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一种合成的三酰化假二肽分子可促进Th1/调节性T细胞免疫反应,并通过舌下途径增强耐受性诱导。

A synthetic triacylated pseudo-dipeptide molecule promotes Th1/TReg immune responses and enhances tolerance induction via the sublingual route.

作者信息

Mascarell Laurent, Van Overtvelt Laurence, Lombardi Vincent, Razafindratsita Alain, Moussu Hélène, Horiot Stéphane, Chabre Henri, Limal David, Moutel Stéphane, Bauer Jacques, Chiavaroli Carlo, Moingeon Philippe

机构信息

Stallergènes SA, Research and Development, 6 rue Alexis de Tocqueville, 92160 Antony, France.

出版信息

Vaccine. 2007 Dec 21;26(1):108-18. doi: 10.1016/j.vaccine.2007.10.050. Epub 2007 Nov 9.

Abstract

In this study, we tested two triacylated pseudo-dipeptidic molecules, OM-197-MP-AC and OM-294-BA-MP as candidate adjuvants for allergy vaccines. Both molecules induce human dendritic cell (h-DC) maturation and polarize naïve T cells toward the Th1 type with IFNgamma production. Only OM-294-BA-MP induces IL10 gene expression both in monocyte-derived DCs and CD4+ naïve T cells. Sublingual administration of OM-294-BA-MP plus the antigen enhances tolerance induction in BALB/c mice with established asthma to ovalbumin with an impact on both airways hyperresponsiveness and lung inflammation. Given its Th1/Treg polarizing properties, OM-294-BA-MP is a valid candidate for sublingual allergy vaccines.

摘要

在本研究中,我们测试了两种三酰化假二肽分子OM-197-MP-AC和OM-294-BA-MP作为过敏疫苗的候选佐剂。这两种分子均可诱导人树突状细胞(h-DC)成熟,并使初始T细胞向Th1型极化,产生IFNγ。只有OM-294-BA-MP可在单核细胞衍生的DC和CD4+初始T细胞中诱导IL10基因表达。对已患哮喘的BALB/c小鼠经舌下给予OM-294-BA-MP加抗原可增强对卵清蛋白的耐受性诱导,对气道高反应性和肺部炎症均有影响。鉴于其Th1/Treg极化特性,OM-294-BA-MP是舌下过敏疫苗的有效候选物。

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