Tuberculosis, hepatitis B and herpes zoster in tofacitinib-treated patients with rheumatoid arthritis

Zhuoya Zhang1, Wei Deng2, Qizhe Wu2

  • 1Department of Rheumatology & Immunology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, China, 210008.

Immunotherapy
|January 12, 2019
PubMed

Insights

Tofacitinib, a targeted drug for rheumatoid arthritis, may increase infection risks like tuberculosis and hepatitis B, particularly in East Asia. This review examines these risks, including reactivation, during tofacitinib treatment.

Area of Science:

  • Rheumatology
  • Infectious Diseases
  • Pharmacology

Background:

  • Targeted synthetic disease-modifying antirheumatic drugs (DMARDs), like tofacitinib, are increasingly used for rheumatoid arthritis.
  • East Asian countries face high endemic rates of tuberculosis (TB) and hepatitis B virus (HBV) infections.
  • Concerns exist regarding the risk of infections, including reactivation, with Janus kinase (JAK) inhibitors.

Purpose of the Study:

  • To review available data on the risk of TB, HBV, and herpes zoster infections during tofacitinib treatment.
  • To focus specifically on the risk of infection recurrence or reactivation in East Asian populations.
  • To assess the safety profile of tofacitinib concerning infectious complications.

Main Methods:

  • Literature review of studies on tofacitinib and infection risks.
  • Analysis of data focusing on tuberculosis, hepatitis B virus, and herpes zoster.
  • Emphasis on studies conducted in or relevant to East Asian populations.

Main Results:

  • Tofacitinib is effective for rheumatoid arthritis but carries potential infection risks.
  • Data suggests an increased risk of TB, HBV, and herpes zoster reactivation with tofacitinib use.
  • These risks are of heightened concern in East Asian regions due to high background infection rates.

Conclusions:

  • Healthcare providers should carefully consider the risk of TB, HBV, and herpes zoster reactivation in patients on tofacitinib, especially in East Asia.
  • Monitoring and prophylactic measures may be necessary for patients initiating tofacitinib in endemic areas.
  • Further research is warranted to fully elucidate and manage infection risks associated with JAK inhibitors.

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