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Induction of interferon-α production in plasmacytoid dendritic cells by immune complexes containing nucleic acid released by necrotic or late apoptotic cells and lupus IgG

Lövgren, Tanja (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper
Eloranta, Maija-Leena (författare)
Båve, Ullvi (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper
visa fler...
Alm, Gunnar V. (författare)
Rönnblom, Lars (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper
visa färre...
 (creator_code:org_t)
2004-06-03
2004
Engelska.
Ingår i: Arthritis and Rheumatism. - : Wiley. - 0004-3591 .- 1529-0131. ; 50:6, s. 1861-1872
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVE: To investigate the release of interferon-alpha (IFN alpha)-inducing material by necrotic or apoptotic cells, its properties, and the necessity of autoantibodies from systemic lupus erythematosus (SLE) patients for the interferogenic activity. METHODS: U937 monocytic leukemia cells or peripheral blood mononuclear cells (PBMCs) were rendered necrotic by freeze-thawing or apoptotic by treatment with ultraviolet light. Cell culture supernatants from these cells and IgG from SLE patients (SLE IgG) were added to cultures of normal PBMCs or purified plasmacytoid dendritic cells (PDCs). The importance of nucleic acids for IFN alpha induction was investigated by RNase and DNase treatment. The IFN alpha levels were measured by immunoassay. RESULTS: Both necrotic and apoptotic U937 cells released material that, combined with SLE IgG, induced IFN alpha production in PDCs. The release from apoptotic cells occurred with a 16-hour delay, in late apoptosis. Also, normal PBMCs released IFN alpha-inducing material, but only during necrosis. The interferogenic activity of the necrotic material required the presence of RNA, while both RNA and DNA were important in the apoptotic material. In both cases, the presence of SLE IgG was necessary, and its activity correlated with the presence of antibodies to RNA-binding proteins, but not anti-DNA antibodies. CONCLUSION: Necrotic and late apoptotic cells release material that, combined with SLE IgG, induces production of IFN alpha in PDCs. The IFN alpha inducers probably consist of immune complexes (ICs) containing RNA and possibly DNA as essential interferogenic components. The presence of such interferogenic ICs could explain the ongoing production of IFN alpha in SLE and could be of etiopathogenic importance.

Nyckelord

Antigen-Antibody Complex/*genetics/immunology
Apoptosis/*immunology
DNA/metabolism
Dendritic Cells/*immunology/metabolism
Deoxyribonucleases/pharmacology
Freezing
Humans
Immunoglobulin G/metabolism
Interferon-alpha/genetics/*metabolism
Leukocytes; Mononuclear/cytology/immunology
Lupus Erythematosus; Systemic/*immunology/metabolism/physiopathology
Necrosis
RNA/metabolism
Research Support; Non-U.S. Gov't
Ribonucleases/pharmacology
U937 Cells
Ultraviolet Rays

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