Antiviral potential of cathelicidins

被引:72
作者
Barlow, Peter G. [1 ]
Findlay, Emily Gwyer [2 ]
Currie, Silke M. [2 ]
Davidson, Donald J. [2 ]
机构
[1] Edinburgh Napier Univ, Edinburgh EH11 4BN, Midlothian, Scotland
[2] Univ Edinburgh, MRC, Ctr Inflammat Res, Queens Med Res Inst, Edinburgh EH16 4TJ, Midlothian, Scotland
关键词
adenovirus; antimicrobial peptide; cationic host defense peptide; herpes simplex virus; HIV; influenza; innate immunity; respiratory syncytial virus; vaccinia virus; virus; ANTIMICROBIAL PEPTIDE LL-37; HOST-DEFENSE PEPTIDES; BRONCHIAL EPITHELIAL-CELLS; GRAM-NEGATIVE BACTERIA; HUMAN DENDRITIC CELLS; RECEPTOR-LIKE; ANTIBACTERIAL PEPTIDE; INNATE IMMUNITY; VITAMIN-D; IN-VITRO;
D O I
10.2217/fmb.13.135
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The global burden of morbidity and mortality arising from viral infections is high; however, the development of effective therapeutics has been slow. As our understanding of innate immunity has expanded over recent years, knowledge of natural host defenses against viral infections has started to offer potential for novel therapeutic strategies. An area of current research interest is in understanding the roles played by naturally occurring cationic host defense peptides, such as the cathelicidins, in these innate antiviral host defenses across different species. This research also has the potential to inform the design of novel synthetic antiviral peptide analogs and/or provide rationale for therapies aimed at boosting the natural production of these peptides. In this review, we will discuss our knowledge of the antiviral activities of cathelicidins, an important family of cationic host defense peptides, and consider the implications for novel antiviral therapeutic approaches.
引用
收藏
页码:55 / 73
页数:19
相关论文
共 194 条
[1]  
Achtman A.H., 2012, Sci. Transl. Med, V4, p135ra64
[2]   FALL-39, A PUTATIVE HUMAN PEPTIDE ANTIBIOTIC, IS CYSTEINE-FREE AND EXPRESSED IN BONE-MARROW AND TESTIS [J].
AGERBERTH, B ;
GUNNE, H ;
ODEBERG, J ;
KOGNER, P ;
BOMAN, HG ;
GUDMUNDSSON, GH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (01) :195-199
[3]   The human antimicrobial and chemotactic peptides LL-37 and α-defensins are expressed by specific lymphocyte and monocyte populations [J].
Agerberth, B ;
Charo, J ;
Werr, J ;
Olsson, B ;
Idali, F ;
Lindbom, L ;
Kiessling, R ;
Jörnvall, H ;
Wigzell, H ;
Gudmundsson, GH .
BLOOD, 2000, 96 (09) :3086-3093
[4]   AMINO-ACID-SEQUENCE OF PR-39 - ISOLATION FROM PIG INTESTINE OF A NEW MEMBER OF THE FAMILY OF PROLINE-ARGININE-RICH ANTIBACTERIAL PEPTIDES [J].
AGERBERTH, B ;
LEE, JY ;
BERGMAN, T ;
CARLQUIST, M ;
BOMAN, HG ;
MUTT, V ;
JORNVALL, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 202 (03) :849-854
[5]   The antimicrobial peptide LL-37 modulates the inflammatory and host defense response of human neutrophils [J].
Alalwani, Sadek M. ;
Sierigk, Johannes ;
Herr, Christian ;
Pinkenburg, Olaf ;
Gallo, Richard ;
Vogelmeier, Claus ;
Bals, Robert .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2010, 40 (04) :1118-1126
[6]   LL-37 enhances adaptive antitumor immune response in a murine model when genetically fused with M-CSFRJ6-1 DNA vaccine [J].
An, LL ;
Yang, YH ;
Ma, XT ;
Lin, YM ;
Li, G ;
Song, YH ;
Wu, KF .
LEUKEMIA RESEARCH, 2005, 29 (05) :535-543
[7]  
[Anonymous], 2011, PLoS One, DOI 10.1371/
[8]  
Arts E. J., 2012, COLD SPRING HARB PER, V2
[9]   CDNA SEQUENCES OF 3 SHEEP MYELOID CATHELICIDINS [J].
BAGELLA, L ;
SCOCCHI, M ;
ZANETTI, M .
FEBS LETTERS, 1995, 376 (03) :225-228
[10]   Rhesus monkey (Macaca mulatta) mucosal antimicrobial peptides are close homologues of human molecules [J].
Bals, R ;
Lang, C ;
Weiner, DJ ;
Vogelmeier, C ;
Welsch, U ;
Wilson, JM .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (02) :370-375