Repurposing Miltefosine for the Treatment of Immune-Mediated Disease?

被引:8
作者
Verhaar, Auke P. [1 ,2 ]
Wildenberg, Manon E. [1 ]
Peppelenbosch, Maikel P. [3 ]
Hommes, Daniel W. [2 ,4 ]
van den Brink, Gijs R. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Tytgat Inst Liver & Intestinal Res, Dept Gastroenterol & Hepatol, NL-1105 AZ Amsterdam, Netherlands
[2] Leiden Univ, Dept Gastroenterol & Hepatol, Med Ctr, Leiden, Netherlands
[3] Erasmus Univ, Dept Gastroenterol & Hepatol, Med Ctr, Rotterdam, Netherlands
[4] Univ Calif Los Angeles, Ctr Inflammatory Bowel Dis, Los Angeles, CA USA
关键词
INDIAN VISCERAL LEISHMANIASIS; INFLAMMATORY-BOWEL-DISEASE; RAFT MODULATOR MILTEFOSINE; AZAR DERMAL LEISHMANIASIS; TUMOR-NECROSIS-FACTOR; MAST-CELL ACTIVATION; ORAL MILTEFOSINE; PHASE-II; DOUBLE-BLIND; LIPID RAFTS;
D O I
10.1124/jpet.113.212654
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Miltefosine is an ether lipid that was initially developed for cancer treatment in the early 1980s. Miltefosine largely failed development for oncology, although it was approved for the topical treatment of breast cancer metastasis. It was subsequently discovered that miltefosine is a highly effective treatment of visceral Leishmaniasis, a parasitic disease that affects millions worldwide and causes an estimated 30,000 fatalities each year. Oral treatment with miltefosine is generally well tolerated and has relatively few adverse effects. The exact mechanism of action of miltefosine treatment is still under investigation. Its close resemblance to phospholipids allows it to be quickly taken up by cell membranes and affect related processes, such as lipid metabolism and signaling through lipid rafts. These processes play an important role in the immune response and it comes as no surprise that miltefosine has been successfully tested for the treatment of a number of immune-mediated diseases in preclinical models of disease. Drug repurposing of miltefosine for immune-mediated diseases may provide an opportunity to expand the limited number of drugs that are currently available for therapeutic use.
引用
收藏
页码:189 / 195
页数:7
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