INSERM: Vincent Sauzeau, Inserm researcher and his team located at the Nantes Thorax Institute
(Inserm, CNRS, University of Nantes, Nantes University Hospital) have
recently discovered the major role played by the Rac1 protein in the
development of bronchial hyperresponsiveness associated with allergic
asthma. Researchers will use this new therapeutic target to reduce
bronchoconstriction and pulmonary inflammation in patients. This article
has been published in The Journal of Allergy and Clinical Immunology.
Allergic asthma is a major public health problem, which currently
affects 8 to 10% of the global population. It represents 70% of the
various types of asthma, and is responsible for more than 250,000 deaths
per year. Asthma attacks are triggered by an allergen, which induces
excessive contraction of muscle cells in the bronchial wall (bronchial
hyperresponsiveness). This reduces the diameter of the bronchi and
causes breathing difficulties in the patient (sense of suffocation,
shortness of breath, cough, wheezing, etc.).
Vincent Sauzeau, Inserm researcher and his team have recently
evidenced the essential role played by the Rac1 protein in bronchial
muscle contraction and bronchial hyperresponsiveness associated with
allergic asthma, making Rac1 a new therapeutic target in allergic
asthma.
A promising avenue for treating patients
The researchers used a dust-mite sensitized asthmatic mouse model to
imitate the human disease, in order to determine the role of Rac1 in
bronchial hyperresponsiveness. They noted that inhalation of a Rac1
inhibitor prevents bronchial hyperresponsiveness in this allergic
asthmatic mouse model. Furthermore, bronchial inflammation and the
infiltration of certain white blood cells into the lungs (which promote
bronchial hyperresponsiveness in allergic asthma) are also reduced by
long-term administration of the Rac1 inhibitor. The research team
observed a 70 to 80% reduction in bronchial contraction due to Rac1
inhibition, on bronchial samples taken from lung transplant patients.
“Blocking the activity of Rac1 made it possible to both limit
bronchial contraction during an asthma attack, and also to reduce local
inflammation during maintenance therapy,” clarifies Vincent
Sauzeau, Inserm researcher leading these studies. The inhibitors used in
these studies are research instruments, which can only be used in a
laboratory setting. Hence, the researchers are currently developing new
molecules for clinical applications.
This research team, in partnership with the Pulmonology Department at the Thorax Institute
based at Nantes University Hospital has recently obtained funding to
verify the relationship between bronchial hyperresponsiveness and
abnormal Rac1 activation in the bronchi in patients suffering from
allergic asthma. “If this relationship is confirmed, this will
validate the significance of developing a new Rac1 inhibitor for
therapeutic purposes in humans. It would then be administered by
inhalation, for a targeted action in the bronchi,” concludes
Vincent Sauzeau. At present, 5 to 10% of patients suffering from
allergic asthma do not gain any relief from standard anti-inflammatory
and bronchodilator treatments. Rac1 inhibitors could offer new
therapeutic solutions.
[1] (http://www.umr1087.univ-nantes.fr/)