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Antimicrobial peptide LL-37 and recombinant human mannose-binding lectin express distinct age- and pathogen-specific antimicrobial activity in human newborn cord bloodin vitro

机译:抗菌肽LL-37和重组人甘露糖结合凝集素在人新生儿脐带血中表达不同的年龄和病原体特异性抗菌活性体外

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摘要

>Background: There is a need to prevent and treat infection in newborns. One approach is administration of antimicrobial proteins and peptides (APPs) such as LL-37, a membrane-active cathelicidin antimicrobial peptide, and mannose-binding lectin (MBL), a pattern-recognition protein that binds to microbial surface polysaccharides resulting in opsonization and complement activation. Low plasma/serum levels of LL-37 and of MBL have been correlated with infection and exogenous administration of these agents may enhance host defense. >Methods: The antimicrobial activity of LL-37 (15 µg/ml) or rMBL (0.5, 2 and 10 µg/ml) was tested in hirudin-anticoagulated preterm and term human cord blood (N = 12–14) against Staphylococcus aureus (SA) USA 300 (2x10 4 CFU/ml), Staphylococcus epidermis (SE) 1457 (2x10 4 CFU/ml) and Candida albicans (CA) SC5314 (1x10 4 CFU/ml). After incubation (1, 45, or 180 min), CFUs were enumerated by plating blood onto agar plates. Supernatants were collected for measurement of MBL via ELISA. >Results: Preterm cord blood demonstrated impaired endogenous killing capacity against SA and SE compared to term blood. Addition of LL-37 strongly enhanced antimicrobial/antifungal activity vs SA, SE and CA in term blood and SE and CA in preterm blood. By contrast, rMBL showed modest fungistatic activity vs CA in a sub-analysis of term newborns with high basal MBL levels. Baseline MBL levels varied within preterm and term cohorts with no correlation to gestational age. In summary, exogenous LL-37 demonstrated significant antimicrobial activity against SA, SE and CA in term and SE and CA in preterm human blood tested in vitro. rMBL demonstrated modest antifungal activity in term cord blood of individuals with high baseline MBL levels. >Conclusions: To the extent that our in vitro results predict the effects of APPs in vivo, development of APPs for prevention and treatment of infection should take into account host age as well as the target pathogen.
机译:>背景:有必要预防和治疗新生儿感染。一种方法是施用抗菌蛋白和肽(APP),例如LL-37(膜活性cathelicidin抗菌肽)和甘露糖结合凝集素(MBL),其是一种模式识别蛋白,与微生物表面多糖结合,导致调理和补体激活。 LL-37和MBL的血浆/血清水平低与感染相关,这些药物的外源给药可能增强宿主防御能力。 >方法:在水rud素抗凝早产和足月人脐带血(N = 12)中测试了LL-37(15 µg / ml)或rMBL(0.5、2和10 µg / ml)的抗菌活性。 –14)针对美国金黄色葡萄球菌(SA)300(2x10 4 CFU / ml),表皮葡萄球菌(SE)1457(2x10 4 CFU / ml)和白色念珠菌( CA)SC5314(1x10 4 CFU / ml)。温育(1、45或180分钟)后,通过将血液铺板到琼脂板上来枚举CFU。收集上清液以通过ELISA测量MBL。 >结果:与足月血液相比,早产脐血显示出对SA和SE的内源性杀伤能力受损。与足月血液中的SA,SE和CA和足月血液中的SE和CA相比,添加LL-37可以显着增强抗菌/抗真菌活性。相比之下,在具有较高基础MBL水平的足月新生儿的亚分析中,rMBL与CA相比显示出适度的抑菌活性。基线MBL水平在早产和足月队列中变化,与胎龄无关。总之,外源LL-37足月对SA,SE和CA以及体外测试的早产人血液中的SE和CA表现出显着的抗菌活性。 rMBL在高基线MBL水平的个体的足月脐血中显示出适度的抗真菌活性。 >结论:就我们的体外研究结果预测APP在体内的作用而言,在开发用于预防和治疗感染的APP时应考虑宿主年龄以及目标病原体。

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