CD45RA-depleted DLI for the Prevention of Viral Infections in High-risk Patients After Haploidentical Transplantation (CD45RADLIPx)
CD45RA-depleted DLI for the Prevention of Viral Infections in High-risk Patients After Transplantation: a Prospective, Multicenter, Single-arm, Pragmatic Clinical Study
The goal of this clinical trial is to learn whether giving patients a special type of donor immune cells (called CD45RA Depleted DLI) can help prevent viral infections after a stem cell transplant. It will also learn about the safety of this treatment. The main questions it aims to answer are:
Does this treatment lower the chance of getting serious viral infections after transplant? What medical problems do patients have when receiving this treatment?
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Following allogeneic hematopoietic stem cell transplantation (allo-HSCT), delayed immune reconstitution and long-term use of immunosuppressants leave patients in a prolonged immunocompromised state, predisposing them to various infections, which represent a leading cause of transplant-related mortality. Conventional antiviral agents such as ganciclovir and valganciclovir are associated with hematologic toxicities, including neutropenia and anemia, potentially complicating post-transplant management. Meanwhile, newer antivirals such as cidofovir have not yet been approved in China, limiting patient access. Antiviral cell therapies, represented by virus-specific T cells (VSTs), are expensive and require prolonged culture periods. Therefore, there is an urgent need to identify effective strategies to prevent viral infections after HSCT, especially in high-risk patients.
Previous studies suggest that adoptive donor lymphocyte infusion (DLI) can facilitate immune reconstitution; however, the CD45RA-positive naïve T cells contained in conventional DLI are a major cause of graft-versus-host disease (GvHD). By depleting naïve T cells from donor lymphocytes ex vivo while retaining donor memory T cells (Tm), it is possible to promote post-transplant immune reconstitution without increasing the risk of GvHD. This study plans to conduct a prospective, multicenter, single-arm pragmatic clinical trial. Using the CliniMACS® cell selection system, we will selectively deplete CD45RA-positive T cells ex vivo and infuse the CD45RA-depleted donor lymphocytes (i.e., CD45RA Depleted DLI) to prevent viral infections in high-risk patients after transplantation. The efficacy, safety, and impact on post-transplant immune reconstitution of this regimen will be evaluated.
Primary objective: To evaluate the efficacy and safety of CD45RA Depleted DLI in preventing viral infections in high-risk patients after transplantation.
Secondary objective: To evaluate the impact of CD45RA Depleted DLI on immune reconstitution after transplantation.
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
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SH
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Shanghai, SH, Chine, 200025
- Ruijin Hospital
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Contact:
- Xiaoxia Hu, MD, PhD
- Numéro de téléphone: 008613795437259
- E-mail: hu_xiaoxia@126.com
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
Accepte les volontaires sains
La description
Inclusion Criteria:
Participants must meet all of the following criteria:
- Patients undergoing allogeneic hematopoietic stem cell transplantation (any conditioning regimen or graft source is allowed).
- Presence of at least one high-risk factor for post-transplant viral infection (any of the following):
- Age ≥50 years or ≤14 years
- Non-sibling matched transplantation
- In vivo or ex vivo T-cell depletion
- Myeloablative conditioning
- Conditioning containing radiotherapy
- Second transplantation
- CMV IgG or EBV IgG donor/recipient mismatch (donor positive, recipient negative)
- History of grade II or higher acute graft-versus-host disease (aGVHD) after transplantation and use of high-dose corticosteroids (prednisone equivalent ≥1 mg/kg/day)
- Availability of a suitable lymphocyte donor (see "Donor Selection Criteria").
- Adequate organ function meeting the following laboratory criteria:
- Liver function: ALT and AST ≤10× upper limit of normal (ULN); total bilirubin ≤5× ULN
- Renal function: BUN and creatinine ≤1.25× ULN
- No cardiac dysfunction on electrocardiogram or echocardiogram
- Pulmonary function: oxygen saturation >90% without supplemental oxygen
- The patient or legal guardian has the desire and request to receive treatment, signs the informed consent form before treatment, and is willing to comply with the treatment plan, follow-up schedule, and laboratory tests.
Exclusion Criteria:
Patients meeting any of the following criteria will be excluded from this study:
- Active grade II-IV acute graft-versus-host disease (aGVHD)
- Active aGVHD requiring prednisone or equivalent corticosteroid >0.5 mg/kg/day
- Active viral infection
- Uncontrolled or relapsed malignancy
- Other serious acute or chronic physical or psychiatric conditions, or laboratory abnormalities, that may compromise patient safety or compliance, or affect informed consent, study participation, follow-up, or interpretation of results.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Prevention Group
Prophylactic CD45RA-depleted DLI
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CD45RA Depleted DLI by ex vivo CliniMACS® prepared from mononuclear cell leukapheresis
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Cumulative Incidence of Overall Viral Infection After CD45RA-Depleted DLI
Délai: Up to 3 months after the first CD45RA-depleted DLI, assessed at Days 14, 28, 60, and 90.
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Overall viral infection is defined as the first occurrence of any qualifying viral infection or reactivation detected by quantitative PCR after the first CD45RA-DLI infusion. Viruses assessed include CMV, EBV, ADV, BKV, HHV6, JCV, and B19. A participant will be considered to have a qualifying viral event if any of the following thresholds are met: CMV DNA ≥250 IU/mL, EBV DNA ≥250 IU/mL, ADV DNA ≥1,000 copies/mL, BKV DNA ≥5,000 copies/mL, HHV6 DNA ≥1,000 copies/mL, JCV DNA ≥1,000 copies/mL, or B19 DNA ≥1,000 copies/mL. The outcome will be reported as the cumulative incidence, expressed as the percentage of participants with at least one qualifying viral infection or reactivation event during the assessment period. |
Up to 3 months after the first CD45RA-depleted DLI, assessed at Days 14, 28, 60, and 90.
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Cumulative Incidence of Virus-Specific Infections After CD45RA-Depleted DLI
Délai: Up to 3 months after first infusion
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Report cumulative incidence separately for CMV, EBV, ADV, BKV, HHV6, JCV, and B19 using the protocol-defined PCR thresholds.
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Up to 3 months after first infusion
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Absolute Counts of Peripheral Blood Lymphocyte Subsets as Measured by Flow Cytometry
Délai: Up to 1 year after the first CD45RA-depleted DLI
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Immune reconstitution will be assessed by flow cytometric enumeration of peripheral blood lymphocyte subsets, including CD3+ T cells, CD4+ T cells, CD8+ T cells, CD19+ B cells, CD56+ NK cells, and CD4+CD25+CD127- regulatory T cells.
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Up to 1 year after the first CD45RA-depleted DLI
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Virus-Specific T-Cell Immune Responses After CD45RA-Depleted DLI
Délai: Up to 3 months after the first CD45RA-depleted DLI, assessed at Days 14, 28, 60, and 90.
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Virus-specific immune reconstitution will be assessed by measuring virus-specific T-cell responses against CMV, EBV, ADV, BKV, B19, HHV6, and JCV using the protocol-defined virus-specific T-cell assay.
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Up to 3 months after the first CD45RA-depleted DLI, assessed at Days 14, 28, 60, and 90.
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- RJ-BMT-Prophylaxis 1.0
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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