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Stefan Bauer

Researcher at University of Marburg

Publications -  151
Citations -  24529

Stefan Bauer is an academic researcher from University of Marburg. The author has contributed to research in topics: Innate immune system & Immune system. The author has an hindex of 57, co-authored 141 publications receiving 23272 citations. Previous affiliations of Stefan Bauer include Technische Universität München & University of Mainz.

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Species-Specific Recognition of Single-Stranded RNA via Toll-like Receptor 7 and 8

TL;DR: It is shown that guanosine (G)- and uridine (U)-rich ssRNA oligonucleotides derived from human immunodeficiency virus–1 (HIV-1) stimulate dendritic cells and macrophages to secrete interferon-α and proinflammatory, as well as regulatory, cytokines, and these data suggest that ssRNA represents a physiological ligand for TLR7 and TLR8.
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Activation of NK Cells and T Cells by NKG2D, a Receptor for Stress-Inducible MICA

TL;DR: An activating immunoreceptor-MHC ligand interaction that may promote antitumor NK and T cell responses is defined.
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Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition

TL;DR: It is shown that human TLR9 expression in human immune cells correlates with responsiveness to bacterial deoxycytidylate-phosphate-deoxyguanylate (CpG)-DNA, and data suggest that hTLR9 conveys CpG-DNA responsiveness to human cells by directly engaging immunostimulating Cpg-DNA.
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Recognition of Stress-Induced MHC Molecules by Intestinal Epithelial γδ T Cells

TL;DR: In this paper, the expression and recognition of a major histocompatibility complex (MHC) class I-related molecule, MICA, matches this localization, and the closely related MICB were recognized by intestinal epithelial T cells expressing diverse Vδ1 γδ TCRs.
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An activating immunoreceptor complex formed by NKG2D and DAP10.

TL;DR: In natural killer (NK) and T cells, DAP10 was identified as a cell surface adaptor protein in an activating receptor complex with NKG2D, a receptor for the stress-inducible and tumor-associated major histocompatibility complex molecule MICA.