Summary of Asthma
Transcript for Asthma
Asthma comes from the Greek word for “panting”, which makes sense because it causes chronic inflammation of the airways, making them narrow and more difficult to breathe through.
People with asthma can have asthma exacerbation or asthma attacks, which are usually triggered by something in the environment which causes immune cells to generate inflammation in the lungs which can make them even narrower and potentially be life-threatening.
So, if we take a look at the lungs, you’ve got the trachea, which branches off into right and left bronchi, and then continues to branch into thousands of bronchioles.
In the bronchioles you’ve got the lumen, the mucosa, which includes the inner lining of epithelial cells, as well as the lamina propria, and the submucosa which is where the smooth muscle lives.
The molecular pathway that leads to asthma is actually pretty complex but it is often initiated by an environmental trigger.
In asthma there is often an excessive reaction from type 2 helper cells or Th2 cells against specific allergens.
What can happen with asthma is allergens from environmental triggers, like cigarette smoke, are picked up by dendritic cells which present them to a Th2 cell which produce cytokines like IL-4 and IL-5 leading to a number of features of asthma.
For example IL-4 leads the production of IgE antibodies which coat mast cells and stimulate them to release granules containing things like histamines, leukotrienes and prostaglandins. IL-5, on the other hand, activates eosinophils which promote an immune response by releasing more cytokines and leukotrienes.
In this case, since IgE antibodies are being produced this is an example of a Type 1 hypersensitivity reaction.n
This leads to two series of events. Early on, minutes after the exposure to the allergen, smooth muscle around the bronchioles start to spasms and there is increased mucus secretion.
This narrows the airways making it difficult to breathe, and this is why asthma is considered to be a type of obstructive pulmonary disease.
There is also an increase in vascular permeability and and recruitment of additional immune cells from the blood.
So, a few hours after exposure, these immune cells, particularly eosinophils, release chemical mediators that physically damage the endothelium of the lungs.
Initially these inflammatory changes are completely reversible, but over the years irreversible changes start to take place—edema, scarring, and fibrosis build up, leading to thickening of the epithelial basement membrane, which permanently reduces the airway diameter.
Although the specific causes of asthma are ultimately unknown, it’s thought to be caused by a combination of genetic and environmental factors, since certain genes have been identified that increase the risk of developing asthma and having a family history of asthma seems to increase risk as well.
For environmental factors, there’s the hygiene hypothesis, which suggests that reduced early immune-system exposure to bacteria and viruses which might actually increase the risk of later developing asthma, possibly by altering the overall proportion of immune cell subtypes.
In general, causes of childhood asthma diagnosed before age 12 are thought to be due to a stronger genetic influence, whereas later onset asthma is more likely to be largely due to environmental factors.