Key result
Treatment with pleconaril and IVIG resulted in complete recovery and viral clearance in a patient with susceptible echovirus 13, but failed in a patient with resistant echovirus 11.
Why the study?
Does pleconaril and IVIG improve clinical outcomes and clear HEV in patients with chronic enteroviral meningitis?
Case Report (n=2)
Does pleconaril and IVIG improve clinical outcomes and clear HEV in patients with chronic enteroviral meningitis?
Clinical response to pleconaril in chronic enteroviral meningitis correlates with in vitro susceptibility of the viral isolate.
May support susceptibility testing before pleconaril-IVIG in chronic enteroviral meningitis; leaves open efficacy in controlled trials.
BACKGROUND: Human enteroviruses (HEVs) can cause severe infections, especially in patients with a deficient humoral immune response, such as X-linked agammaglobulinemia. In this patient group, chronic enteroviral meningitis (CEMA) is feared because of extensive morbidity and high fatality rate. Treatment options consist of intravenous immunoglobulin (IVIG), with various outcomes. Pleconaril is an antiviral agent with in vitro activity against HEVs that has been used in the treatment of HEV infections. METHODS: The efficacy of pleconaril and IVIG against HEV isolated from the patients was assessed in vitro in two patients with CEMA. RESULTS: Echovirus 11 was found in the cerebrospinal fluid (CSF) of case 1. Treatment with high-dose IVIG and pleconaril did not provide any clinical improvement and HEV PCR in CSF remained positive. Case 2 (echovirus 13 positive in CSF) was also treated with IVIG and pleconaril. The patient recovered completely and HEV PCR in CSF became negative. Recent IVIG batches contained low titres of neutralizing antibodies against the patient strains. Echovirus 11 (case 1) was resistant to pleconaril in vitro, whereas echovirus 13 (case 2) was susceptible, in accordance with virological response after treatment and subsequent clinical results. CONCLUSIONS: This is the first report that evaluates efficacy of antiviral treatment in CEMA patients in relation to in vitro susceptibility of clinical virus isolates. Since pleconaril is no longer available for compassionate use we strongly propagate that new drugs should be developed against these potential life threatening HEV infections.
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Wildenbeest et al. (2011) conducted a case report in Chronic enteroviral meningoencephalitis (CEMA) (n=2). Pleconaril and IVIG was evaluated on Clinical improvement and HEV PCR in CSF. Treatment with pleconaril and IVIG resulted in complete recovery and viral clearance in a patient with susceptible echovirus 13, but failed in a patient with resistant echovirus 11.
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