Medical Journals

Kshv/Hhv-8 Infection of Human Hematopoietic Progenitor (Cd34+) Cells: Persistence of Infection During Hematopoiesis in Vitro and in Vivo.

Authors:
  • Wu William
  • Vieira Jeffrey
  • Fiore Nancy
  • Banerjee Prabal
  • Sieburg Michelle
  • Rochford Rosemary
  • Harrington William
  • Feuer Gerold

From: Department of Microbiology and Immunology, State University New York (SUNY) Upstate Medical University, Syracuse, NYUSA.

Blood

  • Publish Date: Jul 2006
  • ISSN: 0006-4971
  • Volume: 108
  • Issue: 1
  • Pages: 141-51
  • Medium: Print
  • Language: English
  • Citation (JAMA): Wu William, Vieira Jeffrey, Fiore Nancy, et al. Kshv/Hhv-8 Infection of Human Hematopoietic Progenitor (Cd34+) Cells: Persistence of Infection During Hematopoiesis in Vitro and in Vivo.. Blood Jul 2006;108:141-51

Abstract

The cellular reservoir for Kaposi sarcoma-associated herpesvirus (KSHV) infection in the hematopoietic compartment and mechanisms governing latent infection and reactivation remain undefined. To determine susceptibility of human CD34+ hematopoietic progenitor cells (HPCs) to infection with KSHV, purified HPCs were exposed to KSHV, and cells were differentiated in vitro and in vivo. Clonogenic colony-forming activity was significantly suppressed in KSHV-infected CD34+ cells, and viral DNA was predominantly localized to granulocyte-macrophage colonies differentiated in vitro. rKSHV.219 is a recombinant KSHV construct that expresses green fluorescent protein from a cellular promoter active during latency and red fluorescent protein from a viral lytic promoter. Infection of CD34+ HPCs with rKSHV.219 showed similar patterns of infection, persistence, and hematopoietic suppression in vitro in comparison with KSHV. rKSHV.219 infection was detected in human CD14+ and CD19+ cells recovered from NOD/SCID mouse bone marrow and spleen following reconstitution with rKSHV.219-infected CD34+ HPCs. These results suggest that rKSHV.219 establishes persistent infection in NOD/SCID mice and that virus may be disseminated following differentiation of infected HPCs into the B-cell and monocyte lineages. CD34+ HPCs may be a reservoir for KSHV infection and may provide a continuous source of virally infected cells in vivo.

Mesh Headings (Keywords): Animals, Antigens, CD34, Cell Line, Disease Models, Animal, Gene Expression Regulation, Viral, Hematopoietic Stem Cells, Herpesviridae Infections, Herpesvirus 8, Human, Humans, Mice, Mice, SCID, Reverse Transcriptase Polymerase Chain Reaction, Transplantation, Heterologous, Virus Replication


Check for Full Text / PubMed Unique Identifier (PMID): 16543476


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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