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:A decade of CD4+ chimeric antigen receptor T-cell evolution in two chronic lymphocytic leukemia patients: were chronic lymphocytic leukemia cells present?
A decade of CD4+ chimeric antigen receptor T-cell evolution in two chronic lymphocytic leukemia patients: were chronic lymphocytic leukemia cells present?
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2022年2月2日,《Nature》发表题为“CD4+ CAR-T 细胞持久存在伴随长达十年的白血病缓解”的论文(Nature. 2022;602:503–509. doi:10.1038/s41586-021-04390-6)。根据文中结果,有人可能认为“嵌合抗原受体(CAR)T细胞确实可以治愈慢性淋巴细胞白血病(CLL)患者”。CAR-T 细胞在输注十多年后仍可检测到;免疫球蛋白重链(IGH)重排深度测序显示两名患者均持续维持深度分子缓解(CAR-T 输注6个月后及此后均未检测到CLL克隆型)。
然而,两名患者目前的实际疾病状态仍不明确,因为尚不清楚:(1)在初始抗白血病应答期,即CAR-T 输注后不久,CAR-T 是否已杀灭全部白血病细胞;(2)是否仍有少量CLL细胞存活,但持续存在的CAR-T 能在其达到可检测水平前将其清除。若为第一种情况,可认为两名患者已确定治愈;若为第二种则不能如此判断,其持续十年的深度缓解可能是功能活跃的CD4+ CAR-T 细胞发挥细胞毒作用的结果。第一种解释似乎更有说服力,相关支持论据已纳入一篇全面的评论文章。未来可能出现新的治疗干预,有望全面改善这两名患者的生活质量;此外,CAR-T 细胞研究也可能因此转向更有效的新方向。
On Feb 2, 2022, Nature published the paper titled "Decade-long leukemia remissions with the persistence of CD4+ CAR T-cells" ( Nature . 2022;602:503-9. doi: 10. 1038/s41586-021-04390-6). According to the results presented, it could be argued that "chimeric antigen receptor (CAR) T-cells can actually cure patients with chronic lymphocytic leukemia (CLL)".
CAR T-cells remained detectable more than ten years after infusion, and immunoglobulin heavy chain (IGH) rearrangement deep sequencing showed persistent deep molecular remission for both patients (no CLL clonotypes were detectable six months after CAR T-cell infusion and onwards).
However, the existing actual disease status of both patients remained unclear, as it was unknown: (1) if CAR T-cells killed all leukemia cells during the initial anti-leukemic response phase, that is, soon after CAR T-cell infusion into both patients; (2) if few CLL cells survived, but persistent CAR T-cells had been able to destroy any leukemia cells before they reach detectable levels.
In the first case, both patients could be considered definitely cured; in the second not and their decade-prolonged deep remission could be a consequence of the cytotoxic activity of the functionally active CD4+ CAR T-cells.
The first version appears to be stronger and the supporting arguments have been included in a comprehensive commentary article. A new therapeutic intervention may emerge with the potential to fully improve the quality of life of both patients and in addition, ongoing research into CAR T-cells may turn in a new, more effective direction.
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