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Lymph node removal enhances corneal graft survival in mice at high risk of rejection

BACKGROUND: As shown previously, the submandibular (SM) lymph node (LN) is required for priming the immune response during corneal graft rejection. In this study, we wished to determine whether corneal grafts at "high-risk" of rejection were also protected after selective SM LN removal and...

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Autores principales: Plšková, Jarmila, Holáň, Vladimír, Filipec, Martin, Forrester, John V
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC406505/
https://www.ncbi.nlm.nih.gov/pubmed/15038832
http://dx.doi.org/10.1186/1471-2415-4-3
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author Plšková, Jarmila
Holáň, Vladimír
Filipec, Martin
Forrester, John V
author_facet Plšková, Jarmila
Holáň, Vladimír
Filipec, Martin
Forrester, John V
author_sort Plšková, Jarmila
collection PubMed
description BACKGROUND: As shown previously, the submandibular (SM) lymph node (LN) is required for priming the immune response during corneal graft rejection. In this study, we wished to determine whether corneal grafts at "high-risk" of rejection were also protected after selective SM LN removal and if so to investigate whether this improved corneal graft survival was due to induction of specific regulatory/suppressor cells or was due to immunological "ignorance". METHODS: Two sets of experiments were performed. (1) Adoptive transfer of possible regulatory splenocytes from mice with long-term accepted corneal graft after SM LN removal. (2) SM LN removal and corneal grafts in "high-risk" hosts, which had been (A) subjected to corneal trauma with vascularization or (B) allosensitized by previous corneal graft or (C) allosensitized by previous skin graft. RESULTS: Adoptive transfer of splenocytes from tolerant mice after SM LN removal did not enhance corneal graft survival in naive recipients (p > 0.05). SM LN removal in mice with corneal vascularization enhanced corneal allograft survival compared to grafted controls with/without vascularization (p < 0.0001). The removal of the SM LN in mice, who had already been allosensitized by a previous corneal graft, did not statistically prolong corneal graft survival (p > 0.05). SM LN removal procedure did not delay rejection of corneal grafts in mice allosensitized by a previous skin transplant with the same strain combination (p > 0.05). CONCLUSION: The results suggest that removal of the SM LN in "high-risk" mice prevents rejection by mechanisms involving immune "ignorance", since prior allosensitization prevents graft acceptance after LN removal. In allosensitized recipients the stronger the allosensitization (skin- vs. corneal graft-presensitization) the greater the possibility of priming for rejection at alternative draining LN sites.
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spelling pubmed-4065052004-05-13 Lymph node removal enhances corneal graft survival in mice at high risk of rejection Plšková, Jarmila Holáň, Vladimír Filipec, Martin Forrester, John V BMC Ophthalmol Research Article BACKGROUND: As shown previously, the submandibular (SM) lymph node (LN) is required for priming the immune response during corneal graft rejection. In this study, we wished to determine whether corneal grafts at "high-risk" of rejection were also protected after selective SM LN removal and if so to investigate whether this improved corneal graft survival was due to induction of specific regulatory/suppressor cells or was due to immunological "ignorance". METHODS: Two sets of experiments were performed. (1) Adoptive transfer of possible regulatory splenocytes from mice with long-term accepted corneal graft after SM LN removal. (2) SM LN removal and corneal grafts in "high-risk" hosts, which had been (A) subjected to corneal trauma with vascularization or (B) allosensitized by previous corneal graft or (C) allosensitized by previous skin graft. RESULTS: Adoptive transfer of splenocytes from tolerant mice after SM LN removal did not enhance corneal graft survival in naive recipients (p > 0.05). SM LN removal in mice with corneal vascularization enhanced corneal allograft survival compared to grafted controls with/without vascularization (p < 0.0001). The removal of the SM LN in mice, who had already been allosensitized by a previous corneal graft, did not statistically prolong corneal graft survival (p > 0.05). SM LN removal procedure did not delay rejection of corneal grafts in mice allosensitized by a previous skin transplant with the same strain combination (p > 0.05). CONCLUSION: The results suggest that removal of the SM LN in "high-risk" mice prevents rejection by mechanisms involving immune "ignorance", since prior allosensitization prevents graft acceptance after LN removal. In allosensitized recipients the stronger the allosensitization (skin- vs. corneal graft-presensitization) the greater the possibility of priming for rejection at alternative draining LN sites. BioMed Central 2004-03-23 /pmc/articles/PMC406505/ /pubmed/15038832 http://dx.doi.org/10.1186/1471-2415-4-3 Text en Copyright © 2004 Plšková et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Plšková, Jarmila
Holáň, Vladimír
Filipec, Martin
Forrester, John V
Lymph node removal enhances corneal graft survival in mice at high risk of rejection
title Lymph node removal enhances corneal graft survival in mice at high risk of rejection
title_full Lymph node removal enhances corneal graft survival in mice at high risk of rejection
title_fullStr Lymph node removal enhances corneal graft survival in mice at high risk of rejection
title_full_unstemmed Lymph node removal enhances corneal graft survival in mice at high risk of rejection
title_short Lymph node removal enhances corneal graft survival in mice at high risk of rejection
title_sort lymph node removal enhances corneal graft survival in mice at high risk of rejection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC406505/
https://www.ncbi.nlm.nih.gov/pubmed/15038832
http://dx.doi.org/10.1186/1471-2415-4-3
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