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Clinical Utility of CMV-Specific CD8+ T-Cell Immune Competence Score in Lung and Heart-Lung Transplant Recipients at Risk of Cytomegalovirus Infection

A. Meesing,1 R. Abraham,2 R. Razonable.1

1Division of Infectious Diseases, Mayo Clinic, Rochester, MN
2Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.

Meeting: 2018 American Transplant Congress

Abstract number: C251

Keywords: Cytomeglovirus, Infection

Session Information

Session Name: Poster Session C: Lung: All Topics

Session Type: Poster Session

Date: Monday, June 4, 2018

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Hall 4EF

Introduction: Cytomegalovirus (CMV) is a common infection that causes significant morbidity among lung and heart-lung (LHL) transplant recipients. We determined the clinical utility of global CD8+ T cell and CMV-specific CD8+ T cell assay as predictor of CMV infection after LHL transplantation.

Methods: During a 10-year period, selected LHL transplant recipients underwent analysis of CMV-specific CD8+ T cells (CMV-CD8+; quantitatively and functionally) using MHC class I tetramers with CMV peptides (n=5). Functional assessment included measurement of interferon-gamma (IFNg) production and CD107a/b degranulation after stimulation with either CMV peptides (antigen-specific) or PMA/ionomycin (global CD8+ T cell). A T cell immune competence (TIC) score was derived from the CMV-CD8+ quantitative and functional data. CMV infection was diagnosed by PCR in blood and other clinical samples or histopathology. Per protocol, valganciclovir prophylaxis was given for 6 months (CMV R+) or at least one year (CMV D+/R-).

Results: Sixty-four LHL transplant patients positive for MHC Class I alleles HLA A1, A2, B7, B8, and/or B35 were tested for TIC score. The median age is 60 years (IQR: 42-64), and most (56%) were male. The majority was CMV R+ (60%); 30% were CMV D+/R-. CMV infection occurred in 27 patients (42.2%) at a median of 15.9 months (IQR: 10-6-22.6) post-transplant. CMV infection developed in 41% of patients with impaired TIC score or global CD8+ T cell function. Normal TIC score was associated with shorter duration of CMV viremia compared to impaired TIC score (18.7 vs. 31.6 days, p=0.01) (Figure 1). Likewise, normal TIC score and global CD8+ T cell function was associated with a lower rate of CMV relapse (13 vs. 75%, p=0.03).

Conclusion: Monitoring for TIC score and global CD8+ T cell function can be useful clinical guide in managing LHL transplant patients at risk of CMV infection. An impaired TIC score and global CD8+ T cell function is associated with a high rate of CMV infection, longer duration of viremia, and high rate of relapse.

CITATION INFORMATION: Meesing A., Abraham R., Razonable R. Clinical Utility of CMV-Specific CD8+ T-Cell Immune Competence Score in Lung and Heart-Lung Transplant Recipients at Risk of Cytomegalovirus Infection Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Meesing A, Abraham R, Razonable R. Clinical Utility of CMV-Specific CD8+ T-Cell Immune Competence Score in Lung and Heart-Lung Transplant Recipients at Risk of Cytomegalovirus Infection [abstract]. https://atcmeetingabstracts.com/abstract/clinical-utility-of-cmv-specific-cd8-t-cell-immune-competence-score-in-lung-and-heart-lung-transplant-recipients-at-risk-of-cytomegalovirus-infection/. Accessed May 16, 2025.

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