基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CD8 immunoPET imaging to stratify response and guide combination immunotherapy and radiation in triple negative breast cancer.
CD8 immunoPET imaging to stratify response and guide combination immunotherapy and radiation in triple negative breast cancer.
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放射治疗增强了肿瘤中 CD8+的表达,CD8 immunoPET 能有效筛选出更可能对后续免疫治疗产生应答的肿瘤。CD8 immunoPET 为优化三阴性乳腺癌放射治疗后的联合免疫治疗提供了一种方法。
靶向免疫细胞的PET成像可用于动态监测组织内肿瘤免疫调节。已知放射治疗会改变肿瘤免疫微环境;因此,本研究展示CD8免疫PET成像如何通过分层筛选在放射治疗后最可能从免疫治疗中获益的肿瘤,来优化联合免疫治疗和放射治疗。
通过对放射敏感的亲本4T1细胞系进行重复照射,直至分离出放射抗性亚克隆(RR-4T1),在体内研究之前建立了一株放射抗性三阴性乳腺癌细胞系。采用CD8 immunoPET成像对放射敏感和放射抗性4T1乳腺癌模型中响应分次放疗的免疫细胞浸润进行成像。在这一基因匹配的放射敏感和放射抗性模型中,我们利用流式细胞术探讨放射抗性如何改变放射诱导的免疫调节和CD8 T细胞运输,同时在放射敏感亲本4T1模型中评估了对放疗联合免疫治疗的反应。利用CD8 immunoPET,基于放疗后CD8组织浸润的变化,对免疫治疗的长期治疗反应进行分层。
放射敏感的亲本4T1肿瘤在接受放射治疗后,相对于对照肿瘤,显示出CD8 immunoPET信号(SUV)增加(p < 0.01),而放射抵抗的4T1肿瘤在放射治疗后未见变化(p = 0.99),这一点通过流式细胞术得到验证。当肿瘤按CD8 minibody摄取高低进行分层时,CD8高的放射敏感亲本4T1肿瘤接受放射和免疫治疗后,与CD8低的放射敏感亲本4T1肿瘤相比,对免疫治疗的敏感性显著增加(p < 0.05)。
PET imaging targeting immune cells can be used to dynamically monitor intratumoral immune modulation in tissues. Radiation therapy is known to alter the tumor immune microenvironment; therefore, this study demonstrates how CD8 immunoPET imaging can optimize combination immunotherapy and radiation therapy by stratifying tumors who could derive the greatest benefit from immunotherapy following radiation therapy. EXPERIMENTAL DESIGN: A radiation resistant triple negative breast cancer cell line was derived through repeat irradiation of the radiosensitive parental 4T1 cell line prior to in vivo studies, until a radiation resistant subclone (RR-4T1) was isolated. CD8 immunoPET imaging was used to image immune cell infiltration in response to fractionated radiotherapy in radiation sensitive and radiation resistant 4T1 breast cancer models. In this genetically matched radiation sensitive and resistant model, we explore how radiation resistance alters radiation-induced immune modulation and CD8 T cell trafficking with flow cytometry, while response to combination radiation and immunotherapy was assessed in the radiosensitive parental 4T1 model. CD8 immunoPET was utilized to stratify for long-term therapeutic response to immunotherapy based on post-radiation therapy changes in CD8 tissue infiltration.
Radiosensitive parental 4T1 tumors show increased CD8 immunoPET signal (SUV) when treated with radiation therapy, relative to control tumors (p < 0.01) whereas radiation resistant 4T1 tumors showed no change following radiation therapy (p = 0.99), which was validated with flow cytometry. When tumors were stratified for high or low CD8 minibody uptake, CD8-high radiosensitive parental 4T1 tumors treated with radiation and immunotherapy had significantly increased sensitivity to immunotherapy compared to CD8-low radiosensitive parental 4T1 tumors (p < 0.05).
Radiation therapy enhanced CD8 + expression in tumors and CD8 immunoPET effectively stratifies tumors that are more likely to respond to subsequent immunotherapy. CD8 immunoPET provides an approach to optimize combination immunotherapy following radiation treatment in triple-negative breast cancer.
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