Immune checkpoint inhibitors and the orbit; two cases of reactive dacryoadenitis.

Pub Date : 2024-08-07 DOI:10.1080/01676830.2024.2385010
Matthew Fenech, Ayodeji Ajanaku, James Hsuan, Austin McCormick, Simon Shamas, Nima Ghadiri
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Abstract

Immune checkpoints refer to mechanisms entrusted with the modulation of immune responses in peripheral tissues and are required for minimising collateral damage. Immune checkpoint inhibitors (ICPi) work through numerous pathways, including the anti-CTLA-4 (cytotoxic T-lymphocyte-associated protein 4), anti-PD-1 (programmed cell death protein 1) and the PD-L1 (protein cell death protein-ligand-1) pathways. They are proving to be an exciting therapeutic avenue in the attempt to activate anti-tumour activity. Ipilimumab is a fully human monoclonal antibody working on the anti-CTLA-4 pathway, while nivolumab and pembrolizumab are humanised monoclonal IgG4 antibodies that work on the PD-1 pathway. Despite a growing body of research pertinent to these novel therapies, early indications show that they are limited by their side effect profile. Furthermore, their efficacy appears to be greater in cancers with a high mutational burden. We present two female patients with bilateral reactive dacryoadenitis secondary to ICPi therapy, a finding that to the best of our knowledge was not previously described in the literature.

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免疫检查点抑制剂与眼眶;两例反应性泪腺炎。
免疫检查点是指负责调节外周组织免疫反应的机制,是将附带损害降至最低的必要条件。免疫检查点抑制剂(ICPi)通过多种途径发挥作用,包括抗CTLA-4(细胞毒性T淋巴细胞相关蛋白4)、抗PD-1(程序性细胞死亡蛋白1)和PD-L1(蛋白细胞死亡蛋白-配体-1)途径。事实证明,它们是激活抗肿瘤活性的一种令人兴奋的治疗途径。伊匹单抗(Ipilimumab)是一种作用于抗CTLA-4途径的全人源单克隆抗体,而nivolumab和pembrolizumab则是作用于PD-1途径的人源化单克隆IgG4抗体。尽管有关这些新型疗法的研究越来越多,但早期迹象表明,这些疗法受到副作用的限制。此外,在突变负荷较高的癌症中,它们的疗效似乎更大。我们介绍了两名继发于 ICPi 治疗的双侧反应性泪腺炎的女性患者,据我们所知,此前的文献中从未描述过这一发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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