TY - JOUR
T1 - Emerging pharmacotherapy for inflammatory bowel diseases
AU - Luo, Hua
AU - Cao, Guiqing
AU - Luo, Chun
AU - Tan, Dechao
AU - Vong, Chi Teng
AU - Xu, Yinyue
AU - Wang, Sicen
AU - Lu, Haitao
AU - Wang, Yitao
AU - Jing, Wanghui
N1 - Funding Information:
This work was funded by the Science and Technology Development Fund of Macau (FDCT/007/2020/ALC), the Research Fund of University of Macau (CPG2022-00005-ICMS), the National Natural Science Foundation of China (82174059), the Natural Science Foundation of Shaanxi Province (2022SF-123), Open fund of the State Key Laboratory of Quality Research in Chinese Medicine, University of Macau (SKL-QRCM (UM)-2020–2022, QRCM-OP21007), the National Key Research and Development Program of China (2017YFC1308600 and 2017YFC1308605), Natural Science Foundation of Shanghai Grant (21ZR1431600).
Publisher Copyright:
© 2022 Elsevier Ltd. All rights reserved.
PY - 2022/4
Y1 - 2022/4
N2 - Inflammatory bowel disease (IBD) refers to a gamut of disorders that are characterized by chronic intestinal inflammation, including ulcerative colitis (UC) and Crohn's disease (CD), which often leads to mucosal ulceration and progressive loss of intestinal function. The etiopathogenesis of IBD has not been completely clarified, although multiple factors involving genetic modifications, host immune dysfunction, intestinal dysbiosis and environmental effects have been implicated. Currently, pharmacotherapies including both non-targeted and targeted biological agents are widely used for the clinical treatment of IBD. In addition, novel therapeutic approaches that target the intestinal microorganisms, such as fecal microbiota transplantation, antibiotics, probiotics and microbial metabolite inhibitors, are also under development. However, these treatments are either accompanied by side effects or cannot achieve complete clinical remission when used alone. The efficacy and safety of drugs are currently a clinical challenge. Thus, advanced drug delivery systems are needed for targeted delivery of drugs to the inflammatory sites and avoid absorption by healthy tissues. In this review, we have summarized the latest research on the pathogenesis of IBD and the emerging pharmacotherapies, and discussed potential therapeutic targets for innovative therapies.
AB - Inflammatory bowel disease (IBD) refers to a gamut of disorders that are characterized by chronic intestinal inflammation, including ulcerative colitis (UC) and Crohn's disease (CD), which often leads to mucosal ulceration and progressive loss of intestinal function. The etiopathogenesis of IBD has not been completely clarified, although multiple factors involving genetic modifications, host immune dysfunction, intestinal dysbiosis and environmental effects have been implicated. Currently, pharmacotherapies including both non-targeted and targeted biological agents are widely used for the clinical treatment of IBD. In addition, novel therapeutic approaches that target the intestinal microorganisms, such as fecal microbiota transplantation, antibiotics, probiotics and microbial metabolite inhibitors, are also under development. However, these treatments are either accompanied by side effects or cannot achieve complete clinical remission when used alone. The efficacy and safety of drugs are currently a clinical challenge. Thus, advanced drug delivery systems are needed for targeted delivery of drugs to the inflammatory sites and avoid absorption by healthy tissues. In this review, we have summarized the latest research on the pathogenesis of IBD and the emerging pharmacotherapies, and discussed potential therapeutic targets for innovative therapies.
KW - Emerging pharmacotherapy
KW - IBD
KW - Molecular pathogenesis
KW - Therapeutic targets
UR - http://www.scopus.com/inward/record.url?scp=85125547030&partnerID=8YFLogxK
U2 - 10.1016/j.phrs.2022.106146
DO - 10.1016/j.phrs.2022.106146
M3 - Review article
C2 - 35227890
SN - 1043-6618
VL - 178
JO - Pharmacological Research
JF - Pharmacological Research
M1 - 106146
ER -