抗炎药物的发展:广泛性还是特异性趋化因子受体拮抗剂?

Remo Castro Russo, Cristiana Couto Garcia, Mauro Martins Teixeira
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引用次数: 0

摘要

趋化因子和趋化因子受体形成了一个复杂而多样的系统,已知与白细胞激活和运输有关。人们对开发抗炎药物以拮抗趋化因子或其受体的功能非常感兴趣。然而,将动物模型的结果转化为人类疾病并不简单,该领域的药物开发在许多情况下都失败了,这导致了一个问题,即针对几种趋化因子是否比针对单一趋化因子或受体更有用。这个问题没有简单的答案。趋化因子系统的复杂性可能导致功能冗余,这不是绝对的。然而,这种复杂性可能对免疫系统的生理机能很重要。未来针对趋化因子及其受体的治疗方法的成功开发需要对人类慢性炎症疾病和感染系统的多样性和复杂性有一个完整的了解。
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Anti-inflammatory drug development: Broad or specific chemokine receptor antagonists?

Chemokines and chemokine receptors form a complex and diverse system known to be relevant for leukocyte activation and trafficking. There has been significant interest in the development of anti-inflammatory drugs that antagonize the function of chemokines or their receptors. However, the translation of results from animal models to human disease has not been simple, and drug development in the field has failed in many instances, leading to the question of whether targeting several chemokines may be more useful than targeting a single chemokine or receptor. This question has no simple answer. The complexity of the chemokine system may result in functional redundancy, which is not absolute. However, this complexity is likely important for the physiology of the immune system. The success of future development of therapies targeting chemokines and their receptors requires a complete understanding of the diversity and complexity of the system in human chronic inflammatory diseases and infection.

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