Imagine a seasonal jab of antibodies that could neutralise the HIV virus. Such an injection could prove to be next best alternative to an HIV vaccine, which has proven elusive to date.
American and German researchers have demonstrated that by injecting macaques with neutralising antibodies, they successfully shielded the monkeys from HIV infection for as long as six months.
After infection, HIV methodically weakens the immune system to the extent that a simple cold can escalate to fatal pneumonia.
But what if you could give your body some warning of HIV infection in advance by training the immune system with anti-HIV antibodies?
This was the thinking of the researchers behind this study. They purified four antibodies produced by patients infected with HIV, and then injected the macaques each with a different type.
The macaques were then exposed to the monkey equivalent of HIV, named appropriately SIV (simian immunodeficiency virus). Results showed that the antibodies were able to provide the macaques with protection for three to six months, even after the monkeys were repeatedly exposed to SIV.
Associate Professor Sarah Palmer, from The Westmead Institute for Medical Research, who was not involved in the study, said although the research was conducted in a monkey model, the findings showed promise in preventing new HIV infections in humans.
“This is potentially significant,” she said. “The study indicates that an injectable antibody product given once every three to four months could effectively protect high-risk individuals from HIV infection.”
University of Melbourne professor and director of the Doherty Institute, Sharon Lewin, agreed. She also said that what set the study apart was the use of a macaque monkey model to evaluate each antibody separately.
“It indeed looks very impressive, namely protection from infection in monkeys after multiple challenges,” she said.
However, the approach of using neutralising antibodies to pre-emptively prime the immune system is not novel.
“The potency of each of these antibodies has been reported before. There has been an explosion of work regarding broadly neutralising antibodies in the last few years, in vitro [in cell models], in mice and in macaques, and also humans,” said Prof Lewin.
In addition, Assoc Prof Palmer emphasised that the study provides only a small fraction of the answers to developing a highly effective HIV treatment.
“Currently we have very limited clinical data as to the effectiveness of passively transfused anti-HIV antibodies to protect from new HIV infections and, more importantly, repeated exposures to HIV,” she said.
“We do not know what dosage of antibody is required to protect against HIV infection or whether these injectable antibodies are available in human tissues such as the mucosal.”
According to Assoc Prof Palmer, the next step is for additional proof-of-concept trials in humans.
“They are needed to provide important data as to how effective these antibodies are in preventing HIV-1 infection,” she said.
Prof Lewin said the study showcased how a strategy using neutralising antibodies could also protect against HIV infection for a limited time following a single dose, albeit in an animal model.
But the need for continual injections every eight weeks showed that antibody injections still had their limitations.
“I doubt these antibodies will ever be used as a single passive administration in practise,” she said.
Prof Lewin said that the next logical step for the study would be to generate the same response and antibody levels without it waning over time, referring to the Hepatitis A vaccine as a success story.
“We need a way to continually have the antibody there without having to have repeated injections,” she said.
The study was published last week in Nature.