| Literature DB >> 33530489 |
Michael P Bachmann1,2,3,4, Tabea Bartsch1, Claudia C Bippes5, Dominik Bachmann2, Edinson Puentes-Cala1,6, Jennifer Bachmann2, Holger Bartsch5, Claudia Arndt1, Stefanie Koristka1, Liliana R Loureiro1, Alexandra Kegler1, Markus Laube1, Joanne K Gross7, Tim Gross7, Biji T Kurien7, R Hal Scofield7, A Darise Farris7, Judith A James7, Marc Schmitz3,4,5, Anja Feldmann1.
Abstract
Since the first description of nuclear autoantigens in the late 1960s and early 1970s, researchers, including ourselves, have found it difficult to establish monoclonal antibodies (mabs) against nuclear antigens, including the La/SS-B (Sjögrens' syndrome associated antigen B) autoantigen. To date, only a few anti-La mabs have been derived by conventional hybridoma technology; however, those anti-La mabs were not bona fide autoantibodies as they recognize either human La specific, cryptic, or post-translationally modified epitopes which are not accessible on native mouse La protein. Herein, we present a series of novel murine anti-La mabs including truly autoreactive ones. These mabs were elicited from a human La transgenic animal through adoptive transfer of T cells from non-transgenic mice immunized with human La antigen. Detailed epitope and paratope analyses experimentally confirm the hypothesis that somatic hypermutations that occur during T cell dependent maturation can lead to autoreactivity to the nuclear La/SS-B autoantigen.Entities:
Keywords: La/SS-B autoantigen; anti-La/SS-B antibodies; autoimmunity; primary Sjögren’s syndrome; systemic lupus erythematosus
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Year: 2021 PMID: 33530489 PMCID: PMC7865296 DOI: 10.3390/ijms22031198
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923