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[ intro ]
Our immune systems are awesome.
I mean, while we're sitting on the couch
shoving our faces full of Doritos or whatever,
they're recognizing pathogens and other things that don't belong,
and ousting them from our bodies.
And on top of that,
they remember previous intruders,
and make it harder for them to invade again—
all while leaving our cells and the microbes that help us alone.
Basically, our immune systems are like really good bouncers
for the happening clubs that are our bodies.
Except for when they're not.
Sometimes, a body's immune system mistakenly decides
its own tissues are foreign—
what immunologists call autoimmunity.
Currently, there are more than
80 autoimmune conditions defined by doctors.
These include a slew of well-known conditions like lupus,
rheumatoid arthritis, and multiple sclerosis,
as well as lots of more rare ones.
They tend to be chronic and are often debilitating.
And taken together,
they're a leading cause of death and disability worldwide—
it's estimated that from three to ten percent of people
have an autoimmune condition at some point.
But if you were to put all of the people with autoimmune conditions in one room,
you'd notice something.
They're almost all women.
A whopping 75% of U.S. cases of autoimmunity
are in people who identify as women,
and rates are similar in other countries.
And for some autoimmune conditions,
the disparity is even higher.
Which is not only super unfair,
it's also a scientific enigma.
This gender bias of autoimmunity is considered one of the great mysteries of medicine.
And it's one that researchers are fervently trying to solve,
because it could reveal new ways of treating these usually incurable and often devastating
conditions.
Now, we'd be remiss if we didn't mention that part of the reason—
perhaps even a lot of the reason—
we don't fully understand these immunological betrayals is cultural.
Conditions that predominantly affect women have been historically understudied,
and studied in sexist ways when researchers have looked at them.
And, historically,
clinicians as a group just haven't taken women as seriously—
an issue that persists today.
But also, early work in the field of immunology
threw scientists off for decades.
At the turn of the twentieth century,
biologist and Nobel laureate Paul Ehrlich performed a series of experiments in animals
which found the animals didn't develop antibodies
in response to their own tissues.
Those are the Y-shaped proteins your immune system uses to recognize
and neutralize things like bacteria, viruses, and parasites.
And if Ehrlich wasn't seeing them, clearly,
autoimmune conditions couldn't be a thing.
He even coined a term based on his results:
horror autotoxicus—
which literally means the horror of self-toxicity.
But the thing with Nobel prize winners is that sometimes scientists heed them,
when they're wrong.
And that's what researchers say happened with horror autotoxicus and the immunology
community.
Still, over time,
the evidence became too clear to ignore.
Like, in 1946,
a British immunologist developed a test that could detect self-targeting
or autoantibodies attached
to the surface of a person's red blood cells.
Then there was the discovery of rheumatoid factor—
a type of autoantibody that occurs in rheumatoid arthritis
and some other autoimmune diseases.
Long story short,
these findings piled up until finally, in 1964,
the global immunology community rang in their acceptance of autoimmunity
as an actual thing with an international conference.
Research into autoimmunity in the decades since has come a long way.
But the mystery of why these conditions are so much more prevalent in women remains.
And, just to be clear,
we do mean women,
not just people with two X chromosomes or a uterus and ovaries.
It's true that the bulk of autoimmune research
has been conducted on people whose sex assigned at birth matches their gender identity.
But it's also been shown that some autoimmune conditions are more common
than expected in transgender women.
Often, these conditions are associated with medical transitioning,
but not always.
And some occur at higher rates in people with what are sometimes called
differences of sex development or intersex traits—
where parts of their biology like their chromosomes or genitals
diverge from the typical definitions of male and female.
In fact, including transgender people and people with hormonal, developmental, or chromosomal
variations in immunological research
has been an important part of evaluating the hypotheses
for the bias in autoimmunity we're about to discuss.
You see, researchers have been searching for the root cause of autoimmunity—
one or two nearly universal or nearly universal things
that are to blame for the immune system going rogue.
Yes, environmental factors like diet are a big part of the equation,
but the thinking is that there has to be something physiological
that makes some people more likely to develop autoimmunity
when exposed to those environmental factors.
Find that something,
and you'll find the best way to manage or even cure autoimmunity.
And that something, presumably,
tends to differ between men and women, and therefore,
can explain why women are so much more prone.
This is what led to the earliest and perhaps most immediately obvious hypothesis:
that autoimmunity has something to do with sex hormones—
the hormones involved in sexual differentiation and reproduction.
If that's true, it could mean autoimmune conditions could be better treated
by tweaking a person's hormone levels or the pathways those hormones interact with.
But researchers don't always agree on which sex hormones are most important,
and overall, results are mixed.
Like, some think it's all about testosterone
or other hormones that generally occur at higher levels in men.
And There is pretty solid evidence
that testosterone suppresses immune function.
And scientists know for sure that increasing a person's testosterone level
reduces the number of B cells in their body—
a type of white blood cell that recognizes foreign stuff,
and the only type of cell that produces antibodies.
So the idea has been that since testosterone reduces B cells,
and B cells produce antibodies, that may be why men generally have weaker
immune responses than women...
...the upside to which could be that a less aggressive immune system
is also less likely to misplace its attacks.
Like, one 2018 study looked at hormones and key components of the immune system
in cisgender and transgender volunteers
as well as people with atypical sex chromosomes.
The researchers found that even when accounting for different combinations of sex chromosomes,
higher testosterone levels were associated with less interfereon alpha—
an immunological protein suspected to play a role in autoimmune conditions like rheumatoid
arthritis.
But that's just one study,
and research connecting hormone levels to autoimmune conditions is kind of all over
the place.
Other studies have suggested estrogens
or other hormones that tend to be higher in women matter more.
And some studies have pointed out that even if hormones modulate these conditions,
they're probably not what causes them.
So many researchers think there's something else at play—
like, perhaps, sex chromosomes.
Those are the chromosomes which help steer sex development and sex hormone levels.
Males usually have an X and a Y chromosome, while females usually have two Xs.
But these chromosomes don't just affect the differentiation of gonads or levels of
hormones.
For example, the human X chromosome has more immune system related genes
than any other chromosome.
And it's possible that autoimmunity somehow stems from those genes
in a way that isn't dependent on sex hormones.
That would explain why anyone can develop autoimmunity,
because everyone has an X chromosome.
And, if X-linked genes are somehow the ultimate cause of autoimmunity,
it would also make sense that people with two Xs are more prone to it—
whether or not they're women.
There is evidence that's the case, too.
For example, autoimmune conditions are also more common in men with Klinefelter's syndrome—
where they have two X chromosomes and a Y chromosome.
In fact, the proportion of people with Kleinfelter's syndrome is 17 times higher