Enterovirus RNA persisted in the explanted myocardium of 28.6% of patients with end-stage dilated cardiomyopathy versus 5.3% with other heart diseases, in the absence of an immune response.
Observational (n=40)
End-stage dilated cardiomyopathy (n=40)
Enterovirus RNA detection vs Other specific heart muscle diseases
Presence of enterovirus-specific RNA in myocardium
Absolute Event Rate: 28.6% vs 5.3%
Tissue from the explanted hearts of 21 patients with idiopathic dilated cardiomyopathy or 19 patients with other specific heart muscle diseases were investigated for presence of enterovirus-specific RNA with an enterovirus group-specific cDNA probe. This was complementary to coxsackievirus B2 RNA sequences between nucleotide numbers 6,550 and 7,400, which are highly conserved between enteroviruses. Hearts from six patients with dilated cardiomyopathy and one patient with ischemic heart disease were found to contain virus RNA. Serology revealed that only one patient (dilated cardiomyopathy group) was positive for coxsackievirus B-specific IgM but negative for virus RNA in the myocardium. Quantitation of leukocytes and T-lymphocytes in the myocardium and expression of major histocompatibility locus antigens revealed no significant differences associated with persistence of virus RNA. These data demonstrate that enterovirus RNA persists in myocardium of a significant proportion of patients with end-stage dilated cardiomyopathy in the absence of a continuing cell-mediated or humoral immune response.
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Neil E. Bowles
Northwestern University
Marlene L. Rose
Harefield Hospital
Peter C. Taylor
South African Medical Research Council
Circulation
Charing Cross Hospital
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Bowles et al. (Wed,) conducted a observational in End-stage dilated cardiomyopathy (n=40). Enterovirus RNA detection vs. Other specific heart muscle diseases was evaluated on Presence of enterovirus-specific RNA in myocardium. Enterovirus RNA persisted in the explanted myocardium of 28.6% of patients with end-stage dilated cardiomyopathy versus 5.3% with other heart diseases, in the absence of an immune response.
synapsesocial.com/papers/6a0f18481cf410a932425b26 — DOI: https://doi.org/10.1161/01.cir.80.5.1128