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三重混合与肿瘤抗原 mRNA 电穿孔树突状细胞疫苗接种联合伊匹单抗:晚期黑色素瘤中 T 细胞激活与临床应答之间的联系。

TriMix and tumor antigen mRNA electroporated dendritic cell vaccination plus ipilimumab: link between T-cell activation and clinical responses in advanced melanoma.

机构信息

eTheRNA immunotherapies, Niel, Belgium

eTheRNA immunotherapies, Niel, Belgium.

出版信息

J Immunother Cancer. 2020 Feb;8(1). doi: 10.1136/jitc-2019-000329.

Abstract

BACKGROUND

We previously reported that dendritic cell-based mRNA vaccination plus ipilimumab (TriMixDC-MEL IPI) results in an encouraging rate of tumor responses in patients with pretreated advanced melanoma. Here, we report the TriMixDC-MEL IPI-induced T-cell responses detected in the peripheral blood.

METHODS

Monocyte-derived dendritic cells electroporated with mRNA encoding CD70, CD40 ligand, and constitutively active TLR4 (TriMix) as well as the tumor-associated antigens tyrosinase, gp100, MAGE-A3, or MAGE-C2 were administered together with IPI for four cycles. For 18/39 patients, an additional vaccine was administered before the first IPI administration. We evaluated tumor-associated antigen specific T-cell responses in previously collected peripheral blood mononuclear cells, available from 15 patients.

RESULTS

Vaccine-induced enzyme-linked immunospot assay responses detected after in vitro T-cell stimulation were shown in 12/15 patients. Immune responses detected in patients with a complete or partial response were significantly stronger and broader, and exhibited a higher degree of multifunctionality compared with responses in patients with stable or progressive disease. CD8+ T-cell responses from patients with an ongoing clinical response, either elicited by TriMixDC-MEL IPI or on subsequent pembrolizumab treatment, exhibited the highest degree of multifunctionality.

CONCLUSIONS

TriMixDC-MEL IPI treatment results in robust CD8+ T-cell responses in a meaningful portion of stage III or IV melanoma patients, and obviously in patients with a clinical response. The levels of polyfunctional and multiantigen T-cell responses measured in patients with a complete response, particularly in patients evidently cured after 5+ years of follow-up, may provide a benchmark for the level of immune stimulation needed to achieve a durable clinical remission.

TRIAL REGISTRATION NUMBER

NCT01302496.

摘要

背景

我们之前报道过基于树突状细胞的 mRNA 疫苗联合伊匹单抗(TriMixDC-MEL IPI)治疗可使预处理的晚期黑色素瘤患者的肿瘤反应率达到令人鼓舞的水平。在此,我们报告 TriMixDC-MEL IPI 诱导的外周血中的 T 细胞反应。

方法

电穿孔转染编码 CD70、CD40 配体和组成型激活 TLR4(TriMix)以及肿瘤相关抗原酪氨酸酶、gp100、MAGE-A3 或 MAGE-C2 的单核细胞来源的树突状细胞与 IPI 一起使用,共进行四个周期。对于 18/39 例患者,在第一次 IPI 给药前额外给予疫苗。我们评估了来自 15 例患者的先前收集的外周血单个核细胞中的肿瘤相关抗原特异性 T 细胞反应。

结果

在体外 T 细胞刺激后检测到疫苗诱导的酶联免疫斑点测定反应,在 15 例患者中有 12 例。完全或部分缓解患者的免疫反应明显更强且更广泛,与稳定或进展性疾病患者的反应相比,多功能性更高。具有持续临床缓解的患者(无论是由 TriMixDC-MEL IPI 还是后续的 pembrolizumab 治疗引起的)的 CD8+T 细胞反应表现出最高的多功能性。

结论

TriMixDC-MEL IPI 治疗可使相当一部分 III 期或 IV 期黑色素瘤患者产生强烈的 CD8+T 细胞反应,并且在具有临床反应的患者中明显如此。在完全缓解患者中测量的多反应性和多抗原 T 细胞反应的水平,特别是在随访 5 年以上被明显治愈的患者中,可能为达到持久临床缓解所需的免疫刺激水平提供基准。

试验注册号

NCT01302496。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf2/7057443/c165b32825b5/jitc-2019-000329f01.jpg

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