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A Mouse Model of Vascularized Heterotopic Spleen Transplantation for Studying Spleen Cell Biology and Transplant Immunity
Published on: June 11, 2019
Alterations of the immune system following splenectomy in childhood
E Kreuzfelder1, U Obertacke, J Erhard
1Institut für Medizinische Virologie und Immunologie, Universitätsklinikum-GHS-Essen, F.R., Germany.
Insights
Children who undergo splenectomy for trauma exhibit T-cell immunodeficiency, with lower T-cell counts and proliferation. This may be linked to impaired lymphocyte maturation and altered B-lymphocyte levels post-surgery.
Area of Science:
- Immunology
- Pediatric Traumatology
Background:
- Splenectomy is a common procedure for blunt abdominal trauma in children.
- The spleen plays a crucial role in immune function, particularly in managing encapsulated bacteria.
Purpose of the Study:
- To investigate the impact of splenectomy on T-cell immunodeficiency in children.
- To compare immune cell profiles and function in splenectomized children versus healthy controls.
Main Methods:
- Comparative analysis of peripheral blood T-cell subsets (CD3, CD4CD29) and T-cell proliferation (PHA-induced).
- Assessment of B-lymphocyte counts in splenectomized children and age/sex-matched controls.
Main Results:
- Splenectomized children showed significantly lower CD3 T-cell counts and PHA-induced T-cell proliferation compared to controls.
- A notable deficit in CD4CD29 T-helper inducer cells was observed in splenectomized children.
- Elevated B-lymphocyte counts were found in splenectomized children, suggesting a loss of splenic reservoir function.
Conclusions:
- Splenectomy in children leads to a restricted pattern of T-cell immunodeficiency.
- Impaired maturation of CD4CD29 T-cells may contribute to reduced T-cell proliferation post-splenectomy.
- Altered B-lymphocyte levels indicate a compromised immune surveillance following spleen removal.
Abstract:
After splenectomy due to blunt abdominal trauma, splenectomized children showed a restricted pattern of T-cell immunodeficiency compared to age and sex-matched normal children. Peripheral blood total (CD3) T-cell counts of 11 splenectomized children of 43%, double positive helper (CD4) inducer subpopulation (CD29) cell counts of nine splenectomized children of 7%, and phytohemagglutinin (PHA)-induced T-cell proliferation of 11 splenectomized children of 53,206 c.p.m. were significantly (p less than 0.05) lower than values of normal children (61% CD3 cells, n = 12; 13% CD4CD29 cells, n = 11; 107,832 c.p.m. PHA-induced proliferation, n = 12). The deficit of CD4CD29 cell numbers may be due to impaired maturation of these particular CD4 lymphocytes and may explain diminished PHA-induced proliferation in small children. The significantly higher B-lymphocyte counts of splenectomized children (21%, n = 11; 558 cells/mm3, n = 10) compared with 12 normal children (14%; 329 cells/mm3) may be due to loss of the reservoir function of the spleen.
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