Skin-derived aeroallergen-specific T-cell clones of Th2 phenotype in patients with atopic dermatitis

T-cell lines have been derived from aeroallergen-induced eczematous patch test sites of patients with atopic dermatitis (AD). Biopsy specimens were obtained 24 hours after allergen application to the skin, and only in vivo-activated T cells were propagated. From one patient, the T-cell lines were su...

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Published inJournal of allergy and clinical immunology Vol. 90; no. 2; pp. 184 - 193
Main Authors van Reijsen, F.C., Bruijnzeel-Koomen, C.A.F.M., Kalthoff, F.S., Maggi, E., Romagnani, S., Westland, J.K.T., Mudde, G.C.
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.08.1992
Elsevier
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Abstract T-cell lines have been derived from aeroallergen-induced eczematous patch test sites of patients with atopic dermatitis (AD). Biopsy specimens were obtained 24 hours after allergen application to the skin, and only in vivo-activated T cells were propagated. From one patient, the T-cell lines were subcloned at 0.3 cells per well. With allergen-induced interleukin (IL) production, all clones tested (n = 13) were found to be specific for the allergen, producing IL-4 and granulocyte-macrophage-colony-stimulating factor. No IL-2 or interferon-γ was found. The allergen-specific proliferative response of these clones, although the response was dependent on exogenous IL-2 or IL-4, also proved that all clones were allergen specific. Under optimal stimulation (aCD3 plus phorbol myristate acetate), 15% of the clones appeared to be of Th0 phenotype and 70% of Th2 phenotype. In 15% of the clones, IL-4 was produced in the absence of IL-2, IL-5, or interferon-γ. Supernatants of all clones tested induced IgE production by B cells from normal non-atopic donors. The T-cell lines of the other patient demonstrated similar results; allergen-specific proliferation was dependent on exogenous IL-2 or IL-4 and stimulation with aCD3 plus phorbol myristate acetate demonstrated that the T cells in these lines were of the Th2 phenotype. In conclusion, our data reveal that, in AD, percutaneous sensitization to aeroallergens may occur and indicate that allergen-specific Th2 type T cells may be responsible for the high levels of (specific) IgE found in 80% of patients with AD.
AbstractList T-cell lines have been derived from aeroallergen-induced eczematous patch test sites of patients with atopic dermatitis (AD). Biopsy specimens were obtained 24 hours after allergen application to the skin, and only in vivo-activated T cells were propagated. From one patient, the T-cell lines were subcloned at 0.3 cells per well. With allergen-induced interleukin (IL) production, all clones tested (n = 13) were found to be specific for the allergen, producing IL-4 and granulocyte-macrophage - colony-stimulating factor. No IL-2 or interferon- gamma was found. The allergen-specific proliferative response of these clones, although the response was dependent on exogenous IL-2 or IL-4, also proved that all clones were allergen specific. Our data reveal that, in AD, percutaneous sensitization to aeroallergens may occur and indicate that allergen-specific Th2 type T cells may be responsible for the high levels of (specific) IgE found in 80% of patients with AD.
T-cell lines have been derived from aeroallergen-induced eczematous patch test sites of patients with atopic dermatitis (AD). Biopsy specimens were obtained 24 hours after allergen application to the skin, and only in vivo-activated T cells were propagated. From one patient, the T-cell lines were subcloned at 0.3 cells per well. With allergen-induced interleukin (IL) production, all clones tested (n = 13) were found to be specific for the allergen, producing IL-4 and granulocyte-macrophage-colony-stimulating factor. No IL-2 or interferon-γ was found. The allergen-specific proliferative response of these clones, although the response was dependent on exogenous IL-2 or IL-4, also proved that all clones were allergen specific. Under optimal stimulation (aCD3 plus phorbol myristate acetate), 15% of the clones appeared to be of Th0 phenotype and 70% of Th2 phenotype. In 15% of the clones, IL-4 was produced in the absence of IL-2, IL-5, or interferon-γ. Supernatants of all clones tested induced IgE production by B cells from normal non-atopic donors. The T-cell lines of the other patient demonstrated similar results; allergen-specific proliferation was dependent on exogenous IL-2 or IL-4 and stimulation with aCD3 plus phorbol myristate acetate demonstrated that the T cells in these lines were of the Th2 phenotype. In conclusion, our data reveal that, in AD, percutaneous sensitization to aeroallergens may occur and indicate that allergen-specific Th2 type T cells may be responsible for the high levels of (specific) IgE found in 80% of patients with AD.
T-cell lines have been derived from aeroallergen-induced eczematous patch test sites of patients with atopic dermatitis (AD). Biopsy specimens were obtained 24 hours after allergen application to the skin, and only in vivo-activated T cells were propagated. From one patient, the T-cell lines were subcloned at 0.3 cells per well. With allergen-induced interleukin (IL) production, all clones tested (n = 13) were found to be specific for the allergen, producing IL-4 and granulocyte-macrophage-colony-stimulating factor. No IL-2 or interferon-gamma was found. The allergen-specific proliferative response of these clones, although the response was dependent on exogenous IL-2 or IL-4, also proved that all clones were allergen specific. Under optimal stimulation (aCD3 plus phorbol myristate acetate), 15% of the clones appeared to be of Th0 phenotype and 70% of Th2 phenotype. In 15% of the clones, IL-4 was produced in the absence of IL-2, IL-5, or interferon-gamma. Supernatants of all clones tested induced IgE production by B cells from normal non-atopic donors. The T-cell lines of the other patient demonstrated similar results; allergen-specific proliferation was dependent on exogenous IL-2 or IL-4 and stimulation with aCD3 plus phorbol myristate acetate demonstrated that the T cells in these lines were of the Th2 phenotype. In conclusion, our data reveal that, in AD, percutaneous sensitization to aeroallergens may occur and indicate that allergen-specific Th2 type T cells may be responsible for the high levels of (specific) IgE found in 80% of patients with AD.
Author van Reijsen, F.C.
Romagnani, S.
Maggi, E.
Mudde, G.C.
Westland, J.K.T.
Bruijnzeel-Koomen, C.A.F.M.
Kalthoff, F.S.
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Thu May 23 23:55:38 EDT 2024
Fri Nov 25 01:05:35 EST 2022
Fri Feb 23 02:37:03 EST 2024
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords TCR
RT
Dpr
epicutaneous patch tests
GaH-IgE-biot
INF-γ
EFT
GaM
ABS
FITC
FcR
rIL
Atopic dermatitis
GM-CSF
a-alpha/beta TCR
PBS
AD
a-IL
EBV-B
PMA
allergen-specific Th2 cells
GP
CM
LST
Dermatophagoides pteronyssinus
APC
LC
FCS
a-IgE
AP-strept
Human
Immunopathology
Allergy
Skin disease
Pathogenesis
Helper cell
Phenotype
Specificity
T-Lymphocyte
Aerosols
Skin
Allergen
Clone
Language English
License CC BY 4.0
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PublicationDate 1992-08-01
PublicationDateYYYYMMDD 1992-08-01
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  year: 1992
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PublicationPlace New York, NY
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PublicationTitle Journal of allergy and clinical immunology
PublicationTitleAlternate J Allergy Clin Immunol
PublicationYear 1992
Publisher Mosby, Inc
Elsevier
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Mudde, Van Reijsen, Boland, De Gast, Bruijnzeel, Bruijnzeel-Koomen (BIB10) 1990; 69
Paliard, De Vries, Spits (BIB26) 1991; 135
Langhoff, Steinman (BIB13) 1989; 169
Reinhold, Kukel, Goeden, Neumann, Wehrmann, Kreysel (BIB24) 1991; 96
Norris, Schofield, Camp (BIB4) 1988; 118
Bruijnzeel-Koomen, Van der Donk, Bruijnzeel, Capron, De Gast, Mudde (BIB8) 1988; 74
Swain, Weinberg, English, Huston (BIB22) 1990; 145
Juhlin, Johansson, Bennich, Hogman, Thyresson (BIB1) 1969; 100
Mudde, Van Dam, De Gast (BIB20) 1986; 64
Mitchell, Chapman, Pope, Crow, Jouhal, Platts-Mills (BIB5) 1982; 1
Firestein, Roeder, Laxer (BIB21) 1989; 143
Adinoff, Tellez, Clark (BIB7) 1988; 81
Wierenga, Snoek, Bos, Jansen, Kapsenberg (BIB32) 1990; 20
Wierenga, Snoek, De Groot (BIB31) 1990; 144
Kalthoff, Rossiter, Liehl (BIB23) 1991; 27
Del Prete, De Carli, Mastromauro (BIB15) 1991; 88
Reitamo, Visa, Kahonen, Kyhk, Stubb, Salo (BIB6) 1986; 114
Hanifin, Rajka (BIB12) 1980; 92
Ramb-Lindhauer, Feldmann, Rotte, Neumann (BIB28) 1991; 283
MacKie, Cobb, Cochrane, Thompson (BIB2) 1979; 4
Bruijnzeel-Koomen, Boland, Mudde (BIB9) 1988
Rolink, Melchers, Palacios (BIB17) 1989; 169
Bruijnzeel-Koomen, Wichen v, Spry, Venge, Bruijnzeel (BIB3) 1988; 118
Parronchi, Macchia, Piccinni (BIB16) 1991; 88
Chrétien, Helm, Marsh, Padlan, Wijdenes, Banchereau (BIB11) 1988; 141
Mudde, Van Reijsen, Bruijnzeel-Koomen (BIB27) 1992
Van der Heijden, Wierenga, Bos, Kapsenberg (BIB29) 1991; 97
Chang, Shea, Urioste, Thompson, Boom, Abbas (BIB30) 1990; 145
Maggi, Del Prete, Macchia (BIB18) 1988; 18
Vercelli, Jabara, Arai, Geha (BIB19) 1989; 169
Walker, Pichler, Koponen, Domzig, De Weck (BIB14) 1986; 101
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Snippet T-cell lines have been derived from aeroallergen-induced eczematous patch test sites of patients with atopic dermatitis (AD). Biopsy specimens were obtained 24...
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SubjectTerms allergen-specific Th2 cells
Allergens - immunology
Allergic diseases
Antigens - immunology
Atopic dermatitis
B-Lymphocytes - immunology
Biological and medical sciences
Cell Division - drug effects
Clone Cells
Cytokines - metabolism
Dermatitis, Atopic - genetics
Dermatitis, Atopic - immunology
Dermatitis, Atopic - pathology
Dermatophagoides pteronyssinus
epicutaneous patch tests
Epitopes
Humans
Immunoglobulin E - biosynthesis
Immunopathology
Interleukin-2 - pharmacology
Medical sciences
Phenotype
Reference Values
Skin - immunology
Skin - pathology
Skin allergic diseases. Stinging insect allergies
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
Title Skin-derived aeroallergen-specific T-cell clones of Th2 phenotype in patients with atopic dermatitis
URI https://dx.doi.org/10.1016/0091-6749(92)90070-I
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