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Published on: September 7, 2022
Reference values of lymphocyte subsets in healthy, HIV-negative children in Cameroon
Bertrand Sagnia1, Francis Ateba Ndongo, Suzie Ndiang Moyo Tetang
1Chantal BIYA International Reference Centre for Research on HIV/AIDS Prevention and Management (CIRCB), BP 3077, Messa-Yaounde, Cameroon. bertrysagnia@yahoo.fr
Insights
Reference values for lymphocyte subsets in Cameroonian children are needed for diagnosing infectious diseases. This study establishes baseline immunological profiles for children aged 0-6 years, revealing significant differences from Caucasian and some African populations, crucial for accurate health assessments.
Area of Science:
- Immunology
- Pediatrics
- Hematology
Background:
- Accurate lymphocyte subset reference values are crucial for monitoring infectious diseases like HIV/AIDS, tuberculosis, and malaria in children.
- Existing reference values, often derived from Caucasian cohorts, may not be appropriate for African populations, potentially leading to misdiagnosis.
- There is a lack of established pediatric lymphocyte subset reference ranges for Cameroon.
Purpose of the Study:
- To determine the immunological profile of healthy children aged 0-6 years in Cameroon.
- To compare these values with those from other African and Caucasian populations.
- To provide initial reference guidelines for clinical use in Cameroon.
Main Methods:
- A cohort of 352 healthy children aged 0-6 years in Cameroon was studied.
- Peripheral blood samples were analyzed for relative and absolute counts of T-cell subsets, B cells, and NK lymphocytes.
- Flow cytometry was used with BD Multitest reagents and Trucount tubes, analyzed via CellQuest-Pro and FlowJo software.
Main Results:
- Significant age-dependent differences (P < 0.05) were observed in absolute and percentage values of approximately 23 lymphocyte subsets, peaking between 6-12 months.
- B-cell values were higher than those reported in developed countries.
- Differences in activated and differentiated T cells were noted in children aged 1-6 years, with CD8(+) T-cell count and CD4(+)/CD8(+) ratio potentially influenced by gender.
Conclusions:
- Normal lymphocyte subset values in Cameroonian children differ significantly from Caucasian and some other African populations.
- Observed variations may be attributed to genetic, environmental, and methodological factors.
- The established values serve as initial national reference guidelines pending further data accumulation.
Abstract:
Lymphocyte subset reference values used to monitor infectious diseases, including HIV/AIDS, tuberculosis, malaria, or other immunological disorders in healthy children in Cameroon, are lacking. Values for Caucasian cohorts are already being utilized for clinical decisions but could be inappropriate for African populations. We report here the immunological profile for children aged from birth through 6 years in Cameroon and also compare our values to data from other African and Caucasian populations. In a cohort of 352 healthy children, aged 0 to 6 years, the relative and absolute numbers of T-cell subsets, B cells, and NK lymphocytes were determined from peripheral blood collected in EDTA tubes. Samples were stained with BD Multitest reagents in Trucount tubes and analyzed by using CellQuest-Pro and FlowJo software. We evaluated about 23 different lymphocyte subsets in which the absolute number and percentage values differed significantly (P < 0.05) with age and peaked between 6 and 12 months. B-cell values were higher compared to reported values from developed countries. Differences in activated and differentiated T cells were observed in subjects between 1 and 6 years of age. The absolute CD8(+) T-cell count and the CD4(+)/CD8(+) ratio seem to depend on gender. Normal lymphocyte subsets values among children from Cameroon differ from reported values in Caucasian and some African populations. The differences observed could be due to genetic and environmental factors coupled with the methodology used. These values could be used as initial national reference guidelines as more data are assembled.

