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Anti-NMDAR Encephalitis After Neonatal HSV-1 Infection in a Child With Low TLR-3 Function
Monica Manglani1,2, Marian Poley3, Ashutosh Kumar4
1College of Medicine, Pennsylvania State, Hershey, Pennsylvania.
Insights
Neonatal herpes simplex virus encephalitis (HSVE) can lead to autoimmune anti-N-methyl-D-aspartate receptor encephalitis (NMDARe). Early immunodeficiency screening is crucial for infants with neonatal herpes to prevent long-term neurological damage.
Area of Science:
- Neuroimmunology
- Pediatric Neurology
- Infectious Diseases
Background:
- Neonatal herpes simplex virus encephalitis (HSVE) frequently causes lasting neurodevelopmental deficits.
- Children with herpes simplex virus are at higher risk for developing autoimmune anti-N-methyl-D-aspartate receptor encephalitis (NMDARe).
Observation:
- A case of neonatal disseminated herpes infection is presented, where HSVE developed after acyclovir cessation.
- Following HSVE resolution, the patient exhibited rapid neurological decline, including behavioral changes and seizures, indicative of NMDARe.
- The patient was diagnosed with NMDARe and low toll-like receptor-3 function.
Findings:
- Review of pediatric NMDARe post-HSVE cases highlights presentation, risk factors, outcomes, and the role of immunodeficiency.
- Neonatal herpes virus exposure poses unique risks to the developing immune system and brain.
- Low toll-like receptor-3 function may be a predisposing factor in HSVE-mediated NMDARe.
Implications:
- Early immunodeficiency screening in infants with neonatal herpes is vital.
- Understanding the immune response in HSVE-mediated NMDARe can guide therapeutic strategies.
- Mitigating long-term neurological disability and improving quality of life for affected children is a key goal.
Abstract:
Neonatal herpes simplex virus encephalitis (HSVE) often results in long-lasting neuro-disability in affected children. In addition to primary HSVE and HSVE relapses, children with herpes simplex virus are at increased risk of developing anti-N-methyl-d-aspartate receptor encephalitis (NMDARe), an autoimmune encephalitis. In this study, we describe a patient with neonatal disseminated herpes infection, who developed HSVE after discontinuation of 2 years of acyclovir suppressive therapy. After resolution of HSVE, the patient rapidly deteriorated with significant behavioral and neurologic changes including emotional outbursts, fearfulness, involuntary movements, and focal seizures. The patient was diagnosed with anti-NMDARe and was later found to have low toll-like receptor-3 function. In this study, we review published pediatric cases of anti-NMDARe after HSVE as well as previous literature and primary data examining the presentation, predisposing risk factors, predictive outcomes, future directions, and the role of immunodeficiency in HSVE-mediated anti-NMDARe. The neonatal immune system and developing brain are disproportionately vulnerable to early viral exposure; therefore, it is important to recognize the value of early immunodeficiency screening in patients with neonatal herpes simplex virus. By understanding the immune landscape within this patient population, we can mitigate long-term neurologic disability and improve the quality of life of affected children.
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