The role of CD8+ T cells during allograft rejection

Detalhes bibliográficos
Autor(a) principal: Bueno, Valquiria [UNIFESP]
Data de Publicação: 2002
Outros Autores: Pestana, Jose Osmar Medina [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0100-879X2002001100001
http://repositorio.unifesp.br/handle/11600/1544
Resumo: Organ transplantation can be considered as replacement therapy for patients with end-stage organ failure. The percent of one-year allograft survival has increased due, among other factors, to a better understanding of the rejection process and new immunosuppressive drugs. Immunosuppressive therapy used in transplantation prevents activation and proliferation of alloreactive T lymphocytes, although not fully preventing chronic rejection. Recognition by recipient T cells of alloantigens expressed by donor tissues initiates immune destruction of allogeneic transplants. However, there is controversy concerning the relative contribution of CD4+ and CD8+ T cells to allograft rejection. Some animal models indicate that there is an absolute requirement for CD4+ T cells in allogeneic rejection, whereas in others CD4-depleted mice reject certain types of allografts. Moreover, there is evidence that CD8+ T cells are more resistant to immunotherapy and tolerance induction protocols. An intense focal infiltration of mainly CD8+CTLA4+ T lymphocytes during kidney rejection has been described in patients. This suggests that CD8+ T cells could escape from immunosuppression and participate in the rejection process. Our group is primarily interested in the immune mechanisms involved in allograft rejection. Thus, we believe that a better understanding of the role of CD8+ T cells in allograft rejection could indicate new targets for immunotherapy in transplantation. Therefore, the objective of the present review was to focus on the role of the CD8+ T cell population in the rejection of allogeneic tissue.
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spelling The role of CD8+ T cells during allograft rejectionTransplantationRejectionT cellsCytokinesChemokinesOrgan transplantation can be considered as replacement therapy for patients with end-stage organ failure. The percent of one-year allograft survival has increased due, among other factors, to a better understanding of the rejection process and new immunosuppressive drugs. Immunosuppressive therapy used in transplantation prevents activation and proliferation of alloreactive T lymphocytes, although not fully preventing chronic rejection. Recognition by recipient T cells of alloantigens expressed by donor tissues initiates immune destruction of allogeneic transplants. However, there is controversy concerning the relative contribution of CD4+ and CD8+ T cells to allograft rejection. Some animal models indicate that there is an absolute requirement for CD4+ T cells in allogeneic rejection, whereas in others CD4-depleted mice reject certain types of allografts. Moreover, there is evidence that CD8+ T cells are more resistant to immunotherapy and tolerance induction protocols. An intense focal infiltration of mainly CD8+CTLA4+ T lymphocytes during kidney rejection has been described in patients. This suggests that CD8+ T cells could escape from immunosuppression and participate in the rejection process. Our group is primarily interested in the immune mechanisms involved in allograft rejection. Thus, we believe that a better understanding of the role of CD8+ T cells in allograft rejection could indicate new targets for immunotherapy in transplantation. Therefore, the objective of the present review was to focus on the role of the CD8+ T cell population in the rejection of allogeneic tissue.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Disciplina de NefrologiaUNIFESP, EPM, Disciplina de NefrologiaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Bueno, Valquiria [UNIFESP]Pestana, Jose Osmar Medina [UNIFESP]2015-06-14T13:29:49Z2015-06-14T13:29:49Z2002-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1247-1258application/pdfhttp://dx.doi.org/10.1590/S0100-879X2002001100001Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 35, n. 11, p. 1247-1258, 2002.10.1590/S0100-879X2002001100001S0100-879X2002001100001.pdf0100-879XS0100-879X2002001100001http://repositorio.unifesp.br/handle/11600/1544WOS:000179717100001engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T22:57:41Zoai:repositorio.unifesp.br/:11600/1544Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-05T22:57:41Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv The role of CD8+ T cells during allograft rejection
title The role of CD8+ T cells during allograft rejection
spellingShingle The role of CD8+ T cells during allograft rejection
Bueno, Valquiria [UNIFESP]
Transplantation
Rejection
T cells
Cytokines
Chemokines
title_short The role of CD8+ T cells during allograft rejection
title_full The role of CD8+ T cells during allograft rejection
title_fullStr The role of CD8+ T cells during allograft rejection
title_full_unstemmed The role of CD8+ T cells during allograft rejection
title_sort The role of CD8+ T cells during allograft rejection
author Bueno, Valquiria [UNIFESP]
author_facet Bueno, Valquiria [UNIFESP]
Pestana, Jose Osmar Medina [UNIFESP]
author_role author
author2 Pestana, Jose Osmar Medina [UNIFESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Bueno, Valquiria [UNIFESP]
Pestana, Jose Osmar Medina [UNIFESP]
dc.subject.por.fl_str_mv Transplantation
Rejection
T cells
Cytokines
Chemokines
topic Transplantation
Rejection
T cells
Cytokines
Chemokines
description Organ transplantation can be considered as replacement therapy for patients with end-stage organ failure. The percent of one-year allograft survival has increased due, among other factors, to a better understanding of the rejection process and new immunosuppressive drugs. Immunosuppressive therapy used in transplantation prevents activation and proliferation of alloreactive T lymphocytes, although not fully preventing chronic rejection. Recognition by recipient T cells of alloantigens expressed by donor tissues initiates immune destruction of allogeneic transplants. However, there is controversy concerning the relative contribution of CD4+ and CD8+ T cells to allograft rejection. Some animal models indicate that there is an absolute requirement for CD4+ T cells in allogeneic rejection, whereas in others CD4-depleted mice reject certain types of allografts. Moreover, there is evidence that CD8+ T cells are more resistant to immunotherapy and tolerance induction protocols. An intense focal infiltration of mainly CD8+CTLA4+ T lymphocytes during kidney rejection has been described in patients. This suggests that CD8+ T cells could escape from immunosuppression and participate in the rejection process. Our group is primarily interested in the immune mechanisms involved in allograft rejection. Thus, we believe that a better understanding of the role of CD8+ T cells in allograft rejection could indicate new targets for immunotherapy in transplantation. Therefore, the objective of the present review was to focus on the role of the CD8+ T cell population in the rejection of allogeneic tissue.
publishDate 2002
dc.date.none.fl_str_mv 2002-11-01
2015-06-14T13:29:49Z
2015-06-14T13:29:49Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0100-879X2002001100001
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 35, n. 11, p. 1247-1258, 2002.
10.1590/S0100-879X2002001100001
S0100-879X2002001100001.pdf
0100-879X
S0100-879X2002001100001
http://repositorio.unifesp.br/handle/11600/1544
WOS:000179717100001
url http://dx.doi.org/10.1590/S0100-879X2002001100001
http://repositorio.unifesp.br/handle/11600/1544
identifier_str_mv Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 35, n. 11, p. 1247-1258, 2002.
10.1590/S0100-879X2002001100001
S0100-879X2002001100001.pdf
0100-879X
S0100-879X2002001100001
WOS:000179717100001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brazilian Journal of Medical and Biological Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1247-1258
application/pdf
dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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