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Cytomegalovirus Spread and Reactivation in Blood Cells
This study has been completed.
First Received: September 28, 2000   Last Updated: January 27, 2006   History of Changes
Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)
ClinicalTrials.gov Identifier: NCT00006314
  Purpose

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.


Condition
Blood Disease
Cytomegalovirus Infections

MedlinePlus related topics: Cytomegalovirus Infections
U.S. FDA Resources
Study Type: Observational
Study Design: Natural History

Further study details as provided by National Heart, Lung, and Blood Institute (NHLBI):

Study Start Date: July 1999
Estimated Study Completion Date: June 2004
Detailed Description:

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.

  Eligibility

Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

No eligibility criteria

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00006314

Sponsors and Collaborators
Investigators
Investigator: Stephen St. Jeor University of Nevada
  More Information

Publications:
Study ID Numbers: 922
Study First Received: September 28, 2000
Last Updated: January 27, 2006
ClinicalTrials.gov Identifier: NCT00006314     History of Changes
Health Authority: United States: Federal Government

Study placed in the following topic categories:
Virus Diseases
Hematologic Diseases
Cytomegalic Inclusion Disease
Cytomegalovirus Infections
DNA Virus Infections
Cytomegalovirus
Herpesviridae Infections

Additional relevant MeSH terms:
Virus Diseases
Hematologic Diseases
Cytomegalovirus Infections
DNA Virus Infections
Infection
Herpesviridae Infections

ClinicalTrials.gov processed this record on May 06, 2009