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一种新的治疗性克氏锥虫病疫苗的临床前进展和免疫生理学。

Preclinical advances and the immunophysiology of a new therapeutic Chagas disease vaccine.

机构信息

Texas Children's Hospital Center for Vaccine Development, Department of Pediatrics, Division of Tropical Medicine, Baylor College of Medicine, Houston, Texas, USA.

Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Expert Rev Vaccines. 2022 Sep;21(9):1185-1203. doi: 10.1080/14760584.2022.2093721. Epub 2022 Jul 4.

DOI:10.1080/14760584.2022.2093721
PMID:35735065
Abstract

INTRODUCTION

Chronic infection with the protozoal parasite leads to a progressive cardiac disease, known as chronic Chagasic cardiomyopathy (CCC). A new therapeutic Chagas disease vaccine is in development to augment the existing antiparasitic chemotherapy drugs.

AREAS COVERED

We report on our current understanding of the underlying immunologic and physiologic mechanisms that lead to CCC, including parasite immune escape mechanisms that allow persistence and the subsequent inflammatory and fibrotic processes that lead to clinical disease. We report on vaccine design and the observed immunotherapeutic effects including induction of a balanced T1/T2/T17 immune response that leads to reduced parasite burdens and tissue pathology. Furthermore, we report vaccine-linked chemotherapy, a dose-sparing strategy to further reduce parasite burdens and tissue pathology.

EXPERT OPINION

Our vaccine-linked chemotherapeutic approach is a multimodal treatment strategy, addressing both the parasite persistence and the underlying deleterious host inflammatory and fibrotic responses that lead to cardiac dysfunction. In targeting treatment towards patients with chronic indeterminate or early determinate Chagas disease, this vaccine-linked chemotherapeutic approach will be highly economical and will reduce the global disease burden and deaths due to CCC.

摘要

简介

原生动物寄生虫 的慢性感染可导致进行性心脏疾病,即慢性恰加斯心肌病(CCC)。目前正在开发一种新的治疗性克氏锥虫病疫苗,以增强现有的抗寄生虫化学疗法药物。

涵盖领域

我们报告了导致 CCC 的潜在免疫和生理机制的最新认识,包括寄生虫免疫逃避机制,允许寄生虫持续存在,以及随后导致临床疾病的炎症和纤维化过程。我们报告了疫苗设计和观察到的免疫治疗效果,包括诱导平衡的 T1/T2/T17 免疫反应,从而减少寄生虫负担和组织病理学。此外,我们报告了疫苗相关化疗,这是一种节省剂量的策略,可进一步减少寄生虫负担和组织病理学。

专家意见

我们的疫苗相关化疗方法是一种多模式治疗策略,针对寄生虫持续存在以及导致心脏功能障碍的潜在有害宿主炎症和纤维化反应。通过将治疗针对慢性不确定或早期确定性恰加斯病患者,这种疫苗相关化疗方法将具有很高的经济性,并将降低全球因 CCC 导致的疾病负担和死亡人数。

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