通过 DNA 纹身进行皮内裸 DNA 疫苗接种,为 IV 期黑色素瘤患者建立肿瘤特异性免疫:I 期临床试验。

IF 2 4区 医学 Q3 ONCOLOGY Oncology Research and Treatment Pub Date : 2024-04-05 DOI:10.1159/000537896
M. G. Geukes Foppen, M. Rohaan, J. Borgers, Daisy Philips, F. Vyth-Dreese, Jos H. Beijnen, B. Nuijen, J. H. van den Berg, J. B. Haanen
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引用次数: 0

摘要

简介:裸DNA疫苗接种是一种强大而安全的抗原特异性细胞免疫策略。我们设计了一项 I 期临床试验,研究编码肿瘤相关抗原 MART-1 的 CD8+ T 细胞表位的裸 DNA 疫苗对晚期黑色素瘤患者的毒性。方法这项剂量递增的 Ia 期临床试验研究了在晚期黑色素瘤患者(无法手术的 IIIC-IV 期,AJCC 第 7 版)中使用编码肿瘤相关抗原 MART-1 的 CD8+ T 细胞表位的裸 DNA 疫苗的毒性和免疫反应。疫苗通过永久化妆或纹身设备进行皮内注射。根据 CTCAE v.3.0 对安全性进行了监测,并采集了皮肤活检和血液样本进行免疫学监测。中位随访时间为5.9个月,DNA疫苗接种是安全的,没有出现与治疗相关的死亡病例。常见的任何级别的治疗突发不良反应是接种部位的皮肤反应(100%)和疼痛(56%)。一名患者出现了四级毒性,很可能与肿瘤进展有关。一名患者(11%)病情稳定,持续了 353 天。免疫分析表明,5 名患者外周血中疫苗诱导的 T 细胞反应没有增加,但在纹身给药部位出现了 MART-1 特异性 CD8+ T 细胞反应。由于缺乏临床活性,最大给药剂量为 2 毫克。要想证明 DNA 疫苗接种可能带来的临床益处,还需要对改进后的疫苗形式进行进一步研究。
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Intradermal naked DNA vaccination by DNA tattooing for mounting tumor-specific immunity in stage IV melanoma patients: a phase I clinical trial.
INTRODUCTION Naked DNA vaccination could be a powerful and safe strategy to mount antigen-specific cellular immunity. We designed a phase I clinical trial to investigate the toxicity of naked DNA vaccines encoding CD8+ T-cell epitope from tumor-associated antigen MART-1 in patients with advanced melanoma. METHODS This dose escalating phase Ia clinical trial investigates the toxicity and immunological response upon naked DNA vaccines encoding a CD8+ T-cell epitope from the tumor-associated antigen MART-1, genetically linked to the gene encoding domain 1 of subunit-tetanus toxin fragment C in patients with advanced melanoma (inoperable stage IIIC-IV, AJCC 7th edition). The vaccine was administrated via intradermal application using a permanent make-up or tattoo device. Safety was monitored according to CTCAE v.3.0 and skin biopsies and blood samples were obtained for immunologic monitoring. RESULTS Nine pretreated, HLA-A*0201-positive patients with advanced melanoma expressing MART-1 and MHC class I, with a good performance status, and adequate organ function, were included. With a median follow-up of 5.9 months, DNA vaccination was safe, without treatment-related deaths. Common treatment-emergent adverse events of any grade were dermatologic reactions at the vaccination site (100%) and pain (56%). One patient experienced grade 4 toxicity, most likely related to tumor progression. One patient (11%) achieved stable disease, lasting 353 days. Immune analysis showed no increase in vaccine-induced T cell response in peripheral blood of five patients, but did show a MART-1 specific CD8+ T cell response at the tattoo administration site. The maximum dose administered was 2 mg due to lack of clinical activity. CONCLUSION We showed that the developed DNA vaccine, applied using a novel intradermal application strategy, can be administered safely. Further research with improved vaccine formats is required to show possible clinical benefit of DNA vaccination.
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
84
期刊介绍: With the first issue in 2014, the journal ''Onkologie'' has changed its title to ''Oncology Research and Treatment''. By this change, publisher and editor set the scene for the further development of this interdisciplinary journal. The English title makes it clear that the articles are published in English – a logical step for the journal, which is listed in all relevant international databases. For excellent manuscripts, a ''Fast Track'' was introduced: The review is carried out within 2 weeks; after acceptance the papers are published online within 14 days and immediately released as ''Editor’s Choice'' to provide the authors with maximum visibility of their results. Interesting case reports are published in the section ''Novel Insights from Clinical Practice'' which clearly highlights the scientific advances which the report presents.
期刊最新文献
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