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Betaherpesviruses in transplant recipients
P D Griffiths1, D A Clark, V C Emery
1Department of Virology, Royal Free and University College Medical School, UK. p.griffiths@rfc.ucl.ac.uk
The Journal of Antimicrobial Chemotherapy
|June 16, 2000
Summary
Cytomegalovirus (CMV) and human herpesviruses 6 and 7 (HHV-6, HHV-7) can cause opportunistic infections post-transplant. High CMV viral load is linked to disease and graft rejection, suggesting a greater role for betaherpesviruses.
Area of Science:
- Virology
- Transplantation Immunology
- Infectious Diseases
Background:
- Betaherpesviruses, including cytomegalovirus (CMV) and human herpesviruses 6 and 7 (HHV-6, HHV-7), are known human pathogens.
- These viruses can cause opportunistic infections in immunocompromised individuals, particularly after organ transplantation.
Purpose of the Study:
- To investigate the clinical significance of betaherpesviruses, specifically CMV, HHV-6, and HHV-7, in the context of organ transplantation.
- To determine the association between viral load and the development of CMV disease and allograft rejection.
Main Methods:
- Quantitative analysis of viral loads for CMV, HHV-6, and HHV-7 in transplant recipients.
- Correlation of viral loads with clinical outcomes, including end-organ disease and biopsy-proven graft rejection.
Main Results:
- Patients with overt CMV disease exhibit significantly higher CMV viral loads compared to asymptomatic individuals.
- High CMV viral load is a major determinant of risk factors for CMV disease, such as pre-transplant serostatus and post-transplant viremia.
- CMV is implicated in allograft rejection, which can be mitigated by antiviral prophylaxis.
- Quantitative studies reveal that HHV-6 and CMV are independently associated with graft rejection after liver transplantation.
Conclusions:
- The clinical significance of betaherpesviruses in transplantation may be underestimated.
- Viral load quantification is crucial for understanding the pathogenesis of CMV disease and its complications.
- HHV-6 and CMV are significant contributors to graft rejection in liver transplant recipients.