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Antiviral T-Cell Frequencies in a Healthy Population: Reference Values for Evaluating Antiviral Immune Cell Profiles in Immunocompromised Patients.

Authors :
Schulze Lammers FC
Bonifacius A
Tischer-Zimmermann S
Goudeva L
Martens J
Lepenies B
von Karpowitz M
Einecke G
Beutel G
Skripuletz T
Blasczyk R
Beier R
Maecker-Kolhoff B
Eiz-Vesper B
Source :
Journal of clinical immunology [J Clin Immunol] 2022 Apr; Vol. 42 (3), pp. 546-558. Date of Electronic Publication: 2022 Jan 06.
Publication Year :
2022

Abstract

Viral infections and reactivations are major causes of morbidity and mortality after hematopoietic stem cell (HSCT) and solid organ transplantation (SOT) as well as in patients with immunodeficiencies. Latent herpesviruses (e.g., cytomegalovirus, Epstein-Barr virus, and human herpesvirus 6), lytic viruses (e.g., adenovirus), and polyomaviruses (e.g., BK virus, JC virus) can cause severe complications. Antiviral drugs form the mainstay of treatment for viral infections and reactivations after transplantation, but they have side effects and cannot achieve complete viral clearance without prior reconstitution of functional antiviral T-cell immunity. The aim of this study was to establish normal ranges for virus-specific T-cell (VST) frequencies in healthy donors. Such data are needed for better interpretation of VST frequencies observed in immunocompromised patients. Therefore, we measured the frequencies of VSTs against 23 viral protein-derived peptide pools from 11 clinically relevant human viruses in blood from healthy donors (nā€‰=ā€‰151). Specifically, we determined the VST frequencies by interferon-gamma enzyme-linked immunospot assay and classified their distribution according to age and gender to allow for a more specific evaluation and prediction of antiviral immune responses. The reference values established here provide an invaluable tool for immune response evaluation, intensity of therapeutic drugs and treatment decision-making in immunosuppressed patients. This data should make an important contribution to improving the assessment of immune responses in immunocompromised patients.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1573-2592
Volume :
42
Issue :
3
Database :
MEDLINE
Journal :
Journal of clinical immunology
Publication Type :
Academic Journal
Accession number :
34989946
Full Text :
https://doi.org/10.1007/s10875-021-01205-1