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RESEARCH PRODUCT

HBV viral load within subpopulations of peripheral blood mononuclear cells in HBV infection using limiting dilution PCR.

Guido GerkenMartin TripplerKarl-herrmann Meyer Zum Büschenfelde

subject

MaleHepatitis B virusmedicine.disease_causePeripheral blood mononuclear cellPolymerase Chain ReactionVirusHepatitis B ChronicOrthohepadnavirusVirologymedicineHumansPoisson DistributionHepatitis B virusbiologyImmunomagnetic Separationvirus diseasesViral Loadbiology.organism_classificationHepatitis BVirologydigestive system diseasesGlobinsHepadnaviridaeImmunologyDNA ViralLeukocytes MononuclearFemaleViral diseaseViral loadCD8

description

Abstract Extrahepatic viral load in peripheral blood mononuclear cells (PBMCs) of patients with hepatitis B virus (HBV) is still under debate. In this study, HBV infection rates and viral titers were examined within all PBMC subpopulations using limiting dilution-PCR (LD-PCR). PBMCs of patients with acute or chronic hepatitis B were separated by magnetic beads in monocytes, B-cells, CD4+ T-cells, CD8+ T-cells, and NK cells. Using two-round nested PCR, HBV-DNA sequences were detected in all patients examined within each PBMC subpopulation. The frequencies of HBV-positive cells and viral loads were calculated by Poisson analysis of HBV PCR results from serial dilutions of cells and cell lysates. Highest infection rates were found in monocytes and B-cells followed by CD8+ T-cells, NK cells, and CD4+ T-cells. Concerning all subsets, frequencies of HBV-positive cells were 50- to 500-fold higher in chronic than in acute hepatitis B. Viral loads were mostly estimated at about one HBV genome per HBV-positive cell. Moreover, slightly elevated HBV titers were seen in B-cells, CD4+ T-cells, and NK cells in both acute and chronic hepatitis B. It was demonstrated that beside a generally more latent HBV infection in PBMCs, elevated HBV titers point to replication or selective viral uptake within particular PBMC subsets. Therefore, the data suggest that HBV-infected PBMCs may participate in persistence of HBV.

10.1016/s0166-0934(98)00172-4https://pubmed.ncbi.nlm.nih.gov/10204703