We selected 102 NMOSD patients treated with inebilizumab or rituximab between January 1, 2016, and August 31, 2024. Liver function tests, HBV serology tests, and interferon-gamma release assay (IGRA) were performed to identify pOBI or LTBI. For pOBI patients, liver function, HBV serology, and HBV-DNA were continuously monitored to ascertain hepatitis B reactivation. For LTBI patients, IGRA was tested during subsequent treatments, and clinical and radiographic manifestations were used to assess tuberculosis reactivation.