<?xml version="1.0" encoding="UTF-8"?>
<clinical_study>
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    http://clinicaltrials.gov/ct2/html/images/info/public.xsd
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  <required_header>
    <download_date>Information obtained from ClinicalTrials.gov on May 19, 2013</download_date>
    <link_text>Link to the current ClinicalTrials.gov record.</link_text>
    <url>http://clinicaltrials.gov/show/NCT00006314</url>
  </required_header>
  <id_info>
    <org_study_id>922</org_study_id>
    <nct_id>NCT00006314</nct_id>
  </id_info>
  <brief_title>Cytomegalovirus Spread and Reactivation in Blood Cells</brief_title>
  <sponsors>
    <lead_sponsor>
      <agency>National Heart, Lung, and Blood Institute (NHLBI)</agency>
      <agency_class>NIH</agency_class>
    </lead_sponsor>
  </sponsors>
  <source>National Heart, Lung, and Blood Institute (NHLBI)</source>
  <oversight_info>
    <authority>United States: Federal Government</authority>
  </oversight_info>
  <brief_summary>
    <textblock>
      To investigate the relationship between HCMV and bone marrow progenitor cells to understand
      whether HCMV is latent in CD34 + bone marrow progenitors and the mechanism by which the
      virus remains in a latent state.
    </textblock>
  </brief_summary>
  <detailed_description>
    <textblock>
      BACKGROUND:

      Despite progress in understanding the pathophysiology of human cytomegalovirus (HCMV)
      infections, its manifestations in the immune compromised host are frequently associated with
      high morbidity and mortality.  In this setting, HCMV disease can develop e.g. following
      immune suppression as a result of reactivation of latent HCMV acquired earlier in life.  The
      mechanisms leading to establishment of latent infections and their subsequent reactivation
      are not clear.  It is also unknown whether HCMV exists in a latent form with limited viral
      gene expression or as a persistent infection with normal virus transcription.

      DESIGN NARRATIVE:

      The specific aims of the study were to: 1) examine the percentage of HCMV positive donors
      whose bone marrow progenitors contained HCMV DNA using nested PCR and determine if virus
      could be rescued from those cells. 2) Analyze the HCMV life cycle in hematopoietic
      progenitor and stem cells. 3) identify and analyze HCMV gene expression in in vivo infected
      leukocytes. Bone marrow progenitors containing HCMV DNA detectable by nested PCR were
      isolated from human donors and used as as source of mRNA to prepare Cdna libraries. 4)
      Determine if gene(s) expressed in bone marrow progenitors were important in either
      establishing or maintaining a latent infection or in the lytic cycle of HCMV. Information
      provided from the above studies yielded information important in planning future approaches
      for the therapy of HCMV infections.
    </textblock>
  </detailed_description>
  <overall_status>Completed</overall_status>
  <start_date>July 1999</start_date>
  <completion_date>June 2004</completion_date>
  <phase>N/A</phase>
  <study_type>Observational</study_type>
  <study_design>Observational Model:  Natural History</study_design>
  <condition>Blood Disease</condition>
  <condition>Cytomegalovirus Infections</condition>
  <eligibility>
    <criteria>
      <textblock>
        No eligibility criteria
      </textblock>
    </criteria>
    <gender>Male</gender>
    <minimum_age>N/A</minimum_age>
    <maximum_age>N/A</maximum_age>
    <healthy_volunteers>No</healthy_volunteers>
  </eligibility>
  <overall_official>
    <last_name>Stephen St. Jeor</last_name>
    <affiliation>University of Nevada, Las Vegas</affiliation>
  </overall_official>
  <reference>
    <citation>Crapnell K, Zanjani ED, Chaudhuri A, Ascensao JL, St Jeor S, Maciejewski JP. In vitro infection of megakaryocytes and their precursors by human cytomegalovirus. Blood. 2000 Jan 15;95(2):487-93.</citation>
    <PMID>10627453</PMID>
  </reference>
  <reference>
    <citation>Rizvanov AA, van Geelen AG, Morzunov S, Otteson EW, Bohlman C, Pari GS, St Jeor SC. Generation of a recombinant cytomegalovirus for expression of a hantavirus glycoprotein. J Virol. 2003 Nov;77(22):12203-10.</citation>
    <PMID>14581557</PMID>
  </reference>
  <reference>
    <citation>Khaiboullina SF, Maciejewski JP, Crapnell K, Spallone PA, Dean Stock A, Pari GS, Zanjani ED, Jeor SS. Human cytomegalovirus persists in myeloid progenitors and is passed to the myeloid progeny in a latent form. Br J Haematol. 2004 Aug;126(3):410-7.</citation>
    <PMID>15257715</PMID>
  </reference>
  <reference>
    <citation>Bego M, Maciejewski J, Khaiboullina S, Pari G, St Jeor S. Characterization of an antisense transcript spanning the UL81-82 locus of human cytomegalovirus. J Virol. 2005 Sep;79(17):11022-34.</citation>
    <PMID>16103153</PMID>
  </reference>
  <verification_date>January 2006</verification_date>
  <lastchanged_date>January 27, 2006</lastchanged_date>
  <firstreceived_date>September 28, 2000</firstreceived_date>
  <has_expanded_access>No</has_expanded_access>
  <condition_browse>
    <!-- CAUTION:  The following MeSH terms are assigned with an imperfect algorithm  -->
    <mesh_term>Cytomegalovirus Infections</mesh_term>
    <mesh_term>Hematologic Diseases</mesh_term>
  </condition_browse>
  <!-- Results have not yet been posted for this study                                -->
</clinical_study>
