B7-H3和CSPG4共靶向泛car -t细胞治疗三阴性乳腺癌

IF 10.3 1区 医学 Q1 IMMUNOLOGY
Simone Stucchi, Roberto Borea, Susana Garcia-Recio, Manuela Zingarelli, Patrick D Rädler, Elena Camerini, Caroline Marnata Pellegry, Siobhan O'Connor, H Shelton Earp, Lisa A Carey, Charles M Perou, Barbara Savoldo, Gianpietro Dotti
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引用次数: 0

摘要

目的:嵌合抗原受体T (CAR-T)细胞治疗转移性三阴性乳腺癌(TNBC)的临床研究。然而,为了避免毒性和防止肿瘤逃逸,鉴定可靶向抗原仍然是当务之急。实验设计:在这里,我们分析了北卡罗来纳大学(UNC) AURORA US网络和快速尸检RNA测序数据集中鉴定的98例TNBC样本中B7-H3 (CD276)和硫酸软骨素蛋白多糖4 (CSPG4)的基因表达。然后,我们对在UNC收集的151例TNBC样本进行了B7-H3和CSPG4蛋白表达的免疫组织化学分析。最后,在临床相关的TNBC患者来源的异种移植(PDX)模型中测试了所提出的B7-H3和CSGP4共同靶向的有效性。结果:我们观察到CD276和CSPG4基因在TNBC样本中广泛表达,且在肿瘤转移中基因表达普遍保守。分析的TNBC均不符合CSPG4和CD276基因同时低表达的标准。免疫组化分析显示,B7-H3表达的h值中位数为138(105-168,上下四分位数),CSPG4表达的h值中位数为33(上下四分位数分别为14-78)。值得注意的是,在B7-H3 h值≤105的TNBC核心中,49%的CSPG4 h值超过中位数,而在B7-H3低表达的TNBC核心中,分别有37%和18%的CSPG4表达高于中位数h值或超过其上四分位数,这证实了这两种蛋白中至少有一种在94%的分析肿瘤中表达。最后,优化后的双特异性B7-H3和CSPG4 CAR-T细胞在TNBC PDX模型中根除了混合抗原表达的肿瘤。结论:这些数据强调了所提出的方法的临床潜力,该方法可适用于绝大多数TNBC患者以及大多数乳腺癌患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
B7-H3 and CSPG4 co-targeting as Pan-CAR-T cell treatment of triple-negative breast cancer.

Purpose: Chimeric antigen receptor T (CAR-T) cell therapy is under clinical investigation in patients with metastatic triple-negative breast cancer (TNBC). However, the identification of targetable antigens remains a high priority to avoid toxicity and prevent tumor escape.

Experimental design: Here we analyzed the gene expression of B7-H3 (CD276) and chondroitin sulfate proteoglycan 4 (CSPG4) in 98 TNBC samples identified in the AURORA US Network and Rapid Autopsy RNA sequencing data set at University of North Carolina (UNC). We then performed immunohistochemistry analysis for B7-H3 and CSPG4 protein expression in 151 TNBC samples collected at UNC. Finally, the validity of the proposed B7-H3 and CSGP4 co-targeting was tested in clinically relevant TNBC patient derived xenograft (PDX) models.

Results: We observed that CD276 and CSPG4 genes are broadly and comparably expressed in TNBC samples, and gene expression is generally conserved in tumor metastases. None of the TNBC analyzed met the criteria for simultaneous low expression of CSPG4 and CD276 genes. Immunohistochemistry analysis showed a median H-score of 138 (105-168, lower and upper quartile, respectively) for B7-H3 expression and a median H-score of 33 (14-78 lower and upper quartile, respectively) for CSPG4 expression. Notably, 49% of the TNBC cores with B7-H3 H-score ≤105 exhibited a CSPG4 H-score exceeding its median value, and 37% and 18% of the TNBC cores with low B7-H3 expression scored CSPG4 expression above its median H-score or exceeded its upper quartile, respectively, confirming that at least one of these two proteins is expressed in 94% of the analyzed tumors. Finally, optimized dual-specific B7-H3 and CSPG4 CAR-T cells eradicated tumors with mixed antigen expression in TNBC PDX models.

Conclusions: These data highlight the clinical potential of the proposed approach that could be applicable to the great majority of patients with TNBC as well as most of patients with breast cancer in general.

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来源期刊
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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