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http://hdl.handle.net/10400.7/843
Título: | Route of Antigen Presentation Can Determine the Selection of Foxp3-Dependent or Foxp3-Independent Dominant Immune Tolerance |
Autor: | Agua-Doce, Ana Caridade, Marta Oliveira, Vanessa G Bergman, Lisa Lafaille, Maria C Lafaille, Juan J Demengeot, Jocelyne Graca, Luis |
Palavras-chave: | Aluminum Hydroxide Animals Antibodies Antigen Presentation CD4 Antigens Cell Differentiation Cells, Cultured Clonal Selection, Antigen-Mediated Forkhead Transcription Factors Interleukin-10 Interleukin-2 Lymphocyte Activation Mice Mice, Knockout Mice, Transgenic Ovalbumin T-Lymphocyte Subsets T-Lymphocytes, Regulatory Immune Tolerance Skin Transplantation |
Data: | 1-Jan-2018 |
Editora: | American Association of Immunologists |
Citação: | Route of Antigen Presentation Can Determine the Selection of Foxp3-Dependent or Foxp3-Independent Dominant Immune Tolerance Ana Agua-Doce, Marta Caridade, Vanessa G. Oliveira, Lisa Bergman, Maria C. Lafaille, Juan J. Lafaille, Jocelyne Demengeot, Luis Graca The Journal of Immunology January 1, 2018, 200 (1) 101-109; DOI: 10.4049/jimmunol.1601886 |
Resumo: | It has been shown that dominant tolerance, namely in transplantation, requires Foxp3+regulatory T cells. Although most tolerance-inducing regimens rely on regulatory T cells, we found that induction of tolerance to proteins in aluminum hydroxide can be achieved in Foxp3-deficient mice using nondepleting anti-CD4 Abs. This type of tolerance is Ag specific, and tolerant mice retain immune competence to respond to unrelated Ags. We demonstrated with chicken OVA-specific TCR-transgenic mice that the same tolerizing protocol (CD4 blockade) and the same target Ag (OVA) achieves Foxp3-dependent transplantation tolerance to OVA-expressing skin grafts, but Foxp3-independent tolerance when the Ag is provided as OVA-aluminum hydroxide. In the latter case, we found that tolerance induction triggered recessive mechanisms leading to elimination of effector cells and, simultaneously, a dominant mechanism associated with the emergence of an anergic and regulatory CTLA-4+IL-2lowFoxp3-T cell population, where the tolerance state is IL-10 dependent. Such Foxp3-independent mechanisms can improve the efficacy of tolerance-inducing protocols. |
Descrição: | This deposit is composed by a publication in which the IGC' authors have had the role of collaboration (it's a collaboration publication). This type of deposit in ARCA is in restrictedAccess (it can't be in open access to the public), and could only be accessed by two ways: either by requesting a legal copy to the author (the email contact present in this deposit) or by visiting the following link: http://www.jimmunol.org/content/200/1/101.long#ack-1 This publication hasn't any creative commons license associated. |
Peer review: | yes |
URI: | http://hdl.handle.net/10400.7/843 |
DOI: | 10.4049/jimmunol.1601886 |
Versão do Editor: | http://www.jimmunol.org/content/200/1/101 |
Aparece nas colecções: | LP - Artigos |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
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Graca_J.Immunol_(2018).pdf | main article | 1,56 MB | Adobe PDF | Ver/Abrir Acesso Restrito. Solicitar cópia ao autor! |
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