Antimicrobial peptides as therapeutic agents: opportunities and challenges

被引:335
作者
Mahlapuu, Margit [1 ]
Bjorn, Camilla [2 ]
Ekblom, Jonas [1 ]
机构
[1] Promore Pharma AB, Karolinska Inst Sci Pk,Fogdevreten 2, SE-17165 Solna, Sweden
[2] RISE Res Inst Sweden, Boras, Sweden
关键词
AMP; antimicrobial peptide; anti-infectives; antibiotic resistance; therapeutic agents; HOST-DEFENSE PEPTIDES; MEMBRANE INTERACTIONS; ADHESION FORMATION; POLYMYXIN-B; LACTOFERRIN; MECHANISMS; LL-37; PATHOGENS; IMMUNITY; CARRIERS;
D O I
10.1080/07388551.2020.1796576
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The rapid development of microbial resistance to conventional antibiotics has accelerated efforts to find anti-infectives with a novel mode-of-action, which are less prone to bacterial resistance. Intense nonclinical and clinical research is today ongoing to evaluate antimicrobial peptides (AMPs) as potential next-generation antibiotics. Currently, multiple AMPs are assessed in late-stage clinical trials, not only as novel anti-infective drugs, but also as innovative product candidates for immunomodulation, promotion of wound healing, and prevention of post-operative scars. The efforts to translate AMP-based research findings into pharmaceutical product candidates are expected to accelerate in coming years due to technological advancements in multiple areas, including an improved understanding of the mechanism-of-action of AMPs, smart formulation strategies, and advanced chemical synthesis protocols. At the same time, it is recognized that cytotoxicity, low metabolic stability due to sensitivity to proteolytic degradation, and limited oral bioavailability are some of the key weaknesses of AMPs. Furthermore, the pricing and reimbursement environment for new antimicrobial products remains as a major barrier to the commercialization of AMPs.
引用
收藏
页码:978 / 992
页数:15
相关论文
共 131 条
[1]   Vitamin D and antimicrobial peptide levels in patients with atopic dermatitis and atopic dermatitis complicated by eczema herpeticum: A pilot study [J].
Albenali, Lujain H. ;
Danby, Simon ;
Moustafa, Manar ;
Brown, Kirsty ;
Chittock, John ;
Shackley, Fiona ;
Cork, Michael J. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 138 (06) :1715-+
[2]   Mechanisms and consequences of bacterial resistance to antimicrobial peptides [J].
Andersson, D. I. ;
Hughes, D. ;
Kubicek-Sutherland, J. Z. .
DRUG RESISTANCE UPDATES, 2016, 26 :43-57
[3]   Cyclization Improves Membrane Permeation by Antimicrobial Peptoids [J].
Andreev, Konstantin ;
Martynowycz, Michael W. ;
Ivankin, Andrey ;
Huang, Mia L. ;
Kuzmenko, Ivan ;
Meron, Mati ;
Lin, Binhua ;
Kirshenbaum, Kent ;
Gidalevitz, David .
LANGMUIR, 2016, 32 (48) :12905-12913
[4]  
[Anonymous], 2006, GUID IND CHRON CUT U
[5]   Antimicrobial Peptides [J].
Bahar, Ali Adem ;
Ren, Dacheng .
PHARMACEUTICALS, 2013, 6 (12) :1543-1575
[6]   Advances in Fmoc solid-phase peptide synthesis [J].
Behrendt, Raymond ;
White, Peter ;
Offer, John .
JOURNAL OF PEPTIDE SCIENCE, 2016, 22 (01) :4-27
[7]   Anti-infective efficacy of the lactoferrin-derived antimicrobial peptide HLR1r [J].
Bjorn, Camilla ;
Mahlapuu, Margit ;
Mattsby-Baltzer, Inger ;
Hakansson, Joakim .
PEPTIDES, 2016, 81 :21-28
[8]   Cubosomes post-loaded with antimicrobial peptides: characterization, bactericidal effect and proteolytic stability [J].
Boge, Lukas ;
Umerska, Anita ;
Matougui, Nada ;
Bysell, Helena ;
Ringstad, Lovisa ;
Davoudi, Mina ;
Eriksson, Jonny ;
Edwards, Katarina ;
Andersson, Martin .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 526 (1-2) :400-412
[9]   Membrane interactions of mesoporous silica nanoparticles as carriers of antimicrobial peptides [J].
Braun, Katharina ;
Pochert, Alexander ;
Linden, Mika ;
Davoudi, Mina ;
Schmidtchen, Artur ;
Nordstrom, Randi ;
Malmsten, Martin .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2016, 475 :161-170
[10]   Antiviral Activities of Human Host Defense Peptides [J].
Brice, David C. ;
Diamond, Gill .
CURRENT MEDICINAL CHEMISTRY, 2020, 27 (09) :1420-1443