Publication
Human FOXN1-deficiency is associated with αβ double-negative and FoxP3+ T-cell expansions that are distinctly modulated upon thymic transplantation
| dc.contributor.author | Albuquerque, A. S. | |
| dc.contributor.author | Marques, J. G. | |
| dc.contributor.author | Silva, S. L. | |
| dc.contributor.author | Ligeiro, D. | |
| dc.contributor.author | Devlin, B. H. | |
| dc.contributor.author | Dutrieux, J. | |
| dc.contributor.author | Cheynier, R. | |
| dc.contributor.author | Pignata, C. | |
| dc.contributor.author | Victorino, R. M. | |
| dc.contributor.author | Markert, M. L. | |
| dc.contributor.author | Sousa, A. E. | |
| dc.date.accessioned | 2015-02-03T16:35:06Z | |
| dc.date.available | 2015-02-03T16:35:06Z | |
| dc.date.issued | 2002 | |
| dc.description | © 2012 Albuquerque et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | por |
| dc.description.abstract | Forkhead box N1 (FOXN1) is a transcription factor crucial for thymic epithelium development and prevention of its involution. Investigation of a patient with a rare homozygous FOXN1 mutation (R255X), leading to alopecia universalis and thymus aplasia, unexpectedly revealed non-maternal circulating T-cells, and, strikingly, large numbers of aberrant doublenegative ab T-cells (CD4negCD8neg, DN) and regulatory-like T-cells. These data raise the possibility that a thymic rudiment persisted, allowing T-cell development, albeit with disturbances in positive/negative selection, as suggested by DN and FoxP3+ cell expansions. Although regulatory-like T-cell numbers normalized following HLA-mismatched thymic transplantation, the abDN subset persisted 5 years post-transplantation. Involution of thymus allograft likely occurred 3 years post-transplantation based on sj/bTREC ratio, which estimates intrathymic precursor T-cell divisions and, consequently, thymic explant output. Nevertheless, functional immune-competence was sustained, providing new insights for the design of immunological reconstitution strategies based on thymic transplantation, with potential applications in other clinical settings. | por |
| dc.description.sponsorship | This work was supported by grants from ‘‘Fundação para a Ciência e a Tecnologia’’ (FCT) and by ‘‘Programa Operacional Ciência e Inovação 2010’’ (POCI2010) to RMMV and AES. ASA received a scholarship from FCT. Thymus transplantation performed at the Duke University Medical Center, Durham, USA was financially supported by the Portuguese National Health Services. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. | por |
| dc.identifier.citation | PLoS ONE May 2012 | Volume 7 | Issue 5 | e37042 | por |
| dc.identifier.issn | 1932-6203 | |
| dc.identifier.uri | http://dx.doi.org/ 10.1371/journal.pone.0037042 | |
| dc.identifier.uri | http://hdl.handle.net/10451/15877 | |
| dc.language.iso | eng | por |
| dc.peerreviewed | yes | por |
| dc.publisher | Public Library of Science | por |
| dc.title | Human FOXN1-deficiency is associated with αβ double-negative and FoxP3+ T-cell expansions that are distinctly modulated upon thymic transplantation | por |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.title | PLoS ONE | por |
| rcaap.rights | openAccess | por |
| rcaap.type | article | por |