Table 1.
Medication
|
Mechanism
|
Definition of HBV reactivation
|
Study population
|
Reactivation rate
|
Methotrexate | Suppressive HBV specific cytotoxic T cell response and the production of proinflammatory cytokines | HBV DNA > 103 (copies/mL) | HBsAg-positive | Low risk[29,30] |
HBsAg-negative | Low risk[30] | |||
Leflunomide | Inhibition of the growth of activated lymphocytes by inhibition of dihydro-lactate dehydrogenase | 10-fold rise in HBV-DNA compared to baseline or a switch from undetectable to detectable | HBsAg-positive | High risk, contraindicated[31] |
HBsAg-negative | No data | |||
Corticosteroids | Immunomodulatory and anti-inflammatory | Switch from undetectable HBV DNA to detectable or a 10-fold increase compared with baseline[34] | HBsAg-positive | High risk (> 10 mg, > 4 wk); medium risk (< 10 mg, > 4 wk); low risk (< 10 mg, < 1 wk) |
HBsAg-negative | 1%-1.8%[34,36] | |||
TNF inhibitor | Dampening of the cytokine cascade and suppression of the cytotoxic CD8+ T-cell responses against HBV | An increase of serum HBV DNA levels by greater than 1 logs10 IU/mL or conversion from HBsAg- to HBsAg+ | HBsAg-positive | Medium-high risk (9.1%-75%)[23,38] |
HBsAg-negative | Low risk (0-8.3%)[22,39] | |||
Tocilizumab | Blocks IL-6 signaling by inhibiting its receptor | HBV-DNA level higher than 2.0 log copies/mL | HBsAg-positive | No data |
HBsAg-negative | Low risk (8%)[40] | |||
Tofacitinib | Inhibition of JAK signal pathway | An increase in HBV DNA by greater than 1 to 2 logs10 IU/mL or a reappearance of HBsAg | HBsAg-positive | High risk (100%)[41] |
HBsAg-negative | Low risk (0) | |||
Abatacept | Blocks co-stimulation of T lymphocytes | Conversion from HBsAg- to HBsAg+ | HBsAg-positive | Medium risk[34] |
HBsAg-negative | Low risk[34] |
HBsAg: Hepatitis B surface antigen; HBV: Hepatitis B virus.