CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Liquid biopsy: current technology and clinical applications.
Liquid biopsy: current technology and clinical applications.
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液体活检越来越多地用于癌症分子分型,从而支持精准肿瘤学方法。循环细胞外核酸(游离DNA;cfDNA)、循环肿瘤DNA(ctDNA)和循环肿瘤细胞(CTCs)可从血液及其他体液中分离。本综述将聚焦液体活检的当前技术和临床应用。ctDNA/cfDNA已通过多种技术分离和分析,例如微滴数字聚合酶链反应、磁珠、乳液、扩增和磁性(BEAMing)、标记扩子深度测序(TAm-Seq)、通过深度测序进行癌症个性化分析(CAPP-Seq)、全基因组亚硫酸氢盐测序(WGBS-Seq)、全外显子组测序(WES)和全基因组测序(WGS)。CTCs已通过基于生物标志物的细胞捕获,以及基于生物物理和其他特性的阳性或阴性富集进行分离。
ctDNA/cfDNA和CTCs正在多种临床应用中加以利用:使用连续样本区分独特的免疫检查点阻断反应模式;基于基线液体活检特征预测免疫检查点阻断反应;基于连续采样预测对靶向治疗和化疗以及免疫治疗(包括CAR-T 细胞)的反应和耐药;评估来自多个转移部位的脱落DNA;评估潜在可操作的改变;分析预后和肿瘤负荷,包括手术后;探查难以活检的肿瘤;以及在早期阶段检测癌症。后者可能受限于肿瘤来源成分释放入循环的量较少;此外,所有癌症中的 cfDNA 评估都可能受到意义未明的克隆性造血的影响,尤其是在老年人中。CTCs 在技术上比 cfDNA 更难分离,但可用于功能检测,以及评估 CTC 来源的 DNA、RNA 和蛋白质,包括单细胞分析。血液活检比组织活检侵入性更小,因此适合连续采集,这可以实时提供关键的分子信息。
总之,液体活检是一种强大的工具,该技术的显著进步已影响精准肿瘤学的多个方面,从早期诊断到难治性转移性疾病的管理。未来的研究可能会关注血液以外的液体,如腹水、积液、尿液和脑脊液,以及甲基化模式和外泌体等要素。
Liquid biopsies are increasingly used for cancer molecular profiling that enables a precision oncology approach. Circulating extracellular nucleic acids (cell-free DNA; cfDNA), circulating tumor DNA (ctDNA), and circulating tumor cells (CTCs) can be isolated from the blood and other body fluids. This review will focus on current technologies and clinical applications for liquid biopsies. ctDNA/cfDNA has been isolated and analyzed using many techniques, e. g. , droplet digital polymerase chain reaction, beads, emulsion, amplification, and magnetics (BEAMing), tagged-amplicon deep sequencing (TAm-Seq), cancer personalized profiling by deep sequencing (CAPP-Seq), whole genome bisulfite sequencing (WGBS-Seq), whole exome sequencing (WES), and whole genome sequencing (WGS). CTCs have been isolated using biomarker-based cell capture, and positive or negative enrichment based on biophysical and other properties.
ctDNA/cfDNA and CTCs are being exploited in a variety of clinical applications: differentiating unique immune checkpoint blockade response patterns using serial samples; predicting immune checkpoint blockade response based on baseline liquid biopsy characteristics; predicting response and resistance to targeted therapy and chemotherapy as well as immunotherapy, including CAR-T cells, based on serial sampling; assessing shed DNA from multiple metastatic sites; assessing potentially actionable alterations; analyzing prognosis and tumor burden, including after surgery; interrogating difficult-to biopsy tumors; and detecting cancer at early stages.
The latter can be limited by the small amounts of tumor-derived components shed into the circulation; furthermore, cfDNA assessment in all cancers can be confounded by clonal hematopoeisis of indeterminate potential, especially in the elderly.
CTCs can be technically more difficult to isolate that cfDNA, but permit functional assays, as well as evaluation of CTC-derived DNA, RNA and proteins, including single-cell analysis. Blood biopsies are less invasive than tissue biopsies and hence amenable to serial collection, which can provide critical molecular information in real time.
In conclusion, liquid biopsy is a powerful tool, and remarkable advances in this technology have impacted multiple aspects of precision oncology, from early diagnosis to management of refractory metastatic disease. Future research may focus on fluids beyond blood, such as ascites, effusions, urine, and cerebrospinal fluid, as well as methylation patterns and elements such as exosomes.
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