Evidence map›Paper›PMID 28056841›Full record

ArticleBMC infectious diseases2017

Thymus activity measured by T-cell receptor excision circles in patients with different severities of respiratory syncytial virus infection.

Kiran Aftab Gul, Tonje Sonerud, Hans O Fjærli, Britt Nakstad, Tore Gunnar Abrahamsen, Christopher S Inchley

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Article in BMC infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Kiran Aftab GulDepartment of Pediatric Research, Women and Children's Division, Oslo University Hospital Rikshospitalet, Oslo, Norway. Kiran.aftab.gul@rr-research.no.
Tonje SonerudDepartment of Pediatric and Adolescent Medicine, Akershus University Hospital, Lørenskog, Norway.
Hans O FjærliDepartment of Pediatric and Adolescent Medicine, Akershus University Hospital, Lørenskog, Norway.
Britt NakstadDepartment of Pediatric and Adolescent Medicine, Akershus University Hospital, Lørenskog, Norway.
Tore Gunnar AbrahamsenInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Christopher S InchleyDepartment of Pediatric and Adolescent Medicine, Akershus University Hospital, Lørenskog, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRespiratory syncytial virus (RSV) infection is an important cause of hospitalization in previously healthy infants. Immunological mechanisms predisposing infants to severe disease are poorly understood. Early biomarkers for disease severity may assist clinical decisions. We investigated T-cell receptor excision circles (TREC), episomal DNA made during thymic T-cell receptor rearrangement, and a marker for thymus activity, both during disease and in neonatal screening cards as a risk factor for RSV disease severity.

methodsOne hundred thirteen patients hospitalized with RSV infection <12 months of age, grouped by disease severity, were available for this investigation, in which we conducted both a prospective and a case-control study. The prospective study included 47 RSV positive infants (mild n = 13, moderate n = 10, severe n = 24). TREC counts were determined by PCR of DNA extracted from EDTA-blood collected on hospitalization, and corrected for lymphocytes using ANCOVA. The case-control study included 85 newborns who later in infancy became RSV positive (mild n = 32, moderate n = 24, severe n = 29) and 47 newborns who never developed RSV disease as healthy controls included from health centres in the same catchment area. TRECs were measured using DNA extracted from dry blood spots from stored neonatal screening cards, followed by PCR. Student's T-test compared patients with controls, ANOVA compared disease severity groups.

resultsDuring RSV infection patients in the severe disease group had significantly lower (p = 0.017) TREC/200 μL blood compared to the other two disease groups, after correction for lymphocyte count. Newborn TREC levels, were significantly higher in RSV patients compared to controls (p < 0.0001). No significant differences in TREC copies at birth were found between disease severities.

conclusionDuring acute RSV infection a lower number of TREC is found in the severe disease group. TREC has potential as an immunological marker for severe RSV infection. Higher neonatal TREC counts indicate that infants later presenting with severe RSV do not have reduced thymic activity at birth and probably no congenital T-cell defect.

Indexed as

Case-Control StudiesDNADried Blood Spot TestingFemaleHumansInfantInfant, NewbornLymphocyte CountMaleProspective StudiesReceptors, Antigen, T-CellRespiratory Syncytial Virus InfectionsThymus GlandDNAReceptors, Antigen, T-CellBronchiolitisChildrenRespiratory syncytial virusT-cell receptor excision circlesThymus

Identifiers

PMID28056841
PMCPMC5217228

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