Tat是HIV-1病毒进行转录和复制的一个十分重要的蛋白质,同时,Tat也与HIV-1感染引起的严重病理学程度密切相关.Tat 的生物学性质和功能决定了其是一个理想的开发抗AIDS疫苗和药物的靶蛋白.基于Tat自身及其作用的TAR RNA,可以设计Tat疫苗、细胞外结合Tat的拮抗剂、抗Tat的反义核酸、抗TAR的反义核酸、抗Tat的细胞内抗体和细胞内Tat协同因子的抑制剂等.传统的抗病毒药物及蛋白酶抑制剂与新的细胞内和细胞外Tat拮抗剂联合使用,多靶点地抑制HIV-1的复制将是一个有效的抗AIDS的治疗方案.这一治疗方案能够防止HIV病毒耐药株的产生,减少单一作用靶点药物的用药剂量和降低相应的毒性,最终治愈AIDS相关的病理学变化.
Tat is a HIV-1 transaction transcriptional activator protein and plays a pivotal role in viral replication and in several AIDS-associated pathologies. Its biological properties and functions make it as a good candidate for the development of an anti-AIDS vaccine and/or drug. Strategies designing vaccines and drugs for anti-AIDS include vaccines derived from Tat, extracellular Tat-binding antagonists, inhibitors of Tat-activated intracellular second messengers, anti-Tat antisense, anti-TAR antisense, decoy and antagonists, anti-Tat intracellular intrabody, inhibitors of intracellular Tat cofactors and so on. An effective anti-AIDS therapy will require a multi-targeted approach in which classic antiviral drugs and protease inhibitors are combined with novel extracellular and intracellular Tat antagonists. This approach could prevent the development of drug-resistant HIV strains and decrease the dosage and related toxicity of each single drug and lead to a cure for AIDS-associated pathologies.
梁伟,王亚芹,DAVALIAN DARIUSH.一个新的HIV-1治疗靶——Tat转录激活蛋白(英)[J].生物化学与生物物理进展,2004,31(9):772-776
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