Lin I-Ping, Hsu Yu-Shen, Kang Ssu-Wei, Hsieh Miao-His, Wang Jiu-Yao
Institute of Microbiology & Immunology, College of Medical, National Cheng-Kung University, Tainan, Taiwan; Development Center for Biotechnology, Taipei, Taiwan.
Development Center for Biotechnology, Taipei, Taiwan.
PLoS One. 2014 Mar 17;9(3):e90293. doi: 10.1371/journal.pone.0090293. eCollection 2014.
Various mutant forms of Escherichia coli heat-labile enterotoxin (LT) have been used as a mucosal adjuvant for vaccines, as it enhances immune responses to specific antigens including antigen-specific IgA antibodies when administrated intranasally or orally. We hypothesized that a detoxified mutant form of LT, LTS61K, could modulate dendritic cell (DC) function and alleviate allergen-induced airway inflammation. Two protocols, preventative and therapeutic, were used to evaluate the effects of LTS61K in a Dermatophagoides pteronyssinus (Der p)-sensitized and challenged murine model of asthma. LTS61K or Der p-primed bone marrow-derived dendritic cells (BMDCs) were also adoptively transferred into Der p-sensitized and challenged mice. Intranasal inoculations with LTS61K or LTS61K/Der p decreased allergen-induced airway inflammation and alleviated systemic TH2-type immune responses. Bronchoalveolar lavage fluid (BALF) and sera from LTS61K/Der p-treated mice also had higher concentrations of Der p-specific immunoglobulin (Ig) A than those of other groups. In vitro, BMDCs stimulated with Der p underwent cellular maturation and secreted proinflammatory cytokines interleukin (IL)-6 and tumor necrosis factor (TNF)α In contrast, Der p-stimulated BMDCs that were pretreated with LTS61K showed decreased IL-6 and TNFα production and were less mature. Intratracheal adoptive transfer of LTS61K- or LTS61K/Der p-primed BMDCs into Der p-sensitized mice reduced inflammatory cell infiltration and TH2-type chemokines in BALF and alleviated airway inflammation in treated mice. LTS61K influenced DC maturation and decreased inflammatory cytokine production. Moreover, LTS61K/Der p induced increased Der p-specific IgA production to decrease allergic TH2 cytokine responses and alleviated airway inflammation in Der p-sensitized mice. These results suggest that the immunomodulatory effects of LTS61K may have clinical applications for allergy and asthma treatment.
大肠杆菌热不稳定肠毒素(LT)的多种突变形式已被用作疫苗的黏膜佐剂,因为经鼻内或口服给药时,它能增强对包括抗原特异性IgA抗体在内的特定抗原的免疫反应。我们推测,一种解毒的LT突变形式LTS61K可以调节树突状细胞(DC)功能,并减轻变应原诱导的气道炎症。采用预防性和治疗性两种方案,在屋尘螨(Der p)致敏和激发的小鼠哮喘模型中评估LTS61K的作用。LTS61K或Der p致敏的骨髓来源树突状细胞(BMDC)也被过继转移到Der p致敏和激发的小鼠体内。鼻内接种LTS61K或LTS61K/Der p可减少变应原诱导的气道炎症,并减轻全身TH2型免疫反应。LTS61K/Der p处理的小鼠的支气管肺泡灌洗液(BALF)和血清中Der p特异性免疫球蛋白(Ig)A的浓度也高于其他组。在体外,用Der p刺激的BMDC发生细胞成熟并分泌促炎细胞因子白细胞介素(IL)-6和肿瘤坏死因子(TNF)α。相反,用LTS61K预处理的Der p刺激的BMDC显示IL-6和TNFα的产生减少,且成熟度较低。将LTS61K或LTS61K/Der p致敏的BMDC经气管过继转移到Der p致敏的小鼠体内,可减少BALF中的炎性细胞浸润和TH2型趋化因子,并减轻治疗小鼠的气道炎症。LTS61K影响DC成熟并减少炎性细胞因子的产生。此外,LTS61K/Der p诱导Der p特异性IgA产生增加,以减少过敏性TH2细胞因子反应,并减轻Der p致敏小鼠的气道炎症。这些结果表明,LTS61K的免疫调节作用可能在过敏和哮喘治疗中具有临床应用价值。