TSRI scientists get first-ever glimpse of ‘teenage’ HIV-neutralizing antibody

Research revelations expand the knowledge of the evolution and key traits of anti-HIV antibodies and could help researchers design a vaccine to prevent AIDS

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LA, JOLLA, Calif.—So many of us are conditioned to think of “trouble” and “angst” when we think of teens that the headline above might already have you fidgeting. But fear not, these “teenagers” don’t live under your roof—they may live in your immune system, though.
I’m not making things better, am I? So let me get to the point: Scientists at The Scripps Research Institute (TSRI) and collaborating institutions recently described the first-ever immature or “teenage” antibody found in a powerful class of immune molecules effective against HIV. This represents new knowledge of the evolution and key traits of anti-HIV antibodies and, in the end, these revelations could help researchers design a vaccine to prevent AIDS.
The research was an international collaboration, also led by Yuxing Li of the University of Maryland, Yiming Shao of the Chinese Center for Disease Control and Prevention (China CDC), Peking University and Nankai University and Ian Wilson of TSRI—it was published April 5, 2016, online ahead of print, where it was to be featured as the cover story of the journal Immunity.
It’s no secret that HIV has been hard to combat because of the ability not only to rapidly mutate but because of a kind of “force field” of glycan molecules on the surface of its envelope glycoproteins—those protected glycoproteins, in turn, are the viral machinery used to make initial contact and subsequently infect human host cells.
These formidable defenses are why researchers haven’t been able to develop an HIV vaccine using traditional methods. Instead, explained TSRI biologist Jiang Zhu, who served as co-senior author of the study, they have to “reverse engineer” the right vaccine candidates using rare effective antibodies from HIV-positive patients as guides.
Having described this teenage antibody, though, researchers might be able to better carry out that reverse engineering.
“This is actually the first example of how we can go back to the really early stage to see how this antibody lineage was born and can develop,” said Zhu.
The antibody in the new study came from a patient in China who was what scientists call an “elite” controller, meaning the patient’s immune system had managed to create antibodies with some ability to fight the disease. The patient was among the top 5 percent of neutralizers assessed in a screening of hundreds of Chinese HIV patients by China CDC scientists.
Genetically, the antibody found in this donor resembled members of the VRC01 class of antibodies, which are “broadly neutralizing antibodies,” named for their ability to target a key site of vulnerability on many strains of the virus. However, there was “something a little bit weird about this antibody,” said Zhu, in part because it lacked one of the key structural traits of VRC01 antibodies. Further studies into the antibody’s genetics and structure showed that it was a precursor to mature VRC01 antibodies—it was, in essence, a middle stage in the evolution of this class of HIV killers.
Zhu called the antibody a “teenager” and said it gives scientists a unique view of the steps needed to prompt the immune system to effectively target HIV.
The researchers studied samples taken from the patient over five years, starting in 2006 when Zhu said the antibody was a “toddler.” Each sample showed the antibody in a different stage of development, giving researchers a possible guide for how to elicit these antibodies with a vaccine. Zhu and his colleagues were surprised to find that the antibody evolved rapidly between 2006 and 2008, gaining many of the traits it would need to fight HIV. This finding contradicts previous studies suggesting that it can take up to 10 to 15 years for VRC01 antibodies to develop useful traits.
 “Now we know these specialized antibodies can evolve in just one or two years,” noted TSRI Research Associate Yajing Chen, who served as co-first author of the study.
Zhu said this discovery is encouraging, since an HIV vaccine will also need to prompt the body to make antibodies quickly.
The scientists also spotted a hurdle they will have to overcome as they engineer their own antibodies: The teenage VRC01 has a slightly longer amino acid chain at one site than the mature version, and this chain clashes with part of the glycoprotein shield (gp120) on HIV and prevents the antibody from effectively neutralizing the virus.
The researchers managed to tweak the immature antibody to make it into a broadly neutralizing antibody. “As long as you have some of those VRC01 signatures, a teenage-stage antibody can become a killer for HIV,” said Zhu.
The researchers also noted that this is the first time a VRC01-like antibody has been isolated from a patient of Asian descent—the other VRC01s had come from African or Caucasian patients. This means people with different genetic backgrounds may benefit from a vaccine that harnesses a person’s ability to make VRC01s.
“This could be important for developing a universal HIV vaccine,” Zhu said.
As long as we’re on the topic of the immune system, TSRI also announced around the same time as the news above that a new study led by some of its other scientists has uncovered a previously unknown type of immune cell, opening up possibilities for the creation of novel therapies for autoimmune diseases, such as type 1 diabetes.
The newly discovered cells resemble conventional T cells, yet are biased toward becoming T regulatory cells, which protect the body from autoimmune disease.
“This study was eye-opening,” said study senior author and TSRI biologist Oktay Kirak. “You wouldn’t expect these cells to have this ability. The best analogy I have is Clark Kent turning into Superman. Clark Kent looks like an Average Joe, so no one would expect him to have the same abilities as Superman.”

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