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Discovery of a Zika antibody offers hope for a vaccine

Zika domain

Researchers have found natural antibodies that prevent Zika infection by latching onto a part of the virus. Credit: Jennifer R. Keeffe, Anthony P. West, Jr., and Pamela J. Bjorkman

 

 

A research team based at The Rockefeller University has identified a potent new weapon against the Zika virus in the blood of people who have been infected by it. This discovery could lead to new ways of fighting the disease, including a vaccine.

In blood samples taken from subjects in Mexico and Brazil, the scientists found antibodies—proteins produced by the immune system—that block the virus from initiating an infection. The antibodies appeared to have been initially generated in response to an earlier infection by a related virus that causes dengue.

“In the near future, these antibodies could be very useful. One could envision, for example, administering them to safely prevent Zika among pregnant women or others at risk of contracting the disease,” says Davide F. Robbiani, a research associate professor in Michel C. Nussenzweig’s lab. He and Leonia Bozzacco, a research affiliate in Charles M. Rice’s lab, led the study, which appeared in Cell on May 4.

The team’s detailed examination of the interaction between this antibody and the virus also revealed a new potential strategy for developing a vaccine.

A precise target

A mosquito-borne virus, Zika usually causes mild symptoms in those who contract it. However, dramatic effects can appear in the next generation. Babies born to women infected during pregnancy are at risk of devastating neurodevelopmental abnormalities. The only way to prevent Zika is to avoid mosquito bites; there are currently no vaccines or other medical measures.

An infection begins when the virus, traveling in a spherical particle studded with the viral envelope protein, latches onto a host cell and forces its way in. Faced with a viral threat, the human immune system generates antibodies that recognize the virus and stop it from invading cells. The team set out to find antibodies tuned to a particular target: a part of Zika’s envelope protein, which the virus needs to launch an attack.

Five out of six

Through collaborators working in Pau da Lima, Brazil, and Santa Maria Mixtequilla, Mexico, they obtained blood samples from more than 400 people, collected shortly after Zika was circulating.

Individual responses to the same pathogen can vary greatly. Yet a deeper analysis of samples from six of the volunteers with the most promising antibodies revealed a surprise: Five of them contained the same species of nearly identical antibodies. This similarity suggested these molecules were particularly good at fighting the virus.

When the team examined these closely related antibodies’ performance against Zika, one, obtained from a Mexican volunteer’s blood, stood out. When this antibody, called Z004, was given to mice rendered vulnerable to Zika, it protected them from developing serious infections.

A shared ridge

To get a closer look at the interaction between the antibody and a fragment of the virus’ envelope protein, scientists in Pamela J. Bjorkman’s lab at Caltech determined the molecular structure formed as the two units interacted. Their detailed maps revealed how the antibody pinches a ridge on the virus when it binds to it.

While some efforts to develop a vaccine use all or most of the virus to stimulate the immune system, the researchers believe it could be safer to employ only a tiny fragment containing this ridge.

Zika isn’t the only virus to sport the ridge, as it is also present in envelopes of other viruses in the same family. The dengue 1 virus, a close relative of Zika and one of four types of dengue, has a ridge that is remarkably similar to Zika’s. When pitted against dengue 1, Z004 neutralized this virus as well.

A look back at samples from the Brazilians, collected six months before Zika arrived by a team led by Albert Ko of Yale University, revealed evidence of prior dengue 1 infections in some—and a potential explanation as to why certain people’s immune systems fared better against Zika.

“Even before Zika, their blood samples likely had antibodies that could interact with this same spot on the envelope protein,” says Margaret R. MacDonald, a research associate professor in Rice’s lab. “It appears that, much like a vaccine, dengue 1 can prime the immune system to respond to Zika.”

Nussenzweig is the Zanvil A. Cohn and Ralph M. Steinman Professor and Rice is the Maurice R. and Corinne P. Greenberg Professor in Virology.

Michel C. Nussenzweig
Senior Physician
Investigator of  Howard Hughes Medical Institute
Zanvil A. Cohn and Ralph M. Steinman
Laboratory of Molecular Immunology 

Nussenzweig studies molecular aspects of adaptive and innate immune responses with a focus on HIV-1.

Charles M. Rice
Maurice R. and Corinne P. Greenberg
Professor in Virology
Laboratory of Virology Infectious Disease 

Rice studies pathogenic viruses and innate antiviral immune mechanisms.


Related publication

Cell
Recurrent Potent Human Neutralizing Antibodies to Zika Virus in Brazil and Mexico

Davide F. Robbiani, Leonia Bozzacco, Priscilla C. Olsen, Anna Gazumyan, Dennis Schaefer-Babajew, Lilian Nogueira, Roshni Patel, Stephanie A. Azzopardi, Lion F.K. Uhl, Mohsan Saeed, Marianna Agudelo, Kai-Hui Yao, Jovana Golijanin, Arlene Hurley, Marina Caskey, Joy Pai, Thiago Oliveira, Neena M. Thomas, Thomas Eisenreich, Antonio R.P. de Almeida, Charles M. Rice, Margaret R. MacDonald, and Michel C. Nussenzweig


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