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Confirmed primary HHV-6 infection in children with suspected encephalitis
J O Virtanen1, E Herrgård, P Valmari
1Department of Virology, Haartman Institute, University of Helsinki, Helsinki, Finland. oskari.virtanen@helsinki.fi
Insights
Human herpes virus 6 (HHV-6) primary infection is linked to neurological issues in young children. An IgG-avidity test can help diagnose acute HHV-6 infections from a single blood sample.
Area of Science:
- Virology
- Pediatric Neurology
- Immunology
Background:
- Human herpes virus 6 (HHV-6) infection is associated with neurological symptoms in children.
- Two variants, HHV-6A and HHV-6B, exist, but their role in neurological infections remains unclear.
Purpose of the Study:
- To investigate the association between HHV-6A and HHV-6B primary infections and neurological symptoms in children.
- To evaluate the utility of indirect immunofluorescence and IgG-avidity tests in diagnosing acute HHV-6 infections.
Main Methods:
- Studied 53 children with suspected encephalitis for HHV-6A and HHV-6B antibodies using indirect immunofluorescence.
- Employed IgG-avidity testing to differentiate primary from past HHV-6 infections.
- Utilized PCR to detect HHV-6 DNA in patients with confirmed primary infections.
Main Results:
- Forty-one out of 53 children showed IgG antibodies to HHV-6.
- Six children had low IgG avidity, indicating acute primary infection (4 HHV-6A, 1 HHV-6B, 1 mixed).
- HHV-6 was suggested as the viral etiology in 11.3% of cases; HHV-6 DNA was detected in serum/CSF of primary infection cases. Children with primary HHV-6 infection were significantly younger (2.3 vs. 6.4 years).
Conclusions:
- Primary HHV-6 infection is an important potential cause of neurological infections in young children.
- The IgG-avidity test is a valuable tool for diagnosing acute HHV-6 infection using a single serum specimen.
Abstract:
HHV-6 infection has been associated with neurological symptoms in children. Two variants of human herpes virus 6, HHV-6A and HHV-6B, have been identified. Their role in neurological infections is poorly understood. We studied 53 children with suspected encephalitis for HHV-6A (strain GS) and HHV-6B (strain Z29) antibodies using an indirect immunofluorescence test. Primary infection was separated from past infection by an IgG-avidity test. The identified primary infections were studied for HHV-6 specific DNA by PCR. Forty-one children of 53 had IgG antibodies to HHV-6. Six children had low avidity of HHV-6 IgG antibodies indicating acute primary infection; four to type A, one to B, and one to both types. By serology, HHV-6 viral etiology was suggested in 6/53 (11.3%) of cases. One of the six patients with primary infection had HHV-6 DNA in serum and two in CSF. The children with primary HHV-6 infection were significantly younger than the whole series, 2.3 years vs. 6.4 years. We conclude that primary HHV-6 infection appears to be an important associated or causative agent in neurological infections of young children, and it can be confirmed from a single serum specimen using the IgG-avidity test.
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