乙型肝炎的治疗和预防进展。

Niraj James Shah, Mark M Aloysius, Neil Rohit Sharma, Kumar Pallav
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引用次数: 2

摘要

慢性乙型肝炎(CHB)继续在世界范围内显著增加发病率和死亡率。科学家、临床医生、制药公司和卫生组织投入了大量的智力和金钱资源来寻找治疗方法,提高免疫接种率,减轻慢性乙型肝炎的全球负担。国家和国际健康相关组织,包括疾病控制中心,国家卫生研究所,美国肝病研究协会(AASLD),欧洲肝脏研究协会(EASL),亚太肝脏研究协会(APASL)和世界卫生组织发布疾病预防和治疗的定期建议。我们回顾了EASL、AASLD、APASL和台湾肝脏研究协会的最新指南,发现绝大多数被引用的研究都是在2018年之前发表的。我们回顾了2018年以来发表的与乙肝相关的文献,以确定可能指导未来根除乙肝努力的最新进展和当前的障碍。我们对乙肝病毒生命周期的理解取得了突破,由此产生的药物开发令人鼓舞,并有进一步进展的巨大空间。高危人群最容易受到乙型肝炎感染和再激活的破坏性影响,来自这些人群的数据仍然很少。利用系统方法,优化实验模型,鉴定和验证下一代生物标志物,以及精确调节人类免疫反应将是未来创新的关键。在可预见的未来,新疗法可能会补充而不是取代传统疗法。最重要的是,必须优先考虑与慢性乙型肝炎相关的人口健康挑战的务实管理,以产生实际结果。
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Advances in treatment and prevention of hepatitis B.

Chronic hepatitis B (CHB) continues to contribute to worldwide morbidity and mortality significantly. Scientists, clinicians, pharmaceutical companies, and health organizations have dedicated substantial Intellectual and monetary resources to finding a cure, increasing immunization rates, and reducing the global burden of CHB. National and international health-related organizations including the center for disease control, the national institute of health, the American Association for the study of liver disease (AASLD), The European association for the study of the Liver (EASL), The Asia Pacific association for the study of the Liver (APASL) and the world health organization release periodic recommendations for disease prevention and treatment. Our review of the most recent guidelines by EASL, AASLD, APASL, and Taiwan Association for the Study of the Liver revealed that an overwhelming majority of cited studies were published before 2018. We reviewed Hepatitis B-related literature published 2018 onwards to identify recent developments and current barriers that will likely direct future efforts towards eradicating hepatitis B. The breakthrough in our understanding of the hepatitis B virus life cycle and resulting drug development is encouraging with significant room for further progress. Data from high-risk populations, most vulnerable to the devastating effects of hepatitis B infection and reactivation remain sparse. Utilization of systems approach, optimization of experimental models, identification and validation of next-generation biomarkers, and precise modulation of the human immune response will be critical for future innovation. Within the foreseeable future, new treatments will likely complement conventional therapies rather than replace them. Most Importantly, pragmatic management of CHB related population health challenges must be prioritized to produce real-world results.

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