Release of LL-37 by activated human Vγ9Vδ2 T cells:: A microbicidal weapon against Brucella suis

被引:41
作者
Dudal, Sherri [1 ]
Turriere, Chrystell [1 ]
Bessoles, Stephanie [1 ]
Fontes, Pascaline [1 ]
Sanchez, Francoise [1 ]
Liautard, Janny [1 ]
Liautard, Jean-Pierre [1 ]
Lafont, Virginie [1 ]
机构
[1] Univ Montpellier 2, Inst Natl Sante & Rech Med, Unite 431, F-34095 Montpellier 05, France
关键词
D O I
10.4049/jimmunol.177.8.5533
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human V gamma 9V delta 2 T cells play a crucial role in early immune response to intracellular pathogens. Moreover, in brucellosis, these cells are drastically increased in the peripheral blood of patients during the acute phase of infection. In vitro, V gamma 9V delta 2 T cells are capable of inhibiting Brucella growth and development through a combination of mechanisms: 1) cytotoxicity, 2) macrophage activation and bactericidal activity through cytokine and chemokine secretion, and 3) antibacterial effects. We previously described that antibacterial factors were found in supernatants from activated V gamma 9V delta 2 T cells. In this study, we show that V gamma 9V delta 2 T cells express the human cathelicidin hCAP18 and its mature form, known as LL-37, is released upon activation of V gamma 9V delta 2 T cells. We also show that LL-37 has an antibacterial effect on Brucella suis. Overall, our results demonstrate that LL-37 is a soluble factor responsible for a part of the bactericidal activity of V gamma 9V delta 2 T cells.
引用
收藏
页码:5533 / 5539
页数:7
相关论文
共 39 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]   An innate view of gamma delta T cells [J].
Boismenu, R ;
Havran, WL .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :57-63
[3]   Immunomodulatory activities of small host defense peptides [J].
Bowdish, DME ;
Davidson, DJ ;
Scott, MG ;
Hancock, REW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (05) :1727-1732
[4]   Impact of LL-37 on anti-infective immunity [J].
Bowdish, DME ;
Davidson, DJ ;
Lau, YE ;
Lee, K ;
Scott, MG ;
Hancock, REW .
JOURNAL OF LEUKOCYTE BIOLOGY, 2005, 77 (04) :451-459
[5]   Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria? [J].
Brogden, KA .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (03) :238-250
[6]   Vγ2Vδ2+ T cells and anti-microbial immune responses [J].
Chen, ZW ;
Letvin, NL .
MICROBES AND INFECTION, 2003, 5 (06) :491-498
[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]  
DETEJADA GM, 1995, INFECT IMMUN, V63, P3054
[9]  
Dieli F, 2000, EUR J IMMUNOL, V30, P1512, DOI 10.1002/(SICI)1521-4141(200005)30:5<1512::AID-IMMU1512>3.0.CO
[10]  
2-3