Peron Jean Pierre Schatzmann, de Brito Auriléia Aparecida, Pelatti Mayra, Brandão Wesley Nogueira, Vitoretti Luana Beatriz, Greiffo Flávia Regina, da Silveira Elaine Cristina, Oliveira-Junior Manuel Carneiro, Maluf Mariangela, Evangelista Lucila, Halpern Silvio, Nisenbaum Marcelo Gil, Perin Paulo, Czeresnia Carlos Eduardo, Câmara Niels Olsen Saraiva, Aimbire Flávio, Vieira Rodolfo de Paula, Zatz Mayana, de Oliveira Ana Paula Ligeiro
Neuroimmune Interactions Laboratory, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, SP, Brazil.
Laboratory of Pulmonary and Exercise Immunology-LABPEI, Nove de Julho University (UNINOVE), São Paulo, SP, Brazil.
PLoS One. 2015 Aug 31;10(8):e0136942. doi: 10.1371/journal.pone.0136942. eCollection 2015.
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.
香烟烟雾诱导的慢性阻塞性肺疾病是一种非常使人衰弱的疾病,在全球范围内患病率极高,会导致巨大的经济和社会负担。因此,治疗这些患者的新疗法具有毋庸置疑的重要性。间充质基质细胞(MSCs)的应用是一种创新且可行的治疗肺部急慢性疾病的方法,主要是因为其具有重要的免疫调节、抗纤维化、抗凋亡和促血管生成作用。此外,应测试旨在增强其功能或与之协同作用的辅助疗法。低强度激光(LLL)疗法是一种相对新颖且有前景的方法,成本极低,无侵入性且无副作用。在此,我们旨在研究人支气管来源的间充质基质细胞(htMSCs)细胞疗法联合30mW/3J - 660nm低强度激光照射对实验性香烟烟雾诱导的慢性阻塞性肺疾病的疗效。因此,将C57BL/6小鼠每天两次暴露于香烟烟雾中75天,并在第76天进行所有实验。实验组单独或联合接受腹腔内或鼻内注射htMSCS和/或低强度激光照射。我们发现联合治疗可显著减轻肺部炎症,减少细胞浸润和促炎细胞因子分泌(IL - 1β、IL - 6、TNF - α和KC),随后黏液分泌、胶原蛋白积累和组织损伤减少。这些发现似乎继发于肺组织中NF - κB和NF - AT激活的减少以及IL - 10的同时增加。总之,我们的数据表明,MSCs + LLLT联合使用可能是治疗如慢性阻塞性肺疾病等肺部炎症性疾病的一种有前景的治疗方法。