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Cytomegalovirus in Neonates

Cytomegalovirus in Neonates. David K. Hong, MD Pediatrics/Infectious Diseases & Immunology/Allergy Stanford University Medical School Santa Clara Valley Medical Center. Objectives. 1.  Describe the clinical features of congenital infection with CMV

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Cytomegalovirus in Neonates

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  1. Cytomegalovirus in Neonates David K. Hong, MD Pediatrics/Infectious Diseases & Immunology/Allergy Stanford University Medical School Santa Clara Valley Medical Center

  2. Objectives 1.  Describe the clinical features of congenital infection with CMV 2.  Review current treatment options for congenital CMV infections 3.  Discuss the unique features of CMV infections in premature infants

  3. Cytomegalovirus Beta herpesvirus - dsDNA Co-evolved with humans Largest virus to infect humans – 230 proteins CMV infection is not cleared. Chronic infection leads to intermittent viral shedding 1956 – Margaret Smith isolated virus from human salivary gland 1965 – 1st recognized CMV disease in a healthy adult (Br Med J. 1965;1099:102)

  4. CMV - Pathology • Cell enlargement with intranuclear inclusions • “Cytomegalic inclusion disease” • Cytomegalia in viscera and parotid glands. • “salivary gland virus” Margaret Smith. Proc Soc Exp Biol Med 1956, 92:424

  5. Historical Interest Thomas Weller named virus Cytomegalovirus Virologic and Clinical Observations on Cytomegalic Inclusion Disease. Thomas Weller and JB Hanshaw. NEJM 1962

  6. Clinical Manifestations of acute CMV infection Immunocompetent Individuals • Primary CMV infection in immunocompetent children and adults is usually asymptomatic • Clinical features of acute infection overlap with EBV • Mononucleosis syndrome – more common in EBV • fever, lymphadenopathy, lymphocytosis • Mean duration of fever is 2 weeks • Sore throat with enlarged exudate-covered tonsils – more common in EBV • Low level elevation of liver transaminases common (>90%)

  7. CMV infection is very Common Prevalence of CMV by Age Group and Ethnic Group Mexican American females Mexican American males Non-Hispanic white females Non-Hispanic white males Bates SL et al, CID 2010 vol. 50 (11) pp. 1439-1447

  8. CMV is the most common congenital infection Stagno S et al, Clin Obstet Gynecol. 1982 Sep;25(3):563-76 Stanford/El Camino Hospital/SCVMC – 0.6%

  9. Stagno S et al, N Engl J Med 1982; 306:945-9

  10. Multiple studies have shown maternal acquisition of CMV leads to fetal infection from 33—75% Disease rates may be as high as 50% if infection occurs during first half of pregnancy

  11. Disease manifestations – Congenital CMV 90% 10%

  12. Congenital CMV Newborn infected with CMV 10% 90% Symptomatic at birth Asymptomatic 5-10% 90% 10% Death No symptoms Progressive hearing loss Survival ~3% with bilateral hearing loss 3% 50% 55% 52% Sensorineural hearing loss IQ < 70 Microcephaly, seizures, paralysis IQ < 70, Microcephaly, seizures, paralysis ~33% with bilateral hearing loss

  13. Clinical abnormalities in symptomatic congenital CMV Boppana SB et al, Pediatr Infect Dis J. 1992 Feb;11(2):93-9

  14. Laboratory abnormalities in symptomatic congenital CMV Boppana SB et al, Pediatr Infect Dis J. 1992 Feb;11(2):93-9

  15. 10% die 45% - 90% will have CNS sequelae Sequelae Sensorineural hearing loss Developmental & cognitive deficits Chorioretinitis Symptomatic Congenital CMV

  16. Congenital CMV Risk Factors • Caring for preschool children in the year before delivery • Onset of sexual activity <2yrs before delivery • Sexually transmitted diseases during pregnancy • Household size > 3 people • Maternal age < 25 • Seroconversionbetween children and delivery of subsequent child within 2 years • HIV infection • Pre-term delivery • Lower socioeconomic status • Black race • Fowler KB, Pass RF Pediatrics (2006) 118:e286; Fowler KB, Stagno S, Pass RF. ClinInfect Dis 2004; 38:1035–1037; KennesonA, Cannon MJ. Rev Med Virol2007; 17:253–276.

  17. Diagnosis of Congenital CMV • Virus should be isolated within the first 2-3 weeks of life • Isolation of CMV after this time may represent acquisition at birth or post-natally • Options for isolation of virus include viral culture or PCR from saliva or urine • CMV IgM lacks adequate sensitivity or specificity compared with culture or PCR

  18. CMV-infect infants shed virus in their urine for many months Stagno S et al, N Engl J Med 1982; 306:945-9

  19. CMV viral testing • Conventional viral culture can take 2-4 weeks to isolate CMV • CMV shell vial – identification can occur in 24-48 hours • CMV PCR in urine is available at LPCH Specimen is centrifuged onto cover slip covered with fibroblasts to accelerate virus entry CMV is detected with fluorescent antibodies against early CMV proteins

  20. How many CMV urine tests are needed? 1st test 2nd test 3rd test Two CMV urine tests are adequate to screen for CMV infection Courtesy N. Srinivas, LPCH

  21. Treatment of Congenital CMV • Antiviral against CMV is available • Ganciclovir - IV • Which patients do you treat? • How long do you treat? • How do you know if it worked?

  22. J Pediatr 2003; 143:16-25 • Enrolled 100 patients with symptomatic CMV disease involving the CNS • Patients received 6 weeks of IV ganciclovir • Patients were followed for 1 year and had hearing evaluations at 6 months and 1 year • Found less hearing loss at 6 months and possibly less hearing loss at 1 year

  23. Kimberlin DW. J Pediatr 2003, 143:16;

  24. Ganciclovir therapy appears to be beneficial • After 6 weeks of IV ganciclovir… • At 6 months, 84% (21/25) improved or maintained hearing status • 59% (10/17) controls • At 12 months, 21% (5/24) worse hearing • 68% (13/19) controls Kimberlin DW. J Pediatr 2003, 143:16;

  25. Major caveats… • 100 subjects enrolled; 42 with full follow-up for analysis • 63% (29/46) grade 3 or 4 neutropenia • Dosage modifications 14/29 patients • GCSF in 2 patients • Gram negative sepsis in 1 patient • What about mildly symptomatic or asymptomatic patients? • How do you know 6 weeks is enough? • CMV can be detected in inner ear fluid (perilymph/endolymph) in patients getting cochlear implants

  26. 3 Reasons for Prolonged Ganciclovir Therapy 2. Viral load in blood increases after treatment 1. Virus in the urine increases after treatment 3. CMV genome detected in perilymph Whitley RJ, et al. JID 1997, 175:1080; KImberlin DW, et al. JID, 2008, Mar 15; Bauer PW, et al. Laryngoscope 2005, 115:223Sugiura S, et al. J mEd Virol 2003, 69:72

  27. J Infect Dis (2008) 197:836-45 Valganciclovir is a form of ganciclovir that can be given orally Dosing information is now available for infants

  28. CASG 112

  29. CASG 112

  30. CASG 112

  31. Congenital CMV Newborn infected with CMV 10% 90% Symptomatic at birth Asymptomatic 5-10% 90% 10% Death No symptoms Progressive hearing loss Survival ~3% with bilateral hearing loss 3% 50% 55% 52% Sensorineural hearing loss IQ < 70 Microcephaly, seizures, paralysis IQ < 70, Microcephaly, seizures, paralysis ~33% with bilateral hearing loss

  32. Asymptomatic congenital CMV • 90% of infants infected with CMV have no symptoms • 5-10% will progress to sensorineural hearing loss • We do not know… • Which infants will have progressive hearing loss. • If ganciclovir treatment would prevent hearing loss • If treatment is helpful, how long would you need to treat? • Routine screening of newborns and treatment of newborns is NOT recommended at this time

  33. Can anti-CMV immunoglobulin prevent severe congenital infection? 1 (3%) 7 (50%) 19 (40%) 6 (16%) Congenital CMV disease Nigro G et al, N Engl J Med 2005 vol. 353 (13) pp. 1350-1362

  34. A Randomized Trial to Prevent Congenital Cytomegalovirus (CMV) - NCT01376778 • Prospective, double-blind, placebo-controlled randomized controlled trial evaluating the effectiveness of CMV hyperimmune globulin (Cytogam) at preventing congenital CMV infection in babies born to moms with primary CMV infection during the first half of pregnancy • Inclusion Criteria: • Primary CMV infection in a mother prior to : • 24wks gestational age • Singleton pregnancy • Intervention: • Cytogam – 100mg/kg – how many doses? • Primary outcome measures: • fetal loss (spontaneous or termination) • confirmed fetal CMV infection from amniocentesis • neonatal congenital CMV infection diagnosed by urine or saliva collected by 3 weeks of age that is positive for CMV by culture (the intent will be to obtain in the first two days of life)

  35. CMV Vaccine? The ideal vaccine would: • induce high levels of CMV neutralizing antibodies • Would be targeted at women of child-bearing age • Would have to induce immunity better than natural immunity

  36. CMV glycoprotein B vaccine with MF59 • recent phase 2 trial showed 50% vaccine efficacy at preventing CMV infection in CMV-seronegative women over 42 months • 1 infant had congenital CMV in vaccine group (1%), while 3 infants had congenital CMV in placebo group (3%) – more women became pregnant in the placebo group Pass RF et al, N Engl J Med (2009) 360:1191

  37. Acquired CMV infection in premature infants Perinatal infections can be acquired from exposure to virus in maternal genital secretions, breast milk, or transfusion Incubation period is 4-12 weeks Most infections are asymptomatic with no long-term sequelae Premature infants (750-1500g) at greater risk of symptomatic postnatal CMV infection • CMV from maternal source led to hepatosplenomegaly, neutropenia, lymphocytosis, thrombocytopenia. Longer oxygen requirement Yeager AS et al, J Pediatr (1983)102:918 Transfusion associated CMV occurred in 13.5% of 74 infants of seronegative mothers who were exposed to blood donors with CMV Severe or fatal CMV disease in infants born to seronegative mothers who received CMV+ blood – all were 1200g or less (<28 wks) Yeager AS et al, J Pediatr (1981)98:281-287

  38. What about CMV acquisition via breastmilk in ELBW and VLBW babies? CMV is shed intermittently in breast milk Rates of symptomatic infection in VLBW and ELBW infants from breast-milk associated infections range from 0.6 – 18% Symptoms are variable – asymptomatic infection to severe sepsis Lower birthweight infants and younger infants were more likely to be infected with CMV Some data suggests that administering anti-CMV immunoglobulin prophylaxis can decrease symptomatic disease from CMV acquisition • Maschmann J et al, Clin Infect Dis (2001) 33:1998; Hamele M et al, PIDJ (2010) 29:84; Capretti MG et al, J Pediatr (2009) 154:842

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