Clinical Pharmacology & Early Clinical Development, Takeda Development Center Americas, Inc., Cambridge, MA 02142, USA.
Immunotherapy. 2024;16(13):879-894. doi: 10.1080/1750743X.2024.2382081. Epub 2024 Sep 26.
Immunoglobulin G (IgG) therapies have been used for decades as standard treatment for patients with primary antibody deficiencies. Monitoring the pharmacokinetics (PK) of IgG is a key component in guiding treatment regimens. Despite the wealth of clinical experience, substantial gaps exist in our understanding of the true nature of IgGs and their disposition in humans. Furthermore, intrinsic and extrinsic factors may alter the PK of IgG, necessitating an individualized approach for patients. A comprehensive literature review was performed in order to summarize the PK of IgGs, examine the mechanisms of IgG disposition (including catabolism), outline considerations for special patient populations and discuss knowledge gaps and future perspectives for improving our understanding of IgG PK in relation to the individualized treatment paradigm.
免疫球蛋白 G(IgG)疗法已被使用数十年,作为原发性抗体缺陷患者的标准治疗方法。监测 IgG 的药代动力学(PK)是指导治疗方案的关键组成部分。尽管有丰富的临床经验,但我们对 IgG 的真实性质及其在人体内的处置仍存在很大的差距。此外,内在和外在因素可能会改变 IgG 的 PK,因此需要为患者采取个体化的方法。为了总结 IgG 的 PK,检查 IgG 处置的机制(包括分解代谢),概述特殊患者人群的注意事项,并讨论有关改善我们对与个体化治疗模式相关的 IgG PK 的理解的知识空白和未来展望,我们进行了全面的文献回顾。