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Boosting Type 2 Immunity: When OX40L Comes from ILC2s
Marina Babic1, Chiara Romagnani1
1Innate immunity, German Rheumatism Research Centre (DRFZ), a Leibniz Association, Berlin, Germany; Medical Department I, Charité-Universitätsmedizin, Berlin, Germany.
Abstract:
Accumulating evidence supports a role for the innate lymphoid cells (ILCs) in the modulation of T cell responses. In this issue of Immunity, Halim et al. (2018) identify a role for the costimulatory OX40-OX40L axis in ILC2-mediated regulation of adaptive type 2 immunity during helminth infection and allergen exposure.
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Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in the regulation of gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
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