{"title":"多糖在炎症中的治疗潜力:目前的见解和未来的方向。","authors":"Thananjeyan Balasubramaniyam , Hye-Bin Ahn , Juhee Lim , Abhishikta Basu , Jacek Z. Kubiak , Shailima Rampogu , Vinod Kumar Nathan","doi":"10.1016/j.intimp.2025.115538","DOIUrl":null,"url":null,"abstract":"<div><div>Polysaccharides from plants, microorganisms, algae, and animals exhibit significant anti-inflammatory potential, offering safe and effective therapeutic options for diseases like inflammatory bowel disease and arthritis. This review synthesizes their sources, structural modifications, and mechanisms, including modulation of NF-κB and MAPK pathways. In vitro models (e.g., RAW264.7 macrophages, THP-1 cells) demonstrate reductions in pro-inflammatory cytokines (e.g., TNF-α and IL-1β by 30–40 % at doses of 50–200 μg/mL), while in vivo models (e.g., DSS-induced colitis, collagen-induced arthritis) show decreased Disease Activity Index and improved histopathological outcomes at doses of 50–200 mg/kg. Chemical modifications, such as sulfation, enhance bioactivity, though challenges like bioavailability, inconsistent methodologies, and variable dosing persist. A comprehensive Table 3 summarizes sources, compounds, models, doses, and effects, while critical evaluations highlight methodological limitations and propose standardized assays (e.g., ELISA, qPCR). Future directions include nanotechnology for improved delivery, bioinformatics for structural optimization, and randomized clinical trials to validate preclinical findings, paving the way for novel polysaccharide-based therapies.</div></div>","PeriodicalId":13859,"journal":{"name":"International immunopharmacology","volume":"166 ","pages":"Article 115538"},"PeriodicalIF":4.7000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Therapeutic potential of polysaccharides in inflammation: current insights and future directions\",\"authors\":\"Thananjeyan Balasubramaniyam , Hye-Bin Ahn , Juhee Lim , Abhishikta Basu , Jacek Z. Kubiak , Shailima Rampogu , Vinod Kumar Nathan\",\"doi\":\"10.1016/j.intimp.2025.115538\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Polysaccharides from plants, microorganisms, algae, and animals exhibit significant anti-inflammatory potential, offering safe and effective therapeutic options for diseases like inflammatory bowel disease and arthritis. This review synthesizes their sources, structural modifications, and mechanisms, including modulation of NF-κB and MAPK pathways. In vitro models (e.g., RAW264.7 macrophages, THP-1 cells) demonstrate reductions in pro-inflammatory cytokines (e.g., TNF-α and IL-1β by 30–40 % at doses of 50–200 μg/mL), while in vivo models (e.g., DSS-induced colitis, collagen-induced arthritis) show decreased Disease Activity Index and improved histopathological outcomes at doses of 50–200 mg/kg. Chemical modifications, such as sulfation, enhance bioactivity, though challenges like bioavailability, inconsistent methodologies, and variable dosing persist. A comprehensive Table 3 summarizes sources, compounds, models, doses, and effects, while critical evaluations highlight methodological limitations and propose standardized assays (e.g., ELISA, qPCR). Future directions include nanotechnology for improved delivery, bioinformatics for structural optimization, and randomized clinical trials to validate preclinical findings, paving the way for novel polysaccharide-based therapies.</div></div>\",\"PeriodicalId\":13859,\"journal\":{\"name\":\"International immunopharmacology\",\"volume\":\"166 \",\"pages\":\"Article 115538\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International immunopharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1567576925015292\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International immunopharmacology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567576925015292","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Therapeutic potential of polysaccharides in inflammation: current insights and future directions
Polysaccharides from plants, microorganisms, algae, and animals exhibit significant anti-inflammatory potential, offering safe and effective therapeutic options for diseases like inflammatory bowel disease and arthritis. This review synthesizes their sources, structural modifications, and mechanisms, including modulation of NF-κB and MAPK pathways. In vitro models (e.g., RAW264.7 macrophages, THP-1 cells) demonstrate reductions in pro-inflammatory cytokines (e.g., TNF-α and IL-1β by 30–40 % at doses of 50–200 μg/mL), while in vivo models (e.g., DSS-induced colitis, collagen-induced arthritis) show decreased Disease Activity Index and improved histopathological outcomes at doses of 50–200 mg/kg. Chemical modifications, such as sulfation, enhance bioactivity, though challenges like bioavailability, inconsistent methodologies, and variable dosing persist. A comprehensive Table 3 summarizes sources, compounds, models, doses, and effects, while critical evaluations highlight methodological limitations and propose standardized assays (e.g., ELISA, qPCR). Future directions include nanotechnology for improved delivery, bioinformatics for structural optimization, and randomized clinical trials to validate preclinical findings, paving the way for novel polysaccharide-based therapies.
期刊介绍:
International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome.
The subject material appropriate for submission includes:
• Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders.
• Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state.
• Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses.
• Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action.
• Agents that activate genes or modify transcription and translation within the immune response.
• Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active.
• Production, function and regulation of cytokines and their receptors.
• Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.