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Publication : Cytosolic Recognition of RNA Drives the Immune Response to Heterologous Erythrocytes.

First Author  Loetsch C Year  2017
Journal  Cell Rep Volume  21
Issue  6 Pages  1624-1638
PubMed ID  29117566 Mgi Jnum  J:254874
Mgi Id  MGI:6104142 Doi  10.1016/j.celrep.2017.10.044
Citation  Loetsch C, et al. (2017) Cytosolic Recognition of RNA Drives the Immune Response to Heterologous Erythrocytes. Cell Rep 21(6):1624-1638
abstractText  The archetypal T cell-dependent antigen is sheep red blood cells (SRBCs), which have defined much of what we know about humoral immunity. Early studies using solubilized or sonicated SRBCs argued that the intact structure of SRBCs was important for optimal antibody responses. However, the reason for the requirement of intact SRBCs for the response to polyvalent protein antigen remained unknown. Here, we report that the immune response to SRBCs is driven by cytosolic recognition of SRBC RNA through the RIG-I-like receptor (RLR)-mitochondrial anti-viral signaling adaptor (MAVS) pathway. Following the uptake of SRBCs by antigen-presenting cells, the MAVS signaling complex governs the differentiation of both T follicular cells and antibody-producing B cells. Importantly, the involvement of the RLR-MAVS pathway precedes that of endosomal Toll-like receptor pathways, yet both are required for optimal effect.
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