In the long battle to create an effective HIV vaccine, scientists have made a major leap forward. A new study shows that a series of vaccines can coax the immune system to produce powerful antibodies capable of blocking a wide range of HIV strains-including those that are typically the hardest to stop.
A team of scientists at Scripps Research and Sweden's Karolinska Institute presented a strong demonstration that broadly neutralizing antibodies (bNAbs)-long considered a key goal for HIV vaccination-can be successfully induced in nonhuman primates. It also points to a new target on the HIV spike protein that future antibodies may be able to successfully bind to block the virus.
Because HIV rapidly mutates and there are literally millions of different strains circulating in humans around the world, scientists have focused their research efforts on creating vaccines that can stimulate the body to produce bNAbs that simultaneously recognize many strains at once. While some people spontaneously produce bNAbs after exposure to HIV, it has been a challenge to create a vaccine that reliably induces bNAbs in nonhuman primates or humans.
A Two Step Strategy.
In the new work, Wyatt and his team first designed a mimic for the HIV spike protein-a key section of HIV's machinery that antibodies target to block infection. Unlike earlier designs, the new "spike mimics" don't fall apart after injection and closely resemble the HIV spike protein's structure.
Then, the group turned to a two-step vaccination strategy. First, they primed the immune system with a version of the spike mimic that lacked key sugar molecules, which normally coat the protein and make it harder to recognize. This helped expose a critical, conserved region of the spike: the CD4 binding site, where the spike protein attaches to human immune cells.
After two sequential doses of the priming vaccine, five boosters were administered, each about twelve weeks apart. This booster series of spike proteins from different HIV strains-now with their sugar coat intact-retrained the immune system to recognize the same region even when it was partially hidden.
The deliberate sequence of vaccines, the researchers say, was key to success. "We weren't just vaccinating at random," says Javier Guenaga, a senior staff scientist at Scripps Research and co-first author of the new paper. "This was a rational, structure-guided approach to elicit the right kinds of antibodies."
"What sets this work apart is that we didn't just see initial signs of a promising response; we actually isolated functional broadly neutralizing antibodies and pinpointed exactly where they bind on the surface of the virus. This tells us not only that the approach works, but also specifically why it works."
Richard Wyatt, senior author, Professor, Department of Immunology and Microbiology, Scripps Research.
A team of scientists at Scripps Research and Sweden's Karolinska Institute presented a strong demonstration that broadly neutralizing antibodies (bNAbs)-long considered a key goal for HIV vaccination-can be successfully induced in nonhuman primates. It also points to a new target on the HIV spike protein that future antibodies may be able to successfully bind to block the virus.
Because HIV rapidly mutates and there are literally millions of different strains circulating in humans around the world, scientists have focused their research efforts on creating vaccines that can stimulate the body to produce bNAbs that simultaneously recognize many strains at once. While some people spontaneously produce bNAbs after exposure to HIV, it has been a challenge to create a vaccine that reliably induces bNAbs in nonhuman primates or humans.
A Two Step Strategy.
In the new work, Wyatt and his team first designed a mimic for the HIV spike protein-a key section of HIV's machinery that antibodies target to block infection. Unlike earlier designs, the new "spike mimics" don't fall apart after injection and closely resemble the HIV spike protein's structure.
Then, the group turned to a two-step vaccination strategy. First, they primed the immune system with a version of the spike mimic that lacked key sugar molecules, which normally coat the protein and make it harder to recognize. This helped expose a critical, conserved region of the spike: the CD4 binding site, where the spike protein attaches to human immune cells.
After two sequential doses of the priming vaccine, five boosters were administered, each about twelve weeks apart. This booster series of spike proteins from different HIV strains-now with their sugar coat intact-retrained the immune system to recognize the same region even when it was partially hidden.
The deliberate sequence of vaccines, the researchers say, was key to success. "We weren't just vaccinating at random," says Javier Guenaga, a senior staff scientist at Scripps Research and co-first author of the new paper. "This was a rational, structure-guided approach to elicit the right kinds of antibodies."
"What sets this work apart is that we didn't just see initial signs of a promising response; we actually isolated functional broadly neutralizing antibodies and pinpointed exactly where they bind on the surface of the virus. This tells us not only that the approach works, but also specifically why it works."
Richard Wyatt, senior author, Professor, Department of Immunology and Microbiology, Scripps Research.
