Ni Guoying, Liu Xiaosong, Li Hejie, Fogarty Conor E, Chen Shu, Zhang Pingping, Liu Ying, Wu Xiaolian, Wei Ming Q, Chen Guoqiang, Zhang Ping, Wang Tianfang
Cancer Research Institute, First People's Hospital of Foshan, Foshan, China.
Genecology Research Centre, University of the Sunshine Coast, Maroochydore DC, QLD, Australia.
Front Oncol. 2021 Nov 11;11:754770. doi: 10.3389/fonc.2021.754770. eCollection 2021.
The development of topical cream drugs that increase the immune activation of tumour-infiltrating lymphocytes against tumour and chronic viral infection-associated lesions is of great immunotherapeutic significance. This study demonstrates that the topical application of a temperature-sensitive gel containing caerin 1.1 and 1.9 peptides reduces nearly 50% of the tumour weight of HPV16 E6/E7-transformed TC-1 tumour-bearing mice improving the tumour microenvironment. Confocal microscopy confirms the time-dependent penetration of caerin 1.9 through the epidermal layer of the ear skin structure of mice. Single-cell transcriptomic analysis shows that the caerin 1.1/1.9 gel expands the populations with high immune activation level and largely stimulates the pro-inflammatory activity of NK and dendritic cells. Closely associated with INFα response, seems to play a key role in altering the function of all macrophages in the caerin group. In addition, the caerin gel treatment recruits almost two-fold more activated CD8 T cells to the TME, relative to the untreated tumour, which shows a synergistic effect derived from the regulation of S1pr1, , and family expression. The TMT10plex-labelling proteomic quantification further demonstrates the activation of interferon-alpha/beta secretion and response to cytokine stimulus by the caerin gel, while the protein contents of several key regulators were elevated by more than 30%, such as , , , and . Computational integration of the proteome with the single-cell transcriptome consistently suggested greater activation of NK and T cells with the topical application of caerin peptide gel.
开发能够增强肿瘤浸润淋巴细胞对肿瘤及慢性病毒感染相关病变免疫激活的外用乳膏药物具有重大的免疫治疗意义。本研究表明,局部应用含有凯林1.1和1.9肽的温度敏感凝胶可使携带HPV16 E6/E7转化的TC-1肿瘤的小鼠肿瘤重量减轻近50%,改善肿瘤微环境。共聚焦显微镜证实凯林1.9可随时间穿透小鼠耳部皮肤结构的表皮层。单细胞转录组分析表明,凯林1.1/1.9凝胶可扩大具有高免疫激活水平的细胞群体,并在很大程度上刺激自然杀伤细胞和树突状细胞的促炎活性。与INFα反应密切相关,似乎在改变凯林组所有巨噬细胞功能中起关键作用。此外,相对于未治疗的肿瘤,凯林凝胶治疗使肿瘤微环境中募集的活化CD8 T细胞增加了近两倍,这显示出由S1pr1、 、 和 家族表达调控产生的协同效应。TMT10plex标记蛋白质组定量进一步证明了凯林凝胶激活干扰素-α/β分泌并对细胞因子刺激产生反应,同时几种关键调节因子的蛋白质含量升高了30%以上,如 、 、 、 和 。蛋白质组与单细胞转录组的计算整合一致表明,局部应用凯林肽凝胶可使自然杀伤细胞和T细胞得到更大程度的激活。