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Published on: January 26, 2016
Helminth-derived molecules: Pathogenic and pharmacopeial roles
Yu Zhang1, Chunxiang Shen1, Xinyi Zhu1
1State Key Laboratory of Reproductive Medicine and Offspring Health, Department of Pathogen Biology, National Vaccine Innovation Platform, Nanjing Medical University, Nanjing, Jiangsu 211166, China.
Helminth molecules modulate host immunity, suppressing infections but also aiding autoimmune and allergic conditions. Understanding these dual roles is key for developing new therapies.
Area of Science:
- Immunology
- Parasitology
- Molecular Biology
- Metabolic Homeostasis
Background:
- Parasitic helminths (trematodes, cestodes, nematodes) are widespread multicellular invertebrates causing chronic infections.
- Helminths produce diverse molecules involved in host immune and metabolic interactions.
- These molecules mediate immune evasion for parasite survival and chronic infection establishment.
Purpose of the Study:
- To review the properties of helminth-derived molecules.
- To provide an overview of recent scientific knowledge on their pathogenic and pharmacopeial roles.
- To explore their impact on host immune-metabolic homeostasis.
Main Methods:
- Literature review focusing on helminth-derived molecules.
- Analysis of scientific knowledge regarding host-helminth interactions.
- Examination of immune and metabolic regulatory mechanisms.
Main Results:
- Helminth molecules exhibit potent immunosuppressive effects, facilitating parasite survival.
- These molecules also ameliorate autoimmune and allergic responses.
- They promote metabolic homeostasis through immune cell reprogramming (e.g., alternatively activated macrophages, T helper 2 cells, regulatory T cells).
Conclusions:
- Helminth-derived molecules possess dual roles in host immunity, impacting both infection and non-infectious inflammatory diseases.
- Further exploration of their immunopathogenic and immune regulatory mechanisms is crucial.
- This knowledge can guide the development of novel therapeutic strategies for various diseases.
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