Stem cells collected from human amniotic membrane (one of the two fetal membranes forming the amniotic sac) can slow the progression of scarring in pulmonary fibrosis, according to a pre-clinical study published in Stem Cells Translational Medicine (SCTM)
“Mesenchymal stromal cells derived from human amniotic membrane (hAMSCs) display a marked ability to affect the body’s immune system,” she explained. “They have been shown to reduce lung fibrosis in mice, possibly by creating a microenvironment that limits the evolution of chronic inflammation which leads to scarring. However, the ability of hAMSCs to modulate the immune cells – and specifically B cells- involved in pulmonary inflammation has yet to be clearly described. That’s what we sought to do in our study.”
A team led by researchers at the Eugenia Menni Research Centre (CREM) in Brescia, Italy, conducted a study on mice, beginning by inducing lung scarring with the drug bleomycin, which intra-tracheally instilled produces injury to the alveoli (the tiny air sacs in the lungs) and a consequent lung fibrosis. They then injected one group of animals with freshly isolated hAMSCs and another group with hAMSCs expanded in vitro, to address the important question of how in vitro expansion affects the hAMSCs’ therapeutic capabilities. A third group of animals, the control group, was treated with the saline solution used to inject hAMSCs but without the cells.
In order to explore whether treatment with hAMSCs may affect the immune cells that bleomycin-induced injury recruit into the lungs, the immune cells were collected at four, seven, nine and 14 days after treatment, from the alveolar spaces of the animals of treated and control groups. The animals’ immune cells were identified and quantified by a technique called flow cytometry. Lung tissues were also collected at the same times and analyzed for gene expression of markers associated with different immune cell types.
“We found that both the freshly collected and the expanded hAMSCs were able to control the recruitment, retention and maturation of B cells in the diseased lungs. This is important because in IPF patients, B cells form pulmonary aggregates with T cells, and continuously activate T cells creating a self-maintaining inflammatory condition.
“By modulating the B cells, the hAMSCs were able to break this loop and, thus, help blunt the progression of lung inflammation and, consequently, scarring, too,” Dr. Cargnoni explained. “We believe these key insights into the therapeutic potential of hAMSCs provide further evidence for the potential clinical use of hAMSCs in treating IPF and other inflammation-related fibrotic diseases.”
“This pre-clinical study demonstrates that stem cells derived from the amniotic fluid have the ability to hamper inflammation and slow scarring in lung tissue.” said Anthony Atala, M.D., Editor-in-Chief of Stem Cells Translational Medicine and director of the Wake Forest Institute for Regenerative Medicine. “These cells could eventually be used for new treatments of a deadly lung disease for which there is still no known cause or cure.”
Worldwide, IPF affects 13 to 20 out of every 100,000 people, according to the National Institutes of Health. While current medications (and in some instances, a lung transplant) can extend a patient’s life beyond the three to five years previously predicted from time of diagnosis until death, there is no cure.