Abstract

Cytomegalovirus (CMV) is one of the most pathogenic viruses in human. After a primary infection, CMV resides in the host for life as a latent infection. When immunity is reduced, CMV can escape the suppressive effects of the immune system and lead to viremia and antigenemia. This reactivation, first seen in transplant patients, has also been documented in non-immunocompromised CMV-seropositive critically ill patients and is associated with higher morbidity and mortality. In the latter, it is not clear whether CMV reactivation is an innocent bystander or the cause of this observed worse outcome. Two studies showed no difference in the outcome of CMV-seropositive and seronegative patients. In addition, proof-of-concept studies investigating prophylactic antiviral treatment to prevent CMV reactivation during critical illness, failed to show a beneficial effect on interleukin levels or clinical outcome. Further research is necessary to resolve the question whether CMV replication impairs the prognosis in non-immunocompromised critically ill patients. We here give a concise overview on the available data and propose strategies to further unravel this question. First, post-mortem investigation may be useful to evaluate the effect of viral replication on organ inflammation and function. Second, further research should focus on the question whether the level of viremia needs to exceed a threshold to be associated with worse outcome. Third, clinical and biochemical assessments may help to identify patients at high risk for reactivation. Fourth, preemptive treatment based upon early detection of the virus is currently under investigation. Finally, immune-stimulating biologicals may be beneficial in high-risk groups.

Highlights

  • The human cytomegalovirus (CMV) is a beta herpes virus that only infects human after transmission by body fluids such as saliva, blood and urine [1]

  • Reactivation occurred more frequently in the ganciclovir group (11.9%) than in the valganciclovir group of the CCCC trial (2.2%). This may be explained by the higher risk of the studied population, as 88% had sepsis upon admission and reactivation in blood occurred in 38.9% of the placebo-treated patients as compared to 27.3% of the non-treated patients in the CCCC trial

  • This study has evaluated the effect of treating herpes simplex virus oropharyngeal reactivation in mechanically ventilated patients, and found no increase in the ventilator-free days at day 60 as compared to placebo

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Summary

INTRODUCTION

The human cytomegalovirus (CMV) is a beta herpes virus that only infects human after transmission by body fluids such as saliva, blood and urine [1]. Reactivation can occur and viral antigens spread into the blood [1, 2] This reactivation has first been identified as an important cause of morbidity and mortality in transplant recipients [5] and HIV-infected patients [6]; and later it has been increasingly encountered in nonimmunocompromised critically ill patients. Lung transplant recipients and CMV-naive patients who received a CMV infected organ are at highest risk of reactivation and in those, guidelines advise to use the prophylactic strategy.

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