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Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives
Cytomegalovirus infection is one of most frequent infectious complications after renal transplantation, and can be classified as primo-infection, when the transmission occurs through the graft, or reactivation, when the recipient is cytomegalovirus seropositive. After transplantation, cytomegaloviru...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto de Ensino e Pesquisa Albert Einstein
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946822/ https://www.ncbi.nlm.nih.gov/pubmed/25993081 http://dx.doi.org/10.1590/S1679-45082015RW3175 |
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author | Requião-Moura, Lúcio Roberto de Matos, Ana Cristina Carvalho Pacheco-Silva, Alvaro |
author_facet | Requião-Moura, Lúcio Roberto de Matos, Ana Cristina Carvalho Pacheco-Silva, Alvaro |
author_sort | Requião-Moura, Lúcio Roberto |
collection | PubMed |
description | Cytomegalovirus infection is one of most frequent infectious complications after renal transplantation, and can be classified as primo-infection, when the transmission occurs through the graft, or reactivation, when the recipient is cytomegalovirus seropositive. After transplantation, cytomegalovirus can appear as an infection, when the patient presents with evidence of viral replication without symptoms or disease, which has two clinical spectra: typical viral syndrome or invasive disease, which is a less common form. Their effects can be classified as direct, while the disease is developed, or indirect, with an increase of acute rejection and chronic allograft dysfunction risks. Diagnosis must be made based on viremia by one of the standardized methods: antigenemia or PCR, which is more sensitive. The risk factors related to infection after transplantation are the serologic matching (positive donor and negative recipient) and anti-lymphocyte antibody drugs. One of the strategies to reduce risk of disease should be chosen for patients at high risk: preemptive treatment or universal prophylaxis. Recent clinical research has described ganciclovir resistance as an emergent problem in management of cytomegalovirus infection. Two types of mutation that cause resistance were described: UL97 (most frequent) and UL54. Today, sophisticated methods of immunologic monitoring to detect specific T-cell clones against cytomegalovirus are used in clinical practice to improve the management of high-risk patients after renal transplantation. |
format | Online Article Text |
id | pubmed-4946822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Instituto de Ensino e Pesquisa Albert Einstein |
record_format | MEDLINE/PubMed |
spelling | pubmed-49468222016-08-10 Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives Requião-Moura, Lúcio Roberto de Matos, Ana Cristina Carvalho Pacheco-Silva, Alvaro Einstein (Sao Paulo) Review Cytomegalovirus infection is one of most frequent infectious complications after renal transplantation, and can be classified as primo-infection, when the transmission occurs through the graft, or reactivation, when the recipient is cytomegalovirus seropositive. After transplantation, cytomegalovirus can appear as an infection, when the patient presents with evidence of viral replication without symptoms or disease, which has two clinical spectra: typical viral syndrome or invasive disease, which is a less common form. Their effects can be classified as direct, while the disease is developed, or indirect, with an increase of acute rejection and chronic allograft dysfunction risks. Diagnosis must be made based on viremia by one of the standardized methods: antigenemia or PCR, which is more sensitive. The risk factors related to infection after transplantation are the serologic matching (positive donor and negative recipient) and anti-lymphocyte antibody drugs. One of the strategies to reduce risk of disease should be chosen for patients at high risk: preemptive treatment or universal prophylaxis. Recent clinical research has described ganciclovir resistance as an emergent problem in management of cytomegalovirus infection. Two types of mutation that cause resistance were described: UL97 (most frequent) and UL54. Today, sophisticated methods of immunologic monitoring to detect specific T-cell clones against cytomegalovirus are used in clinical practice to improve the management of high-risk patients after renal transplantation. Instituto de Ensino e Pesquisa Albert Einstein 2015 /pmc/articles/PMC4946822/ /pubmed/25993081 http://dx.doi.org/10.1590/S1679-45082015RW3175 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Requião-Moura, Lúcio Roberto de Matos, Ana Cristina Carvalho Pacheco-Silva, Alvaro Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
title | Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
title_full | Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
title_fullStr | Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
title_full_unstemmed | Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
title_short | Cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
title_sort | cytomegalovirus infection in renal transplantation: clinical aspects, management and the perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946822/ https://www.ncbi.nlm.nih.gov/pubmed/25993081 http://dx.doi.org/10.1590/S1679-45082015RW3175 |
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