<p>Physicians rely on reference values from healthy populations to guide clinical decisions regarding B-cell subpopulations in primary immunodeficiency. While age-dependent reference ranges have been reported in several populations, no study has established these values for Malaysian children. Given that B-cell subpopulation distributions may vary between populations, we aimed to define reference ranges for total B cells, transitional B cells, naïve B cells, total memory B cells, switched and non-switched memory B cells, and plasmablasts in Malaysian children aged 2 to 15 years. Blood samples taken from 85 children aged 2 to 15 years were evaluated for the distribution of B cell subsets. Absolute numbers and percentages were determined for total B cells (CD19<sup>+</sup>), transitional B cells (CD19<sup>+</sup>CD27<sup>−</sup>CD24<sup>+ bright</sup>CD38<sup>+bright</sup>), naïve B cells (CD19<sup>+</sup>CD27<sup>−</sup>IgD<sup>+</sup>), total memory B cells (CD19<sup>+</sup>CD27<sup>+</sup>), class-switched memory B cells (CD19<sup>+</sup>CD27<sup>+</sup>IgM<sup>−</sup>IgD<sup>−</sup>), non-classical switched memory B cells(CD19<sup>+</sup>CD27<sup>−</sup>IgM<sup>−</sup>IgD<sup>−</sup>), non-switched memory B cells (CD19<sup>+</sup>CD27<sup>+</sup>IgM<sup>+</sup>IgD<sup>+</sup>), and plasmablasts (CD19<sup>+</sup>CD27<sup>+</sup>CD38<sup>+ bright</sup>). We observed age-dependent variations in most B-cell subpopulations, with naïve B cells being predominant, followed by memory B cells, while plasmablasts were present in trace amounts across all ages. Additionally, certain of B-cell subpopulations (total memory B cells and class-switched memory B cells) were observed at higher frequencies in female children compared to males. This study provides age-specific reference values for B cell subsets in a paediatric population, which may serve as a valuable guideline for diagnosing children with suspected immunodeficiency.</p>

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Preliminary reference range for B cell subpopulations in peripheral blood of healthy Malaysian children aged 2–15 years

  • Jalilah Jamaluddin,
  • Intan Hakimah Ismail,
  • Mohd Azri Zainal Abidin,
  • Siti Mardhiana Mohamad,
  • Hasni Mahayidin

摘要

Physicians rely on reference values from healthy populations to guide clinical decisions regarding B-cell subpopulations in primary immunodeficiency. While age-dependent reference ranges have been reported in several populations, no study has established these values for Malaysian children. Given that B-cell subpopulation distributions may vary between populations, we aimed to define reference ranges for total B cells, transitional B cells, naïve B cells, total memory B cells, switched and non-switched memory B cells, and plasmablasts in Malaysian children aged 2 to 15 years. Blood samples taken from 85 children aged 2 to 15 years were evaluated for the distribution of B cell subsets. Absolute numbers and percentages were determined for total B cells (CD19+), transitional B cells (CD19+CD27CD24+ brightCD38+bright), naïve B cells (CD19+CD27IgD+), total memory B cells (CD19+CD27+), class-switched memory B cells (CD19+CD27+IgMIgD), non-classical switched memory B cells(CD19+CD27IgMIgD), non-switched memory B cells (CD19+CD27+IgM+IgD+), and plasmablasts (CD19+CD27+CD38+ bright). We observed age-dependent variations in most B-cell subpopulations, with naïve B cells being predominant, followed by memory B cells, while plasmablasts were present in trace amounts across all ages. Additionally, certain of B-cell subpopulations (total memory B cells and class-switched memory B cells) were observed at higher frequencies in female children compared to males. This study provides age-specific reference values for B cell subsets in a paediatric population, which may serve as a valuable guideline for diagnosing children with suspected immunodeficiency.