaccine based on his more than 20 years of experience working with MVA and animal models to develop an HIV/AIDS vaccine. He and his Yerkes-based research team tested two MVA SARS-CoV-2 vaccines in mice. One of them, MVA/S, used the complete spike protein of coronavirus to induce strong neutralizing antibodies against SARS-CoV-2. In addition, this vaccine also induced a strong killer CD8 T cell response.
According to Amara, a researcher in Yerkes and the Emory Vaccine Center, “Generating neutralizing antibodies is an important component of a successful COVID-19 vaccine because the antibodies can block the virus from entering the body’s cells. It’s as important to activate CD8 T cells that can clear infected cells, so this allows us to approach halting the virus two ways simultaneously. The CD8 T cells also provide ongoing value because they are key to working against other variants of the virus, especially if antibodies fail.”
Based on the encouraging study results in mice, the Amara team advanced the MVA/S COVID-19 vaccine into a study with 10 rhesus monkeys at Yerkes. For five animals, the researchers gave two doses of the vaccine a month apart and then challenged them with SARS-CoV-2. The researchers also challenged a group of five monkeys that received a placebo MVA vaccine, which did not contain any genes from the COVID-19 virus. The virus grew to high levels in the lungs of all five placebo animals by the second day, but was below detection limits in all five MVA/S-vaccinated animals. “These results are even more promising because the MVA/S-vaccinated animals did not show any signs of inflammation in the lungs such as what medical professional are seeing in humans who have COVID-19,” says Amara.
Amara is working with Emory’s Office of Technology Transfer to license the vaccine for production.
He will continue his work on COVID-19 vaccines. One study focuses on the effectiveness of a single dose of the Emory MVA COVID-19 vaccine. A single dose could prove especially valuable to ensure vaccination compliance and, therefore, effectiveness, which can help drive a reduction in COVID-19 diagnoses and hospitalizations. In a second study, Amara’s team is focusing on inducing broader T cell responses capable of fighting new COVID-19 variants and other human coronaviruses."
Amara’s research team includes Nandakishore Routhu (postdoc), Sailaja Gangadhara (research associate), Narayanaiah Cheedarla (postdoc), and Venkata Satish Bollimpelli (postdoc), all four co-lead authors, as well as Ayalensh Shiferaw (research specialist). Amara and his team worked in close collaboration with the laboratories of Mehul Suthar and Steve Bosinger. Results from this NIH-funded study published online in Immunity. |