TY - JOUR
T1 - Successful experience of rituximab therapy for systemic sclerosis-associated interstitial lung disease with concomitant systemic lupus erythematosus
AU - Sumida, Hayakazu
AU - Asano, Yoshihide
AU - Tamaki, Zenshiro
AU - Aozasa, Naohiko
AU - Taniguchi, Takashi
AU - Takahashi, Takehiro
AU - Toyama, Tetsuo
AU - Ichimura, Yohei
AU - Noda, Shinji
AU - Akamata, Kaname
AU - Miyazaki, Miki
AU - Kuwano, Yoshihiro
AU - Yanaba, Koichi
AU - Sato, Shinichi
PY - 2014/5
Y1 - 2014/5
N2 - Previous studies have demonstrated that B cells play critical roles in autoimmune disorders including systemic sclerosis (SSc) and systemic lupus erythematosus (SLE). However, the effectiveness of rituximab (RTX), a chimeric anti-CD20 antibody, for SSc-associated interstitial lung disease (ILD) or SLE disease activity remains controversial. We herein report an SSc patient with severely progressed ILD and concomitant SLE treated by two cycles of RTX at baseline and half a year later. This treatment improved ILD and SLE activities, along with reduction of dermal sclerosis and serum anti-topoisomerase I antibody levels. In addition, our detailed time-course data indicate that half a year may be appropriate as an interval between each cycle of RTX therapy aimed at SSc-associated ILD or SLE. Overall, the current report could pave the way to establish RTX as a disease-modifying drug for patients with SSc and/or SLE showing resistance to other already approved medications.
AB - Previous studies have demonstrated that B cells play critical roles in autoimmune disorders including systemic sclerosis (SSc) and systemic lupus erythematosus (SLE). However, the effectiveness of rituximab (RTX), a chimeric anti-CD20 antibody, for SSc-associated interstitial lung disease (ILD) or SLE disease activity remains controversial. We herein report an SSc patient with severely progressed ILD and concomitant SLE treated by two cycles of RTX at baseline and half a year later. This treatment improved ILD and SLE activities, along with reduction of dermal sclerosis and serum anti-topoisomerase I antibody levels. In addition, our detailed time-course data indicate that half a year may be appropriate as an interval between each cycle of RTX therapy aimed at SSc-associated ILD or SLE. Overall, the current report could pave the way to establish RTX as a disease-modifying drug for patients with SSc and/or SLE showing resistance to other already approved medications.
KW - B cells
KW - interstitial lung disease
KW - rituximab
KW - systemic lupus erythematosus
KW - systemic sclerosis
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U2 - 10.1111/1346-8138.12461
DO - 10.1111/1346-8138.12461
M3 - Article
C2 - 24801917
AN - SCOPUS:84900009349
SN - 0385-2407
VL - 41
SP - 418
EP - 420
JO - Journal of Dermatology
JF - Journal of Dermatology
IS - 5
ER -