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阿米巴病中的宿主-病原体相互作用及疫苗研发进展

Host-pathogen interaction in amebiasis and progress in vaccine development.

作者信息

Huston C D, Petri W A

机构信息

Department of Internal Medicine, University of Vermont College of Medicine, Burlington 05401, USA.

出版信息

Eur J Clin Microbiol Infect Dis. 1998 Sep;17(9):601-14. doi: 10.1007/BF01708342.

Abstract

Entamoeba histolytica, the causative organism of invasive intestinal and extraintestinal amebiasis, infects approximately 50 million people each year, causing an estimated 40 to 100 thousand deaths annually. Because amebae only infect humans and some higher non-human primates, an anti-amebic vaccine could theoretically eradicate the organism. Uncontrolled epidemiologic studies indicate that acquired immunity to amebic infection probably occurs and that such a vaccine might be feasible. Application of molecular biologic techniques has led to rapid progress towards understanding how Entamoeba histolytica causes disease, and to the identification of several amebic proteins associated with virulence. These proteins are now being evaluated as potential vaccine components. Parenteral and oral vaccine preparations containing recombinant amebic proteins have been effective in preventing disease in a gerbil model of amebic liver abscess. Although systemic and mucosal cellular and humoral immunity both appear to play a role in protection against Entamoeba histolytica, the relative importance of each in the human immune response remains unknown. No animal model of intestinal amebiasis currently exists, moreover, so it has been impossible to evaluate protection against colonization and colitis. Further investigation of the fundamental mechanisms by which Entamoeba histolytica causes disease and of the human immune response to amebic infection is necessary to assess the true feasibility of an anti-amebic vaccine.

摘要

溶组织内阿米巴是侵袭性肠道和肠道外阿米巴病的病原体,每年感染约5000万人,估计每年导致4万至10万人死亡。由于阿米巴仅感染人类和一些高等非人类灵长类动物,理论上一种抗阿米巴疫苗可以根除这种病原体。未经控制的流行病学研究表明,对阿米巴感染的获得性免疫可能会发生,并且这种疫苗可能是可行的。分子生物学技术的应用已在理解溶组织内阿米巴如何致病以及鉴定几种与毒力相关的阿米巴蛋白方面取得了快速进展。这些蛋白目前正在作为潜在的疫苗成分进行评估。含有重组阿米巴蛋白的肠外和口服疫苗制剂在预防阿米巴肝脓肿的沙鼠模型疾病方面已证明有效。虽然全身和黏膜的细胞免疫和体液免疫似乎都在抵御溶组织内阿米巴中发挥作用,但它们在人类免疫反应中的相对重要性仍然未知。此外,目前不存在肠道阿米巴病的动物模型,因此无法评估针对定植和结肠炎的保护作用。有必要进一步研究溶组织内阿米巴致病的基本机制以及人类对阿米巴感染的免疫反应,以评估抗阿米巴疫苗的真正可行性。

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