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FIGHT AUTOIMMUNE DISEASES
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Just three months ago, Reagan Williams, 9,
was dangerously sick with extremely high
levels of sugar in her blood. Today she's
back on her feet and enjoying her first days
in fourth grade.
Last week, Kylynn Welsh,
18, was in critical condition on a ventilator in
a New Jersey hospital, unable to breathe on her
own because of swelling that closed her throat.
On Sunday, she was released from the hospital
and will soon be starting college.
These young people have
very different illnesses with one thing in
common: Their immune systems have gone awry. Immune
System
Scientists say immune
disorders, which range from common diseases such
as juvenile diabetes or lupus to some so unusual
that many doctors have never heard of them, are
among the most mysterious of ailments,
genetically complex and so diverse that
estimating their true prevalence is a guessing
game. But with major advances in genetics and
exponential growth of knowledge about the immune
system, scientists say important discoveries are
tantalizingly within reach.
"The capacity to explore
the human genome has reached the worker bee,"
says John Harley of the Arthritis and Immunology
Research Program at the Oklahoma Medical
Research Foundation in Oklahoma City. "It has
filtered down far enough that we now have the
capacity to do experiments we only dreamed of 10
years ago."
Now, he says, "the whole
range of human disease is going to be studied
using this approach and will produce new clues
that will be utterly transforming in our ability
to manipulate the fundamental disease process."
Disorders of the immune
system can be debilitating and expensive, and
are likely to be much more common than
previously realized.
But just how many people
have them is not known, because such diseases
are not tracked. The National Institutes of
Health estimated in a 2005 report that 5% to 8%
of Americans, up to 23.5 million, have one or
more autoimmune diseases, which occur when the
immune system launches an attack on healthy
cells within its own body.
In the current issue of
the Journal of Clinical Immunology,
researchers estimate, based on a random
telephone survey, that another group of immune
disorders called primary immune deficiency
diseases may afflict as many as one in 1,200. In
these diseases, caused by an inborn genetic
defect, the body can't mount an effective immune
response to infection.
"Almost every autoimmune
disease, with the exception of rheumatoid
arthritis, seems to be going up," says
immunologist Noel Rose, director of the Johns
Hopkins Autoimmune Diseases Research Center. But
whether that's because of an increase in disease
or better recognition of cases is not certain.
Wonder of nature
The immune system is
nature's built-in security force. When working
properly, it detects an incoming attack upon the
body, whether by viruses or other organisms, and
mounts a protective response. When the invader
is vanquished, it calls off the troops. But when
that system malfunctions, the body's internal
security force can lay down its arms or even
turn on itself.
In some cases, diagnosis
is a slam-dunk because symptoms are hard to
miss. But for others, it's not so clear. Pain or
fatigue is hard to measure, and other symptoms,
such as inflammation or weight loss, can have
many causes.
"When you have type 1
diabetes, there's a relatively clear boundary
between when you have it and when you don't,"
says Josiah Wedgwood, chairman of the Autoimmune
Diseases Coordinating Committee at the National
Institutes of Health. "With most of the other
autoimmune diseases, there isn't a clear
boundary like that. There's a problem called an
ascertainment bias: You identify the sickest
patients always, but like an iceberg, are you
only looking at the surface? And what's
beneath?"
Often, patients go from
doctor to doctor, desperate for a diagnosis.
"We know from surveys
there's a really unacceptable time from onset of
symptoms to diagnosis of primary immune
deficiency, as high as nine years," says
pediatric immunologist Jordan Orange of the
University of Pennsylvania and Children's
Hospital of Philadelphia.
'A car without a
brake'
For Kylynn Welsh, it took
more than 12 years.
The teenager is missing a
blood protein needed to stop the immune
response. If she gets a cut or a bump or if she
catches a cold, her body's immune system swings
into gear, sending white blood cells and fluids
to the affected area, causing inflammation and
swelling. But her body can't turn off the
response. "It's like driving a car without a
brake pedal," Wedgwood says.
As a child, Kylynn would
have unexplained bouts of swelling, says her
mother, Sandra Welsh. After gym one day, her
legs swelled painfully. Sometimes her belly
would puff up, causing agonizing pain.
"One time, her face was
so distorted that her scalp swelled down over
her eyes and she couldn't open her eyes," Welsh
says.
After four
hospitalizations and dozens of medical
evaluations, doctors pinpointed the disease as
hereditary angioedema, a disorder that is
usually inherited but can result from a genetic
mutation before birth. No one in her family has
had it, Welsh says. "I said, 'OK, now I know
what devil I'm playing with.' "
In her most recent
hospitalization, Kylynn went to Cooper Medical
Center in Camden, N.J., about 20 minutes from
her family's home in Delanco, N.J., to have
dental work done, which requires that she be
intubated and given plasma infusions because of
her immune system disease. But "her throat
started to bother her the day we were coming in
for the procedure, and before we could get a
(hospital) bracelet on her arm, her throat
closed," her mother says.
It was a moment of panic.
"She was dying in front of me," Welsh says. A
critical-care doctor recognized the signs of
distress and said, " 'Let's go, let's go,' "
Welsh says. He inserted a fiber-optic scope
through Kylynn's nose and throat to see where
the swelling was, so he could insert a breathing
tube.
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