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Selective depletion of plasma cells in vivo based on the specificity of their secreted antibodies.
Cheng, Qingyu; Pelz, Andreas; Taddeo, Adriano; Khodadadi, Laleh; Klotsche, Jens; Hoyer, Bimba F; Alexander, Tobias; Thiel, Andreas; Burmester, Gerd-R; Radbruch, Andreas; Hiepe, Falk.
Afiliação
  • Cheng Q; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
  • Pelz A; Charité - Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Medizinische Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Berlin, Germany.
  • Taddeo A; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
  • Khodadadi L; Charité - Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Medizinische Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Berlin, Germany.
  • Klotsche J; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
  • Hoyer BF; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
  • Alexander T; Charité - Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Medizinische Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Berlin, Germany.
  • Thiel A; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
  • Burmester GR; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
  • Radbruch A; Charité - Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Medizinische Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Berlin, Germany.
  • Hiepe F; Deutsches RheumaForschungszentrum Berlin - a Leibniz Institute, Berlin, Germany.
Eur J Immunol ; 50(2): 284-291, 2020 02.
Article em En | MEDLINE | ID: mdl-31714996
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasmócitos / Anticorpos / Formação de Anticorpos Limite: Animals Idioma: En Revista: Eur J Immunol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasmócitos / Anticorpos / Formação de Anticorpos Limite: Animals Idioma: En Revista: Eur J Immunol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha
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