CD8+ T cells in asthma: Friend or foe?

被引:42
作者
Betts, Richard J.
Kemeny, D. Michael [1 ]
机构
[1] Natl Univ Singapore, Program Immunol, Ctr Life Sci, Singapore 119074, Singapore
关键词
Allergy; Asthma; T lymphocyte; CD8 T cell; CD4 T cell; IgE; ALLERGIC AIRWAY RESPONSES; BROWN-NORWAY RATS; HOMOCYTOTROPIC ANTIBODY FORMATION; OBSTRUCTIVE PULMONARY-DISEASE; SYNCYTIAL VIRUS-INFECTION; SOLUBLE-PROTEIN ANTIGENS; PERIPHERAL-BLOOD CD4(+); INHIBIT IGE RESPONSES; GAMMA-DELTA RECEPTOR; INTERFERON-GAMMA;
D O I
10.1016/j.pharmthera.2008.09.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
While it is well established that CD4(+) T lymphocytes play a crucial role in the initiation, progression and persistence of asthma, the role of CD8(+) T cells is less understood. CD8(+) T cells form functionally similar subsets which exhibit similar cytokine profiles as Th1 and Th2 cells, known as Tc1 and Tc2. Evidence from animal studies suggest that CD8(+) T cells are capable of regulating IgE production through the induction of IL-12 and IL-18 production in dendritic cells, and that CD8(+) T cells may act to moderate Th2 polarisation within the localised lymph nodes during allergic sensitisation. Such findings have led to the suggestion that Th1 polarising, CD8(+) T cell-inducing vaccines would inhibit the development of airway hyperresponsiveness (AHR) and Th2 cell infiltration. Despite these positive findings, the role of CD8(+) T cells within the lung remains poorly understood. While CD8(+) T cells, particularly those expressing the Tc1 phenotype, are capable of moderating inflammation and suppressing AHR, it has been postulated that Tc2 CD8(+) T cells predominate within established asthma and may act to amplify the inappropriate immune response which defines the condition. Within the clinic, the association between CD8(+) T cells and asthma is almost universally defined as injurious, further suggesting a prejudicial role for these cells within the established disease. CD8(+) T cells may be a valuable potential target for therapeutic intervention, either by potentiating their regulatory effects prior to the development of sensitisation, or through suppressing their pro-inflammatory properties within established atopy. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:123 / 131
页数:9
相关论文
共 123 条
[91]   Preferential expression of very late antigen-4 on type 1 CTL cells plays a critical role in trafficking into central nervous system tumors [J].
Sasaki, Kotaro ;
Zhu, Xinmei ;
Vasquez, Cecilia ;
Nishimura, Fumihiko ;
Dusak, Jill E. ;
Huang, Jian ;
Fujita, Mitsugn ;
Wesa, Amy ;
Potter, Douglas M. ;
Walker, Paul R. ;
Storkus, Walter J. ;
Okada, Hideho .
CANCER RESEARCH, 2007, 67 (13) :6451-6458
[92]   Tc2 cells respond to soluble antigen in the respiratory tract and induce lung eosinophilia and bronchial hyperresponsiveness [J].
Sawicka, E ;
Noble, A ;
Walker, C ;
Kemeny, DM .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (09) :2599-2608
[93]   CD8+ T cell contributions to allergen induced pulmonary inflammation and airway hyperreactivity [J].
Schaller, MA ;
Lundy, SK ;
Huffnagle, GB ;
Lukacs, NW .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (07) :2061-2070
[94]  
Schwarze J, 1999, J IMMUNOL, V163, P5729
[95]   Respiratory syncytial virus infection results in airway hyperresponsiveness and enhanced airway sensitization to allergen [J].
Schwarze, J ;
Hamelmann, E ;
Bradley, KL ;
Takeda, K ;
Gelfand, EW .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (01) :226-233
[96]  
SEDER RA, 1992, J IMMUNOL, V148, P1652
[97]   SUPPRESSION OF IGE RESPONSES IN INBRED RATS BY REPEATED RESPIRATORY-TRACT EXPOSURE TO ANTIGEN - RESPONDER PHENOTYPE INFLUENCES ISOTYPE SPECIFICITY OF INDUCED TOLERANCE [J].
SEDGWICK, JD ;
HOLT, PG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1984, 14 (10) :893-897
[98]   Correlation between peripheral blood T-cell profiles and airway inflammation in atopic asthma [J].
Shirai, Toshihiro ;
Inui, Naoki ;
Suda, Takafumi ;
Chida, Kingo .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 118 (03) :622-626
[99]   Revival of CD8+ Treg-mediated suppression [J].
Smith, Trevor R. F. ;
Kumar, Vipin .
TRENDS IN IMMUNOLOGY, 2008, 29 (07) :337-342
[100]   γδ T cells, allergen recognition and airway inflammation [J].
Spinozzi, F ;
Agea, E ;
Bistoni, O ;
Forenza, N ;
Bertotto, A .
IMMUNOLOGY TODAY, 1998, 19 (01) :22-26