Does MHC Heterozygosity Promote IgA Plasmablast Diversity in the Gut?
نویسندگان
چکیده
Abstract The diversity of protein antigens the adaptive immune system can respond to is governed by polymorphic major histocompatibility complex (MHC) molecules. Because MHC alleles are co-dominantly expressed, heterozygosity should allow for a wider activate T cells. B cells present antigen via molecules cells, and through ensuing cell interaction, differentiate into plasma this, result in generation pool able generate antibodies that target array antigens. To investigate this claim, we compared selection dynamics between homozygote heterozygote congenic mice within germinal centers (GCs) Peyer’s patches; secondary lymphoid tissues gut where develop response microbiota. I have observed differences distribution GC dark zone (DZ) light (LZ) GCs. Specifically, heterozygotes found greater abundance LZ lower DZ from mice, which suggests more capable interacting with heterozygotes. also significantly higher GC-T FHcells their patches. show enhanced binding IgA SI-resident bacteria. Future experiments seek sort-purify IgA-bound bacteria homozygotes 16S analysis determine if bind diverse bacterial species. We will perform IgH-sequencing define effect on repertoire populations. Supported grants NIH (R21AI142409, R01AII55887)
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ژورنال
عنوان ژورنال: Journal of Immunology
سال: 2023
ISSN: ['1550-6606', '0022-1767']
DOI: https://doi.org/10.4049/jimmunol.210.supp.218.04