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Active Human Herpesvirus 6 Infection in Patients With Multiple Sclerosis
Roberto Álvarez-Lafuente, MD;
Carlos Martín-Estefanía, PhD;
Virginia de las Heras, PhD;
Carmen Castrillo, PhD;
Juan José Picazo, MD;
Eduardo Varela de Seijas, MD;
Rafael Arroyo González, MD
Arch Neurol. 2002;59:929-933.
Context Human herpesvirus 6 (HHV-6) has been linked with multiple sclerosis
(MS).
Objectives To determine HHV-6 viral load in patients with MS, and to analyze separately
its 2 variants, HHV-6A and HHV-6B.
Patients and Methods We analyzed 149 blood and serum samples; 103 were from patients with
relapsing-remitting MS (33 during an MS relapse and 70 during remission),
and 46 were from healthy blood donors. To determine whether the HHV-6 genome
and its variants were present, we analyzed viral DNA using quantitative real-time
polymerase chain reaction, which has a sensitivity of 1 copy.
Results We found HHV-6 DNA in the peripheral blood mononuclear cells of 53.4%
of patients and 30.4% of healthy blood donors; HHV-6A was found in 20.4% of
patients and 4.4% of controls, and HHV-6B was found in 33.0% vs 26.1%, respectively.
Mean viral load in both groups was 7.4 copies of HHV-6 per microgram of DNA
(range, 1-15 copies). Analysis of serum samples showed that none of the healthy
blood donors were positive for HHV-6, although 14.6% of patients were positive
for the virus, specifically the HHV-6A variant. There was no difference between
patients during remission or relapse. Mean viral load was 26.3 copies/µg
microgram of DNA (range, 1-86 copies).
Conclusions Despite the low viral load and the lack of clinical correlation, and
given the biological characteristics of the virus, our results suggest that
there was active HHV-6A infection in 14.6% of patients with MS. Further quantitative
real-time polymerase chain reaction studies will help us understand the clinical
significance of such a low viral load.
From the Departments of Clinical Microbiology (Drs Álvarez-Lafuente
and Picazo) and Neurology (Drs Martín-Estefanía, de las Heras,
Castrillo, Varela de Seijas, and Arroyo González), San Carlos Hospital,
Madrid, Spain.
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