Abstract |
Mycoplasma pneumoniae (Mp) may cause immune cell reactions as pivotal aspects of this clinically common respiratory pathogen. Our aim is to determine if Mp extract induces a cellular immune response associated with interleukin (IL)-17, leading to lung inflammation and lung injury. BALB/c mice were immunized with Mp extract intraperitoneally followed by its intratracheal administration, to mimic repeated Mp infection found in humans (repeated inoculation, RI group). Those with a single inoculation were compared as single inoculation group (SI group). Analysis of bronchoalveolar lavage fluid (BALF) demonstrated that keratinocyte-derived cytokine, tumor necrosis factor-α, and IL-6 were produced and peaked on days 0.5 or 1, followed by IL-17 on day 2. Levels of these mediators in BALF were higher in RI group than SI group (P < 0.05). Further, significantly more neutrophils were recruited to the lungs of the RI group (P < 0.05). These observations suggest that IL-17 is involved in the prolonged induction of neutrophils in mice treated with Mp extract.
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Authors | Daisuke Kurai, Kazuhide Nakagaki, Hiroo Wada, Takeshi Saraya, Shigeru Kamiya, Yasunori Fujioka, Koh Nakata, Hajime Takizawa, Hajime Goto |
Journal | Inflammation
(Inflammation)
Vol. 36
Issue 2
Pg. 285-93
(Apr 2013)
ISSN: 1573-2576 [Electronic] United States |
PMID | 23001692
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Interleukin-17
- Interleukin-23
- Interleukin-6
- Tumor Necrosis Factor-alpha
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Topics |
- Animals
- Bronchoalveolar Lavage Fluid
(chemistry, cytology)
- Cells, Cultured
- Female
- Immunization
- Inflammation
- Interleukin-17
(biosynthesis, immunology)
- Interleukin-23
(metabolism)
- Interleukin-6
(biosynthesis, immunology)
- Lung
(immunology, microbiology)
- Mice
- Mice, Inbred BALB C
- Mycoplasma pneumoniae
(immunology, metabolism)
- Neutrophils
(immunology)
- Pneumonia, Mycoplasma
(immunology, microbiology)
- Tumor Necrosis Factor-alpha
(biosynthesis, immunology)
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