Herpesvirus Immunology in Solid Organ Transplant Recipients - Liver Transplant Study

NCT ID: NCT05532540

Last Updated: 2025-04-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-01-01

Study Completion Date

2033-01-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Liver transplantation is the only curative treatment of end-stage liver disease, and every year, around 60 patients undergo liver transplantation in Denmark. Immunosuppressive therapy is necessary to avoid rejection of the transplanted organ.

Over 90% of adults have been infected with at least one herpesvirus, and it is characteristic for herpesviruses that after a first-time infection, the virus remains dormant in the body and may reactivate, particularly if the host is immunosuppressed. An effective immune response against reactivation depends highly on T cells, but T cells are suppressed by immunosuppressive drugs given to organ transplant recipients. Infections caused by herpesviruses are therefore very common in organ transplant recipients, and particularly two herpesviruses, cytomegalovirus (CMV) and varicella-zoster virus (VZV) pose challenges after transplantation.

CMV causes significant morbidity in transplant recipients, contributes to increased mortality and may contribute to loss of the transplanted organ. CMV infections occur in around 40% of liver transplant recipients within a year of transplantation. VZV causes chickenpox at first-time infection and shingles at reactivation. VZV is the second-most common infection in transplant recipients and occurs in around 9% of liver transplant recipients each year. Organ transplant recipients are at higher risk for disseminated disease with complications compared to immunocompetent persons.

A limited number of drugs exist that reduce the risk of and treat CMV infection, but they may cause significant adverse events, and drug resistance is emerging. To avoid CMV infection, some liver transplant recipients receive prophylactic therapy, but due to toxicity, new treatment modalities are warranted. This requires knowledge about herpesvirus specific T cell function in liver transplant recipients, which currently is limited.

The aim of this study is to provide an in-depth description of the protective immune response and immunological risk factors for CMV and VZV infections in liver transplant recipients and to identify patients at high risk in order to provide a platform for future treatment modalities against CMV and VZV infections in liver transplant recipients.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The Herpesvirus Immunology in Solid Organ Transplant Recipients - Liver Transplant Study (HISTORY) is a prospective cohort study that aims to provide in-depth characterisation of the protective immune response and immunological risk factors for CMV and VZV infections in liver transplant recipients and to identify patients at high risk of infection based on clinical and immunological risk factors. All adult patients enlisted for liver transplantation at the Copenhagen University Hospital - Rigshospitalet will be invited to participate regardless of indication for transplantation.

At study entry, participants will fill out a questionnaire regarding health and medication use. Blood samples will be collected at study entry when enlisted for transplantation, at pre-defined intervals after transplantation, and if primary infection with or reactivation of CMV or VZV occurs during follow-up. Health data will be collected from hospital records and national registries.

Blood samples will be separated into peripheral blood mononuclear cells (PBMC) and plasma and stored in a biobank for analysis of PBMC phenotype and function, concentrations of inflammatory markers and mediators, CMV and VZV viral load and serology and other in-depth immunological analyses. Analyses will be performed at the Technical University of Denmark.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cytomegalovirus Infections Varicella Zoster Virus Infection Liver Transplant; Complications

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Liver transplant recipients

All adults enlisted for liver transplantation at Copenhagen University Hospital - Rigshospitalet (N = around 60 per year) will be invited to participate regardless of indication for liver transplantation. These participants are expected to undergo a liver transplantation and will continue in the study after the procedure.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Enlisted for liver transplantation at Copenhagen University Hospital - Rigshospitalet
* Aged 18 years or older

Exclusion Criteria

* Inability to understand the study information
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Technical University of Denmark

OTHER

Sponsor Role collaborator

Rigshospitalet, Denmark

OTHER

Sponsor Role collaborator

Susanne Dam Nielsen, MD, DMSc

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Susanne Dam Nielsen, MD, DMSc

Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Susanne D Nielsen, Professor, MD, DMSc

Role: PRINCIPAL_INVESTIGATOR

Department of Infectious Diseases, Copenhagen University Hospital - Rigshospitalet

Sine R Hadrup, Professor, MSc, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Health Technology, Technical University of Denmark

Moises Alberto Suarez Zdunek, MD

Role: STUDY_DIRECTOR

Department of Infectious Diseases, Copenhagen University Hospital - Rigshospitalet

Sebastian R Hamm, BSc

Role: STUDY_DIRECTOR

Department of Infectious Diseases, Copenhagen University Hospital - Rigshospitalet

Annemette Hald, RN

Role: STUDY_DIRECTOR

Department of Infectious Diseases, Copenhagen University Hospital - Rigshospitalet

Sunil K Saini, MSc, PhD

Role: STUDY_DIRECTOR

Department of Health Technology, Technical University of Denmark

Allan Rasmussen, MD

Role: STUDY_DIRECTOR

Department of Surgical Gastroenterology, Copenhagen University Hospital - Rigshospitalet

Jens G Hillingsø, MD, PhD

Role: STUDY_DIRECTOR

Department of Surgical Gastroenterology, Copenhagen University Hospital - Rigshospitalet

Christian R Pedersen, MD

Role: STUDY_DIRECTOR

Department of Surgical Gastroenterology, Copenhagen University Hospital - Rigshospitalet

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Infectious Diseases, Copenhagen University Hospital - Rigshospitalet

Copenhagen, , Denmark

Site Status

Department of Surgical Gastroenterology, Copenhagen University Hospital - Rigshospitalet

Copenhagen, , Denmark

Site Status

Department of Health Technology, Technical University of Denmark

Lyngby, , Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

References

Explore related publications, articles, or registry entries linked to this study.

Suarez-Zdunek MA, Saini SK, Pedersen CR, Hamm SR, Hald A, Rasmussen A, Hillingso JG, Hadrup SR, Nielsen SD. Herpesvirus immunology in solid organ transplant recipients - liver transplant study (HISTORY): a retrospective and prospective observational cohort study. BMC Infect Dis. 2023 Apr 6;23(1):214. doi: 10.1186/s12879-023-08153-8.

Reference Type DERIVED
PMID: 37024811 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

0073947

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

H-22039226

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Herpetic Eye Disease Study (HEDS) II
NCT00000139 COMPLETED PHASE3
Shingles Prevention Study
NCT00007501 COMPLETED PHASE3