Selective depletion of plasma cells in vivo based on the specificity of their secreted antibodies

Eur J Immunol. 2020 Feb;50(2):284-291. doi: 10.1002/eji.201948144. Epub 2019 Nov 12.

Abstract

Antibody-mediated diseases affect more than 10% of the human population. For most, no cure is available, particularly when the pathogenic antibodies are secreted by long-lived plasma cells resistant to conventional immunosuppressive therapies. Current therapeutic approaches target not only the plasma cells that secrete pathogenic antibodies, but also those providing protective antibodies. Here, in a murine model bearing long-lived plasma cells secreting anti-OVA and -chicken gamma globulin (CGG) antibodies, we describe the first-time use of an antigen-antibody (OVA/anti-CD138 antibody) conjugate for in vivo labeling and selective ablation of plasma cells that secrete antibodies specific for the antigen OVA. The selective depletion also led to a stable reduction of the corresponding serum anti-OVA antibody levels. In contrast, CGG-specific plasma cells and circulating anti-CGG antibody levels remained unchanged. The method described here should enable the development of unique causative treatment strategies for established antibody-mediated diseases sparing humoral immunity.

Keywords: anti-ovalbumin antibody; antibody-mediated disease; ovalbumin-anti-CD138 antibody conjugate; proof-of-concept study; therapeutic plasma cell targeting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies / immunology*
  • Antibody Formation / immunology*
  • Antigens / immunology
  • Female
  • Immunity, Humoral / immunology
  • Immunosuppression Therapy / methods
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin / immunology
  • Plasma Cells / immunology*
  • gamma-Globulins / immunology

Substances

  • Antibodies
  • Antigens
  • gamma-Globulins
  • Ovalbumin