Deutsche Welle (English edition)

COVID vaccines developed quickly — is a vaccine for HIV next?

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Decades on from the start of the HIV/AIDS pandemic, researcher­s are yet to crack a successful formula for a vaccine. But now we have eight COVID vaccines in 18 months, people are asking: Can we speed things up for HIV?

Decades on from the start of the HIV/AIDS pandemic, researcher­s are yet to crack a successful formula for a vaccine. But now we have eight COVID vaccines in 18 months, people are asking: Can we speed things up for HIV?

It is a search that has so far eluded scientists for 40 years: Finding a safe and effective vaccine to protect people from HIV.

Not a single HIV vaccine has made it beyond Phase III clinical testing in 37 years of research. In comparison to COVID-19, that timeline seems baffling.

Over the last 18 months, more than 32 COVID vaccines have made it to Phase III clinical trials, eight have so far been approved and manufactur­ed, and another 90 are in the Phase I and II pipeline.

"When there's the political will, there is funding and resources," said Hendrik Streeck, virologist and director of the German Center of HIV & AIDS. "And that means there's the ability to be much faster," he told DW

Two 'completely different' viruses

Although HIV vaccine researcher­s have so far been unsuccessf­ul, it's not for lack of trying.

More than 400 HIV vaccine candidates have been tested in Phase I clinical trials, even if only five large-scale Phase III trials have been carried out — each at a cost of more than $100 million.

The world may have firmly turned its attention — and funds — toward finding a vaccine for COVID-19 since the outbreak began in December 2019, but the difference in these timelines is not just about politics and money, Streeck said.

It also has to do with the unique compositio­n of both vi

ruses.

"SARS-CoV-2 [the virus causing COVID] and HIV cannot be compared in terms of structure and complexity," Streeck told DW. The human immunosupp­ressive virus (HIV) is "a completely different virus," he said.

Unlike SARS-CoV-2, which is a very stable virus, the human immunosupp­ressive virus (HIV) is extremely variable — it's constantly mutating. That makes it very difficult for HIV-infected people’s immune systems to make the right antibodies to fend off the virus, as it's usually a step ahead of any response in the body. There are thousands upon thousands of HIV strains circulatin­g in the global population. The HIV genome also integrates into the body's DNA, effectivel­y making itself invisible to the immune system.

These characteri­stics mean our bodies don't usually mount an effective immune response to HIV.

They also make it very difficult to design a broadly effective vaccine.

Most vaccines work by stimulatin­g 'neutralizi­ng antibodies', which are proteins that attack unwanted invaders in the body. But when the target of that attack is constantly changing its appearance, it's very hard to cap

ture.

"Science and the globe have been very fortunate that SARSCoV-2 is an easy target for vaccines," said Jonathan Weber, dean of medicine at Imperial College London and long-term HIV researcher.

All of the methods that vaccine developers have trialed to make a vaccine for COVID — including viral vector, mRNA, and adenovirus — "all of them have worked," Weber said.

"With HIV, the opposite is true. We've tried all those different techniques and none have protected against HIV in an effective way," he said.

Trials of HIV vaccines also tend to take much longer because, at the same time researcher­s want to test whether the vaccines they develop can prevent people from being infected with HIV, they're also actively helping prevent infections with pre-exposure prophylaxi­s (PrEP).

HIV vaccines in progress

To date, only one HIV vaccine, called Uhambo, showedpart­ial protection in human trials, but it was not effective in a recent large trial in South Africa.

Two other large trials, called PrEPVacc and Mosaico are currently underway. Both are using a combinatio­n approach to vaccinatio­n.

Mosaico is based on an adenovirus vaccine followed by a booster that contains a 'mosaic' of proteins from multiple HIV strains. This is similar to the Johnson and Johnson, OxfordAstr­aZeneca and Russian Sputnik COVID-19 vaccines.

Streeck, who's research team is involved in supporting the Mosaico trial in Europe and North and South America, says the researcher­s are "cautiously optimistic" after the vaccine showed promising results in animal testing. The researcher­s expect to have results within the next month.

PrepVacc uses HIV-DNA, a live viral vector and a protein. Researcher­s from the African-led, European-supported trial plan to enroll around 2000 HIV-negative volunteers.

Weber's team is leading the trial, currently being carried out in South Africa, Tanzania and Uganda. Although it began in 2018, progress has been "massively delayed by COVID" he said, and, so far, only about 300 participan­ts have been. signed up. "We think we'll have to run this study until early 2024 to get reliable results on whether the vaccine is effective," Weber told DW.

Meanwhile, vaccine- giant Moderna is working on two mRNA HIV vaccine possibilit­ies. The first, called mRNA-1644, is expected to begin Phase I trials at the end of 2021.

The second, known as mRNA-1574, is being researched in collaborat­ion with the National Institutes of Health (NIH) in the US. Researcher­s working on this second mRNA vaccine type have so far seen some promising results in monkeys, said Peng Zhang, immunologi­st from the National Health Institute in the United States.

"The preliminar­y results were

very exciting. We tested different strains from different regions, from South Africa, Asia and America, and they were all neutralize­d by the monkeys receiving the vaccine," he told DW. The mRNA approach has been used by Moderna and BioNTechPf­izer for their COVID-19 vaccines.

While mRNA vaccines have so far shown to be hugely successful against SARS-CoV-2, Weber cautions that it is too early to hail them as the next big thing in HIV vaccine research.

"My own view at this stage before I have seen any data, is that we still have the problem [with mRNA vaccines] that we don't have the optimal antigen for HIV," he said.

' We need to use this momentum'

Despite the hurdles, Weber is convinced scientists will eventually crack the formula to find a safe and effective HIV vaccine.

"I've gone through my entire career believing we'll get an HIV vaccine. I’m not giving up on that — I only hope I can live to see it," he said.

In the last 40 years, more than 35 million people have died from HIV/AIDS. And according to Streeck, it is a pandemic "we are far from controllin­g."

"Most people that get infected die from this disease," he said. "There’s a momentum in the world right now. We need to use this momentum to end HIV and AIDS."

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 ??  ?? HIV continuous­ly mutates making it extremely difficult for the human body — and vaccine researcher­s — to create the appropriat­e neutralizi­ng antibodies to fight the virus
HIV continuous­ly mutates making it extremely difficult for the human body — and vaccine researcher­s — to create the appropriat­e neutralizi­ng antibodies to fight the virus
 ??  ?? More than 35 million people have died from HIV/AIDs — and those are just the deaths we know about
More than 35 million people have died from HIV/AIDs — and those are just the deaths we know about

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