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Decrease in Gamma Delta T-Cell with Microbiologically Proven Infection in Septic Oncologic Children

Lertbunrian R, MD¹, Chonpaisan K, MD¹, Srisala S, MSc², Anurathapan U, MD¹, Apiwattanakul N, PhD, MD¹

Affiliation : ¹ Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand ² Section for Research Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand


Objective: Predictors determining septic oncologic patients at high or low risk are helpful in guiding of antimicrobial management. As the number of γδ T-cells decreased in septic adult patients and the degree of change significantly associated with disease severity, the authors applied this concept and explored the association between the number of γδ T-cells and sepsis severity in oncologic children. The association of cell counts with microbiologically proven infection was also investigated.
Materials and Methods: Pediatric oncologic patients admitted with sepsis were prospectively enrolled. T-cell subset numbers were performed by flow cytometry method. Each episode of sepsis was categorized as severe sepsis versus non-severe sepsis or microbiologically proven infection versus non-microbiologically proven infection. Comparison of white blood cell count, lymphocyte count, and lymphocyte subset count between groups was performed.
Results: Forty-eight septic episodes were included. No association between the number of γδ T-cells and sepsis severity was noted. However, the percentage of γδ T-cell/total lymphocytes and absolute neutrophil count (ANC) were significantly lower in patients with microbiologically proven infection. A γδ T-cell greater than 3% of total lymphocytes and ANC greater than 100/uL are proposed as factors associated with non-microbiologically proven episodes in patients presenting with mild sepsis.
Conclusion: The authors proposed that percentage of γδ T-cells in septic oncologic patients, along with ANC may be used as a guide for antibiotic management in septic oncologic children.

Keywords : Sepsis, γδ T-cells, Oncologic children


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