z-logo
open-access-imgOpen Access
A Subset of Toll-Like Receptor Ligands Induces Cross-presentation by Bone Marrow-Derived Dendritic Cells
Author(s) -
Sandip K. Datta,
Vanessa Redecke,
Kiley R. Prilliman,
Kenji Takabayashi,
Maripat Corr,
Thomas C. Tallant,
Joseph DiDonato,
Roman Dziarski,
Shizuo Akira,
Stephen P. Schoenberger,
Eyal Raz
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.170.8.4102
Subject(s) - cross presentation , tlr9 , tlr3 , toll like receptor , dendritic cell , tlr7 , microbiology and biotechnology , immune system , endosome , antigen presentation , cpg oligodeoxynucleotide , receptor , acquired immune system , chemistry , biology , immunology , innate immune system , t cell , biochemistry , gene , gene expression , dna methylation
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom