Mahnke Karsten, Ring Sabine, Johnson Theron S, Schallenberg Sonja, Schönfeld Kurt, Storn Volker, Bedke Tanja, Enk Alexander H
Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
Eur J Immunol. 2007 Aug;37(8):2117-26. doi: 10.1002/eji.200636841.
Suppressive functions of CD4+CD25+ regulatory T cells (Treg) are mainly studied by their interaction with conventional T cells. However, there is evidence that Treg also interact with antigen-presenting cells (APC), leading to suppression of APC function in in vitro coculture systems. Studying the in vivo distribution of Treg after injection, we found that Treg are located in direct proximity to dendritic cells (DC) and affect their functional maturation status. After contact to Treg, DC up-regulate the inhibitory B7-H3 molecule and display reduced numbers of MHC-peptide complexes, leading to impaired T cell stimulatory function. When Treg-exposed DC were used to immunize animals against antigens, the DC failed to produce a robust immune response as compared to control DC. Thus, these data indicate that Treg are able to inhibit DC activation and produce an inhibitory phenotype of DC. Accordingly, Treg may recruit DC for the amplification of immunosuppression by restraining their maturation in vivo and inducing an immunosuppressive phenotype of DC.
CD4+CD25+调节性T细胞(Treg)的抑制功能主要通过其与传统T细胞的相互作用来研究。然而,有证据表明Treg也与抗原呈递细胞(APC)相互作用,从而在体外共培养系统中导致APC功能受到抑制。在研究注射后Treg的体内分布时,我们发现Treg位于树突状细胞(DC)的紧邻位置,并影响其功能成熟状态。与Treg接触后,DC上调抑制性B7-H3分子,并显示出数量减少的MHC-肽复合物,导致T细胞刺激功能受损。当用暴露于Treg的DC对动物进行抗原免疫时,与对照DC相比,这些DC未能产生强烈的免疫反应。因此,这些数据表明Treg能够抑制DC的活化并产生DC的抑制表型。相应地,Treg可能通过在体内限制DC的成熟并诱导DC的免疫抑制表型来募集DC以扩大免疫抑制作用。