Welcome to Impact Factor, your weekly dose of commentary on a new medical study.
I’m Dr. F. Perry Wilson of the Yale School of Medicine.
There’s a meme flying around the interwebs that COVID vaccines might render young people
infertile.
Taken on its own, this may seem like run-of-the-mill antivax fear-mongering, and it is, but this
one seems to have some legs.
In fact, a UK survey found that one quarter of young women would decline the vaccine,
citing concerns about fertility.
This is actually a sort of old vaccine trope – it’s been trotted out, without any evidence,
for the polio vaccine, and the HPV vaccine.
And I get why it’s so powerful.
Fertility is obviously a huge issue – a basic human function.
But it also immediately conjures up the long-term – sure, I may be protected from COVID today,
but what if I want to have kids 15 years from now, and find out I can’t.
Handmaids Tale stuff.
Disturbing.
So I want to show how this thing got started, but more importantly, I want to make an argument,
that if you really want to worry about fertility – you should worry about SARS-CoV-2 more
than the SARS-CoV-2 vaccine.
You can trace the earliest emergence of this idea to two guys – Wolfgang Wodarg, a physician
and German politician and Michael Yeadon, an ex-Pfizer scientist.
Yeadon’s Pfizer link lent him credibility, though a perusal of his twitter account – now
deleted - suggests he was not the best COVID prognosticator.
This was tweeted a couple months before the UKs much more deadly second wave.
In any case, their argument centered around the similarity between the spike protein that
the vaccines code for and syncytin-1, a human protein critical for placental development.
Syncytin-1 is known as an endogenous retroviral element.
Basically, code in our DNA that came from an old virus – we have a bunch of these
actually.
This one probably got in there around 25 Million years ago and conferred some selective advantage
leading it to hang around.
The question – is syncytin-1 similar enough to the spike protein of coronavirus that cross-reactive
antibodies might attack the placenta?
The answer, at least according to the geneticists and immunologists I polled, is not really.
They are dramatically different proteins.
The spike protein is complex with 1,273 amino acids.
Syncytin-1 has 538 amino acids.
An alignment search suggests about a 7% overlap – here’s a sample of the sequences to
give you a sense of what that means – syncytyin-1 is red and matches with spike protein are
red underneath.
But I’m told this amount of homology is not surprising.
More importantly, it’s not really the degree of overlap that matters to figure out if an
antibody will be cross-reactive.
It’s actually quite hard to predict and has to do with 3d topology of proteins and
stuff.
If you want to figure out if an antibody will be cross-reactive, just measure it.
Which is what Akiko Iwasaki, here at Yale did.
Her lab tested serum of women with COVID-19 and found no antibodies that bound to syncytin-1.
We also have the empiric data from the vaccine trials that showed no difference in miscarriage
rates between women who became pregnant in the vaccine groups versus the placebo groups.
We also, now, have data on over 100,000 pregnant women who have received the vaccine in the
US.
So far- no safety signals have emerged.
This fertility theory just doesn’t hold up to reality.
And, not to be pedantic here, but even if there was homology between the spike protein
and a human protein, the virus itself HAS the spike protein too – as well as a bunch
of other proteins not present in the vaccine that might also have antibody cross-reactivity
problems.
Maybe better not to get COVID at all?
In fact, if it’s sterility you’re worried about, I honestly think there’s more to
be concerned about with the virus itself than the vaccine.
Here’s why.
The cellular receptor for the coronavirus is ACE-2.
Enter that into a protein expression atlas of your choice and look where ACE-2 is most
robustly expressed.
Nasopharynx and bronchus – no surprises there.
But also testis and placenta.
In fact, ACE-2 is robustly expressed on Sertoli cells, which are the support cells that help
sperm be produced.
This has led to multiple papers – all hypothetical at this point – speculating that SARS-CoV-2
infection may impact male fertility.
To be fair, we haven’t seen much evidence of this either.
I have found a total of one paper – a case report – suggesting that COVID infection
hurt a man’s sperm count.
But the point is this – the vaccines prime your immune system against the spike protein.
But so does COVID.
And COVID, unlike the vaccine, can actually infect cells and kill them – including,
potentially, cells that are important for reproduction.
The anti-vaccination crowd wants to argue that there is biologic plausibility for a
COVID-vaccine / infertility link.
If that’s our standard for evidence, there is a heck of a lot more plausibility for a
COVID / infertility link.
But as I’ve said many times before – biologic plausibility is just the start of research.
Empiric data is necessary in the end.
There is enough empiric data to conclude that it is highly unlikely the vaccines will have
any effect on fertility.
It’s pretty unlikely COVID itself will have an effect either – but it seems to me like
that possibility deserves some deeper investigation.