Experimental Immunotherapy Zaps Two Most Lethal Ebola Virus Strains

First Step Toward All-Inclusive Treatment

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Jan 13, 2016, 06:15 ET

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BRONX, N.Y., Jan. 13, 2016 /PRNewswire-USNewswire/ -- Researchers at Albert Einstein College of Medicine and the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) have engineered the first antibodies that can potently neutralize the two deadliest strains of the virus that causes Ebola hemorrhagic fever. The findings, made in mice, are a significant step toward immunotherapies that are effective against all strains of Ebola virus that cause human disease. The study was published online today in Scientific Reports.

"A broadly effective immunotherapy for Ebola virus would be a tremendous advance, since it's impossible to predict which strain of the virus will cause the next outbreak," said study co-leader Jonathan Lai, Ph.D., associate professor of biochemistry at Einstein. The other study co-leader is John M. Dye, Ph.D., branch chief of viral immunology at USAMRIID.

Zaire Ebola virus (EBOV) was responsible for the 2014 Ebola outbreak in West Africa, the largest in history. The next-most pathogenic strain of Ebola virus is Sudan Ebola virus (SUDV). "This strain is also a concern because outbreaks are occurring more frequently, and it has been responsible for large outbreaks in the past," said Dr. Dye.

Although a Zaire-specific vaccine is in clinical trials, no vaccine has yet been approved for preventing infection from any strain of Ebola virus. And therapies for people who become infected are very limited. ZMapp, a cocktail of three monoclonal antibodies, is the most promising of several experimental immunotherapies for Ebola virus now in development. But ZMapp's antibodies are specific for EBOV and would not work against the other two Ebola strains that have caused major outbreaks. (In addition to Zaire and Sudan, the third major strain is Bundibugyo.)

In previous work, Dr. Lai and his colleagues used a technique called synthetic antibody engineering to create the first humanized antibodies against SUDV. Those antibodies were designed to bind to SUDV's surface glycoprotein, which the virus uses to gain entry into host cells. Since SUDV's glycoprotein shares just 55 percent of amino acid sequences found in EBOV's glycoprotein, antibodies against SUDV do not neutralize EBOV.

In the current study, Dr. Lai's team engineered "bispecific" antibodies that contain key glycoprotein-binding sequences from both the EBOV and SUDV antibodies. The bispecific antibodies effectively neutralized both EBOV and SUDV in tissue culture studies. In addition, the antibodies provided high levels of protection for mice that had been exposed to lethal doses of either of the viruses.

Watch Dr. Lai Discuss His Ebola Research

The bispecific antibodies must still be tested in larger animals and in humans to know whether they'll be effective. If the new immunotherapy proves safe and effective for people, said Dr. Lai, it might best be suited for preventing local outbreaks from getting out of hand, as happened in the recent West Africa Ebola virus epidemic. "It's also possible," he noted, "that a therapy like this could be used prophylactically, to protect health workers or family members who come into contact with Ebola virus patients."

There are currently no plans to further test the new immunotherapy. But if a pharmaceutical company were interested, said Dr. Lai, "it could probably move the antibody fairly rapidly along the evaluation process." Meanwhile, Dr. Lai has broadened his approach to Ebola virus therapy. He is developing antibodies and antibody cocktails aimed at neutralizing the three most dangerous Ebola virus species (Zaire, Sudan and Bundibugyo) as well as Marburg virus, a deadly pathogen closely related to Ebola virus.

The study is titled "Bispecific Antibody Affords Complete Post-Exposure Protection of Mice from Both Ebola (Zaire) and Sudan Viruses." The other contributors are: Ph.D. student Julia Frei, postdoctoral fellow Elisabeth Nyakatura, and Kartik Chandran, Ph.D., all at Einstein, and Samantha Zak and Russell Bakken at USAMRIID.

This work was supported by a grant from the Centers of Excellence for Translational Research, National Institutes of Health (U19 AI109762), an Irma T. Hirschl/Monique Weill-Caulier Career Scientist Award, the NIH Cellular and Molecular Biology and Genetics Training Program, a DAAD (Deutscher Akademischer Austausch Dienst, German Academic Exchange Service) fellowship, and a JSTO-DTRA (Joint Science and Technology Office–Defense Threat Reduction Agency) project (CB3948).

Albert Einstein College of Medicine has filed patent applications related to this research and is seeking licensing partners able to further develop and commercialize this technology. Interested parties can contact the Office of Biotechnology at [email protected].

About Ebola Virus:
Ebola virus is notorious for killing up to 50 percent of the people it infects. Ebola virus disease—the severe, usually fatal disease that Ebola virus causes in humans and in nonhuman primates—was first documented in 1976 in villages along the Ebola River in the Democratic Republic of the Congo, Africa. The recent Ebola epidemic is the largest in recorded history, affecting multiple countries in Western Africa. Through December of this year, there have been over 28,000 total cases of the disease (including suspected, probable, and confirmed) and more than 11,000 deaths, according to the Centers for Disease Control and Prevention. There are no FDA-approved treatments or vaccines for Ebola virus disease.

About Albert Einstein College of Medicine
Albert Einstein College of Medicine is one of the nation's premier centers for research, medical education and clinical investigation. During the 2015-2016 academic year, Einstein is home to 731 M.D. students, 193 Ph.D. students, 106 students in the combined M.D./Ph.D. program, and 278 postdoctoral research fellows. The College of Medicine has more than 1,900 full-time faculty members located on the main campus and at its clinical affiliates. In 2015, Einstein received $148 million in awards from the National Institutes of Health (NIH). This includes the funding of major research centers at Einstein in aging, intellectual development disorders, diabetes, cancer, clinical and translational research, liver disease, and AIDS. Other areas where the College of Medicine is concentrating its efforts include developmental brain research, neuroscience, cardiac disease, and initiatives to reduce and eliminate ethnic and racial health disparities. Its partnership with Montefiore Medical Center, the University Hospital and academic medical center for Einstein, advances clinical and translational research to accelerate the pace at which new discoveries become the treatments and therapies that benefit patients. Through its extensive affiliation network involving Montefiore, Jacobi Medical Center—Einstein's founding hospital, and three other hospital systems in the Bronx, Brooklyn and on Long Island, Einstein runs one of the largest residency and fellowship training programs in the medical and dental professions in the United States. For more information, please visit www.einstein.yu.edu, read our blog, follow us on Twitter, like us on Facebook, and view us on YouTube.