AI Article Synopsis

  • Host cell proteins, like phospholipase B-like 2 (PLBL2), can contaminate therapeutic products like lebrikizumab, potentially affecting safety and effectiveness.
  • Lebrikizumab, an antibody for asthma treatment, was found to have PLBL2 as an impurity, and about 90% of subjects in clinical trials developed immune responses to it.
  • Despite high antibody levels against PLBL2, there was no link to adverse safety issues or effects on the immune response to lebrikizumab, especially with newer formulations having lower PLBL2 levels showing fewer immune responses.

Article Abstract

Host cell proteins are manufacturing process-related impurities that may co-purify with the product despite extensive efforts to optimize the purification process. The risks associated with these impurities can vary and may be patient and/or therapeutic dependent. Therefore, it is critical to monitor and control the levels of these impurities in products and their potential impact on safety and efficacy. Lebrikizumab is a humanized immunoglobulin G4 monoclonal antibody (mAb) that binds specifically to soluble interleukin 13. This mAb is currently in phase III clinical development for the treatment of asthma. Following initial phase III studies, the material used in lebrikizumab clinical trials was found to have a process-related impurity identified as Chinese hamster ovary phospholipase B-like 2 (PLBL2) which co-purified with lebrikizumab. The immunogenic potential of PLBL2 and its potential impact on the immunogenicity of lebrikizumab in clinical studies were therefore evaluated. Data from the clinical studies demonstrated that ∼90% of subjects developed a specific and measurable immune response to PLBL2. Given the high incidence of antibodies to PLBL2 as well as the comparable safety profile observed between placebo- and drug-treated subjects, no correlation between safety events and anti-PLBL2 antibodies could be made. Additionally, no impact on the incidence of anti-lebrikizumab antibodies was observed, suggesting the lack of an adjuvant effect from PLBL2. Interim analysis from ongoing phase III studies using material with substantially reduced levels of PLBL2 with patients having had longer exposure shows significantly less and dose-dependent frequency of immune responses to PLBL2.

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http://dx.doi.org/10.1208/s12248-016-9998-7DOI Listing

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