International Journal of Microbiology Research · 2023 · 13 citations · 25 references
Life SciencesImmunologyPediatricsClinical ImmunologyPediatric HematologyPediatric ImmunologyLymphocyte DevelopmentPediatric Clinical ImmunologyAge-specific Reference RangesDiagnostic ImmunophenotypingFlow Cytometry ImmunophenotypingLymphocyte Function TestingLymphocyte SubtypesMemory T Cell SubsetsNormative Data CollectionNormative Data Establishment
Background & objectives: Accurate diagnosis of immunodeficiencies requires a critical comparison of values with age-matched controls. In India, the existing reference values for rare lymphocyte subsets are currently not available and we rely on the data originating from other countries for the interpretation of the results. Furthermore, there is limited information on normal variation for these rare-subset parameters in Indian children. So, this study aimed to establish normative values for clinically important lymphocyte subsets in Indian children at different age groups. Methods: 148 children aged ≥16 yr were enrolled in this study. The study population included 61 per cent males and 39 per cent females and was divided into the following groups: cord blood (n=18), 0-6 months (n=9), 6-12 months (n=13), 1-2 yr (n=19), 2-5 yr (n=27), 5-10 yr (n=25) and 10-16 yr (n=37). The absolute and relative percentage of lymphocytes, T, B, natural killer cell, along with activated, naïve and memory subsets, was determined by flow cytometry. Results: percentiles were obtained for 34 lymphocyte sub-populations. The T and B naïve compartments showed a decreasing trend, whereas memory cells showed an increase with age. The activated T cell subset shows an increasing pattern up to one year and then declines gradually. Double negative T cells are relatively stable. TCRgd+T cell percentage increases with age. Interpretation & conclusions: This single-centre pilot study provides preliminary data that justifies the need for future large-scale multi centric studies to generate a reference range for interpreting extended immunophenotyping profiles in the paediatric age group, making it possible for clinicians to assess the immunological status in inborn errors of immunity, infectious and autoimmune diseases.
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Stuart G. Tangye, Waleed Al–Herz, Aziz Bousfiha et al. · Journal of Clinical Immunology · 2020 · 1.2K citations · Full text
Life Sciences, Genetics, Immunology +16
Natural killer cell immunotypes related to COVID-19 disease severity
Christopher Maucourant, Iva Filipovic, Andrea Ponzetta et al. · Science Immunology · 2020 · 514 citations · Full text
Paediatric Reference Values for the Peripheral T cell Compartment
Ellen Schatorjé, Eugenie Gemen, Gertjan J. Driessen et al. · Scandinavian Journal of Immunology · 2012 · 205 citations