論文

査読有り 国際誌
2019年

Plasma infliximab monitoring contributes to optimize Takayasu arteritis treatment: a case report.

Journal of pharmaceutical health care and sciences
  • Sho Masui
  • Atsushi Yonezawa
  • Kazushi Izawa
  • Makoto Hayakari
  • Kayoko Asakura
  • Risa Taniguchi
  • Masahiko Isa
  • Hirofumi Shibata
  • Takahiro Yasumi
  • Ryuta Nishikomori
  • Junko Takita
  • Kazuo Matsubara
  • 全て表示

5
開始ページ
9
終了ページ
9
記述言語
英語
掲載種別
DOI
10.1186/s40780-019-0136-4

Background: Infliximab (IFX), a mouse-human chimeric monoclonal antibody against human tumor necrosis factor alpha, is used in refractory cases of Takayasu arteritis. Several factors influence the pharmacokinetics of therapeutic antibodies including IFX. Monitoring plasma levels of IFX could be a useful approach in optimizing treatment via individual dose adjustment. Case presentation: Here, we report the case of a 4-year-old Takayasu arteritis girl who was resistant to standard therapy. IFX was started at 5 mg/kg (day 0). C-reactive protein (CRP) levels decreased from 8.7 (day 0) to 1.6 mg/dL (day 10). CRP levels were thereafter elevated again on day 23 (9.0 mg/dL), and body fluid leakage at the inflammation site in the legs was observed. Trough IFX levels decreased from 23.6 (day 10) to 2.5 μg/mL (day 23). Based on the trough levels, IFX was given biweekly at 8 mg/kg. Plasma IFX levels gradually increased, and CRP levels decreased to around 2 mg/dL. A similar pattern -initial decreases followed by increases- was observed between clinical course of IFX and IgG levels. It was speculated that IgG and IFX losses were due to fluid leakage from the patient's necrotizing legs. Conclusions: Monitoring of plasma IFX levels can be a potential tool to optimize the treatment in Takayasu arteritis patients.

リンク情報
DOI
https://doi.org/10.1186/s40780-019-0136-4
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31073411
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498684
ID情報
  • DOI : 10.1186/s40780-019-0136-4
  • PubMed ID : 31073411
  • PubMed Central 記事ID : PMC6498684

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