Effect of montelukast combined with methylprednisolone for the treatment of mycoplasma pneumonia.

1 Department of Pediatrics, Huai'an Second People's Hospital/The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, Jiangsu Province, PR China. 2 Department of Respiratory Medicine, The Affiliated Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, PR China. 3 Central Laboratory of Huai'an Second People's Hospital/the Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, Jiangsu Province, PR China. 4 Department of Respiratory Medicine, The Affiliated Children's Hospital of Suzhou University, Suzhou, Jiangsu Province, PR China.

The Journal of international medical research. 2019;(6):2555-2561
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Abstract

OBJECTIVE To study the effect of the leukotriene receptor agonist montelukast combined with methylprednisolone on inflammatory response and peripheral blood lymphocyte subset content in children with mycoplasma pneumonia. METHODS Seventy-four children were enrolled and randomly divided into a standard treatment group and a montelukast plus methylprednisolone group. Serum levels of inflammatory cytokines and corresponding cytokines of T lymphocyte subsets were measured, and peripheral blood was collected to determine the T cell subset content. RESULTS At 3 days and 7 days after treatment, serum MCP-1, PCT, ICAM-1, CXCL8, CRP, IFN-γ, and IL-17 levels and peripheral blood Th1 and Th17 content were significantly decreased in both groups, while serum IL-4 and TGF-β levels and peripheral blood Treg and Th2 content were significantly increased. However, serum MCP-1, PCT, ICAM-1, CXCL8, CRP, IFN-γ, and IL-17 levels and peripheral blood Th1 and Th17 content were significantly lower while serum IL-4 and TGF-β levels and peripheral blood Treg and Th2 content were significantly higher in the montelukast plus methylprednisolone group compared with the control group. CONCLUSION Montelukast combined with methylprednisolone for the treatment of mycoplasma pneumonia can inhibit inflammatory responses and regulate levels of Th1/Th2 and Th17/Treg cells.

Methodological quality

Publication Type : Randomized Controlled Trial

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