临床前体外和体内证据表明cd74靶向治疗皮肤T细胞淋巴瘤有效。

IF 11 1区 医学 Q1 DERMATOLOGY
Mariantonia Costanza, Catello Giordano, Ann-Christin von Brünneck, Jing Zhao, Ahmad Makky, Katharina Vinh, Ivonne Aidee Montes-Mojarro, Florian Reisinger, Stephan Forchhammer, Agnieszka Witalisz-Siepracka, Sophie Edtmayer, Dagmar Stoiber, Gang Yin, David Horst, Anja Fischer, Reiner Siebert, Jan P Nicolay, Menghong Yin, Martin Janz, Falko Fend, Jürgen C Becker, Christian M Schürch, Lukas Kenner, Chalid Assaf, Olaf Merkel, Stephan Mathas
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引用次数: 0

摘要

背景:晚期皮肤T细胞淋巴瘤(CTCL)患者的预后和生活质量较差,特别是伴有ssamzary综合征(SS)和晚期蕈样真菌病(MF)的患者。单克隆抗体或抗体-药物偶联物(adc)已被应用于CTCL治疗算法中,但T细胞非霍奇金淋巴瘤(T- nhl)的抗体靶向细胞表面抗原谱是有限的。目的:通过多种方法评估MHC-II伴侣蛋白CD74在CTCL常见亚型中的表达情况,探讨抗CD74抗体-药物偶联物(anti-CD74 antibody-drug conjugate, ADC)在体外和体内靶向CTCL细胞的效果。方法:采用PCR、免疫印迹和流式细胞术等方法全面研究CD74在明确的CTCL细胞系中的表达。通过免疫组织化学、流式细胞术、免疫荧光和“索引联合检测”(CODEX)多重组织成像以及单细胞RNAseq分析,对140多个原发性CTCL样本进行了分析。CTCL细胞系的DNA甲基化是通过一代全基因组甲基化谱来研究的。研究了体外、单独或联合吉西他滨对CTCL细胞株抗CD74的作用,以及NOD-scid Il2rgnull (NSG)小鼠CTCL细胞株异种移植后的体内作用。结果:我们在CTCL细胞系和广泛收集的原代CTCL样本中通过不同的实验方法证明CD74在CTCL细胞中广泛而稳定地表达。此外,CD74在SS和MF中的表达通过单细胞RNA-seq数据分析得到证实,并且在CTCL细胞系中与CD74基因DNA低甲基化相关。CD74在CTCL细胞中迅速内化,ADC STRO-001靶向CD74可有效杀死CTCL来源的细胞系。最后,CD74靶向在体外与常规化疗协同作用,并在体内根除小鼠CTCL细胞系的异种移植。结论:CD74在常见的CTCL亚型中均有表达,CD74靶向在体外和体内均能有效杀伤CTCL细胞。因此,我们的数据确定cd74靶向是CTCL非常有希望的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical in vitro and in vivo evidence for targeting CD74 as an effective treatment strategy for cutaneous T-cell lymphomas.

Background: Prognosis and quality of life in patients with advanced cutaneous T-cell lymphoma (CTCL), particularly in those with Sézary syndrome (SS) or advanced-stage mycosis fungoides (MF), are poor. Monoclonal antibodies or antibody-drug conjugates (ADCs) have been added into CTCL treatment algorithms, but the spectrum of antibody-targetable cell surface antigens in T-cell non-Hodgkin lymphomas (T-NHLs) is limited.

Objectives: To evaluate the expression of the major histocompatibility complex class II chaperone CD74 in common subtypes of CTCL by various methods, and to explore the efficacy of targeting CD74 in CTCL cells with an anti-CD74 ADC in vitro and in vivo.

Methods: We comprehensively investigated the expression of CD74 in well-defined CTCL cell lines by polymerase chain reaction, immunoblotting and flow cytometry. More than 140 primary CTCL samples of all common subtypes were analysed by immunohistochemistry, flow cytometry, immunofluorescence and 'co-detection by indexing' (CODEX) multiplexed tissue imaging, as well as by single-cell RNA sequencing (scRNAseq) analyses. DNA methylation of CTCL cell lines was interrogated by the generation of genome-wide methylation profiling. The effect of a maytansinoid-conjugated humanized ADC against CD74 was investigated in CTCL cell lines in vitro, alone or in combination with gemcitabine, and in vivo after xenotransplantation of CTCL cell lines in NOD-scid Il2rgnull mice.

Results: We demonstrated that CD74 is widely and robustly expressed in CTCL cells. In addition, CD74 expression in SS and MF was confirmed by scRNAseq data analysis and was correlated in CTCL cell lines with CD74 DNA hypomethylation. CD74 was rapidly internalized in CTCL cells and CD74 targeting by the ADC STRO-001 efficiently killed CTCL-derived cell lines. Finally, targeting of CD74 synergized with conventional chemotherapy in vitro and eradicated murine xenotransplants of CTCL cell lines in vivo.

Conclusions: CD74 is expressed in common CTCL subtypes. Targeting CD74 efficiently killed CTCL cells in vitro and in vivo. We therefore suggest the targeting of CD74 to be a highly promising treatment strategy for CTCL.

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来源期刊
British Journal of Dermatology
British Journal of Dermatology 医学-皮肤病学
CiteScore
16.30
自引率
3.90%
发文量
1062
审稿时长
2-4 weeks
期刊介绍: The British Journal of Dermatology (BJD) is committed to publishing the highest quality dermatological research. Through its publications, the journal seeks to advance the understanding, management, and treatment of skin diseases, ultimately aiming to improve patient outcomes.
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