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Lymphocyte immunophenotype reference ranges in healthy Thai adults: implications for management of HIV/AIDS in

H K Webster1, K Pattanapanyasat, P Phanupak

  • 1Becton Dickinson Immunocytometry Systems, San Jose, CA, USA.

Insights

This study established reference ranges for lymphocyte subsets in healthy Thai adults. Thais showed distinct T and NK cell levels compared to Caucasians, impacting HIV/AIDS clinical management.

Area of Science:

  • Immunology
  • Flow Cytometry
  • Clinical Reference Ranges

Background:

  • Establishing accurate lymphocyte immunophenotype reference ranges is crucial for clinical diagnostics.
  • Previous studies primarily focused on Caucasian populations, necessitating data for diverse ethnicities.

Purpose of the Study:

  • To determine lymphocyte immunophenotype reference ranges for healthy adult Thais.
  • To compare Thai reference values with those of Caucasians.
  • To assess the influence of ethnicity, age, and sex on lymphocyte subset distributions.

Main Methods:

  • Multi-center study utilizing flow cytometry on lysed whole blood.
  • Standardized protocols for instrumentation, reagents, and quality control were employed.
  • Analysis included T, B, and NK lymphocyte subsets (CD3, CD4, CD16+56).

Main Results:

  • Significant differences observed in CD3 (T), CD4 (T helper/inducer), and CD16+56 (NK) lymphocyte percentages and CD4 absolute counts between Thais and Caucasians.
  • Thais, especially males, exhibited lower CD3 and CD4 T cell percentages and counts, with higher NK cell percentages.
  • Age and sex demonstrated observable trends, and biological variation in CD4 T lymphocyte distribution was noted.

Conclusions:

  • Ethnicity, age, sex, and environmental factors significantly influence normal lymphocyte immunophenotype reference values.
  • The findings highlight the importance of ethnicity-specific reference ranges for accurate clinical interpretation.
  • These results have critical implications for HIV/AIDS staging and management in Thailand, particularly concerning CD4+ T lymphocyte monitoring.

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