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Longterm clinical and immunological effects of anti-CD20 treatment in patients with refractory systemic lupus erythematosus.

Lindholm, Catharina, 1967 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
Börjesson-Asp, Katharina (författare)
Zendjanchi, Kiandokht (författare)
visa fler...
Sundqvist, Anna-Carin (författare)
Tarkowski, Andrej, 1951 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
Bokarewa, Maria, 1963 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research
visa färre...
 (creator_code:org_t)
2008
2008
Engelska.
Ingår i: The Journal of rheumatology. - 0315-162X. ; 35:5, s. 826-33
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVE: To retrospectively evaluate longterm clinical and immunological effects of anti-CD20 treatment in patients with systemic lupus erythematosus (SLE) with active nephritis or autoantibody-mediated cytopenias refractory to conventional immunosuppressive treatment. METHODS: Anti-CD20 treatment (rituximab) was added to the ongoing immunosuppressive treatment in 31 SLE patients with active nephritis (n = 17), thrombocytopenia (n = 10), and hemolytic anemia (n = 4) refractory to conventional therapy. Disease activity was evaluated by the SLE Disease Activity Index. The median followup time after anti-CD20 treatment was 22 months (range 1-61 mo). RESULTS: Complete B cell depletion was obtained in all patients. In 11 of the 17 lupus nephritis patients complete or partial responses were achieved after 6-12 months. Eight of these patients increased their glomerular filtration rate (GFR) by > 25%. The responders were characterized by having shorter nephritis duration, a baseline GFR > 30 ml/min, and detectable circulating CD19+ B lymphocytes before B cell depletion. Anti-CD20 treatment was highly effective in patients with autoimmune thrombocytopenia, inducing a significant increase of platelet counts after 1 month (p < 0.01). Five of 10 patients achieved complete normalization of their platelet counts within 6 months. The anti-CD20 treatment was followed by a significant reduction of autoantibodies against dsDNA and platelets, in nephritic and in thrombocytopenic patients, respectively. CONCLUSION: Addition of anti-CD20 treatment to conventional immunosuppressive therapy may be a beneficial strategy in refractory lupus nephritis and autoimmune cytopenias, possibly by reducing the levels of pathogenic autoantibodies.

Nyckelord

Adolescent
Adult
Aged
Aged
80 and over
Anemia
Hemolytic
blood
drug therapy
immunology
Antibodies
Monoclonal
pharmacology
therapeutic use
Antigens
CD20
drug effects
Autoantibodies
blood
B-Lymphocytes
drug effects
immunology
pathology
Dose-Response Relationship
Drug
Female
Humans
Immunologic Factors
pharmacology
therapeutic use
Lupus Erythematosus
Systemic
blood
drug therapy
immunology
Lupus Nephritis
blood
drug therapy
immunology
Male
Middle Aged
Purpura
Thrombocytopenic
Idiopathic
blood
drug therapy
immunology
Retrospective Studies
Severity of Illness Index

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