RecruitingNCT07688759

CMV-CMI in csCMVi After HSCT

Study of CMV Specific Immune Reconstitution in Patients With Clinical Significant CMV Infection After Allogeneic Hematopoietic Stem Cell Transplantation (Allo-HSCT)


Sponsor

The First Affiliated Hospital of Soochow University

Enrollment

40 participants

Start Date

Jun 1, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

Cytomegalovirus (CMV) reactivation is a common and serious complication after allogeneic hematopoietic stem cell transplantation (allo-HSCT), and the reconstitution of CMV-specific cell-mediated immunity (CMV-CMI) plays a key role in viral control. This prospective, exploratory study will enroll 40 adult CMV-seropositive patients who experience their first CMV reactivation after allo-HSCT. CMV-specific T cell levels (IFN-γ-producing T cells stimulated by IE-1 and pp65 antigens) will be measured using ELISPOT at four time points: at diagnosis of CMV viremia, 3 weeks after initiating preemptive therapy, at anti-CMV drug withdrawal, and 4 weeks after treatment discontinuation. Patients will be followed for 12 weeks after stopping treatment. The primary objective is to describe the changes in CMV-specific T cell levels over the therapy. Secondary objectives are to explore the relationship between these levels and the occurrence of refractory CMV infection, recurrent CMV infection, and CMV disease. Findings may help identify patients at high risk of progressing to severe or persistent CMV infection at an early stage of preemptive therapy, enabling personalized intervention strategies.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • ≥18 years old and underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT);
  • First CMV reactivation after transplantation;
  • Life expectancy of ≥8 weeks;
  • The participant (or legally acceptable representative, if applicable) has provided written informed consent for the trial.

Exclusion Criteria4

  • Recurrence of CMV infection;
  • primary CMV infection in CMV-seronegative recipients (R-);
  • Resistance to known anti-CMV drugs (ganciclovir, valganciclovir, foscarnet, maribavir, etc.);
  • Currently receiving CMV-CTL treatment or lymphocyte infusion.

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Interventions

DRUGAnti-Cytomegalovirus Therapy

The choice of agent (monotherapy or combination) is at the investigator's discretion and may include ganciclovir, valganciclovir, foscarnet, maribavir, or other approved anti-CMV medications.


Locations(1)

The First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China

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NCT07688759


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