Differentiation stage determines pathologic and protective allergen-specific CD4+ T-cell outcomes during specific immunotherapy

被引:121
|
作者
Wambre, Erik [1 ]
DeLong, Jonathan H. [1 ]
James, Eddie A. [1 ]
LaFond, Rebecca E. [1 ]
Robinson, David [2 ]
Kwok, William W. [1 ,3 ]
机构
[1] Univ Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
[2] Univ Washington, Virginia Mason Med Ctr, Seattle, WA 98101 USA
[3] Univ Washington, Dept Immunol, Seattle, WA 98101 USA
基金
美国国家卫生研究院;
关键词
Immunotherapy; allergy; pollen; T cells; CD4; peptide-MHC class II tetramer; peripheral tolerance; differentiation stage; ex vivo; RESPONSES; EXPRESSION; INDIVIDUALS; MECHANISMS; INDUCTION; EFFECTOR; PROGRAMS; CD8;
D O I
10.1016/j.jaci.2011.08.034
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The main obstacle to elucidating the role of CD4(+) T cells in allergen-specific immunotherapy (SIT) has been the absence of an adequately sensitive approach to directly characterize rare allergen-specific T cells without introducing substantial phenotypic modifications by means of in vitro amplification. Objective: We sought to monitor, in physiological conditions, the allergen-specific CD4(+) T cells generated during natural pollen exposure and during allergy vaccination. Methods: Alder pollen allergy was used as a model for studying seasonal allergies. Allergen-specific CD4(+) T cells were tracked and characterized in 12 subjects with alder pollen allergy, 6 nonallergic subjects, and 9 allergy vaccine-treated subjects by using peptide-MHC class II tetramers. Results: Allergen-specific CD4(+) T cells were detected in all of the subjects with alder pollen allergy and nonallergic subjects tested. Pathogenic responses-chemoattractant receptor homologous molecule expressed on TH- lymphocytes (CRTH2) expression and T(H)2 cytokine production- are specifically associated with terminally differentiated (CD27(-)) allergen-specific CD4(+) T cells, which dominate in allergic subjects but are absent in nonallergic subjects. In contrast, CD27(+) allergen-specific CD4(+) T cells are present at low frequencies in both allergic and nonallergic subjects and reflect classical features of the protective immune response with high expression of IL-10 and IFN-gamma. Restoration of a protective response during SIT appears to be due to the preferential deletion of pathogenic (CD27(-)) allergen-specific CD4(+) T cells accompanied by IL-10 induction in surviving CD27(+) allergen-specific CD4(+) T cells. Conclusions: Differentiation stage divides allergen-specific CD4(+) T cells into 2 distinct subpopulations with unique functional properties and different fates during SIT. (J Allergy Clin Immunol 2012;129:544-51.)
引用
收藏
页码:544 / U411
页数:15
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