Researchers from Rockefeller University, other institutions have discovered hereditary illness that causes defective cell function that was previously unknown.
One of the most significant cells in the body is the macrophage.
This immune cell, dubbed "big eater" in Greek, eats and breaks down
dangerous substances like dust, debris, bacteria, and cancer cells. Macrophages
play a particularly important role in the lungs, where they combat bacterial
infections and remove excess surfactant, a lipid- and protein-rich covering
that is essential for lung health but can accumulate sticky matter if left
unchecked.
The study found that the children are missing half of their alveolar macrophages, which are located in the air sacs of the lungs.
Researchers from Rockefeller University and other institutions have discovered a hereditary illness that causes defective cell function that was previously unknown.
By noticing an unexpected link between a particular subset of sick
kids, the researchers were able to make their breakthrough. These nine
youngsters had fought lifelong battles with life-threatening conditions such as
progressive polycystic lung disease, pulmonary alveolar proteinosis (PAP), and
recurring viral and bacterial infections that frequently left their lungs
riddled with cysts and left them gasping for air.
But as genomic data revealed, the children shared another characteristic: the absence of a chemical receptor that is supposed to call alveolar macrophages into action. It's the first time that this missing receptor, called CCR2, has been linked to disease. The researchers, including Rockefeller's Jean-Laurent Casanova and Institut Imagine's Anna-Lena Neehus, recently published their results in Cell.
The study also found that the children are missing half of their
alveolar macrophages, which are located in the air sacs of the lungs.
"It was surprising to find that CCR2 is so essential for
alveolar macrophages to properly function," said Casanova. "When it
comes to lung defense and clean-up, people without it are operating at a double
loss."
More formally known as C-C motif chemokine receptor 2, CCR2 sits on the surface of alveolar macrophages, a kind of monocyte (or white blood cell). It responds to the presence of a chemical ligand, or binding molecule, known as CCL-2, which is also expressed by monocytes.
The receptor and ligand work together to summon macrophages to the site of an infection, and to maintain the appropriate level of surfactant; too little can lead to collapsed lung tissue, and too much can result in narrowed airways.
It was among these immune cells that first author Neehus, of Casanova's lab at the Institut Imagine in Paris, was seeking evidence of genetic deficiencies that might alter their behaviour. While combing through the genomic data on 15,000 patients in a database, she found two Algerian sisters, then aged 13 and 10, who'd been diagnosed with severe PAP, a syndrome in which surfactant builds up and the gas exchange that takes place in alveoli is hindered.
About 90 per cent of PAP cases are caused by antibodies that cripple a protein that stimulates the growth of infection-fighting white blood cells. The girls, however, didn't have the PAP autoantibodies. Instead, they had no CCR2--a newly identified genetic mutation. Perhaps its lack was connected to their pulmonary conditions, Neehus thought. "It looked interesting and promising," she recalled.
She soon found seven other children in the cohort who had the same CCR2 mutation and serious lung conditions: two more pairs of siblings, and one trio of siblings. They were from the United States and Iran.
To explore the impact the variant might have on the children, the researchers analysed the children's clinical histories, lung tissue samples, and genetic data.
Several key findings emerged. "First we discovered that these
patients have only half the normal counts of pulmonary alveolar macrophages,
which explains the different types of lesions they have across the pulmonary
tissues," says Casanova. With only half a crew, the reduced clean-up unit
couldn't keep up with its workload, leading to tissue injury.
The macrophages were otherwise normal, as were the children's other immune cells.Without CCR2 signalling, monocytes have no idea where they're needed. In the study, a live-imaging analysis of the monocytes from the lungs of a 10-year-old girl with CCR2 deficiency showed the cells milling about aimlessly, unsure where to go. (See gif at top.) In contrast, live imaging of monocytes from a healthy control patient shows them migrating in the same direction, summoned by the teamwork of CCR2 and CCL-2.
This directionlessness also makes those with a CCR2 deficiency more susceptible to mycobacterial infections, because the macrophages can't find their way to the tissue clusters where mycobacteria take up residence, and thus digest the invaders.
This had dire effects for three of the children in the study, who
developed bacterial infections after being vaccinated with a live-attenuated
substrain of Mycobacterium bovis, an agent of tuberculosis. Their immune
systems failed to assemble a legion of macrophages at the vaccination site in
the shoulder, causing tissue destruction or hard nodes that had to be
surgically removed, or lymph node infections. (All of the children were
effectively treated with antibiotics.)
The children inherited the deficiency from their parents--and yet their parents were healthy. "Each of the parents carries one disease copy of the gene, and both parents gave the affected copy to their children," said Neehus. "The parents aren't affected because they each only have one copy, whereas the kids have two."
Several children were the result of consanguineous marriages, in which the parents are related. The offspring of such pairings have a higher risk of inheriting the mutation that causes CCR2 to disappear.
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