γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:Small-scale manufacturing of neoantigen-encoding messenger RNA for early-phase clinical trials.
信使RNA(mRNA)已成为治疗性癌症疫苗策略中一种有前景的工具。
信使RNA(mRNA)已成为治疗性癌症疫苗策略中一种有前景的工具。由于其设计灵活且生产迅速,mRNA是一种有吸引力的抗原递送形式,可用于靶向肿瘤中表达的突变肽——即所谓的新抗原的癌症疫苗。这些新抗原在患者之间很少共享,将这些抗原纳入疫苗需要生产个体化的患者定制mRNA批次。作者开发了MIDRIX NEO,一种靶向肿瘤新抗原的个性化mRNA负载树突状细胞疫苗,目前正在肺癌患者的1期临床研究中进行评估。为促进该研究,作者建立了一套符合药品生产质量管理规范(GMP)的生产工艺,用于制造小批量的个性化新抗原编码mRNA。在本文中,作者描述了完整的mRNA生产流程以及mRNA所接受的广泛质量评估。验证运行表明,该工艺能够产出质量可重现且高质量的mRNA。该工艺现已成功应用于新抗原编码mRNA的生产,用于MIDRIX NEO的临床评估。据作者所知,这是首次描述基于GMP的患者定制新抗原mRNA生产工艺。
Messenger RNA (mRNA) has become a promising tool in therapeutic cancer vaccine strategies. Owing to its flexible design and rapid production, mRNA is an attractive antigen delivery format for cancer vaccines targeting mutated peptides expressed in a tumor-the so-called neoantigens. These neoantigens are rarely shared between patients, and inclusion of these antigens in a vaccine requires the production of individual batches of patient-tailored mRNA. The authors have developed MIDRIX NEO , a personalized mRNA-loaded dendritic cell vaccine targeting tumor neoantigens, which is currently being evaluated in a phase 1 clinical study in lung cancer patients. To facilitate this study, the authors set up a Good Manufacturing Practice (GMP)-compliant production process for the manufacture of small batches of personalized neoantigen-encoding mRNA. In this article, the authors describe the complete mRNA production process and the extensive quality assessment to which the mRNA is subjected. Validation runs have shown that the process delivers mRNA of reproducible, high quality. This process is now successfully applied for the production of neoantigen-encoding mRNA for the clinical evaluation of MIDRIX NEO . To the authors' knowledge, this is the first time that a GMP-based production process of patient-tailored neoantigen mRNA has been described.
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