Granulocytes: New Members of the Antigen-Presenting Cell Family

被引:115
作者
Lin, Ang [1 ,2 ]
Lore, Karin [1 ,2 ]
机构
[1] Karolinska Inst, Immunol & Allergy Unit, Dept Med Solna, Solna, Sweden
[2] Karolinska Inst, Ctr Mol Med, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
antigen presentation; MHC; neutrophil; eosinophil; basophil; MHC CLASS-II; COLONY-STIMULATING FACTOR; COMPLEX CLASS-II; POLYMORPHONUCLEAR NEUTROPHILS; T-CELLS; HLA-DR; AIRWAY EOSINOPHILS; MOUSE NEUTROPHILS; DENDRITIC CELLS; LYMPH-NODES;
D O I
10.3389/fimmu.2017.01781
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Granulocytes, the most abundant types of leukocytes, are the first line of defense against pathogen invasion. However, the plasticity and diversity of granulocytes have been increasingly revealed, especially with regard to their versatile functions in orchestrating adaptive immune responses. A substantial body of recent evidence demonstrates that granulocytes can acquire the function as antigen-presenting cells under pathological or inflammatory conditions. In addition, they can acquire surface expression of MHC class II and costimulatory molecules as well as T cell stimulatory behavior when cultured with selected cytokines. The classic view of granulocytes as terminally differentiated, short-lived phagocytes is therefore changing to phenotypically and functionally heterogeneous cells that are engaged in cross-talk with other leukocyte populations and provide an additional link between innate and adaptive immunity. In this brief review, we summarize the current knowledge on the antigen-presenting capacity of granulocyte subsets (neutrophils, eosinophils, and basophils). Underlying mechanisms, relevant physiological significance and potential controversies are also discussed.
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页数:8
相关论文
共 73 条
[1]   Neutrophils rapidly migrate via lymphatics after Mycobacterium bovis BCG intradermal vaccination and shuttle live bacilli to the draining lymph nodes [J].
Abadie, V ;
Badell, E ;
Douillard, P ;
Ensergueix, D ;
Leenen, PJM ;
Tanguy, M ;
Fiette, L ;
Saeland, S ;
Gicquel, B ;
Winter, N .
BLOOD, 2005, 106 (05) :1843-1850
[2]   Mouse neutrophils are professional antigen-presenting cells programmed to instruct Th1 and Th17 T-cell differentiation [J].
Abdallah, Delbert S. Abi ;
Egan, Charlotte E. ;
Butcher, Barbara A. ;
Denkers, Eric Y. .
INTERNATIONAL IMMUNOLOGY, 2011, 23 (05) :317-326
[3]   Neutrophils efficiently cross-prime naive T cells in vivo [J].
Beauvillain, Celine ;
Delneste, Yves ;
Scotet, Mari ;
Peres, Audrey ;
Gascan, Hugues ;
Guermonprez, Pierre ;
Barnaba, Vincenzo ;
Jeannin, Pascale .
BLOOD, 2007, 110 (08) :2965-2973
[4]   Qualitative differences between naive and memory T cells [J].
Berard, M ;
Tough, DF .
IMMUNOLOGY, 2002, 106 (02) :127-138
[5]   HUMAN-MEMORY T-CELLS EXPRESS INTERCELLULAR-ADHESION MOLECULE-1 WHICH CAN BE INCREASED BY INTERLEUKIN-2 AND INTERFERON-GAMMA [J].
BUCKLE, AM ;
HOGG, N .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (02) :337-341
[6]   Basophils and the T helper 2 environment can promote the development of lupus nephritis [J].
Charles, Nicolas ;
Hardwick, Donna ;
Daugas, Eric ;
Illei, Gabor G. ;
Rivera, Juan .
NATURE MEDICINE, 2010, 16 (06) :701-U107
[7]   Synovial fluid neutrophils transcribe and express class II major histocompatibility complex molecules in rheumatoid arthritis [J].
Cross, A ;
Bucknall, RC ;
Cassatella, MA ;
Edwards, SW ;
Moots, RJ .
ARTHRITIS AND RHEUMATISM, 2003, 48 (10) :2796-2806
[8]   Microbe-Specific Unconventional T Cells Induce Human Neutrophil Differentiation into Antigen Cross-Presenting Cells [J].
Davey, Martin S. ;
Morgan, Matt P. ;
Liuzzi, Anna Rita ;
Tyler, Christopher J. ;
Khan, Mohd Wajid A. ;
Szakmany, Tamas ;
Hall, Judith E. ;
Moser, Bernhard ;
Eberl, Matthias .
JOURNAL OF IMMUNOLOGY, 2014, 193 (07) :3704-3716
[9]  
DELPOZO V, 1992, EUR J IMMUNOL, V22, P1919
[10]   Granulocyte macrophage colony-stimulating factor signaling and proteasome inhibition delay neutrophil apoptosis by increasing the stability of Mcl-1 [J].
Derouet, M ;
Thomas, L ;
Cross, A ;
Moots, RJ ;
Edwards, SW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (26) :26915-26921