Hematopoietic stem cell donor vaccination with cytomegalovirus triplex augments frequencies of functional and durable cytomegalovirus‐specific T cells in the recipient: A novel strategy to limit antiviral prophylaxis

Author:

La Rosa Corinna1ORCID,Aldoss Ibrahim1ORCID,Park Yoonsuh1,Yang Dongyun1,Zhou Qiao1,Gendzekhadze Ketevan2,Kaltcheva Teodora1,Rida Wasima3,Dempsey Shannon1,Arslan Shukaib1ORCID,Artz Andrew1,Ball Brian1ORCID,Nikolaenko Liana1,Pullarkat Vinod A.1ORCID,Nakamura Ryotaro1ORCID,Diamond Don J.1

Affiliation:

1. Department of Hematology and Hematopoietic Cell Transplantation City of Hope National Medical Center Duarte California USA

2. Histocompatibility Laboratory, Department of Hematology and Hematopoietic Cell Transplantation City of Hope National Medical Center Duarte California USA

3. Biostatistics Consultant Arlington Virginia USA

Abstract

AbstractTo 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 × 108 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 < .0001 and p = .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.

Funder

National Cancer Institute

Publisher

Wiley

Subject

Hematology

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