iScience · 2020 · 19 citations · 31 references
Life SciencesImmunologyMolecular BiologyCellular ImmunologyInflammationMolecular ImmunologyAdipose TissueAntigen PresentationMajor Histocompatibility ComplexMetabolic InflammationPeptide AnalysisT Cell ActivationAdipose Tissue Immune CellsHigh-resolution Mass AnalysisHigh-resolution SpectrometryMajor Histocompatibility Complex (Mhc) PresentationMass Spectrometry ImmunopeptidomicsMhc Class I MoleculesObesity-induced InflammationVisceral Adipose Tissue
Adaptive CD8 + T cells were observed to contribute to the initiation and progression of obesity-induced visceral adipose tissue (VAT) chronic inflammation that is critically linked to metabolic disorders. Numerous peptides presented by the major histocompatibility complex (MHC) class I molecules at the cell surface are collectively termed as MHC I-associated immunopeptidome (MIP) for the interaction with CD8 + T cells. We conducted the in-depth mapping of MIP of VAT from lean and obese mice using large-scale high-resolution mass spectrometry and observed that obesity significantly alters the landscape of VAT MIPs. Additionally, the obese VAT-exclusive MIP source proteome reflected a distinct obesity-associated signature. A peptide derived from lactate dehydrogenase A (LDHA) or B chain, named LDHA 237-244 , was identified as an obese VAT-exclusive immunogenic peptide that was capable of eliciting pro-inflammatory CD8 + T cells responses. Our findings suggest that certain immunogenic peptides generated by obesity may trigger CD8 + T cell-mediated VAT inflammation.
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Normalization of obesity-associated insulin resistance through immunotherapy
Shawn Winer, Yin Chan, Geoffrey Paltser et al. · Nature Medicine · 2009 · 1.3K citations · Full text
Medicine, Endocrinology, Immunology +12