Hypochlorous Acid: A Natural Adjuvant That Facilitates Antigen Processing, Cross-Priming, and the Induction of Adaptive Immunity

被引:298
作者
Prokopowicz, Zofia M. [1 ]
Arce, Frederick [1 ]
Biedron, Rafal [2 ]
Chiang, Cheryl L. -L. [1 ]
Ciszek, Marta [2 ]
Katz, David R. [1 ]
Nowakowska, Maria [3 ]
Zapotoczny, Szczepan [2 ]
Marcinkiewicz, Janusz [2 ]
Chain, Benjamin M. [1 ]
机构
[1] UCL, Div Infect & Immun, London W1T 4JP, England
[2] Jagiellonian Univ, Coll Med, Dept Immunol, Krakow, Poland
[3] Jagiellonian Univ, Fac Chem, Dept Phys Chem & Electrochem, PL-30060 Krakow, Poland
基金
英国生物技术与生命科学研究理事会;
关键词
LOW-DENSITY-LIPOPROTEIN; MEDIATED PROTEIN OXIDATION; NECROSIS-FACTOR-ALPHA; DENDRITIC CELLS; T-CELLS; ENHANCES IMMUNOGENICITY; METHIONINE SULFOXIDE; IN-VIVO; MYELOPEROXIDASE; FRAGMENTATION;
D O I
10.4049/jimmunol.0902606
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 production of hypochlorous acid (HOCl) is a characteristic of granulocyte activation, a hallmark of the early phase of innate immune responses. In this study, we show that, in addition to Its Well-established role as a microbicide, HOCl can act as a natural adjuvant of adaptive immunity. HOCl enhances the T cell responses to the model Ag OVA, facilitating the processing and presentation of this protein via the class H MHC pathway. HOCl modification also enhances cross-presentation of the tumor Ag tyrosinase-related protein 2 via class I MHC. The adjuvant effects of HOCl are independent of TLR signaling. The enhanced presentation of HOCl-modified OVA is mediated via modification of the N-linked carbohydrate side chain rather than formation of protein aldehydes or chloramines. HOCl-modified OVA is taken up more efficiently by APCs and is degraded more efficiently by proteinases. Atomic force microscopy demonstrated that enhanced uptake is mediated via specific receptor binding, one candidate for which is the scavenger receptor lectin-like oxidized low-density lipoprotein receptor, which shows enhanced binding to chlorinated OVA. A function of HOCl is therefore to target glycoprotein Ags to scavenger receptors on the APC surface. This additional mechanism linking innate and adaptive immunity suggests novel strategies to enhance immunity to vaccines. The Journal of Immunology, 2010, 184: 824-835.
引用
收藏
页码:824 / 835
页数:12
相关论文
共 49 条
[1]   Effects of oxidised low density lipoprotein on dendritic cells: a possible immunoregulatory component of the atherogenic micro-environment? [J].
Alderman, CJJ ;
Bunyard, PR ;
Chain, BM ;
Foreman, JC ;
Leake, DS ;
Katz, DR .
CARDIOVASCULAR RESEARCH, 2002, 55 (04) :806-819
[2]  
Allison MED, 2000, EUR J IMMUNOL, V30, P2881, DOI 10.1002/1521-4141(200010)30:10<2881::AID-IMMU2881>3.0.CO
[3]  
2-9
[4]  
BAMDEN MJ, 1998, IMMUNOL CELL BIOL, V76, P34
[5]   Toll-dependent selection of microbial antigens for presentation by dendritic cells [J].
Blander, JM ;
Medzhitov, R .
NATURE, 2006, 440 (7085) :808-812
[6]   Efficient targeting of protein antigen to the dendritic cell receptor DEC-205 in the steady state leads to antigen presentation on major histocompatibility complex class I products and peripheral CD8+ T cell tolerance [J].
Bonifaz, L ;
Bonnyay, D ;
Mahnke, K ;
Rivera, M ;
Nussenzweig, MC ;
Steinman, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (12) :1627-1638
[7]   The expression and function of cathepsin E in dendritic cells [J].
Chain, BM ;
Free, P ;
Medd, P ;
Swetman, C ;
Tabor, AB ;
Terrazzini, N .
JOURNAL OF IMMUNOLOGY, 2005, 174 (04) :1791-1800
[8]   Chlorination of bacterial and neutrophil proteins during phagocytosis and killing of Staphylococcus aureus [J].
Chapman, ALP ;
Hampton, MB ;
Senthilmohan, R ;
Winterbourn, CC ;
Kettle, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (12) :9757-9762
[9]  
CHESNUT RW, 1981, J IMMUNOL, V126, P1075
[10]   Oxidation of ovarian epithelial cancer cells by hypochlorous acid enhances immunogenicity and stimulates T cells that recognize autologous primary tumor [J].
Chiang, Cheryl L-L. ;
Ledermann, Jonathan A. ;
Aitkens, Egla ;
Benjamin, Elizabeth ;
Katz, David R. ;
Chain, Benjamin M. .
CLINICAL CANCER RESEARCH, 2008, 14 (15) :4898-4907