Regulatory T cells contribute to the inhibition of radiation-induced acute lung inflammation via bee venom phospholipase A 2 in mice

Dasom Shin, Gihyun Lee, Sung Hwa Sohn, Soojin Park, Kyung Hwa Jung, Ji Min Lee, Jieun Yang, Jaeho Cho, Hyunsu Bae

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10 Citations (Scopus)


Bee venom has long been used to treat various inflammatory diseases, such as rheumatoid arthritis and multiple sclerosis. Previously, we reported that bee venom phospholipase A 2 (bvPLA 2 ) has an anti-inflammatory effect through the induction of regulatory T cells. Radiotherapy is a common anti-cancer method, but often causes adverse effects, such as inflammation. This study was conducted to evaluate the protective effects of bvPLA 2 in radiation-induced acute lung inflammation. Mice were focally irradiated with 75 Gy of X-rays in the lung and administered bvPLA 2 six times after radiation. To evaluate the level of inflammation, the number of immune cells, mRNA level of inflammatory cytokine, and histological changes in the lung were measured. BvPLA 2 treatment reduced the accumulation of immune cells, such as macrophages, neutrophils, lymphocytes, and eosinophils. In addition, bvPLA 2 treatment decreased inflammasome-, chemokine-, cytokine- and fibrosis-related genes’ mRNA expression. The histological results also demonstrated the attenuating effect of bvPLA 2 on radiation-induced lung inflammation. Furthermore, regulatory T cell depletion abolished the therapeutic effects of bvPLA 2 in radiation-induced pneumonitis, implicating the anti-inflammatory effects of bvPLA 2 are dependent upon regulatory T cells. These results support the therapeutic potential of bvPLA 2 in radiation pneumonitis and fibrosis treatments.

Original languageEnglish
Article number131
Issue number5
Publication statusPublished - 2016 May 1


All Science Journal Classification (ASJC) codes

  • Toxicology
  • Health, Toxicology and Mutagenesis

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