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Published on: June 15, 2018
Immunoglobulin subclass concentration in preterm infants treated prophylactically with different intravenous
Insights
This study examined immunoglobulin G (IgG) subclass levels in preterm infants receiving intravenous immunoglobulin (IVIG) therapy. Different IVIG preparations showed distinct subclass level patterns, influencing treatment efficacy.
Area of Science:
- Neonatal immunology
- Immunoglobulin therapy
Background:
- Immature infants have low immunoglobulin G (IgG) subclass concentrations, increasing infection risk.
- Selective IgG subclass deficiency warrants intravenous immunoglobulin (IVIG) substitution.
- IVIG efficacy depends on pharmacokinetics, necessitating study of IgG subclass levels.
Purpose of the Study:
- To investigate peak and trough IgG subclass serum levels in healthy preterm infants over 28 days.
- To compare IgG subclass levels following prophylactic treatment with two different IVIG preparations: Sandoglobulin (SG) and Pentaglobin (PG).
Main Methods:
- Thirty-four healthy preterm infants (30.2 ± 2 weeks GA) received either SG (0.5 g/kg/day) or PG (5 mL/kg/day) for 3 days.
- IgG subclass levels were measured by radioimmundiffusion (RID) on days 1, 3, 5, 7, 14, and 28.
- Paired t-tests were used for statistical analysis.
Main Results:
- Both IVIG preparations increased IgG subclass levels in the first week (days 3, 5, 7) compared to pre-treatment values (p < 0.05).
- During the first week, IgG2 levels were higher with SG, while IgG4 levels were higher with PG (p < 0.05).
- Distinct IgG subclass level patterns were observed 14 days post-treatment, varying by IVIG preparation.
Conclusions:
- Prophylactic IVIG administration influences IgG subclass levels in preterm infants.
- Different IVIG preparations result in varied IgG subclass pharmacokinetic profiles.
- Future clinical trials should assess target serum levels and optimal timing for IVIG administration, considering both total IgG and specific IgG subclasses.
Abstract:
The most immature infants have critically low concentrations of all immunoglobulin G (IgG) subclasses, associated with a higher risk for pyogenic, respiratory, and meningeal infection. Selective IgG subclass deficiency is an established indication for intravenous immunoglobulin (IVIG) substitution. However, considering that therapeutic efficacy of IVIG is dependent on its pharmacokinetics, we studied peak and trough IgG subclass serum levels during the neonatal period (28 days) in a group of 34 healthy preterm babies (30.2 +/- 2 weeks gestational age (GA) and 1065 +/- 210 g birthweight (BW) treated prophylactically with three daily standard doses of two different IVIG preparations: Sandoglobulin (SG) (0.5 g/kg/day) and Pentaglobin (PG) (5 mL/kg/day). IgG subclass levels were assayed by radioimmundiffusion (RID) before treatment (day 1) and at days 3, 5, 7, 14, and 28 of life. Statistical analysis was performed by paired t test. In the first week of life only (days 3, 5, 7), for both IVIG preparations, subclass levels were higher than pretreatment values: IgG1, 4.6 +/- 1.7 versus 5.6 +/- 1.6 g/L; IgG2, 1.6 +/- 0.8 versus 2.1 +/- 0.6 g/L; IgG3, 0.2 +/- 0.7 versus 0.3 +/- 0.1 g/L; IgG4, 0.3 +/- 0.1 versus 0.9 +/- 0.1 g/L (p < 0.05). During this time (7 days) IgG2 levels were higher in the SG group and IgG4 was higher in the PG group (p < 0.05). This study shows pretreatment IgG subclass levels 14 days after treatment and different patterns, depending on the used preparation. We conclude that prospective clinical trials should include the study of target serum levels and timing of IVIG administration not only for IgG but also for IgG subclasses.
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