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Human CD1-restricted T cell recognition of lipids from pollens

Plant pollens are an important source of environmental antigens that stimulate allergic responses. In addition to acting as vehicles for foreign protein antigens, they contain lipids that incorporate saturated and unsaturated fatty acids, which are necessary in the reproduction of higher plants. The...

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Autores principales: Agea, Elisabetta, Russano, Anna, Bistoni, Onelia, Mannucci, Roberta, Nicoletti, Ildo, Corazzi, Lanfranco, Postle, Anthony D., De Libero, Gennaro, Porcelli, Steven A., Spinozzi, Fabrizio
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213012/
https://www.ncbi.nlm.nih.gov/pubmed/16009719
http://dx.doi.org/10.1084/jem.20050773
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author Agea, Elisabetta
Russano, Anna
Bistoni, Onelia
Mannucci, Roberta
Nicoletti, Ildo
Corazzi, Lanfranco
Postle, Anthony D.
De Libero, Gennaro
Porcelli, Steven A.
Spinozzi, Fabrizio
author_facet Agea, Elisabetta
Russano, Anna
Bistoni, Onelia
Mannucci, Roberta
Nicoletti, Ildo
Corazzi, Lanfranco
Postle, Anthony D.
De Libero, Gennaro
Porcelli, Steven A.
Spinozzi, Fabrizio
author_sort Agea, Elisabetta
collection PubMed
description Plant pollens are an important source of environmental antigens that stimulate allergic responses. In addition to acting as vehicles for foreign protein antigens, they contain lipids that incorporate saturated and unsaturated fatty acids, which are necessary in the reproduction of higher plants. The CD1 family of nonpolymorphic major histocompatibility complex–related molecules is highly conserved in mammals, and has been shown to present microbial and self lipids to T cells. Here, we provide evidence that pollen lipids may be recognized as antigens by human T cells through a CD1-dependent pathway. Among phospholipids extracted from cypress grains, phosphatidyl-choline and phosphatidyl-ethanolamine were able to stimulate the proliferation of T cells from cypress-sensitive subjects. Recognition of phospholipids involved multiple cell types, mostly CD4(+) T cell receptor for antigen (TCR)αβ(+), some CD4(−)CD8(−) TCRγδ(+), but rarely Vα24i (+) natural killer–T cells, and required CD1a(+) and CD1d(+) antigen presenting cell. The responding T cells secreted both interleukin (IL)-4 and interferon-γ, in some cases IL-10 and transforming growth factor-β, and could provide help for immunoglobulin E (IgE) production. Responses to pollen phospholipids were maximally evident in blood samples obtained from allergic subjects during pollinating season, uniformly absent in Mycobacterium tuberculosis–exposed health care workers, but occasionally seen in nonallergic subjects. Finally, allergic, but not normal subjects, displayed circulating specific IgE and cutaneous weal and flare reactions to phospholipids.
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spelling pubmed-22130122008-03-11 Human CD1-restricted T cell recognition of lipids from pollens Agea, Elisabetta Russano, Anna Bistoni, Onelia Mannucci, Roberta Nicoletti, Ildo Corazzi, Lanfranco Postle, Anthony D. De Libero, Gennaro Porcelli, Steven A. Spinozzi, Fabrizio J Exp Med Article Plant pollens are an important source of environmental antigens that stimulate allergic responses. In addition to acting as vehicles for foreign protein antigens, they contain lipids that incorporate saturated and unsaturated fatty acids, which are necessary in the reproduction of higher plants. The CD1 family of nonpolymorphic major histocompatibility complex–related molecules is highly conserved in mammals, and has been shown to present microbial and self lipids to T cells. Here, we provide evidence that pollen lipids may be recognized as antigens by human T cells through a CD1-dependent pathway. Among phospholipids extracted from cypress grains, phosphatidyl-choline and phosphatidyl-ethanolamine were able to stimulate the proliferation of T cells from cypress-sensitive subjects. Recognition of phospholipids involved multiple cell types, mostly CD4(+) T cell receptor for antigen (TCR)αβ(+), some CD4(−)CD8(−) TCRγδ(+), but rarely Vα24i (+) natural killer–T cells, and required CD1a(+) and CD1d(+) antigen presenting cell. The responding T cells secreted both interleukin (IL)-4 and interferon-γ, in some cases IL-10 and transforming growth factor-β, and could provide help for immunoglobulin E (IgE) production. Responses to pollen phospholipids were maximally evident in blood samples obtained from allergic subjects during pollinating season, uniformly absent in Mycobacterium tuberculosis–exposed health care workers, but occasionally seen in nonallergic subjects. Finally, allergic, but not normal subjects, displayed circulating specific IgE and cutaneous weal and flare reactions to phospholipids. The Rockefeller University Press 2005-07-18 /pmc/articles/PMC2213012/ /pubmed/16009719 http://dx.doi.org/10.1084/jem.20050773 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Agea, Elisabetta
Russano, Anna
Bistoni, Onelia
Mannucci, Roberta
Nicoletti, Ildo
Corazzi, Lanfranco
Postle, Anthony D.
De Libero, Gennaro
Porcelli, Steven A.
Spinozzi, Fabrizio
Human CD1-restricted T cell recognition of lipids from pollens
title Human CD1-restricted T cell recognition of lipids from pollens
title_full Human CD1-restricted T cell recognition of lipids from pollens
title_fullStr Human CD1-restricted T cell recognition of lipids from pollens
title_full_unstemmed Human CD1-restricted T cell recognition of lipids from pollens
title_short Human CD1-restricted T cell recognition of lipids from pollens
title_sort human cd1-restricted t cell recognition of lipids from pollens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213012/
https://www.ncbi.nlm.nih.gov/pubmed/16009719
http://dx.doi.org/10.1084/jem.20050773
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