Engineering strategies for allogeneic solid tissue acceptance

Detalhes bibliográficos
Autor(a) principal: Sousa, Ana Rita
Data de Publicação: 2021
Outros Autores: Mano, João F., Oliveira, Mariana B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/34363
Resumo: Systemic immunosuppressants have allowed the transplantation of life-saving organs. However, they cause deleterious effects and long-term graft failure. Strategies promoting allogeneic graft acceptance and the maintenance of immunological competence have been proposed. Cell-based tolerance-inducing strategies that preserve immune competence have already extended human allograft acceptance, although toxic side effects or difficult reproduction of observed effects in humans have counteracted their clinical translation. Localized tolerance/immunosuppression mediated through bioengineered setups comprising immunomodulatory biomaterials and/or tissue engineering-inspired tools already achieved allograft acceptance in murine models and are game changing in the field. Such advances have contributed to unveiling the complex interplay of immune cells and allogeneic transplants. Advances in allogeneic transplantation of solid organs and tissues depend on our understanding of mechanisms that mediate the prevention of graft rejection. For the past decades, clinical practice has established guidelines to prevent allograft rejection, which mostly rely on the intake of nontargeted immunosuppressants as the gold standard. However, such lifelong regimens have been reported to trigger severe morbidities and commonly fail in preventing late allograft loss. In this review, the biology of allogeneic rejection and self-tolerance is analyzed, as well as the mechanisms of cellular-based therapeutics driving suppression and/or tolerance. Bioinspired engineering strategies that take advantage of cells, biomaterials, or combinations thereof to prevent allograft rejection are addressed, as well as biological mechanisms that drive their efficacy.
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spelling Engineering strategies for allogeneic solid tissue acceptanceAllogeneic transplantationBioengineering acceptance-inducing strategiesCellular/acellular therapeuticsTissue engineeringSystemic immunosuppressants have allowed the transplantation of life-saving organs. However, they cause deleterious effects and long-term graft failure. Strategies promoting allogeneic graft acceptance and the maintenance of immunological competence have been proposed. Cell-based tolerance-inducing strategies that preserve immune competence have already extended human allograft acceptance, although toxic side effects or difficult reproduction of observed effects in humans have counteracted their clinical translation. Localized tolerance/immunosuppression mediated through bioengineered setups comprising immunomodulatory biomaterials and/or tissue engineering-inspired tools already achieved allograft acceptance in murine models and are game changing in the field. Such advances have contributed to unveiling the complex interplay of immune cells and allogeneic transplants. Advances in allogeneic transplantation of solid organs and tissues depend on our understanding of mechanisms that mediate the prevention of graft rejection. For the past decades, clinical practice has established guidelines to prevent allograft rejection, which mostly rely on the intake of nontargeted immunosuppressants as the gold standard. However, such lifelong regimens have been reported to trigger severe morbidities and commonly fail in preventing late allograft loss. In this review, the biology of allogeneic rejection and self-tolerance is analyzed, as well as the mechanisms of cellular-based therapeutics driving suppression and/or tolerance. Bioinspired engineering strategies that take advantage of cells, biomaterials, or combinations thereof to prevent allograft rejection are addressed, as well as biological mechanisms that drive their efficacy.Cell Press2022-08-01T17:51:09Z2021-06-01T00:00:00Z2021-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/34363eng1471-491410.1016/j.molmed.2021.03.005Sousa, Ana RitaMano, João F.Oliveira, Mariana B.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:06:24Zoai:ria.ua.pt:10773/34363Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:05:44.078267Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Engineering strategies for allogeneic solid tissue acceptance
title Engineering strategies for allogeneic solid tissue acceptance
spellingShingle Engineering strategies for allogeneic solid tissue acceptance
Sousa, Ana Rita
Allogeneic transplantation
Bioengineering acceptance-inducing strategies
Cellular/acellular therapeutics
Tissue engineering
title_short Engineering strategies for allogeneic solid tissue acceptance
title_full Engineering strategies for allogeneic solid tissue acceptance
title_fullStr Engineering strategies for allogeneic solid tissue acceptance
title_full_unstemmed Engineering strategies for allogeneic solid tissue acceptance
title_sort Engineering strategies for allogeneic solid tissue acceptance
author Sousa, Ana Rita
author_facet Sousa, Ana Rita
Mano, João F.
Oliveira, Mariana B.
author_role author
author2 Mano, João F.
Oliveira, Mariana B.
author2_role author
author
dc.contributor.author.fl_str_mv Sousa, Ana Rita
Mano, João F.
Oliveira, Mariana B.
dc.subject.por.fl_str_mv Allogeneic transplantation
Bioengineering acceptance-inducing strategies
Cellular/acellular therapeutics
Tissue engineering
topic Allogeneic transplantation
Bioengineering acceptance-inducing strategies
Cellular/acellular therapeutics
Tissue engineering
description Systemic immunosuppressants have allowed the transplantation of life-saving organs. However, they cause deleterious effects and long-term graft failure. Strategies promoting allogeneic graft acceptance and the maintenance of immunological competence have been proposed. Cell-based tolerance-inducing strategies that preserve immune competence have already extended human allograft acceptance, although toxic side effects or difficult reproduction of observed effects in humans have counteracted their clinical translation. Localized tolerance/immunosuppression mediated through bioengineered setups comprising immunomodulatory biomaterials and/or tissue engineering-inspired tools already achieved allograft acceptance in murine models and are game changing in the field. Such advances have contributed to unveiling the complex interplay of immune cells and allogeneic transplants. Advances in allogeneic transplantation of solid organs and tissues depend on our understanding of mechanisms that mediate the prevention of graft rejection. For the past decades, clinical practice has established guidelines to prevent allograft rejection, which mostly rely on the intake of nontargeted immunosuppressants as the gold standard. However, such lifelong regimens have been reported to trigger severe morbidities and commonly fail in preventing late allograft loss. In this review, the biology of allogeneic rejection and self-tolerance is analyzed, as well as the mechanisms of cellular-based therapeutics driving suppression and/or tolerance. Bioinspired engineering strategies that take advantage of cells, biomaterials, or combinations thereof to prevent allograft rejection are addressed, as well as biological mechanisms that drive their efficacy.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-01T00:00:00Z
2021-06-01
2022-08-01T17:51:09Z
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url http://hdl.handle.net/10773/34363
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1471-4914
10.1016/j.molmed.2021.03.005
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dc.publisher.none.fl_str_mv Cell Press
publisher.none.fl_str_mv Cell Press
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