分枝杆菌衍生药物治疗泌尿和肾癌

Estela Noguera-Ortega, E. Julián
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引用次数: 5

摘要

分枝杆菌是目前用于抗肿瘤免疫治疗的独特细菌群。具体而言,经尿道非肌肉浸润性膀胱癌切除术后,膀胱内灌注牛分枝杆菌卡介苗活细胞是避免疾病复发和进展的最有效治疗方法。在过去的35年里,卡介苗一直用于膀胱癌的治疗,但其他分枝杆菌或分枝杆菌成分目前正在临床前和临床研究中,用于非侵袭性膀胱癌和其他类型的泌尿系统肿瘤的免疫治疗。例如,这些是来自卡介苗或其他分枝杆菌(如细菌性分枝杆菌或indicus pranii分枝杆菌(MIP))的细胞壁提取物或热杀灭形式,甚至是来自非致病性分枝杆菌(如布鲁氏分枝杆菌)的活细胞。将对分枝杆菌成分、非活分枝杆菌和活分枝杆菌用于这些不同癌症的文献进行回顾。在本章中,将分析分枝杆菌作为抗肿瘤剂的功能,使读者对分枝杆菌的有益应用有一个广泛的了解,分枝杆菌通常被介绍为危险的微生物。细菌细胞壁成分负责抗肿瘤作用,但其他部分也触发Th1细胞因子的产生,并刺激外周血细胞对T24 BC细胞的细胞毒活性。来自不同细胞组分的抗原被存在于抗原呈递细胞中的表面受体识别。
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Mycobacteria-Derived Agents for the Treatment of Urological and Renal Cancers
Mycobacteria are the unique group of bacteria that are currently used in antitumoral immunotherapy. Specifically, intravesical instillation of viable cells of Mycobacterium bovis Bacillus Calmette-Guérin (BCG), after transurethral resection of non-muscle invasive bladder cancer, is the most efficacious treatment for avoiding recurrence and progression of the disease. BCG has been used for the last 35 years for bladder cancer treatment, but other mycobacteria or mycobacteria components are currently under pre- clinical and clinical studies for the immunotherapeutic treatment of non-invasive bladder cancer and also of other types of tumors located at the urinary system. Those are, for instance, cell wall extracts or heat-killed forms from BCG or other mycobacteria such as Mycobacterium phlei or Mycobacterium indicus pranii (MIP) or even viable cells from non-pathogenic mycobacteria such us Mycobacterium brumae . A review of the literature in which mycobacteria components, non-viable mycobacteria, and viable mycobacteria have been used for these different cancers will be performed. In this chapter, the func-tion of mycobacteria as antitumor agents will be then analyzed, awarding the audience a broad knowledge of one of the beneficial applications of mycobacteria, which are usually introduced as dangerous microorganisms. bacterial cell wall components are responsible for the antitumor effect but other fractions also triggered the production of Th1 cytokines and stimulated the cytotoxic activity against T24 BC cells by peripheral blood cells. Antigens from different cell fractions are recognized by surface-located receptors present in antigen-presenting cells.
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