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Updated: Mar 7, 2026

Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
Bifidobacterium bifidum OLB6378 Simultaneously Enhances Systemic and Mucosal Humoral Immunity in Low Birth Weight
Katsunori Tanaka1, Takamitsu Tsukahara2, Takahide Yanagi3
1Department of Pediatrics, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga 520-2192, Japan. tanakatsu0124@gmail.com.
Insights
Supplementation with Bifidobacterium bifidum OLB6378 enhanced infant humoral immunity. Non-live OLB6378 showed a more pronounced effect on immunoglobulin levels in low birth weight infants.
Area of Science:
- Immunology
- Microbiology
- Neonatal Health
Background:
- Probiotic supplementation is explored for enhancing humoral immunity.
- Bifidobacterium bifidum OLB6378 (OLB6378) has been linked to reduced late-onset sepsis in infants.
Purpose of the Study:
- To determine the effect of live OLB6378 on infant humoral immunity.
- To investigate if non-live OLB6378 administration yields similar immune-enhancing effects.
Main Methods:
- A non-randomized study involving low birth weight (LBW) infants (1500-2500 g).
- Three groups: no intervention (N), live OLB6378 (L), and non-live OLB6378 (H).
- Intervention from within 48 hours of birth to six months of age.
Main Results:
- Group L showed significantly higher serum immunoglobulin G (IgG) levels compared to Group N.
- Group H exhibited significantly higher serum IgG and intestinal secretory immunoglobulin A (SIgA) levels than Group N.
- No significant differences in mortality or morbidity were observed between groups.
Conclusions:
- OLB6378 administration in LBW infants enhances humoral immunity.
- Non-live OLB6378 demonstrated a more significant impact on immune markers compared to live bacteria.
- Non-live OLB6378 may be a more effective and practical option for immune enhancement in infant nutrition.
Abstract:
Probiotic supplementation has been part of the discussion on methods to enhance humoral immunity. Administration of Bifidobacterium bifidum OLB6378 (OLB6378) reduced the incidence of late-onset sepsis in infants. In this non-randomized study, we aimed to determine the effect of administration of live OLB6378 on infants' humoral immunity. Secondly, we tried to elucidate whether similar effects would be observed with administration of non-live OLB6378. Low birth weight (LBW) infants weighing 1500-2500 g were divided into three groups: Group N (no intervention), Group L (administered live OLB6378 concentrate), and Group H (administered non-live OLB6378 concentrate). The interventions were started within 48 h after birth and continued until six months of age. Serum immunoglobulin G (IgG) levels (IgG at one month/IgG at birth) were significantly higher in Group L than in Group N (p < 0.01). Group H exhibited significantly higher serum IgG levels (p < 0.01) at one month of age and significantly higher intestinal secretory immunoglobulin A (SIgA) levels (p < 0.05) at one and two months of age than Group N. No difference was observed in the mortality or morbidity between groups. Thus, OLB6378 administration in LBW infants enhanced humoral immunity, and non-live OLB6378, which is more useful as a food ingredient, showed a more marked effect than the viable bacteria.
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