肿瘤细胞治疗研究
英文原题:The Chimeric Antigen Receptor T Cell Target Claudin 6 Is a Marker for Early Organ-Specific Epithelial Progenitors and Is Expressed in Some Pediatric Solid Tumor Entities.
The Chimeric Antigen Receptor T Cell Target Claudin 6 Is a Marker for Early Organ-Specific Epithelial Progenitors and Is Expressed in Some Pediatric Solid Tumor Entities.
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研究者利用 500 多份儿童实体瘤样本的 RNA 测序数据,并对 100 多份新鲜冷冻肿瘤样本开展 qRT-PCR 和免疫组化(IHC),分析颅外实体瘤中的 CLDN6 表达。通过 qRT-PCR 检测 32 种不同婴儿组织的正常组织表达,并对来自 4 个年龄组供者的约 290 份组织及胎儿尸检样本进行 IHC 分析。
在胎儿组织中,CLDN6 表达主要见于多个器官的上皮细胞,包括皮肤、肺、肾、肠道和胰腺,但未见于未分化胚芽细胞。出生后最初几周内,仅在上皮祖细胞中发现 CLDN6 阳性表达。在年龄较大的组别中,仍可见散在 CLDN6 阳性祖细胞簇,但数量很少。肿瘤组织中,促纤维增生性小圆细胞肿瘤和生殖细胞肿瘤 CLDN6 表达强且均一。Wilms 瘤的 CLDN6 表达存在异质性,胚芽成分中尤其缺乏表达。
研究结果显示,CLDN6 阳性上皮前体细胞在不同器官中的分布具有特异性,并在出生后数周内大多从终末分化的上皮中消失。因此,数据支持 CLDN6 作为儿童患者可行的治疗靶点,并支持将儿童纳入抗 CLDN6 治疗篮式研究。
Background/Objectives : The oncofetal membrane protein Claudin 6 (CLDN6) is an attractive target for T cell-based therapies. There is a lack of detailed analyses on the age-dependent expression of CLDN6 in normal tissues is lacking, which limits the expansion of CLDN6 CAR-T cell clinical trials to pediatric populations.
Methods : We analyzed CLDN6 expression in extracranial solid tumors and normal tissues of children using RNA-sequencing data from over 500 pediatric solid tumor samples, qRT-PCR and immunohistochemistry (IHC) in more than 100 fresh-frozen tumor samples and, approximately, 250 formalin-fixed paraffin-embedded (FFPE) samples.
We examined normal tissue expression via qRT-PCR in 32 different infant tissues and via IHC in roughly 290 tissues from donors across four age groups, as well as in fetal autopsy samples. Results : In fetal tissues, we detected CLDN6 expression primarily in the epithelial cells of several organs, including the skin, lungs, kidneys, intestinal tract, and pancreas, but not in undifferentiated blastemal cells. Postnatally, we found CLDN6-positive epithelial progenitors only during the first few weeks of life.
In older-age groups, isolated clusters of CLDN6-positive progenitors were present, but in scarce quantities. In tumor tissues, we found strong and homogeneous CLDN6 expression in desmoplastic small round cell tumors and germ cell tumors. Wilms tumors demonstrated heterogeneous CLDN6 expression, notably absent in the blastemal component. Conclusions : These findings highlight an organ-specific presence of CLDN6-positive epithelial precursors that largely disappear in terminally differentiated epithelia within weeks after birth.
Therefore, our data support CLDN6 as a viable therapeutic target in pediatric patients and justify their inclusion in basket studies for anti-CLDN6-based therapies.
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