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Updated: Jun 11, 2026

Quantitative Imaging of Lineage-specific Toll-like Receptor-mediated Signaling in Monocytes and Dendritic Cells from Small Samples of Human Blood
Published on: April 16, 2012
Impact of age, gender, and race on circulating γδ T cells
Cristiana Cairo1, Cheryl L Armstrong, Jean Saville Cummings
1Institute of Human Virology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Insights
Caucasian donors have significantly more Vγ2Vδ2 T cells than African American donors, though age affects both groups similarly. Understanding these differences is crucial for cancer and infectious disease research.
Area of Science:
- Immunology
- Human Genetics
Background:
- A subset of human peripheral blood γδ T cells, expressing the Vγ2Vδ2 T cell receptor, plays a role in responding to malignant and infectious diseases.
- Previous research has not fully elucidated the demographic variations in Vγ2Vδ2 T cell populations.
Purpose of the Study:
- To investigate the impact of race and age on the levels of Vγ2Vδ2 T cells in healthy human peripheral blood.
- To compare Vγ2Vδ2 T cell populations between Caucasian and African American donors.
Main Methods:
- Analysis of peripheral blood samples from healthy Caucasian and African American donors.
- Quantification of Vγ2Vδ2 T cells as a percentage of total lymphocytes.
- Assessment of Vγ2 clonotypes and T cell receptor expression.
Main Results:
- Significant differences observed in Vγ2Vδ2 T cell numbers between Caucasian (3.71% ± 4.37%) and African American (1.18% ± 2.14%) donors (p < 0.0001).
- Age and race were the primary factors influencing Vδ2 cell levels, with age-related effects being consistent across racial groups.
- The Vγ2Vδ2 T cell population was predominantly composed of cells expressing the Vγ2-Jγ1.2 Vδ2 T cell receptor in both groups, indicating strong positive selection.
Conclusions:
- Clinical studies involving Vγ2Vδ2 T cells require age- and race-matched controls due to significant demographic variations.
- Further research is needed to understand the regulatory mechanisms governing circulating Vγ2Vδ2 T cell levels.
Abstract:
A major subset of human peripheral blood γδ T cells expresses the Vγ2Vδ2 T cell receptor and responds to malignant or infectious diseases. We noted significant differences in the numbers of Vγ2Vδ2 T cells in blood samples from healthy Caucasian CA or African American (AA) donors. On average, CA donors had 3.71% ± 4.37% Vδ2 cells (as a percentage of total lymphocytes) compared with 1.18% ± 2.14% Vδ2 cells for AA donors (p < 0.0001). Age and race had the greatest impact on Vδ2 cell levels; the effect of age was similar for both racial groups. The Vδ2 cell population was dominated, for both donor groups, by cells expressing the Vγ2-Jγ1.2 Vδ2 T cell receptor, an apparent result of strong positive selection and there was substantial overlap in the public Vγ2 clonotypes from both racial groups. Mechanisms for selection and amplification of Vδ2 cells are nearly identical for both groups, despite the significant difference in baseline levels. These data show that appropriate controls, matched for age and race, may be required for clinical studies of Vγ2Vδ2 T cells in infectious disease or cancer and raise important questions about the mechanisms regulating the levels of circulating Vδ2 cells.
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