The first and only study to look at isolate HIV-neutralizing antibodies from infants has found that novel antibodies that could protect against many variants of HIV can be produced relatively quickly after infection compared to adults. This suggests that various aspects of HIV-vaccine development, from design to administration, could be improved by mimicking infection and immune response in infants. The work will be published in the journal Cell.
Dr. Julie Overbaugh, a member of the Human Biology Division at Fred Hutchinson Cancer Research Center, Seattle, says that HIV is a wily infection that has found many ways to slip out of the immune system’s grasp, making it a tricky target for a preventive vaccine. A successful vaccine, experts envision, will trigger our bodies to make antibodies, a specialized type of immune protein, which can block a wide swath of HIV variants from infecting target cells. Occasionally, people infected with HIV naturally develop these broadly neutralizing antibodies — but only years after exposure and much tweaking by the immune system. An effective vaccine must protect within months, not decades.
The team drew on samples taken from infants in Nairobi born to HIV-positive mothers prior to the advent of antiretroviral drugs.
They found that infants can produce broadly neutralizing antibodies within the first year of HIV infection, requiring much less somatic hypermutation to generate a broadly neutralizing antibody than would be expected in adults. Additionally, this antibody response is not dominated by just a single antibody, but it appears to be polyclonal, which may make it harder to evade.
In contrast to work in adults, “we could document a case in infants where a broadly neutralizing antibody developed in a time frame and in a way that is something that we could consider mimicking with a vaccine,” Overbaugh said.
Source: Fred Hutchinson Cancer Research Center