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Clinical features and virological findings in children with primary human herpesvirus 7 infection
1Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Insights
Primary human herpesvirus 7 (HHV-7) infection in children presents with fever and rash, similar to human herpesvirus 6 (HHV-6). HHV-7 infection can trigger increased HHV-6 antibody levels.
Area of Science:
- Virology
- Pediatrics
- Infectious Diseases
Background:
- Human herpesvirus 7 (HHV-7) and human herpesvirus 6 (HHV-6) are common childhood viruses.
- Primary infections can present with similar clinical symptoms, making differentiation challenging.
- Understanding the interplay between HHV-7 and HHV-6 is crucial for accurate diagnosis and management.
Purpose of the Study:
- To describe the clinical characteristics of primary HHV-7 infection in infants and children.
- To compare serologic and virologic findings of HHV-7 and HHV-6 infections.
- To investigate the relationship between HHV-7 and HHV-6 during primary infection.
Main Methods:
- Clinical examination and virologic testing of 71 infants and children with acute febrile illness.
- Isolation of HHV-6 and HHV-7 from heparinized blood samples.
- Detection of viral DNA using nested polymerase chain reaction (PCR) and antibody levels via indirect immunofluorescence assay.
Main Results:
- HHV-7 infection was identified in 15 children, presenting with fever (average 38.7°C) and rash (93%) lasting approximately 3 days.
- Clinical features of HHV-7 infection were comparable to HHV-6 infection.
- Elevated HHV-6 antibody titers were observed in 53% of patients with primary HHV-7 infection; HHV-7 DNA was detected in peripheral blood mononuclear cells (MNCs) and plasma.
Conclusions:
- Primary HHV-7 infection in children shares clinical similarities with HHV-6 infection.
- HHV-7 infection can lead to a significant increase in pre-existing HHV-6 antibodies.
- HHV-7 DNA is detectable in peripheral blood MNCs and plasma during acute infection.
Objective:
To elucidate clinical features of patients with primary human herpesvirus 7 (HHV-7) infection and serologic and virologic findings between HHV-7 and human herpesvirus 6 (HHV-6).
Materials And Methods:
During a 19-month observation period, 71 infants and children (35 boys and 36 girls with a mean age of 14.5 months [range, 1 month to 48 months]) who had acute febrile respiratory illness with or without skin rash were examined clinically and virologically. Heparinized blood samples were used for isolation of HHV-6 and HHV-7 and detection of both virus DNA sequences by a nested polymerase chain reaction amplification. Both virus antibody activities were measured by an indirect immunofluorescent assay.
Results:
HHV-7 infection was observed in 15 (6 boys and 9 girls with a mean age of 12.9 months [range, 7 months to 27 months]), 1 of 10 with upper respiratory infection and 14 (28%) of 50 with febrile exanthem, whereas HHV-6 infection was in 22 (44%) of the 50. Fever (37.5 degrees C) was observed in all 15, with an average maximum body temperature of 38.7 degrees C (range, 37.6 degrees C to 39.8 degrees C), which persisted for 2.9 days (range, 1 to 5 days). Papular, macular, or maculopapular rash was observed in 14 (93%) of the 15, which appeared on day 2.9 of fever (range, days 2 to 5) on the face, trunk, and extremities and persisted for 2.7 days (range, 1 to 5 days). A convulsive seizure that persisted for a few minutes developed in 1 patient on the first day of elevation of fever. HHV-6 antibody was demonstrated in 13 (87%), and a simultaneous significant increase to HHV-6 antibody titers was observed in 8 (53%) of the 15 during primary HHV-7 infection. HHV-7 and HHV-6 DNAs were almost always detected in mononuclear cells (MNCs) during acute and convalescent phases, whereas HHV-7 DNA was positive in some plasma samples obtained during the acute phase of the disease.
Conclusions:
Primary HHV-7 infection occurred somewhat later than HHV-6, which was confirmed by the isolation of HHV-7 from blood and/or seroconversion to the virus. Clinical features of a virologically confirmed patient with primary HHV-7 infection were comparable with those of primary HHV-6 infection. Preexisting HHV-6 antibody increased significantly in the half of patients with primary HHV-7 infection. HHV-7 DNA was detected in peripheral blood MNCs and plasma in the acute phase and persisted in MNCs thereafter.
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