# Quantifications of CD4+ T-Lymphocytes levels in adult sickle cell patients: Examining immunological vulnerability and Vaso-Occlusive crises in a low-resource setting, northwestern Nigeria

**Authors:** Abubakar Babangida Usman, Abubakar Hassan Gulma, Kabir Magaji Hamid, Adamu Muhammad Ibrahim, Shuaibu Saidu Musa, Jomar L Aban, Jerico Bautista Ogaya, Kristine Joy Gacutno, Angelica Joyce Gacutno-Evardone, Carina Joane V Barroso, Pearl Irish V De Paz, Mohamed Mustaf Ahmed, Sani Muhammed, Don Eliseo Lucero-Prisno

PMC · DOI: 10.1093/oxfimm/iqaf013 · Oxford Open Immunology · 2026-01-22

## TL;DR

This study examines CD4+ T-lymphocyte levels in adult sickle cell patients in Nigeria, finding lower counts during vaso-occlusive crises, suggesting immunological vulnerability.

## Contribution

The study provides new insights into immunological vulnerability in sickle cell disease patients during crises in a low-resource setting.

## Key findings

- CD4+ T-lymphocyte counts were reduced in patients during vaso-occlusive crises compared to steady states.
- Age group 31–40 had the highest CD4+ counts, while patients aged 40 and above had the lowest.
- No significant correlation was found between CD4+ counts and hemoglobin levels, gender, or age.

## Abstract

Introduction: Sickle Cell Disease (SCD) is a chronic genetic disorder that impairs red blood cell function and contributes to recurrent complications, particularly vaso-occlusive crises. Aim: This study evaluates the level of CD4 + T-lymphocyte counts in adult SCD patients in Northwestern Nigeria, assessing their association with clinical states, and epidemiological factors, to better understand immunological vulnerability. Methods: A descriptive cross-sectional study was conducted at Specialist Hospital Sokoto, 45 adult SCD patients were recruited and stratified by clinical status (steady state versus crisis). CD4 + counts were measured via flow cytometry, and data were analyzed for relationships with haemoglobin levels, gender, and age. Results: Patients in vaso-occlusive crisis observed reduction in CD4 counts compared to those in steady state. However, haemoglobin levels did not show a statistically significant difference between the crisis state (9.43 ± 1.98 g/dL) and steady state (10.08 ± 1.60 g/dL; P = 0.231). Gender-based analysis indicated no significant difference in CD4 + counts (P = 0.403) ++ or haemoglobin levels (P = 0.542) between male and female patients. Age-related analysis showed the highest mean CD4 + count among the 31–40-year age group (1151.80 ± 626.06 cells/µL) and the lowest in patients aged 40 years and above (601.00 ± 0.00 cells/µL). Correlation analysis demonstrated weak and non-significant relationships between CD4 + counts and haemoglobin levels (r = −0.095, P = 0.530), gender (r = −0.126, P = 0.403), and age (r = 0.193, P = 0.198). Conclusion: These findings highlight significant reduced CD4 levels in SCD patients during crises, underscoring the need for regular immunological monitoring.

## Linked entities

- **Diseases:** Sickle Cell Disease (MONDO:0011382)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** SCA (MESH:C565772), SCD (MESH:D000755), multi-organ damage (MESH:D000092124), infectious (MESH:D003141), chronic (MESH:D002908), immune dysregulation (OMIM:614878), HIV (MESH:D015658), VOC (MESH:D001157), bone or joint pain (MESH:D018771), infection (MESH:D007239), immune abnormalities (MESH:D007154), organ dysfunction (MESH:D009102), haemolysis (MESH:D006461), genetic disorder (MESH:D030342), Vaso-Occlusive crises (MESH:D013224), pain (MESH:D010146), inflammation (MESH:D007249), trauma (MESH:D014947), lymphopenia (MESH:D008231)
- **Chemicals:** hydroxyurea (MESH:D006918), EDTA (MESH:D004492)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920040/full.md

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Source: https://tomesphere.com/paper/PMC12920040