The link between antibodies to OxLDL and natural protection against pneumococci depends on DH gene conservation

Author:

Vale Andre M.12,Kapoor Pratibha1,Skibinski Greg A.1,Elgavish Ada1,Mahmoud Tamer I.13,Zemlin Cosima1,Zemlin Michael14,Burrows Peter D.12,Nobrega Alberto2,Kearney John F.1,Briles David E.11,Schroeder Harry W.111

Affiliation:

1. Department of Medicine, Department of Microbiology, Department of Pediatrics, and Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294

2. Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-901, Brazil

3. Department of Microbiology and Immunology, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt

4. Department of Pediatrics, Philipps University Marburg, D-35032 Marburg, Germany

Abstract

Selection and physiological production of protective natural antibodies (NAbs) have been associated with exposure to endogenous antigens. The extent to which this association depends on germline NAb sequence is uncertain. Here we show that alterations in germline DH sequence can sever the association between the production of self-reactive NAbs and NAbs that afford protection against a pathogen. In unmanipulated hosts, the availability of the evolutionarily conserved DFL16.1 gene segment sequence profoundly affected the serum levels of NAbs against bacterial phosphorylcholine but not oxidized low-density lipoprotein. Mice with partially altered DFL16.1 sequence could use N nucleotides to recreate the amino acid sequence associated with the classical protective T15 idiotype–positive NAbs, whereas those without DFL16.1 could not. DFL16.1 gene–deficient mice proved more susceptible to challenge with live Streptococcus pneumoniae. Our findings indicate that although production of self-reactive NAbs can be independent of germline DH sequence, their capacity to provide protection against pathogens cannot. The potential relevance of these findings for the rational design of vaccines is discussed.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference77 articles.

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