Cytotoxic KLRG1+ IL-7R- Effector CD8+ T Cells Distinguish Kidney Transplant Recipients Controlling Cytomegalovirus Reactivation

Overview

Journal Front Immunol

Specialty Allergy & Immunology

Date 2025 Mar 3

PMID 40028342

Authors

Yumeng Sun

Subha Sen

Rajesh Parmar

Janice Arakawa-Hoyt

Monica Cappelletti

Maura Rossetti

David W Gjertson

Tara K Sigdel

Minnie M Sarwal

Joanna M Schaenman

Suphamai Bunnapradist

Lewis L Lanier

Harry Pickering

Elaine F Reed

Affiliations

Soon will be listed here.

Abstract

Introduction: Cytomegalovirus (CMV) viremia remains a major contributor to clinical complications in solid organ transplant (SOT) patients, including organ injury, morbidity and mortality. Given their critical role in antiviral defense, CD8+ T cells are essential for protective immunity against CMV.

Methods: Using single-cell RNA sequencing, we investigated the transcriptional signatures and developmental lineages of CD8+ T cells in eight immunosuppressed kidney transplant recipients (KTRs) who received organs from CMV-seropositive donors. Results were validated in a cohort of 62 KTRs using immunophenotyping.

Results: Our data revealed a significant influence of CMV serostatus on transcriptional variance of CD8+ memory T cells, associating with the first principal component from a global analysis of CD8+ T cells (p =0.0406), forming a continuum with five principal differentiation trajectories driven by CMV primary infection or reactivation. Following CMV primary infection, CD8+ T cells were hallmarked by restrained effector-memory differentiation. CD8+ T cells during CMV reactivation diverged non-linearly into senescent-like cells with signatures of arrested cell cycle, diminished translational activity and downregulated and longitudinally expanding effector cells with robust cytotoxic potential and upregulated , acting as a reservoir for long-lived effector cells supporting long-term protection. Notably, CD28 KLRG1 IL-7R (CD127) HLA-DR CD8+ T cells present prior to the detection of viremia in CMV-seropositive patients emerged as a key feature distinguishing patients who did or did not undergo CMV reactivation after prophylaxis discontinuation (p =0.0163). Frequencies of these cells were also positively correlated with CMV-stimulated secretion of IFN-γ (p =0.0494), TNF-α (p =0.0358), MIP-1α (p =0.0262), MIP-1β (p =0.0043).

Discussion: These results provide insights into the transcriptional regulation that influences the generation of CD8+ T cell immunity to CMV and may inform strategics for monitoring host immune response to CMV to better identify and introduce therapeutic intervention to patients at risk of developing clinically significant CMV viremia.

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