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Production of Autoreactive Heavy Chain-Only Antibodies in Systemic Lupus Erythematosus.
- Source :
-
Frontiers in immunology [Front Immunol] 2020 May 05; Vol. 11, pp. 632. Date of Electronic Publication: 2020 May 05 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Systemic lupus erythematosus (SLE) is characterized by the overproduction of high-affinity autoreactive antibodies. Here, we show that more than 65.8% of 222 recombinant antibodies derived from 8 SLE patients can be secreted as heavy chain-only antibodies (HCAbs) when expressed in HEK-293T cells. The secretion of HCAbs follows the conventional endoplasmic reticulum-Golgi apparatus pathway, despite triggering a weaker unfolded protein response (UPR). Many of the purified SLE HCAbs remain autoreactive and have an even higher affinity for dsDNA, Sm, nucleosome, and cardiolipin than HCAbs from healthy individuals. Extended analyses of the CDR3 region and the heavy chain variable (VH) region of HCAb F3 show that the VH region is responsible for IgH secretion, while the CDR3 region determines its reactivity. Such a high frequency of HCAb secretion cannot fully concur with our current understanding of antibody assembly and secretion. The presence of a large proportion of autoreactive HCAbs in SLE reveals a novel mechanism for the generation of autoreactive antibodies in lupus.<br /> (Copyright © 2020 Xu, Yang, Zhuo, Yu, Liao, Li, Yue, Su and Zhang.)
- Subjects :
- Adult
Amino Acids immunology
Antibody Affinity
Autoantibodies blood
Cardiolipins immunology
DNA immunology
Female
HEK293 Cells
Humans
Immunoglobulin Heavy Chains blood
Immunoglobulin Variable Region
Lupus Erythematosus, Systemic blood
Male
Middle Aged
Nucleosomes immunology
Recombinant Proteins immunology
Young Adult
Autoantibodies immunology
Immunoglobulin Heavy Chains immunology
Lupus Erythematosus, Systemic immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 32431693
- Full Text :
- https://doi.org/10.3389/fimmu.2020.00632