Autophagy, a tightly regulated homeostatic pro-survival mechanism, has also been implicated in pathogen recognition and clearance by macrophages as part of the innate immune response. In the May issue of EJI, Mitroulis et al. shed light into the role of autophagy in human neutrophil biology, associa
Highlights from other journals
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 100 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0265-9247
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โฆ Synopsis
Activation-induced deaminase (AID) deaminates cytosines within the immunoglobulin loci, providing the trigger for both class-switching and IgV somatic hypermutation. Intriguingly, hyper-IgM patients carrying mutations in the C-terminal region of AID retain the ability to hypermutate their IgV genes, although they are deficient in Ig class-switching. Since the AID C-terminus contains a nuclear-export sequence (NES), it has been suggested that interaction of AID with the nuclear export machinery might be essential for Ig class-switching, but not for IgV hypermutation. In a recent article in European Journal of Immunology, Ellyard et al. study the interaction of various AID C-terminal mutants with the export machinery and report that, although the interaction between AID NES and the export machinery is essential for Ig class-switching, the affinity of this interaction does not correlate with the efficacy of Ig class-switching. These results suggest that some -as yet unidentified -interaction involving the AID C-terminus, in addition to the interaction with the export machinery, is also essential for Ig classswitching, but not for IgV hypermutation.
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