Delineating the immunological profile of Algerian children with Down syndrome:A case series.

Authors

  • Linda Mokrane Department of Medical Biology, Rouiba Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria.
  • Azzeddine Tahiat Department of Medical Biology, Rouiba Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria. https://orcid.org/0000-0003-3272-8904 (unauthenticated)
  • Samira Aggoune Department of Pediatrics, El-Harrach Hospital, 16000,Algiers University of Health Sciences, Algiers, Algeria
  • Souad Touri Department of Pediatrics, Blida University Hospital, University of Blida, 09000, Blida, Algeria
  • Hayet Belhadj Department of Pediatrics, Army Mother and Child Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria
  • Chafa Bendahmane5 Department of Pediatrics, Ain Taya Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria
  • Ouardia Ibsaine Department of Pediatrics, Ain Taya Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria
  • Lila Kedji Department of Pediatrics, Blida University Hospital, University of Blida, 09000, Blida, Algeria
  • Réda Belbouab Department of Pediatrics, Mustapha University Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria
  • Rachida Boukari Department of Pediatrics, Mustapha University Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria
  • Kamel Djenouhat Department of Medical Biology, Rouiba Hospital, Algiers University of Health Sciences,16000, Algiers, Algeria.

DOI:

https://doi.org/10.62438/tunismed.v103i11.5770

Keywords:

Down Syndrome, recurrent infections, lymphocyte phenotype, T-cell lymphopenia, Combined immunodeficiency, serum immunoglobulins

Abstract

Purpose:This study aimed to characterize the immunological profile of Algerian children with Down Syndrome (DS).

Methods: Serum immunoglobulin(Ig) levels were measure dusingnephelometry,and lymphocyte Subpopulations were analyzed by flow cytometry (FACSLyric™,BDBiosciences,US). The Lymphocyte phenotype in DS patients was compared to that of patients with combined

immunodeficiency(CID).

Results:Our cohort included 33 patients with DS(20 males),and 40 patients withCID(24 males). All Patients had aclinical history of recurrent or severe infections, including upper and lower respiratory Tract infections in 25 patients(76%).Serum Ig were measured in 29 patients, with normal levels of

IgG,IgA,and Ig Min 83%,73%,and 80% of patients,respectively. Elevated IgG,IgA,and IgM levels. Were found in14%,17%,and 3% of patients,while reduced levels were see nin3%,10%,and17% of patients, respectively. Lymphocyte phenotype analysis revealed CD4l ymphopenia in 24(73%) patients, CD8 lymphopeniain19(58%) patients,B-cell lymphopenia in16(48%) patients, and reduced

NK cells in 7 (21%) patients. Naïve CD4+and CD8+T cells were analyzed in nine patients, with low Percentages observed in three. Patients with DS exhibited significantly milder CD3 and CD4

Lymphopenia compared to those with CID.

Conclusion: Children with D Stypically present withT-andB-cell lymphopenia,while maintaining

Generally normal Ig levels. T-cell lymphopenia in DSis less pronounced thaninCID,and the increased Susceptibility to infections stems from both immunological and non-immunological factors linked to trisomy 21.

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2026-01-22

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