Bioactive molecules of Taenia solium metacestode, a causative agent of neurocysticercosis.

Expert Rev Proteomics

Department of Molecular Parasitology, Sungkyunkwan University School of Medicine and Center for Molecular Medicine, Samsung Biomedical Research Institute, Suwon 440-746, Korea.

Published: October 2010

AI Article Synopsis

  • Neurocysticercosis (NC) is a severe CNS infection caused by the Taenia solium parasite, leading to major public health issues and significant health risks for affected individuals.
  • Effective diagnosis and management of NC are vital, requiring a detailed understanding of the molecular interactions between the parasite and the human host, particularly focusing on bioactive molecules involved.
  • The article reviews existing serological biomarkers and immunoproteomics related to low-molecular-weight proteins, emphasizing the importance of these molecules in understanding NC and potential new treatment approaches.

Article Abstract

Neurocysticercosis (NC), an infection of the CNS with Taenia solium metacestode, exemplifies formidable public health concerns associated with significant morbidity and mortality. The disease is a complex phenomenon involving molecular cell biological cross-talks between the parasite and human host. To effectively combat NC, specific diagnosis and proper management are prerequisites. Bioactive molecules implicated in host-parasite interactions and parasitic homeostasis should be elucidated. This article provides an overview of currently available serological biomarkers, especially those comprising low-molecular-weight proteins, and discusses available immunoproteomics for identification of such molecules. T. solium metacestode bioactive molecules, which might be critically implicated in the progression of NC disease, are summarized. Comprehensive understanding of the biochemical properties and biological functions of bioactive molecules may contribute to the development of novel intervention strategies against NC.

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Source
http://dx.doi.org/10.1586/epr.10.72DOI Listing

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