Related Experiment Video
Updated: Aug 16, 2026

Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
Published on: September 7, 2022
Peripheral blood lymphocyte population in children infected with Helicobacter pylori
E Maciorkowska1, M Kaczmarski, A Stasiak-Barmuta
1III Department of Children's Diseases, Medical University of Białystok, 15-274 Białystok, J. Waszyngtona 17 (PL). emaciorkowska@o2.pl
Insights
In children with Helicobacter pylori infection, peripheral blood T and B lymphocyte levels did not correlate with antrum inflammation. T lymphocytes may play a primary role in this pediatric infection.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Infectious Diseases
Background:
- Helicobacter pylori infection in children causes chronic gastric and duodenal inflammation, potentially leading to ulcers.
- The immune system, particularly T lymphocytes, is implicated in the pathogenesis of chronic gastric inflammation.
Purpose of the Study:
- To quantify peripheral blood T (CD3+, CD4+, CD8+) and B lymphocyte (CD19+) subpopulations in children with H. pylori infection.
- To investigate the relationship between these lymphocyte levels and the severity of antrum mucosa inflammation.
Main Methods:
- Study included 32 children (aged 7-18) with dyspeptic symptoms undergoing upper gastrointestinal endoscopy.
- Gastric and duodenal mucosa were evaluated histologically using the Sydney System.
- H. pylori infection severity was assessed via urease test (CLO-test).
Main Results:
- Moderate antrum inflammation was observed in 41.2% of children.
- Marked inflammation was present in 58.8% of the study group.
- No cases of mild antrum inflammation were recorded.
Conclusions:
- No significant correlation was found between peripheral lymphocyte levels and the degree of antrum inflammation.
- Findings suggest T lymphocytes may have a predominant role in pediatric H. pylori infections.
- Further research is needed to elucidate the specific immune mechanisms involved.
Purpose:
Helicobacter pylori infection in children is associated with a chronic inflammatory process of gastric and duodenal mucosa, which may have a various clinical course ranging from asymptomatic and chronic inflammatory condition to gastric ulceration. The immune system may contribute especially to chronic gastric mucosa inflammation. The aim of our study was to assess the levels of peripheral blood T (CD3+, CD4+, CD8+) and B lymphocyte subpopulation (CD19+) in children with Helicobacter pylori infection and to evaluate their relation to degree of antrum mucosa inflammation.
Material And Methods:
The study was performed in 32 children aged 7-18 years, hospitalized due to dyspeptic symptoms. The endoscopic examination of upper gastrointestinal tract was performed and gastric and duodenal mucosa was estimated in all patients. The endoscopic and histological evaluation of gastric mucosa was performed according to the Sydney System [4]. The urease test (CLO-test-H. pylori) was made to estimate the severity of the infection.
Results:
Moderate antrum mucosa inflammation was found in 41.2% of the examined. The highest percentage of children (58.8%) presented marked inflammation. No mild inflammation was found in children examined.
Conclusions:
No correlation was found between lymphocyte levels and the degree of the inflammatory changes in antrum mucosa. The evaluation of peripheral blood lymphocytes performed in children with Helicobacter pylori infection suggests that T lymphocytes may play a predominant role in this infection.
Related Concept Videos
Disorders of Leukocytes
Leukopenia may result from bone marrow disorders, autoimmune diseases, and infectious diseases. For example, conditions such as multiple myeloma and aplastic anemia can impair the bone marrow's ability to produce adequate leukocytes. Similarly, autoimmune diseases like lupus and viral infections such as HIV can prompt the immune system...
Treating Helicobacter pylori in Peptic Ulcers: Antimicrobial Therapy
Peptic Ulcer
Gastritis II: Pathophysiology

