In Vivo Effect of Recombinant Human Granulocyte Colony-Stimulating Factor on Neutrophilic Expression of CD11b in Septic Neonates: A Randomized Controlled Trial
Autor: | Abeer A. Saad, Mona M. El-Ganzoury, Rania A. El-Farrash, Ashraf G. Mohamed, Inji G. El-Sherbini |
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Rok vydání: | 2012 |
Předmět: |
Myeloid
Neutrophils Granulocyte Neutropenia Sepsis Granulocyte Colony-Stimulating Factor medicine Humans Progenitor cell Cell Proliferation CD11b Antigen medicine.diagnostic_test Neonatal sepsis business.industry Infant Newborn Complete blood count Hematology medicine.disease Anti-Bacterial Agents Blood Cell Count Granulocyte colony-stimulating factor Hospitalization Treatment Outcome medicine.anatomical_structure Oncology Pediatrics Perinatology and Child Health Immunology Absolute neutrophil count business |
Zdroj: | Pediatric Hematology and Oncology. 29:272-284 |
ISSN: | 1521-0669 0888-0018 |
Popis: | Neonates are susceptible to septicemia secondary to quantitative and qualitative neutrophilic defects. Granulocyte colony-stimulating factor (G-CSF) stimulates myeloid progenitor cell proliferation and induces selective neutrophil functions. The authors aimed to evaluate the effect of G-CSF administration in septic neonates on neutrophil production and CD11b expression. Sixty septic neonates were randomized to receive intravenous G-CSF 10 μg/kg/day for 3 days (G-CSF group, n = 30), or not to receive G-CSF (non-G-CSF group, n = 30). Thirty healthy newborns were included as controls. Laboratory investigations included complete blood count, C-reactive protein, blood culture, renal and liver function tests, and assessment of neutrophilic expression of CD11b. Total leukocytes count (TLC), absolute neutrophil count (ANC), and immature myeloid cell count in G-CSF group showed significant difference between post-and pre-G-CSF levels. TLC, ANC, immature myeloid cell count and immature/total myeloid cells ratio were higher in G-CSF group compared to non-G-CSF group on days 1 and 3. Higher neutrophilic expression of CD11b was reported in both septic groups on day 0 compared to control group. On day 5, CD11b was higher in G-CSF group than non-G-CSF group. G-CSF improved CD11b% in neutropenic and non-neutropenic septic neonates. No significant difference was found between pre- and posttreatment renal and liver function tests. Lower duration of antibiotic intake and hospitalization was observed in G-CSF group compared to non-G-CSF group. G-CSF administration as an adjuvant therapy for neonatal septicemia, whether neutropenic or not, improves neutrophilic count and function and contributed to early healing from sepsis. |
Databáze: | OpenAIRE |
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