期刊
RESPIRATORY MEDICINE
卷 105, 期 7, 页码 997-1006出版社
W B SAUNDERS CO LTD
DOI: 10.1016/j.rmed.2010.12.021
关键词
Leukotriene B4; Neutrophils; Innate defense; Rhinitis; Rhinovirus
资金
- LTB4 Sweden AB
Background: Leukotriene B4 (LTB4) recruits and activates neutrophils. Accordingly, this leukotriene is involved in innate defense actions. Objective: To examine if nasal LTB4 can produce neutrophil activity and to explore whether or not LTB4 can condition neutrophils to exert virucidal effects in vitro and in vivo. Methods: 1. Twenty-three healthy subjects received nasal LTB4 in a randomized and sham-controlled design. Symptoms were scored and nasal lavages carried out. Myeloperoxidase (MPO) and alpha-defensins were monitored as indices of neutrophil activity. IL-8, eosinophil cationic protein (ECP) and alpha(2)-macroglobulin were measured as indices of pro-inflammatory cytokine production, eosinophil activity, and plasma exudation. 2. Supernatants from neutrophils activated by LTB4 in vitro were assayed for virucidal activity against respiratory viruses. 3. In 38 healthy individuals, nasal inoculation with human rhinovirus-16 (HRV-16) was performed. In a preliminary study, intervention with LTB4 was given in a randomized and controlled design. Symptoms, virus replication, and antibody-titres were monitored. Results: 1. LTB4 produced statistically significant increases in MPO and alpha-defensins, whereas IL-8, ECP, and alpha(2)-macroglobulin were unaffected. 2. The supernatants efficiently killed human coronavirus, respiratory syncytial virus, and influenza B virus. 3. HRV-16 replication was lower in subjects receiving LTB4, but this difference failed to reach statistical significance. Common cold symptoms and incidence of seroconversion were unaffected. Conclusion: Nasal LTB4 induces a selective recruitment/activation of neutrophils. LTB4 can condition neutrophils to exert virucidal effects in vitro and may reduce virus replication in vivo. We suggest that the condition induced by LTB4 reflects an enhanced state of innate defense. (C) 2010 Elsevier Ltd. All rights reserved.
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