Rodríguez-García Marta, Oliva Harold, Climent Núria, Escribese Maria M, García Felipe, Moran Thomas M, Gatell José M, Gallart Teresa
Service of Immunology, Hospital Clínic Universitari de Barcelona, School of Medicine, University of Barcelona, Barcelona, Spain.
Clin Immunol. 2009 Jun;131(3):374-84. doi: 10.1016/j.clim.2009.01.012. Epub 2009 Feb 23.
alpha-defensins1-3 are potent antimicrobial molecules that also link innate and adaptive immunity, depending on the concentration range. However, their effects on the biology of human DCs remain largely unknown. We analyzed the impact of different concentrations of alpha-defensins1-3 on the maturation and differentiation of monocyte-derived DCs (MDDCs). Low doses of alpha-defensins1-3 up-regulated CD83, CD86 and HLA-DR expression, increased TNF-alpha, IL-1beta, IL-12p40, IL-10 and IL-8 secretion, and slightly augmented allostimulatory capacity. By contrast, high doses down-regulated CD86 and HLA-DR expression, TNF-alpha, IL-1beta, IL-12p40 and IL-10 secretion and allostimulatory capacity, whereas strongly up-regulated IL-8. Furthermore, during the MDDC differentiation process, high doses of alpha-defensins1-3 affected CD14, CD11c and CD86 expression and strongly up-regulated IL-8. Results suggest that alpha-defensins1-3 might modulate the maturation and differentiation of MDDCs in vivo and therefore could be of special interest in the field of vaccine development.
α-防御素1-3是强效抗菌分子,根据浓度范围,它们还能连接天然免疫和适应性免疫。然而,它们对人树突状细胞生物学特性的影响在很大程度上仍不清楚。我们分析了不同浓度的α-防御素1-3对单核细胞衍生树突状细胞(MDDC)成熟和分化的影响。低剂量的α-防御素1-3上调CD83、CD86和HLA-DR的表达,增加肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-12p40、白细胞介素-10和白细胞介素-8的分泌,并略微增强同种异体刺激能力。相比之下,高剂量下调CD86和HLA-DR的表达、肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-12p40和白细胞介素-10的分泌以及同种异体刺激能力,而强烈上调白细胞介素-8。此外,在MDDC分化过程中,高剂量的α-防御素1-3影响CD14、CD11c和CD86的表达,并强烈上调白细胞介素-8。结果表明,α-防御素1-3可能在体内调节MDDC的成熟和分化,因此在疫苗开发领域可能具有特殊意义。