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瑞喹莫德作为免疫佐剂用于高危黑色素瘤患者的 NY-ESO-1 蛋白疫苗接种。

Resiquimod as an immunologic adjuvant for NY-ESO-1 protein vaccination in patients with high-risk melanoma.

机构信息

Cancer Institute, New York University School of Medicine, New York.

Icahn School of Medicine at Mount Sinai Tisch Cancer Institute, Harvard Medical School, New York.

出版信息

Cancer Immunol Res. 2015 Mar;3(3):278-287. doi: 10.1158/2326-6066.CIR-14-0202. Epub 2015 Jan 29.

Abstract

The Toll-like receptor (TLR) 7/8 agonist resiquimod has been used as an immune adjuvant in cancer vaccines. We evaluated the safety and immunogenicity of the cancer testis antigen NY-ESO-1 given in combination with Montanide (Seppic) with or without resiquimod in patients with high-risk melanoma. In part I of the study, patients received 100 μg of full-length NY-ESO-1 protein emulsified in 1.25 mL of Montanide (day 1) followed by topical application of 1,000 mg of 0.2% resiquimod gel on days 1 and 3 (cohort 1) versus days 1, 3, and 5 (cohort 2) of a 21-day cycle. In part II, patients were randomized to receive 100-μg NY-ESO-1 protein plus Montanide (day 1) followed by topical application of placebo gel [(arm A; n = 8) or 1,000 mg of 0.2% resiquimod gel (arm B; n = 12)] using the dosing regimen established in part I. The vaccine regimens were generally well tolerated. NY-ESO-1-specific humoral responses were induced or boosted in all patients, many of whom had high titer antibodies. In part II, 16 of 20 patients in both arms had NY-ESO-1-specific CD4⁺ T-cell responses. CD8⁺ T-cell responses were only seen in 3 of 12 patients in arm B. Patients with TLR7 SNP rs179008 had a greater likelihood of developing NY-ESO-1-specific CD8⁺ responses. In conclusion, NY-ESO-1 protein in combination with Montanide with or without topical resiquimod is safe and induces both antibody and CD4⁺ T-cell responses in the majority of patients; the small proportion of CD8⁺ T-cell responses suggests that the addition of topical resiquimod to Montanide is not sufficient to induce consistent NY-ESO-1-specific CD8⁺ T-cell responses.

摘要

Toll 样受体(TLR)7/8 激动剂瑞喹莫德已被用作癌症疫苗中的免疫佐剂。我们评估了高风险黑色素瘤患者使用全长 NY-ESO-1 与 Montanide(Seppic)联合使用,或联合使用瑞喹莫德治疗的安全性和免疫原性。在研究的第一部分中,患者接受了 100μg 全长 NY-ESO-1 蛋白,与 1.25mL Montanide 混合(第 1 天),随后在第 1 天和第 3 天(第 1 组)或第 1、3 和 5 天(第 2 组)使用 1000mg 0.2%瑞喹莫德凝胶进行局部应用,周期为 21 天。在第二部分中,患者被随机分为两组:一组接受 100μg NY-ESO-1 蛋白加 Montanide(第 1 天),然后使用第一部分建立的给药方案进行局部应用安慰剂凝胶[臂 A(n=8)或 1000mg 0.2%瑞喹莫德凝胶(臂 B(n=12)]。疫苗方案通常耐受性良好。所有患者均诱导或增强了 NY-ESO-1 特异性体液反应,其中许多患者具有高滴度抗体。在第二部分中,两组各 20 名患者中有 16 名患者具有 NY-ESO-1 特异性 CD4+T 细胞反应。仅在臂 B 的 12 名患者中有 3 名患者出现 CD8+T 细胞反应。TLR7 SNP rs179008 的患者更有可能产生 NY-ESO-1 特异性 CD8+反应。总之,NY-ESO-1 蛋白与 Montanide 联合使用,或联合使用局部瑞喹莫德是安全的,可诱导大多数患者产生抗体和 CD4+T 细胞反应;少数 CD8+T 细胞反应表明,将局部瑞喹莫德添加到 Montanide 中不足以诱导一致的 NY-ESO-1 特异性 CD8+T 细胞反应。

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