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Hormone replacement therapy in children with growth hormone deficiency: impact on immune profile
Javier Caballero-Villarraso1,2, Rocío Aguado2,3, M Dolores Cañete2
1Department of Biochemistry and Molecular Biology, Clinical Analyses Service, Córdoba, Spain.
Insights
Growth hormone (GH) treatment in children with GH deficiency positively impacts cellular immunity. However, it led to decreased immunoglobulin G (IgG) and immunoglobulin M (IgM) levels after six months.
Area of Science:
- Pediatric Endocrinology
- Immunology
- Growth Hormone Therapy
Background:
- Growth hormone (GH) plays a role in immune system function.
- Understanding GH's impact on immunity is crucial for treating GH deficiency.
Purpose of the Study:
- To evaluate immune profile changes in pre-pubertal children with GH deficiency after GH treatment.
- To compare immune parameters between treated and untreated children.
Main Methods:
- A two-phase study involving case-control and before-and-after comparisons.
- Analysis of humoral immunity (immunoglobulins, complement) and cell-mediated immunity (lymphocyte subsets, NK cells).
- Measurement of Insulin-like Growth Factor 1 (IGF-1) and IGF-binding Protein 3 (IGFBP-3).
Main Results:
- GH-treated children showed increased CD3+, CD4+, CD19+, NK cells, and CD4+/CD8+ ratio, with lower CD8+ counts compared to untreated children.
- No significant changes in immunoglobulins or complement levels were observed between groups in the first phase.
- After 6 months of GH treatment, a decrease in IgG and IgM, alongside an increase in IGF-1 and monocytes, was noted in previously untreated children.
Conclusions:
- GH treatment alters cellular and humoral immune profiles in children with GH deficiency.
- Further research is needed to understand the long-term implications of these immune changes.
Abstract:
Growth hormone (GH) may influence the immune system. The aim of this study was to assess the immune profile after treatment with GH in pre-pubertal children with a deficiency of this hormone. The study was carried out in two phases. Two groups were included in the first phase: group A) children treated with GH; group B) untreated children, prior to starting treatment. In the second phase, group B children were assessed 6 months after starting treatment. In the first phase, groups A and B were compared (case-control study). In the second phase, group B was compared in terms of baseline and final times (before and after study). We analysed: humoral immunity (immunoglobulin (Ig)A, IgG, IgM, C1 inhibitor, C3, and C4) and cell-mediated immunity (CD3+, CD4+, CD8+, CD4+/CD8+, CD19+ lymphocytes, and natural killer (NK) cells). Insulin-like growth factor 1 (IGF-1) and insulin-like growth factor-binding protein 3 (IGFBP-3) were also determined. In the first phase, CD3+, CD4+, CD19+, and NK cells and CD4+/CD8+ were greater in the treated group. CD8+ was lower in this group. No variations were seen in immunoglobulins and the complement between both groups. There were no changes to the complement in either of the two phases. In the second phase, untreated patients were assessed after 6 months of treatment. When comparing the baseline and final immune profiles, a statistically significant decrease in IgG and IgM was observed, and an increase of IGF-1 levels and monocytes. In conclusion, our study shows changes in the cellular and humoral immune profiles in children with GH deficiency who were treated.
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