Gohal et al.
Allergy Asthma Clin Immunol (2016) 12:10
DOI 10.1186/s13223-016-0115-3
RESEARCH
T-cell receptor phenotype pattern
in atopic children using commercial
fuorescently labeled antibodies against 21
human class-specifc v segments for the tcrβ
chain (vβ) of peripheral blood: a cross sectional
study
Gassem Gohal
1*
, Christine McCusker
1
, Bruce Mazer
2
, Reza Alizadehfar
1
, Duncan Lejtenyi
1
and Moshe Ben-shoshan
1
Abstract
Background: T-cell receptor (TCR) repertoire development is an integral part of the adaptive immune response.
T-cell activation requires recognition of appropriately processed antigens by the TCR. Development of a diverse
repertoire of TCRs is therefore essential to ensure adequate protection from potential threats. The majority of T-cells
in peripheral blood have TCRs composed of an alpha and a beta chain. At the DNA level, the TCR genes are formed
through directed recombination from germline sequences—the so-called VDJ recombination [variable (V) joining
(J) diversity (D) gene segments] which results in variations in the repertoire. The most variable part of TCRs is the Vβ
region (VβTCR), which has multiple V segment families that can be quantitatively measured. However, only sparse
data exists on the normal levels of the VβTCR repertoire in healthy children. We aimed to establish normal values for
the VβTCR repertoire in atopic children without immunodeficiency.
Methods: Fifty-three children were recruited from food allergy, drug allergy, chronic urticaria and anaphylaxis regis-
tries and were divided into groups based on age: >0–2 years, 3–6 years, and 6–18 years. We used commercially avail-
able and fluorescently labeled antibodies against 21 human class-specific V segments of the TCRβ chain (Vβ) to study
in peripheral blood the quantitative pattern of Vβ variation by flow cytometry.
Results: Children of all ages exhibited a similar pattern of TCR Vβ expression. Vβ 2 was the most commonly expressed
family in all three age groups [9.5 % (95 % CI, 8.9, 10 %), 8.8 % (95 % CI, 7.4, 10.2 %) and 7.6 % (7.0, 8.3 %) respectively].
However, the percentage of Vβ 2 decreased in older children and the percentage of Vβ 1 was higher in males. TCR Vβ
expression in our sample of atopic children did not differ substantially from previously published levels in non-atopic
cohorts.
Conclusion: TCR Vβ diversity follows a predictable and comparable pattern in atopic and healthy non-atopic chil-
dren. Establishing normal levels for healthy children with and without atopy will contribute to a better definition of Vβ
receptor deviation in children with primary immunodeficiency and/or immunodysregulation conditions.
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Open Access
Allergy, Asthma & Clinical Immunology
*Correspondence: dr.gassem@gmail.com
1
Division of Allergy and Clinical Immunology, Department of Pediatrics,
Montreal Children’s Hospital, McGill University, 1001 Boulevard Décarie,
Room A 02.2227, Montréal, QC H4A 3J1, Canada
Full list of author information is available at the end of the article