The antimicrobial peptide LL-37 inhibits HIV-1 replication

被引:7
作者
Bergman, Peter
Walter-Jallow, Lilian
Broliden, Kristina
Agerberth, Birgitta
Soderlund, Johan
机构
[1] Karolinska Univ Hosp, Ctr Mol Med, Karolinska Inst, Dept Med, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, Stockholm, Sweden
[3] Karolinska Univ Hosp, Dept Med, Karolinska Inst, Ctr Infect Med, S-17177 Stockholm, Sweden
关键词
antimicrobial peptide; cathelicidin; innate immunity; HIV-1; LL-37; FPRL-1;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The antimicrobial peptide LL-37 is the only cathelicidin that has been described in humans. LL-37 exerts chemotactic, immunomodulatory and angiogenic effects; activities that are mediated through binding to the formyl peptide receptor like (FPRL)-1 receptor. Agonistic ligation of FPRL-1 can also induce down-regulation of HIV-1 chemokine receptors and reduce susceptibility to HIV-1 infection in vitro. Therefore, we have evaluated the capacity of LL-37 to inhibit HIV-1 infection in vitro. Here we demonstrate that LL-37 inhibits HIV-1 replication in PBMC, including primary CD4(+)T cells. This inhibition was readily reproduced using various HIV-1 isolates without detectable changes in the target cell expression of HIV-1 chemokine receptors. Accordingly, the HIV-1 inhibitory effect was shown to be independent of FPRL-1 signalling. Given the epithelial expression of LL-37, it may contribute to the local protection against HIV-1 infection.
引用
收藏
页码:410 / 415
页数:6
相关论文
共 32 条
[1]   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
[2]   RAPID DEVELOPMENT OF ISOLATE-SPECIFIC NEUTRALIZING ANTIBODIES AFTER PRIMARY HIV-1 INFECTION AND CONSEQUENT EMERGENCE OF VIRUS VARIANTS WHICH RESIST NEUTRALIZATION BY AUTOLOGOUS SERA [J].
ALBERT, J ;
ABRAHAMSSON, B ;
NAGY, K ;
AURELIUS, E ;
GAINES, H ;
NYSTROM, G ;
FENYO, EM .
AIDS, 1990, 4 (02) :107-112
[3]   Identification of peptides that antagonize formyl peptide receptor-like 1-mediated signaling [J].
Bae, YS ;
Lee, HY ;
Jo, EJ ;
Kim, JI ;
Kang, HK ;
Ye, RD ;
Kwak, JY ;
Ryu, SH .
JOURNAL OF IMMUNOLOGY, 2004, 173 (01) :607-614
[4]   The human cationic host defense peptide LL-37 mediates contrasting effects on apoptotic pathways in different primary cells of the innate immune system [J].
Barlow, Peter G. ;
Li, Yuexin ;
Wilkinson, Thomas S. ;
Bowdish, Dawn M. E. ;
Lau, Y. Elaine ;
Cosseau, Celine ;
Haslett, Christopher ;
Simpson, A. John ;
Hancock, Robert E. W. ;
Davidson, Donald J. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 80 (03) :509-520
[5]   Structure-function relationships among human cathelicidin peptides: Dissociation of antimicrobial properties from host immunostimulatory activities [J].
Braff, MH ;
Hawkins, MA ;
Di Nardo, A ;
Lopez-Garcia, B ;
Howell, MD ;
Wong, C ;
Lin, K ;
Streib, JE ;
Dorschner, R ;
Leung, DYM ;
Gallo, RL .
JOURNAL OF IMMUNOLOGY, 2005, 174 (07) :4271-4278
[6]   Dual role of α-defensin-1 in anti-HIV-1 innate immunity [J].
Chang, TL ;
Vargas, J ;
DelPortillo, A ;
Klotman, ME .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (03) :765-773
[7]   The cationic antimicrobial peptide LL-37 modulates dendritic cell differentiation and dendritic cell-induced T cell polarization [J].
Davidson, DJ ;
Currie, AJ ;
Reid, GSD ;
Bowdish, DME ;
MacDonald, KL ;
Ma, RC ;
Hancock, REW ;
Speert, DP .
JOURNAL OF IMMUNOLOGY, 2004, 172 (02) :1146-1156
[8]   A synthetic peptide derived from human immunodeficiency virus type 1 gp120 downregulates the expression and function of chemokine receptors CCR5 and CXCR4 in monocytes by activating the 7-transmembrane G-protein-coupled receptor FPRL1/LXA4R [J].
Deng, XY ;
Ueda, H ;
Su, SB ;
Gong, WH ;
Dunlop, NM ;
Gao, JL ;
Murphy, PM ;
Wang, JM .
BLOOD, 1999, 94 (04) :1165-1173
[9]   A novel P2X7 receptor activator, the human cathelicidin-derived peptide LL37, induces IL-1β processing and release [J].
Elssner, A ;
Duncan, M ;
Gavrilin, M ;
Wewers, MD .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4987-4994
[10]   Cutting edge:: Human β defensin 3 -: A novel antagonist of the HIV-1 coreceptor CXCR4 [J].
Feng, Zhimin ;
Dubyak, George R. ;
Lederman, Michael M. ;
Weinberg, Aaron .
JOURNAL OF IMMUNOLOGY, 2006, 177 (02) :782-786