TY - JOUR
T1 - Significance of human herpesviruses to transplant recipients.
AU - Yoshikawa, Tetsushi
PY - 2003/12
Y1 - 2003/12
N2 - PURPOSE OF REVIEW: Despite recent great advances in transplantation techniques, herpesvirus infections remain a major cause of morbidity and mortality in transplant recipients. While improvement in immunosuppressive drug regimens have decreased the risk of graft-versus-host disease and rejection in bone marrow transplant recipients and solid organ transplant recipients, all such drugs carry with them an increased risk of herpesvirus reactivation. The following review consolidates recent findings in this field, covering reports published from January 2002 to August 2003. RECENT FINDINGS: Real-time polymerase chain reaction has improved the ability to distinguish between latent and active herpesvirus infection, which had been a major difficulty in the diagnosis of such conditions. It has been suggested that evaluation of virus-specific cytotoxic T lymphocyte activity is important for prediction of viral diseases. Development of new antiviral drugs has provided other therapeutic options. However, neither prophylactic nor preemptive administration of antiviral drugs can completely abolish the risk of herpesvirus infection. Transfusion of virus-specific cytotoxic T lymphocytes has been suggested to be a useful treatment for recipients with continuous viral replication due to severe immunosuppression. SUMMARY: Recent progress has been made in learning more about the role of virus-specific cytotoxic T lymphocytes, and developing better diagnostic procedures and therapeutic protocols that are efficient and have reduced adverse side effects. Reliable monitoring methods for viral load, in combination with evaluation of virus-specific cytotoxic T cells, has made possible the prediction of viral diseases and furthered understanding of the role of these cells in controlling viral infections. Furthermore, adoptive immunotherapy has been improved by analyzing host immune responses.
AB - PURPOSE OF REVIEW: Despite recent great advances in transplantation techniques, herpesvirus infections remain a major cause of morbidity and mortality in transplant recipients. While improvement in immunosuppressive drug regimens have decreased the risk of graft-versus-host disease and rejection in bone marrow transplant recipients and solid organ transplant recipients, all such drugs carry with them an increased risk of herpesvirus reactivation. The following review consolidates recent findings in this field, covering reports published from January 2002 to August 2003. RECENT FINDINGS: Real-time polymerase chain reaction has improved the ability to distinguish between latent and active herpesvirus infection, which had been a major difficulty in the diagnosis of such conditions. It has been suggested that evaluation of virus-specific cytotoxic T lymphocyte activity is important for prediction of viral diseases. Development of new antiviral drugs has provided other therapeutic options. However, neither prophylactic nor preemptive administration of antiviral drugs can completely abolish the risk of herpesvirus infection. Transfusion of virus-specific cytotoxic T lymphocytes has been suggested to be a useful treatment for recipients with continuous viral replication due to severe immunosuppression. SUMMARY: Recent progress has been made in learning more about the role of virus-specific cytotoxic T lymphocytes, and developing better diagnostic procedures and therapeutic protocols that are efficient and have reduced adverse side effects. Reliable monitoring methods for viral load, in combination with evaluation of virus-specific cytotoxic T cells, has made possible the prediction of viral diseases and furthered understanding of the role of these cells in controlling viral infections. Furthermore, adoptive immunotherapy has been improved by analyzing host immune responses.
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U2 - 10.1097/00001432-200312000-00014
DO - 10.1097/00001432-200312000-00014
M3 - Review article
C2 - 14624112
AN - SCOPUS:2442593067
SN - 0951-7375
VL - 16
SP - 601
EP - 606
JO - Current opinion in infectious diseases
JF - Current opinion in infectious diseases
IS - 6
ER -