The research team, led by Barton F. Haynes, M.D., director of the Duke Human Vaccine Institute, and John Mascola, M.D., acting director of the NIH Vaccine Research Center, have for the first time described the co-evolution of antibodies and virus in a person with HIV whose immune system mounted a broad attack against the pathogen. Findings are published April 3, 2013, in the journal Nature.
Most vaccines work by inducing this antibody response, but the HIV virus has proved to be a difficult vaccine target. When HIV antibodies are produced, they typically have a limited range, and the virus changes rapidly to escape harm, leading to an arms race that the virus usually wins.
The current research was aided by new technologies that can detect early infection and track the subsequent immune response and virus evolution. It fills gaps in knowledge that have impeded development of an effective vaccine for a virus that has killed more than 30 million people worldwide.
“This project could only have been carried out by a multidisciplinary team working closely together,” said Haynes, who led the work as a project of the Duke Center for HIV/AIDS Vaccine Immunology-Immunogen Discovery (CHAVI-ID) consortium, which is funded by the National Institute of Allergy and Infectious Diseases. “For the first time, we have mapped not only the evolutionary pathway of the antibody, but also the evolutionary pathway of the virus, defining the sequence of events involved that induce the broadly neutralizing antibodies.”
The key to this finding was a person in Africa whose HIV infection was detected so early that the virus had not yet mutated to avoid the immune assault. The individual also exhibited a fortuitous trait that occurs in only about 20 percent of people infected with HIV – an immune system that produces broadly neutralizing antibodies. These immune weapons attack vulnerable sites of the virus that are conserved despite mutations. In identifying the early viral infection, the team found the outer envelope, the viral surface glycoprotein, which triggered the start of the broadly neutralizing antibody development.
By tracking the precise virus and antibody pathways involved, the Duke CHAVI-ID and NIH teams now have a detailed road map for development of a potential vaccine, which involves immunogens with an outer envelope specifically selected to stimulate the production of broadly neutralizing antibodies.
“The next step is to use that information to make sequential viral envelopes and test them as experimental vaccines,” Haynes said. “This is a process of discovery and we’ve come a long way with regard to understanding what the problem has been.”
In addition to Haynes, study authors at Duke include lead author Hua-Xin Liao, plus Feng Gao, S. Munir Alam, Kevin Wiehe, Garnett Kelsoe, Guang Yang, Shi-Mao Xia, David C. Montefiori, Robert Parks, Krissey E. Lloyd, Richard M. Scearce, Kelly A. Soderberg, Yue Chen, Fangping Cai and Sheri Chen.
Additional authors include Rebecca Lynch, Tongqing Zhou, Jiang Zhu, Lawrence Shapiro, Mark K. Louder, Lillan M. Tran, Stephanie Moquin, Xiulian Du, M. Gordon Joyce, Sanjay Srivatsan, Baoshan Zhang, Anqi Zheng, Peter D. Kwong and John R. Mascola from the National Institute of Allergy and Infectious Diseases; Thomas B. Kepler from Boston University; Scott D. Boyd, Andrew Z. Fire and Krishna M. Roskin from Stanford University; Chaim A. Schramm and Zhenhai Zhang from Columbia University; James C. Mullikin and the NISC Comparative Sequencing Program at NIH; S. Gnanakaran, Peter Hraber and Bette T.M. Korber of Los Alamos National Laboratory; Myron Cohen of the University of North Carolina; Gift Kamanga of UNC Project, Malawi; George M. Shaw and Beatrice H. Hahn of the University of Pennsylvania.
The NIAID and National Institutes of Health provided funding for the research to the Center for HIV/AIDS Vaccine Immunology (AI067854) and the Center for Vaccine Immunology-Immunogen Discovery (AI100645).