Cytomegalovirus
From IDWiki
Background
Microbiology
- A dsDNA virus and the largest member of the human herpesvirus family
- DNA in the nucleoprotein core is embedded in matrix proteins and pp65 antigen, which is surrounded by lipid envelope
- UL54 encodes DNA polymerase and is highly conserved
- UL97 encodes a phosphotransferase enzymes required to phosphorylate (and therefore activate) ganciclovir
- May have four genotypes
Epidemiology
- Transferred by droplets and blood transfusions
- 80% of people are CMV-IgG positive
Risk Factors
- Crowding
Clinical Presentation
- Often asymptomatic when young
Infectious mononucleosis syndrome
- CMV causes 21% of IM
- Fever, lymphadenopathy, and lymphocytosis
- Often mild liver abnormalities
- Occasionally cold agglutinin disease, RF positivity, cryoglobulinemia, and ANA positivity
- Symptoms can persist or relapse over months (average 2 months, but up to 8)
Stem cell transplantation
- Low risk until day 21 post-transplantation, when cell lines begin to return
- May presents as asymptomatic viremia
- Most common symptomatic presentation is pneumonitis (an interstitial pneumonia)
- Can also present with GI involvement
Solid-organ transplantation
- Tends to reactivate within the transplanted organ
- However, all can have GI involvement
Advanced HIV
- Can cause polyradiculopathy and myopathy
Complications
- Pneumonitis
- Can cause an interstitial pneumonia
- Severe in SCT patients, mild in mononucleosis patients
- Hepatitis
- Usually mild
- Can include granulomatous hepatitis in the context of mononucleosis
- Guillain-Barré syndrome
- Sensory and motor palsies in the extremities and cranial nerves
- Resolves over months
- Meningoencephalitis
- Headache, photophobia, lethargy, and pyramidal tract dysfunction
- May have concurrent motor and sensory palsies
- Myocarditis
- Rare
- Thrombocytopenia and hemolytic anemia
- Common in congenital infection, and occasionally seen in adults
- Rashes
- Can cause maculopapular or rubelliform rashes following treatment with amipicillin
Investigations
- CBC showing leukopenia or pancytopenia
- Mild elevation in liver enzymes
- CMV-IgG positive
- Detectable CMV DNA in peripheral blood, though it can rise during intercurrent illness
Diagnosis
- Serology
- IgG useful for prior exposure (suggesting latent infection)
- IgG avidity can confirm recent infection
- IgM >300 U/mL can help diagnose acute infection
- Quantitative PCR is most useful for diagnosis and monitoring response to treatment
- Can be done on blood, BAL, urine, saliva, etc.
- Standards for reporting are defined by WHO
- However, can shed CMV asymptomatically during an acute illness, so must be taken within the clinical context
- Sensitivity/specificity for CMV disease depends on the laboratory methods and cutoff used
- Microscopy of tissue biopsy or cytology may demonstrate large nuclear inclusions, and can use immunofluorescence to pp65 antigen to confirm diagnosis
- Viral culture can be done with human fibroblast cells, but is slow
Management
- Antivirals
- First-line: valganciclovir or ganciclovir
- Measure baseline CBC first due to risk of cytopenias
- Second-line, if cytopenias: foscarnet
- Third-line: cidofovir, maribavir, letermovir
- First-line: valganciclovir or ganciclovir
- At McMaster, expect 1-log drop within 2 weeks (lab-dependent)
- Continue treatment until PCR is negative
Resistance
- Inherent acyclovir resistance
- Tyrosine kinase mutation UL97? confers resistance to (val)ganciclovir
- Polymerase mutation U54? confers resistance to (val)ganciclovir and foscarnet
- Consider resistance if CMV DNA titres not decreasing despite appropriate treatment
- Resistance genotyping available
Prophylaxis
- Solid-organ transplant
- Donor+/Recipientâ high risk for reactivation, the the donor organ infecting the recipient
- Donorâ/Recipient+ intermediate risk
- Donor+/Recipient+ intermediate risk
- Donorâ/Recipientâ lowest risk
- High and intermediate risk patients get prophylaxis with valganciclovir 900 mg po bid for some amount of duration...
- Hematologic stem cell transplant
- Donor+/Recipient+ high risk for reactivation
- Donorâ/Recipient+ high risk
- Donor+/Recipientâ intermediate risk
- Donorâ/Recipientâ lowest risk
- Preemptive monitoring with weekly CMV DNA PCR starting week 2
- Treat if greater than threshold (1425 at McMaster) or if rising titre with symptoms
Complications
- Even when dormant, can cause mild immunosuppression that predisposes to fungal infections
- Asymptomatic shedding in lungs during intercurrent illness
- Viremia with influenza-like illness
- End-orgam damage
- CMV colitis
- Retinitis in AIDS patient (CD4 < 50-100)
- Organ inflammation of solid-organ transplants
- Pneumonitis in stem cell transplants
References
- ^ Michael J. Cannon, D. Scott Schmid, Terri B. Hyde. Review of cytomegalovirus seroprevalence and demographic characteristics associated with infection. Reviews in Medical Virology. 2010;20(4):202-213. doi:10.1002/rmv.655.
- ^ Jutta K. Preiksaitis, R. P. Bryce Larke, Glory J. Froese. Comparative seroepidemiology of cytomegalovirus infection in the Canadian Arctic and an Urban center. Journal of Medical Virology. 1988;24(3):299-307. doi:10.1002/jmv.1890240307.