生物工程免疫治疗技术治疗选择性继发性免疫缺陷疾病

Alyssa T Dalloo
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引用次数: 0

摘要

免疫系统的内部运作相当复杂。每一个组成部分都勤奋地工作,以保护我们免受病原体、病毒、微生物和真菌等入侵者的侵害。不幸的是,免疫系统可能变得功能失调,这可能导致继发性免疫缺陷疾病。针对这些免疫系统紊乱和疾病的现有治疗方法通常无法治愈,而且相关的副作用往往会加剧病情。作为一种替代方案,免疫治疗领域试图弥补当今医学的局限性。通过这篇综述,深入了解目前可用于选择性继发性免疫缺陷疾病的常规治疗方法,特别是人类免疫缺陷病毒病和系统性红斑狼疮。然后将分析正在进行的现代免疫治疗方法在治疗这些免疫系统缺陷方面的能力和潜力。2-block-ing抗体。使用人源化骨髓-肝脏-胸腺(BLT)小鼠,发现免疫激活降低,T细胞衰竭标志物表达降低,血浆病毒载量降低。IFN-I诱导抗肿瘤反应,促进CD8 + T细胞启动。将这种疗法与抗逆转录病毒疗法联合使用可迅速抑制病毒。也减少了病毒储存库。[14]
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Bioengineered Immunotherapy Techniques for the Treatment of Select Secondary Immunodeficiency Disorders
The inner workings of the immune system are quite complex. Each component works diligently in order to protect us from invaders such as pathogens: viruses, microbes, and fungi. Unfortunately, the immune system may become dysfunctional, which can result in secondary immunodeficiency diseases. The treatments available for these disorders and diseases of the immune system do not typically serve to cure, and much too often the side effects associated can exacerbate the conditions. As an alternative, the area of immunotherapy seeks to remedy the limitations of today’s medicine. Through this review, insight into the current conventional treatments available for select secondary immunodeficiency diseases will be provided, particularly in Human Immunodeficiency Virus disease and Systemic Lupus Erythematosus. The modern immunotherapy approaches that are underway will then be analyzed in their capacity and potential to treat these defects of the immune system. 2-block-ing antibody. With the use of a humanized Bone marrow-liver-thymus (BLT) mouse, it was found that there was decreased immune activation, decreased expression of T cell exhaustion markers and reduced plasma viral loads. IFN-I induces antitumor responses, promotes CD8 + T cell priming. Using this thera- py in conjunction with ART result- ed in rapid viral suppression. Also reduced viral reservoirs. [14]
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