Abstract
The use of parasites or their products for treating chronic inflammation associated diseases (CIADs) has generated significant attention recently. Findings from basic and clinical research have provided valuable information on strengthening the notion that parasites’ molecules can be developed as biotherapeutic agents. Completion of the genome, secreotome, and proteome of the parasites has provided an excellent platform for screening and identifying several host immunomodulatory molecules from the parasites and evaluate their therapeutic potential for CIADs. One of the widely studied host immunomodulatory molecules of the parasites is the cysteine protease inhibitor (cystatin), which is primarily secreted by the parasites to evade host immune responses. In this review, we have attempted to summarize the findings to date on the use of helminth parasite-derived cystatin as a therapeutic agent against CIADs. Although several studies suggest a role for alternatively activated macrophages, other regulatory cells, and immunosuppressive molecules, in this immunoregulatory activity of the parasite-derived cystatin, there is still no clear demonstration as to how cystatin induces its anti-inflammatory effect in suppressing CIADs.
Funder
National Institute of Allergy and Infectious Diseases
Subject
Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy
Reference110 articles.
1. The World Incidence and Prevalence of Autoimmune Diseases is Increasing
2. Potential treatment of inflammatory bowel disease: A review of helminths therapy;Taghipour;Gastroenterol. Hepatol. Bed Bench,2014
3. Brugia malayi abundant larval transcript 2 protein treatment attenuates experimentally-induced colitis in mice;Khatri;Indian J. Exp. Biol.,2015
4. Helminth Regulation of Immunity
5. The tropics, helminth infections and hygiene hypotheses
Cited by
21 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献