AI Article Synopsis

  • Cigarette smoke causes chronic obstructive pulmonary disease (COPD), which is a serious health issue with significant economic and social impacts, highlighting the need for new treatment options.
  • Mesenchymal stromal cells (MSCs) show potential for treating COPD due to their healing properties, and their effectiveness can be enhanced through adjuvant therapies like low-level laser (LLL) therapy, which is safe and affordable.
  • Research using mice exposed to cigarette smoke demonstrated that combining MSC therapy with LLL irradiation significantly reduces lung inflammation, cellular infiltrates, and tissue damage, suggesting this combination could be an effective approach for treating COPD.

Article Abstract

Cigarette smoke-induced chronic obstructive pulmonary disease is a very debilitating disease, with a very high prevalence worldwide, which results in a expressive economic and social burden. Therefore, new therapeutic approaches to treat these patients are of unquestionable relevance. The use of mesenchymal stromal cells (MSCs) is an innovative and yet accessible approach for pulmonary acute and chronic diseases, mainly due to its important immunoregulatory, anti-fibrogenic, anti-apoptotic and pro-angiogenic. Besides, the use of adjuvant therapies, whose aim is to boost or synergize with their function should be tested. Low level laser (LLL) therapy is a relatively new and promising approach, with very low cost, no invasiveness and no side effects. Here, we aimed to study the effectiveness of human tube derived MSCs (htMSCs) cell therapy associated with a 30mW/3J-660 nm LLL irradiation in experimental cigarette smoke-induced chronic obstructive pulmonary disease. Thus, C57BL/6 mice were exposed to cigarette smoke for 75 days (twice a day) and all experiments were performed on day 76. Experimental groups receive htMSCS either intraperitoneally or intranasally and/or LLL irradiation either alone or in association. We show that co-therapy greatly reduces lung inflammation, lowering the cellular infiltrate and pro-inflammatory cytokine secretion (IL-1β, IL-6, TNF-α and KC), which were followed by decreased mucus production, collagen accumulation and tissue damage. These findings seemed to be secondary to the reduction of both NF-κB and NF-AT activation in lung tissues with a concomitant increase in IL-10. In summary, our data suggests that the concomitant use of MSCs + LLLT may be a promising therapeutic approach for lung inflammatory diseases as COPD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554986PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0136942PLOS

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