A novel long-acting C5a-blocking cyclic peptide prevents sepsis-induced organ dysfunction via effective blockade of the inflammatory cascade

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来源: Nature 关键字: mRNA
发布时间: 2025-11-05 11:32
摘要:

Cp1 is a novel long-acting cyclic peptide designed to block C5a, a key mediator in sepsis-induced inflammation. In preclinical studies, it demonstrated significant efficacy in reducing inflammatory responses, improving organ function, and prolonging survival in septic mice. The peptide showed excellent plasma stability and a unique mechanism of action, making it a promising candidate for sepsis therapy.

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关键证据

Cp1 significantly suppressed inflammatory factors and improved survival in septic mice.
The cyclic peptide showed enhanced plasma stability and binding affinity.
Cp1 effectively mitigated organ dysfunction and bacterial burden in sepsis models.

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Cp1 is a novel long-acting cyclic peptide designed to block C5a, a key mediator in sepsis-induced inflammation. In preclinical studies, it demonstrated significant efficacy in reducing inflammatory responses, improving organ function, and prolonging survival in septic mice. The peptide showed excellent plasma stability and a unique mechanism of action, making it a promising candidate for sepsis therapy.

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