Hematopoietic stem cell donor vaccination with CMV Triplex augments frequencies of functional and durable CMV-specific T cells in the recipient: a novel strategy to limit antiviral prophylaxis.
Corinna La RosaIbrahim AldossYoonsuh ParkDongyun YangQiao ZhouKetevan GendzekhadzeTeodora KaltchevaWasima RidaShannon DempseyShukaib ArslanAndrew ArtzBrian J BallLiana NikolaenkoVinod A PullarkatRyotaro NakamuraDon J DiamondPublished in: American journal of hematology (2023)
To enhance protective cytomegalovirus (CMV)-specific T cells in immunosuppressed recipients of an allogeneic hematopoietic cell transplant (HCT), we evaluated post-HCT impact of vaccinating healthy HCT donors with Triplex. Triplex is a viral vectored recombinant vaccine expressing three immunodominant CMV antigens. The vector is modified vaccinia Ankara (MVA), an attenuated, non-replicating poxvirus derived from the vaccinia virus strain Ankara. It demonstrated tolerability and immunogenicity in healthy adults and HCT recipients, in whom it also reduced CMV reactivation. Here, we report feasibility, safety and immunological outcomes of a pilot phase 1 trial (NCT03560752 at ClinicalTrials.gov) including 17 CMV-seropositive recipients who received an HCT from a matched related donor (MRD) vaccinated with 5.1 x10 8 pfu/mL of Triplex before cell harvest (median 15, range 11-28 days). Donor and recipient pairs who committed to participation in the trial resulted in exceptional adherence to the protocol. Triplex was well tolerated with limited adverse events in donors and recipients, who all engrafted with full donor chimerism. On day 28 post-HCT, levels of functional vaccinia- and CMV-specific CD137+CD8+ T cells were significantly higher (p < 0.0001 and p = 0.0174 respectively) in recipients of Triplex vaccinated MRD than unvaccinated MRD (control cohort). Predominantly central and effector memory CMV-specific T cell responses continued to steadily expand through 1-year follow up. CMV viremia requiring antivirals developed in three recipients (18%). In summary, this novel approach represents a promising strategy applicable to different HCT settings for limiting the use of antiviral prophylaxis, which can impair and delay CMV-specific immunity, leading to CMV reactivation requiring treatment This article is protected by copyright. All rights reserved.
Keyphrases
- kidney transplantation
- cell cycle arrest
- hematopoietic stem cell
- randomized controlled trial
- type diabetes
- dendritic cells
- clinical trial
- cell death
- sars cov
- working memory
- epstein barr virus
- cell therapy
- adipose tissue
- cell proliferation
- immune response
- diffuse large b cell lymphoma
- drug induced
- insulin resistance
- nk cells
- wild type