Related Experiment Video
Updated: Sep 7, 2025

14:06
Isolation of Precursor B-cell Subsets from Umbilical Cord Blood
Published on: April 16, 2013
18.2K
Normal B-cell ranges in infants: A systematic review and meta-analysis
Francesco Borriello1, Noemi Pasquarelli2, Lisa Law3
1Generate Biomedicines, Cambridge, Mass.
The Journal of Allergy and Clinical Immunology
|June 21, 2022
Summary
This study establishes the first normal reference ranges for B-cell levels in infants during their first year of life. These findings are crucial for monitoring infant immune system development and the impact of therapies.
Area of Science:
- Immunology
- Pediatrics
- Biostatistics
Background:
- B-cell levels are key indicators of infant immune system development.
- No established reference ranges exist for healthy infants' B-cell counts.
- External factors can impact immune development, necessitating reliable B-cell level benchmarks.
Approach:
- Systematic literature review of studies measuring B-cell levels in infants using flow cytometry and CD19 markers.
- Meta-analysis of 28 studies to estimate normal ranges (2.5th-97.5th percentile) by age.
- Continuous age modeling to identify B-cell level peaks and trends.
Key Points:
- Normal B-cell ranges established for cord blood, 0-1 month, 1-6 months, and >6 months old infants.
- Absolute B-cell levels range from 707 cells/μL (cord blood) to 1493 cells/μL (1-6 months).
- B-cell levels peak around week 26 of infancy, with similar trends for percentage estimates.
Conclusions:
- Provides the first age-specific normal reference ranges for infant B-cell levels.
- Essential for assessing infant immune status and response to treatments.
- Facilitates early detection of immune system abnormalities in infants.
Keywords:
B cellCD19cord bloodflow cytometryinfantslower limit of normalnewbornsnormal rangereference rangeMore Related Videos
Related Concept Videos
Development of Immunocompetence
444
The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
444
B Cell Activation and Differentiation
5.4K
The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
5.4K
Cells of the Adaptive Immune Response
3.9K
The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
3.9K

