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Sökning: WFRF:(Van Vollenhoven Ronald F.) > (2005-2009) > Treatment of refrac...

Treatment of refractory SLE with rituximab plus cyclophosphamide : clinical effects, serological changes, and predictors of response

Jónsdóttir, Thorunn (författare)
Department of Rheumatology, Karolinska University Hospital, Stockholm, Sweden
Gunnarsson, Iva (författare)
Karolinska Institutet
Risselada, Anke (författare)
Department of Rheumatology, Karolinska University Hospital, Stockholm, Sweden
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Welin Henriksson, Elisabet, 1960- (författare)
Karolinska Institutet
Klareskog, Lars (författare)
Karolinska Institutet
van Vollenhoven, Ronald F (författare)
Karolinska Institutet
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 (creator_code:org_t)
2007-10-29
2008
Engelska.
Ingår i: Annals of the Rheumatic Diseases. - : HighWire Press. - 0003-4967 .- 1468-2060. ; 67:3, s. 330-334
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • OBJECTIVE: To evaluate efficacy, serological responses, and predictors of response in patients with severe and refractory systemic lupus erythematosus (SLE) treated with rituximab plus cyclophosphamide.METHODS: 16 patients entered a treatment protocol using rituximab plus cyclophosphamide. Disease activity was assessed by the SLE disease activity index (SLEDAI) and by the British Isles Lupus Assessment Group (BILAG) index.RESULTS: At six months follow up, mean SLEDAI values decreased significantly from (mean (SD)) 12.1 (2.2) to 4.7 (1.1). Clinical improvement (50% reduction in SLEDAI) occurred in all but three patients. All but one patient responded according to BILAG. Remission defined as SLEDAI <3 was achieved in nine of 16 patients. Isotype analysis of anti-dsDNA antibodies revealed preferential decreases of IgG and IgA, but not IgM. Higher absolute numbers of CD19+ cells at baseline were correlated with shorter depletion time (r = -0.6).CONCLUSIONS: The majority of patients improved following rituximab plus cyclophosphamide. The differential downregulation of anti-DNA of the IgG and IgA but not the IgM isotypes supports the hypothesis that cells producing pathogenic autoantibodies are preferentially targeted by the treatment. The fact that greater absolute numbers of CD19+ cells at baseline predict a less impressive clinical and serological response suggests that more flexible dosing could be advantageous.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

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