alexa Susceptibility Loci in C57BL/6 sle1, sle2 and sle3 Contain Genes that Alter Peripheral Selection of the CDR-H3 Sequences Enriched for Arginine | OMICS International| Abstract

ISSN: 2155-9899

Journal of Clinical & Cellular Immunology

  • Review Article   
  • J Clin Cell Immunol 2018, Vol 9(2): 544
  • DOI: 10.4172/2155-9899.1000544

Susceptibility Loci in C57BL/6 sle1, sle2 and sle3 Contain Genes that Alter Peripheral Selection of the CDR-H3 Sequences Enriched for Arginine

Mohamed Khass1,2, Peter D Burrows3 and Harry W Schroeder1*
1Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA
2Genetic Engineering and Biotechnology division, National Research Center, , Cairo, Egypt
3Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL, USA
*Corresponding Author : Harry W Schroeder, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA, Tel: +205-382-2613, Email: [email protected]

Received Date: Feb 18, 2018 / Accepted Date: Mar 09, 2018 / Published Date: Mar 14, 2018

Abstract

Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disease characterized by deposition of ds- DNA binding autoantibodies in various body organs. These antibodies result from failure to control the composition of the B cell repertoire. Development of optimum B cell repertoire depends on the amino acid composition and the physicochemical characteristics at the center of the antigen binding site, the third complementarity determining region heavy chain (CDR-H3). Repertoire control involves positive selection for hydrophilic amino acids such as tyrosine and negative selection of hydrophobic and charged amino acids, specifically those containing arginine within the CDR-H3. Anti-dsDNA antibodies present in SLE patients exist in healthy individuals but at low levels, since dsDNA-specific B cells are deleted from the repertoire, but amplified in SLE patients. These antibodies contain arginine residues in CDR-H3, especially at positions 99-102, where they are positioned to bind negatively charged phosphate groups on the DNA backbone. Three genomic intervals, namely sle1 on chromosome 1, sle2 on chromosome 4, and sle3 on chromosome 7, were found to be associated with SLE susceptibility. We hypothesized that development of ds-DNA binding antibodies in SLE might result from failure to control CDR-H3 amino acid composition. We proposed that the SLE congenic loci might have unique effects in allowing survival/expansion of B cells expressing these auto-reactive antibodies. Our strategy was to change the composition of CDR-H3 by altering the germline composition of the DH gene segments. We created a ΔD-iD altered allele enriched for arginine while depleted of tyrosine at positions 99-102. We then monitored the influence of different SLE loci on the development and maintenance of B cells bearing CDR-H3 arginine. These findings support our hypothesis that peripheral B cell selection is altered by the presence of sle congenic alleles, allowing passage of B cells able to produce autoreactive antibodies binding ds-DNA. These findings may help in developing therapeutics to suppress autoimmunity in SLE.

Keywords: Review; Systemic lupus erythematosus, B cell repertoire; Third complementary determining region heavy chain; CDR-H3; Diversity gene segments DH

Citation: Khass M, Burrows PD, Schroeder HW (2018) Susceptibility Loci in C57BL/6 sle1, sle2 and sle3 Contain Genes that Alter Peripheral Selection of the CDR-H3 Sequences Enriched for Arginine. J Clin Cell Immunol 9: 544. Doi: 10.4172/2155-9899.1000544

Copyright: © 2018 Khass M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium.

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