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Characterization of Adaptive-like γδ T Cells in Ugandan Infants during Primary Cytomegalovirus Infection Tuengel, Jessica; Ranchal, Sanya; Maslova, Alexandra; Aulakh, Gurpreet; Papadopoulou, Maria; Drissler, Sibyl; Cai, Bing; Mohsenzadeh-Green, Cetare; Soudeyns, Hugo; Mostafavi, Sara; van den Elzen, Peter; Vermijlen, David; Cook, Laura; Gantt, Soren
Abstract
Gamma-delta (γδ) T cells are unconventional T cells that help control cytomegalovirus
(CMV) infection in adults. γδ T cells develop early in gestation, and a fetal public γδ T cell receptor
(TCR) clonotype is detected in congenital CMV infections. However, age-dependent γδ T cell
responses to primary CMV infection are not well-understood. Flow cytometry and TCR sequencing
was used to comprehensively characterize γδ T cell responses to CMV infection in a cohort of
32 infants followed prospectively from birth. Peripheral blood γδ T cell frequencies increased during
infancy, and were higher among CMV-infected infants relative to uninfected. Clustering analyses
revealed associations between CMV infection and activation marker expression on adaptive-like Vδ1
and Vδ3, but not innate-like Vγ9Vδ2 γδ T cell subsets. Frequencies of NKG2C⁺CD57⁺ γδ T cells were
temporally associated with the quantity of CMV shed in saliva by infants with primary infection.
The public γδ TCR clonotype was only detected in CMV-infected infants <120 days old and at lower
frequencies than previously described in fetal infections. Our findings support the notion that CMV
infection drives age-dependent expansions of specific γδ T cell populations, and provide insight for
novel strategies to prevent CMV transmission and disease.
Item Metadata
| Title |
Characterization of Adaptive-like γδ T Cells in Ugandan Infants during Primary Cytomegalovirus Infection
|
| Creator | |
| Contributor | |
| Publisher |
Multidisciplinary Digital Publishing Institute
|
| Date Issued |
2021-10-03
|
| Description |
Gamma-delta (γδ) T cells are unconventional T cells that help control cytomegalovirus
(CMV) infection in adults. γδ T cells develop early in gestation, and a fetal public γδ T cell receptor
(TCR) clonotype is detected in congenital CMV infections. However, age-dependent γδ T cell
responses to primary CMV infection are not well-understood. Flow cytometry and TCR sequencing
was used to comprehensively characterize γδ T cell responses to CMV infection in a cohort of
32 infants followed prospectively from birth. Peripheral blood γδ T cell frequencies increased during
infancy, and were higher among CMV-infected infants relative to uninfected. Clustering analyses
revealed associations between CMV infection and activation marker expression on adaptive-like Vδ1
and Vδ3, but not innate-like Vγ9Vδ2 γδ T cell subsets. Frequencies of NKG2C⁺CD57⁺ γδ T cells were
temporally associated with the quantity of CMV shed in saliva by infants with primary infection.
The public γδ TCR clonotype was only detected in CMV-infected infants <120 days old and at lower
frequencies than previously described in fetal infections. Our findings support the notion that CMV
infection drives age-dependent expansions of specific γδ T cell populations, and provide insight for
novel strategies to prevent CMV transmission and disease.
|
| Subject | |
| Genre | |
| Type | |
| Language |
eng
|
| Date Available |
2021-11-25
|
| Provider |
Vancouver : University of British Columbia Library
|
| Rights |
CC BY 4.0
|
| DOI |
10.14288/1.0403827
|
| URI | |
| Affiliation | |
| Citation |
Viruses 13 (10): 1987 (2021)
|
| Publisher DOI |
10.3390/v13101987
|
| Peer Review Status |
Reviewed
|
| Scholarly Level |
Faculty; Researcher
|
| Rights URI | |
| Aggregated Source Repository |
DSpace
|
Item Media
Item Citations and Data
Rights
CC BY 4.0