A lot of very smart people have been working for a very long time on vaccines for HIV/AIDS, and they’ve come up empty. Thanks to broadly neutralizing antibodies (bnAbs) and mRNA vaccine technology, that might be changing. Here’s why we don’t have a vaccine for HIV/AIDS yet.
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So they whipped out vaccines for
COVID-19 in under a year, right? And meanwhile HIV has been a global menace
for decades and there’s no vaccine in sight. So, what gives? But the COVID-19 mRNA
vaccines were a special case. And it’s a fact that
stereotypes and discrimination
00:18:
held up funding for HIV
research in the early days. But the honest truth is that lots of people
really, really want to make a vaccine for HIV and the pesky virus makes it
really, really, REALLY hard to do. Yet researchers haven’t given up, and if anything,
01:34:
the success of COVID vaccines has only
injected new hope into their search. By harnessing biology both
in your body and in the lab, scientists have all sorts of tricks to try
in the search for a vaccine against HIV. Getting diagnosed with HIV used to be
a death sentence, but it isn’t anymore!
01:55:
People with HIV can now live long, full lives thanks to highly effective treatments
in the form of antiretroviral therapy. We even have reliable prevention in the form of pre-exposure prophylaxis, or PrEP for short. But it’s not recommended for
everyone, only those at high risk.
01:11:
But what would be really sweet is a nice little one
and done jab in the arm for absolutely everybody, so we can put a stop to the over a million
new HIV diagnoses worldwide every year. But developing an HIV vaccine has not been easy.
01:25:
There have been many clinical trials
representing various attempts, with the earliest trial starting
all the way back in 1987. But so far, none have shown enough success
to be given the FDA stamp of approval.
02:36:
It turns out, the biological nature of HIV makes
it especially challenging to vaccinate against. In general, when a pathogen enters
your body, or when a vaccine introduces a version of it, your immune system
makes antibodies to fight it off.
02:49:
But with HIV, that immune response
just… doesn’t really happen. When HIV enters your body, it wraps itself
in a trench coat of sugar molecules, shielding its proteins from being
detected by your immune system. This allows it to slip past your natural
defenses without triggering the alarm.
02:06:
Then, HIV turns the tables and dismantles
the cells of your immune system that were supposed to defend against it. And as a second layer of disguise, many of the HIV proteins mimic
human immune cell proteins. Meaning a vaccine targeting those viral proteins
02:21:
might direct your immune system
at your own cells by mistake. As if all that wasn’t challenging enough,
HIV is also a notorious shape-shifter. It mutates quickly, even within the same
person, which means that any antibodies
03:35:
that you might have created against one version
may no longer work after a few mutations. That is, almost any antibodies. Since the early 2000s, much of the
focus for an HIV vaccine has been on a class of antibodies called broadly
neutralizing antibodies, or bnAbs for short.
03:52:
The B cells of your immune system
are the ones in charge of making all of your antibodies, with each B cell
specializing in one specific antibody. But new B cells are pretty much randomly
mixing and matching antibody genes. Your immune system’s not
waiting around for a pathogen
03:07:
to show up and design it a
perfectly custom antibody. There is a method to this madness. Randomly generating as many different B
cells as possible maximizes the chance of at least one of those guys getting a match
that’s close enough to grab onto the pathogen.
03:22:
Once a B cell matches with a pathogen, it
will begin spitting out a bunch of antibodies. Since the initial fit might not have been perfect, those antibodies will get mutated
further to try and improve the match. Even then, those changes are
still random, so your B cells
04:36:
make a lot of duds in order to find the
antibodies that are actually better. So HIV bnAbs happen when your
immune system hits the jackpot and manages to make antibodies against
a less variable part of the virus. So they can bypass its shape shifting
and work against more versions of HIV.
04:54:
And bnAbs are produced naturally in 10-25% of
people living with HIV, but they aren’t perfect. Even if you do have them, there aren’t
usually enough bnAbs in your body to neutralize all of the virus on their own.
04:06:
And there may be a good reason why we don’t
usually have too many of them at the ready. bnAbs are known to show some autoreactivity, meaning that they may be primed to
target some of your body’s own cells. In general, that’s seen as
a bad thing for antibodies,
04:19:
because you don’t want your
immune system to attack you. So your body has checks in place
to destroy autoreactive B cells before they can fully develop. But some of the bnAbs that are the best at neutralizing HIV also tend
to have more autoreactivity.
05:33:
In fact, some research suggests that
the development of anti-HIV powers comes at the inherent cost of picking
up some autoreactive mutations. And this creates a bit of a catch-22: The
better the bnAbs, the more autoreactivity. But that means any bnAb-producing B cells you have
05:50:
might get nuked by your body
before they ever mature. And that includes B cells developing
in response to a vaccine. This has made it really difficult for vaccines
to drum up enough bnAb activity to tackle HIV. Some researchers have found some success
in stimulating the natural precursors
05:06:
that create bnAbs, rather than
trying to get to the bnAbs directly. Scientists wanted to see
if they could get a vaccine to switch on the specific B cells
that go on to make bnAbs against HIV. A phase-1 clinical trial published
in 2022 provided a proof-of-concept
05:22:
that stimulating more bnAb precursors with
a vaccine might be feasible in humans. This study only looked at
people not living with HIV, but the vaccine did successfully stimulate
a type of B cell that makes bnAbs! However, there are some challenges to overcome
06:38:
before we can develop this strategy further. Basically, the strategy wasn’t
specific enough to turn on only the kind of B cells that make bnAbs. It might also switch on other B cells willy-nilly. But while scientists tinker away
at optimizing bnAb technology,
06:53:
there’s another angle that people
are looking at for an HIV vaccine. The COVID-19 pandemic granted fame
and glory to the mRNA vaccine. And it’s inspired high hopes that we
might be able to use that same technology and apply it to different
diseases – including HIV.
06:09:
mRNA refers to a little piece of genetic information that tells your
cells how to make a protein. Unlike traditional vaccines that deliver
viral proteins directly to your body, mRNA vaccines deliver the
instructions to make viral proteins.
06:24:
Once the mRNA gets in, it marches right on
into your cells’ protein-making factories, and the viral protein gets
translated along with all the others. Then, once the viral protein is made, it can be presented to your immune
system to trigger antibody production.
07:38:
Since your body is much better at making
proteins naturally than we can in a lab, this is a great tool to leverage against
the diverse and complicated proteins of HIV. It’s also much faster, safer, and more
cost-effective than traditional vaccine types.
07:52:
Part of the reason why mRNA vaccines
were such a breakthrough for HIV is that our traditional vaccine
options really are not options. Vaccines with a weakened form of the
virus have a tiny chance of accidentally causing the disease, and since HIV is
a chronic disease that has no cure yet,
07:10:
even that tiny chance is
considered way too unsafe. And vaccines that packed a
completely killed version of HIV didn’t generate enough of
an immune response to work. So, enter mRNA vaccines. Since they don’t contain any actual virus,
there’s no way to accidentally cause the disease.
07:27:
And since mRNA molecules are easy to pack, you can pack the instructions
for a bunch of different proteins all into one vaccine way more easily
than you can with traditional approaches! And this is important because
targeting just one HIV protein doesn’t produce a strong enough immune response.
08:42:
So, once again, mRNA vaccines are awesome
for producing a robust immune response against all the various proteins
that are on the surface of HIV. …In theory. In practice, it's again proving trickier. A group of researchers across North
America conducted an initial test
08:58:
of an HIV mRNA vaccine in
rhesus macaques and mice. They found that packaging the mRNA for
two different proteins into one dose got a significantly better immune response
than either of the proteins alone. This vaccine was able to induce bnAb
production in the rhesus macaques,
08:15:
and the monkeys successfully made new
immune cells in response to HIV exposure. Unfortunately, this doesn’t mean it’s
ready to go into human arms just yet. While the vaccine did get an immune response, the level of response wasn’t high
enough to count as fully protective.
08:29:
Plus, this protocol included more than
seven injections in total, which is just… way too many to be practical. And even though HIV mRNA vaccines
have shown promise in animal models, they seem to lose momentum when
translating to human participants. In 2022, three clinical trials were launched
09:46:
to test an mRNA vaccine to protect against HIV. And while the results of these phase 1
trials are not yet published, as of writing this episode, there
have been some initial concerns over some participants experiencing itchiness
and hives after receiving the vaccine.
09:00:
So there’s a bit of a slowdown while the
researchers try to figure out what’s up. Even though itchiness might not be the worst
side effect that could possibly happen, phase 1 trials are all about establishing safety. The researchers want to make sure that
they understand as much as they can
09:14:
about why these skin effects
are happening before moving on. So far, all of these vaccines that
we’ve discussed have been preventative, but what about people who
are already living with HIV? Therapeutic vaccines are also in the works,
09:26:
with the goal of stimulating antibodies
after having already acquired HIV. The hope is that the body can
retroactively develop the immune cells to destroy any of the virus that’s hanging around. While none of the tested therapeutic
vaccines have worked perfectly yet,
10:39:
there’s been a few promising findings. One research group in Europe
tested out a therapeutic vaccine on 45 participants with HIV in a
double-blind, placebo-controlled study. After vaccinating the participants,
they put it to the ultimate test
10:53:
by having the participants stop
taking their HIV medication for up to six months and see how well
their bodies could keep the HIV at bay. And unfortunately, it didn’t seem to work. Well, let’s not be too pessimistic –
it didn’t work well enough yet.
10:08:
None of the participants were able to keep their
HIV levels down after pausing their medication. But the vaccine was able to get
some immune cell activity going, and it didn't cause any major negative effects. So the researchers think it’s still
worth tinkering with this vaccine
10:23:
to see if they can boost that
response to be more effective. The journey to finding a
vaccine for HIV has been long. This sneaky virus has a lot of tricks up its
tiny little sleeves to try to stay one step ahead of our immune systems, but scientists
are closing the gap every day.
11:38:
With our ever-improving knowledge on bnAbs, we’re working on a solution that can
handle all of the strains of HIV. And the promising track record of mRNA vaccines provides an exciting alternative
to traditional technology. So, we're tackling this disease from
multiple angles, and with more testing
11:54:
and a few more hurdles to overcome,
we might soon be able to prevent and treat the transmission of HIV for everyone.