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Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Extremely low birth weight infants have lower Fc gamma RIII (CD 16) plasma levels and their PMN produce less Fc gamma
1Department of Neonatology, Children's Health Care, Minneapolis, MN 55404, USA.
Insights
Extremely low birth weight infants have reduced Fc gamma RIII expression on neutrophils due to decreased receptor synthesis, not shedding. This neutrophil receptor expression is developmentally regulated.
Area of Science:
- Immunology
- Neonatal Research
Background:
- Neutrophils (PMN) play a critical role in infant immunity.
- Fc gamma RIII expression on PMN is crucial for immune responses.
- Extremely low birth weight (ELBW) infants exhibit altered immune function.
Purpose of the Study:
- To investigate the cause of decreased Fc gamma RIII expression on ELBW infant neutrophils.
- To determine if reduced receptor synthesis or increased shedding is responsible.
- To explore the developmental regulation of Fc gamma RIII in ELBW infants.
Main Methods:
- Quantified plasma and cellular Fc gamma RIII using ELISA.
- Measured PMN Fc gamma RIII expression via flow cytometry.
- Compared ELBW infants, larger infants, and adult controls.
Main Results:
- ELBW infants showed significantly lower PMN Fc gamma RIII expression and plasma levels compared to adults.
- Follow-up studies revealed increased PMN Fc gamma RIII expression over time in ELBW infants.
- ELBW infants had lower total PMN-associated Fc gamma RIII than adults, indicating reduced synthesis.
Conclusions:
- Decreased Fc gamma RIII expression in ELBW infants is primarily due to reduced receptor synthesis.
- Fc gamma RIII expression on neutrophils is developmentally regulated in early life.
- Findings highlight an immune deficiency in ELBW infants that improves with maturation.
Abstract:
The purpose of this study was to determine whether decreased Fc gamma RIII expression on the PMN of extremely low birth weight infants (ELBW) is due to decreased receptor synthesis or increased receptor shedding from the PMN surface. 42 ELBW, 12 larger infants and 14 adults were enrolled. Plasma and total cellular Fc gamma RIII were measured by ELISA, and PMN Fc gamma RIII expression was measured by flow cytometry. ELBW PMN plasma membrane expression of Fc gamma RIII as measured by log mean channel fluorescence (5.00 +/- 1.98 vs. 10.68 +/- 1.61, p < 0.050) and plasma Fc gamma RIII levels were both lower (7.5 +/- 6.1 vs. 82.4 +/- 64.8 nM, p < 0.05) than in adult controls. In follow-up studies, 14 ELBW (age = 29 +/- 14 days, range = 14-56 days) increased PMN expression of Fc gamma RIII (p < 0.001) but not plasma Fc gamma RIII. ELBW had lower total PMN-associated Fc gamma RIII than adults (2.3 +/- 0.9 vs. 6.8 +/- 2.2 ng/10(6) PMN, p = 0.006). ELBW's PMN produce less Fc gamma RIII than adults' PMN, and expression of this receptor is developmentally regulated.
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