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表达基于 CD5 的嵌合抗原受体(SRCD5CAR-NK-92)的 NK-92 细胞的转化开发及首次人体同情用药输注:一例多重耐药镰刀菌病患者

英文原题:Translational development and first-in-human compassionate infusion of NK-92 cells expressing a CD5-based chimeric antigen receptor (SRCD5CAR-NK-92) in a patient with multidrug-resistant fusariosis.

PubMed 2026/05/08(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

研究概要

尽管患者最终因基础血液系统恶性肿瘤进展而死亡,但这是SRCD5CAR-NK-92细胞在严重MDR IFI背景下的首次人体使用。结果凸显了其作为一种安全、现货型治疗策略的潜力,同时强调需要进一步研究其疗效和长期结局。

研究思路结论见上方概要

侵袭性真菌感染(IFI)仍然是一个重大的治疗挑战,原因在于抗真菌药物选择有限、多重耐药(MDR)菌株的出现以及高死亡率。这使得开发基于免疫的疗法以恢复和/或增强抗真菌免疫应答成为临床优先事项。这与最近的发现一致,即原发性(脐血来源)NK细胞可通过赋予其靶向β-葡聚糖的基于CD5的第二代嵌合抗原受体(SRCD5CAR)来增强其抗真菌活性,β-葡聚糖是真菌细胞壁的一种组成性且广泛分布的成分。在此基础上,我们旨在探索所报道的白血病来源NK-92细胞的组成性抗真菌活性是否也可通过工程化改造来增强,以进一步潜在用作IFI过继转移治疗中同种异体细胞的均一且即用型来源。

NK-92细胞经慢病毒转导并筛选以获得SRCD5CAR的稳定高水平表达,用于在体外真菌杀伤试验以及体内真菌感染模型中进一步测试。

SRCD5CAR-NK-92细胞显示出比未转导的NK-92细胞 counterpart 更优越的抗真菌活性。SRCD5CAR-NK-92细胞还对一株来自一名血液恶性肿瘤患者的多药耐药 Fusarium petroliphilum 分离株表现出优越的活性,该患者缺乏替代治疗选择。在同情用药批准后,患者接受了递增剂量的辐照SRCD5CAR-NK-92细胞静脉输注,间隔2-5天,未出现显著的局部或全身不良反应(例如细胞因子风暴或同种异体反应性)。

展开英文摘要原文

INTRODUCTION: Invasive fungal infections (IFI) remain a major therapeutic challenge due to limited antifungal options, emergence of multidrug-resistant (MDR) strains and high mortality rates. This has turned up the development of immune-based therapies to restore and/or enhance anti-fungal immune responses into a clinical priority. This is in line with the recent demonstration that antifungal activity of primary (cord blood-derived) NK cells can be potentiated by endowing them with a CD5-based second-generation chimeric antigen receptor (SRCD5CAR) targeting β-glucans, a constitutive and broadly distributed component of fungal cell walls. Building on this, we aimed at exploring whether the reported constitutive antifungal activity of leukemia-derived NK-92 cells can also be potentiated by engineering them for further potential use as a homogeneous and ready-to-use source of allogeneic cells for adoptive transfer therapy in IFI. METHODS: NK-92 cells lentivirally transduced and selected for stable and high-level expression of the SRCD5CAR for further testing in in vitro fungal killing assays, as well as in an in vivo model of fungal infection. RESULTS: SRCD5CAR-NK-92 cells showed superior antifungal activity than untransduced NK-92 cell counterparts. SRCD5CAR-NK-92 cells also exhibited superior activity against a MDR Fusarium petroliphilum isolate from a patient undergoing a hematological malignancy and devoid of alternative therapeutic options. Following compassionate use approval, the patient received escalating intravenous infusions of irradiated SRCD5CAR-NK-92 cells at 2-5 day intervals, without significant local or systemic adverse effects (e.g., cytokine storm or alloreactivity). DISCUSSION: Despite the patient ultimately succumbed due to progression of the underlying hematological malignancy, this represents first-in-human use of SRCD5CAR-NK-92 cells in the context of a severe MDR IFI. The results highlight its potential as a safe and off-the-shelf therapeutic strategy, while underscoring the need for further investigation on efficacy and long-term outcomes.

论文信息

作者
Velasco-de-Andrés M、Puerta-Alcalde P、Eitler J、Krutz L、Chumbita M、Español-Rego M、Català C、Carrillo-Serradell L
单位
Immunoreceptors del sistema innat i adaptatiu, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.Spain
文献类型
病例报告
期刊
Frontiers in immunology2026
原文标识
PubMed 42183292 · DOI 10.3389/fimmu.2026.1772830