Differentiation stage determines pathologic and protective allergen-specific CD4+ T-cell outcomes during specific immunotherapy
被引:121
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作者:
Wambre, Erik
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Univ Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USAUniv Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
Wambre, Erik
[1
]
DeLong, Jonathan H.
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Univ Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USAUniv Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
DeLong, Jonathan H.
[1
]
James, Eddie A.
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Univ Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USAUniv Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
James, Eddie A.
[1
]
LaFond, Rebecca E.
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Univ Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USAUniv Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
LaFond, Rebecca E.
[1
]
Robinson, David
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Univ Washington, Virginia Mason Med Ctr, Seattle, WA 98101 USAUniv Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
Robinson, David
[2
]
Kwok, William W.
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Univ Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
Univ Washington, Dept Immunol, Seattle, WA 98101 USAUniv Washington, Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
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
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.)
机构:
TVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, AustraliaTVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, Australia
Prescott, SL
Macaubas, C
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TVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, AustraliaTVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, Australia
Macaubas, C
Smallacombe, T
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TVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, AustraliaTVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, Australia
Smallacombe, T
Holt, BJ
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机构:
TVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, AustraliaTVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, Australia
Holt, BJ
Sly, PD
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TVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, AustraliaTVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, Australia
Sly, PD
Holt, PG
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机构:
TVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, AustraliaTVW Telethon Inst Child Hlth Res, Div Cell Biol, W Perth, WA 6872, Australia
机构:
TUFTS UNIV,NEW ENGLAND MED CTR,SCH MED,DEPT MED,DIV ALLERGY,750 WASHINGTON ST,BOX 71,BOSTON,MA 02111TUFTS UNIV,NEW ENGLAND MED CTR,SCH MED,DEPT MED,DIV ALLERGY,750 WASHINGTON ST,BOX 71,BOSTON,MA 02111
GURKA, G
OHMAN, J
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机构:
TUFTS UNIV,NEW ENGLAND MED CTR,SCH MED,DEPT MED,DIV ALLERGY,750 WASHINGTON ST,BOX 71,BOSTON,MA 02111TUFTS UNIV,NEW ENGLAND MED CTR,SCH MED,DEPT MED,DIV ALLERGY,750 WASHINGTON ST,BOX 71,BOSTON,MA 02111
OHMAN, J
ROSENWASSER, LJ
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机构:
TUFTS UNIV,NEW ENGLAND MED CTR,SCH MED,DEPT MED,DIV ALLERGY,750 WASHINGTON ST,BOX 71,BOSTON,MA 02111TUFTS UNIV,NEW ENGLAND MED CTR,SCH MED,DEPT MED,DIV ALLERGY,750 WASHINGTON ST,BOX 71,BOSTON,MA 02111