Datta Sandip K, Redecke Vanessa, Prilliman Kiley R, Takabayashi Kenji, Corr Maripat, Tallant Thomas, DiDonato Joseph, Dziarski Roman, Akira Shizuo, Schoenberger Stephen P, Raz Eyal
Department of Medicine and The Sam and Rose Stein Institute for Research on Aging, University of California, La Jolla, CA 92093, USA.
J Immunol. 2003 Apr 15;170(8):4102-10. doi: 10.4049/jimmunol.170.8.4102.
Dendritic cells (DCs) are capable of cross-presenting exogenous Ag to CD8(+) CTLs. Detection of microbial products by Toll-like receptors (TLRs) leads to activation of DCs and subsequent orchestration of an adaptive immune response. We hypothesized that microbial TLR ligands could activate DCs to cross-present Ag to CTLs. Using DCs and CTLs in an in vitro cross-presentation system, we show that a subset of microbial TLR ligands, namely ligands of TLR3 (poly(inosinic-cytidylic) acid) and TLR9 (immunostimulatory CpG DNA), induces cross-presentation. In contrast to presentation of Ag to CD4(+) T cells by immature DCs, TLR-induced cross-presentation is mediated by mature DCs, is independent of endosomal acidification, and relies on cytosolic Ag processing machinery.
树突状细胞(DCs)能够将外源性抗原交叉呈递给CD8(+) 细胞毒性T淋巴细胞(CTLs)。Toll样受体(TLRs)对微生物产物的检测会导致DCs的激活以及随后适应性免疫反应的协调。我们推测微生物TLR配体可以激活DCs,使其将抗原交叉呈递给CTLs。在体外交叉呈递系统中使用DCs和CTLs,我们发现一部分微生物TLR配体,即TLR3的配体(聚肌苷酸-聚胞苷酸)和TLR9的配体(免疫刺激性CpG DNA),可诱导交叉呈递。与未成熟DCs将抗原呈递给CD4(+) T细胞不同,TLR诱导的交叉呈递由成熟DCs介导,不依赖于内体酸化,并且依赖于胞质抗原加工机制。