Flow Cytometry as the Tool to Define Peripheral Blood Leukocyte Signatures in Acute EBV Infection.
Humans
Flow Cytometry
/ methods
Male
Female
Epstein-Barr Virus Infections
/ immunology
Child
Leukocytes
/ immunology
Herpesvirus 4, Human
/ immunology
Adolescent
Adult
Infectious Mononucleosis
/ immunology
Monocytes
/ immunology
Child, Preschool
Neutrophils
/ immunology
Acute Disease
Retrospective Studies
Young Adult
CD16
CD64
EBV
T-large granular lymphocytes
flow cytometry
monocytes
neutrophils
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
03 Jun 2024
03 Jun 2024
Historique:
received:
29
04
2024
revised:
29
05
2024
accepted:
31
05
2024
medline:
19
6
2024
pubmed:
19
6
2024
entrez:
19
6
2024
Statut:
epublish
Résumé
Primary Epstein-Barr virus (EBV) infection which can manifest as infectious mononucleosis (IM) is commonly acquired during childhood. EBV primarily invades B cells leading to a lytic reaction; the control of the infection is handled by natural killer and T cells in immunocompetent individuals. The infection has a wide spectrum of clinical findings and can lead to serious complications in patients with certain underlying immunological dysfunctions. We retrospectively investigated peripheral white blood cell populations' surface marker characteristics in IM using a comprehensive flow cytometry marker panel. Twenty-one cases of IM and seventeen EBV-seropositive cases without IM serving as controls were included. We observed novel alterations in lymphocyte, neutrophil, and monocyte populations. In addition to increased activated cytotoxic T cells and low B cells, we demonstrated high T-large granular lymphocyte (T-LGL) populations in IM cases. Furthermore, despite T cells' increased HLA-DR expression, another activation marker, CD11b, was lower in T-LGL populations. Monocytes showed increased CD16 expression; CD64 was higher in neutrophils. Our findings point to monocyte and neutrophil activation which may account for acute clinical features and may contribute to the understanding of IM immunobiology. Furthermore, they may serve as a useful tool in investigating inherited and post-transplant conditions characterized by deficiencies in controlling EBV infection.
Identifiants
pubmed: 38891094
pii: cells13110963
doi: 10.3390/cells13110963
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Children's Foundation
ID : R2-2019-30