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Bifidobacterium longum subsp. infantis

Bifidobacterium infantis

Research reviewed: Up until 03/2026

Bifidobacterium infantis (Bifidobacterium longum subsp. infantis) is a dietary supplement with 20 published peer-reviewed studies involving 704 participants, researched for IBS Symptom Relief, Infant Microbiome, Anti-inflammatory Effects and 2 more areas.

20
Studies
704
Participants
2005–2025
Research Span

Evidence at a Glance

Strength is scored by study design, sample size, study type, and outcomes

Overall: Strong Evidence

IBS Symptom Relief

Moderate
3 studies 1 of 3 positive 465 participants

Infant Microbiome

Moderate
2 studies 1 of 2 positive 112 participants

Anti-inflammatory Effects

Moderate
2 studies 1 of 2 positive 70 participants

Clinical trials

Moderate
9 studies 0 of 9 positive 57 participants

Systematic reviews

Weak
4 studies 0 of 4 positive 0 participants 0 human

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

11/20
Randomised
10/20
Double-Blind
10/20
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2005)
77
Study 2 (2006)
362
Study 3 (2008)
26
Study 1 (2017)
68
Study 2 (2021)
44
Study 1 (2008)
22
Study 2 (2013)
48
Study 1 (2025)
0

Research Timeline

When the studies were published

1
2005
1
2006
2
2008
1
2013
1
2017
1
2021
2
2024
11
2025

All Studies

Detailed breakdown of each trial. Click to expand.

IBS Symptom Relief

1

To evaluate B. infantis 35624 for IBS symptom relief.

2005 77 participants 8 weeks 10^8 CFU/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate B. infantis 35624 for IBS symptom relief.

Dose

10^8 CFU/day

Participants

77 IBS patients (all subtypes)

Duration

8 weeks

Results

B. infantis 35624 significantly reduced abdominal pain, bloating, and bowel dysfunction compared to placebo. Normalized IL-10/IL-12 ratio indicating anti-inflammatory activity.

How They Measured It

IBS symptom composite score, individual symptoms, cytokine ratios

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2

To determine optimal dose of B. infantis 35624 for IBS across all subtypes.

2006 362 participants 4 weeks 10^6, 10^8, 10^10 CFU/day
Human Study Double-Blind Placebo Positive

Study Type

Large-scale dose-ranging, double-blind, placebo-controlled

Purpose

To determine optimal dose of B. infantis 35624 for IBS across all subtypes.

Dose

10^6, 10^8, 10^10 CFU/day

Participants

362 female IBS patients

Duration

4 weeks

Results

10^8 CFU/day was the most effective dose, significantly improving all IBS symptoms. Both lower and higher doses were less effective.

How They Measured It

IBS-SSS, adequate relief, individual symptom scores

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3

To assess long-term efficacy and safety of B. infantis 35624 for IBS.

2008 26 participants 6 months 10^8 CFU/day
Human Study Mixed

Study Type

Open-label study

Purpose

To assess long-term efficacy and safety of B. infantis 35624 for IBS.

Dose

10^8 CFU/day

Participants

26 IBS patients from prior RCT

Duration

6 months

Results

Sustained improvement in IBS symptoms over 6 months with continued B. infantis supplementation. No adverse effects reported.

How They Measured It

IBS symptom scores, quality of life, safety monitoring

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Infant Microbiome

1

To evaluate B. infantis EVC001 on gut colonization and microbiome in breastfed infants.

2017 68 participants 60 days supplementation + 30 days follow-up 8 × 10^9 CFU/day
Human Study RCT Mixed

Study Type

Randomised controlled trial

Purpose

To evaluate B. infantis EVC001 on gut colonization and microbiome in breastfed infants.

Dose

8 × 10^9 CFU/day

Participants

68 breastfed term infants

Duration

60 days supplementation + 30 days follow-up

Results

B. infantis EVC001 colonized at high levels (>80% of fecal microbiome), efficiently consumed HMOs, lowered fecal pH, and reduced potential pathogens.

How They Measured It

Fecal B. infantis abundance, HMO utilization, fecal pH

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2

To assess B. infantis EVC001 effects on intestinal inflammation and immune development in infants.

2021 44 participants 60 days 8 × 10^9 CFU/day
Human Study RCT Positive

Study Type

Randomised, controlled

Purpose

To assess B. infantis EVC001 effects on intestinal inflammation and immune development in infants.

Dose

8 × 10^9 CFU/day

Participants

44 breastfed infants

Duration

60 days

Results

B. infantis EVC001 significantly reduced intestinal inflammation markers (fecal calprotectin) and promoted anti-inflammatory T-cell responses.

How They Measured It

Fecal calprotectin, cytokine profiles, immune cell phenotyping

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Anti-inflammatory Effects

1

To evaluate B. infantis 35624 on systemic inflammatory markers.

2008 22 participants 6-8 weeks 10^10 CFU/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate B. infantis 35624 on systemic inflammatory markers.

Dose

10^10 CFU/day

Participants

22 patients with psoriasis, 16 with chronic fatigue syndrome, 18 with ulcerative colitis

Duration

6-8 weeks

Results

B. infantis 35624 significantly reduced plasma CRP and TNF-alpha levels across all three inflammatory conditions. Enhanced IL-10 secretion from PBMCs.

How They Measured It

CRP, TNF-alpha, IL-6 levels; cytokine profiles from PBMCs

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2

To assess anti-inflammatory effects of B. infantis in ulcerative colitis.

2013 48 participants 8 weeks 10^9 CFU/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess anti-inflammatory effects of B. infantis in ulcerative colitis.

Dose

10^9 CFU/day

Participants

48 patients with mild-moderate ulcerative colitis

Duration

8 weeks

Results

B. infantis supplementation showed improvement in clinical activity scores and modest reduction in fecal calprotectin. Not statistically significant for endoscopic scores.

How They Measured It

Clinical Activity Index, endoscopic scores, fecal calprotectin

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Clinical trials

1

To investigate the effects of Bifidobacterium infantis in effects of kefir on symptoms, sleep, and gut microbiota in children with adhd: a randomised controlled trial.

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of Bifidobacterium infantis in effects of kefir on symptoms, sleep, and gut microbiota in children with adhd: a randomised controlled trial.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

Evidence indicates the gut microbiome may be altered in ADHD, suggesting that targeting gut bacteria could alleviate symptoms. This study examined the effects of kefir supplementation on ADHD symptoms, sleep, attention, and gut microbiome composition in children diagnosed with ADHD.

How They Measured It

See study for outcome measures

Read full study
2

To investigate the effects of Bifidobacterium infantis in effect of multispecies probiotics on autism symptoms: protocol for a randomized controlled trial (probaut).

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Human Study Mixed

Study Type

Clinical trial

Purpose

To investigate the effects of Bifidobacterium infantis in effect of multispecies probiotics on autism symptoms: protocol for a randomized controlled trial (probaut).

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

n worldwide, negatively impacting the daily functioning and quality of life of patients and their families. New therapeutic approaches for ASD are being investigated. Probiotics have shown promise in modulating gut microbiota and ameliorating ASD symptoms. We aim to evaluate the impact of a 12-week multispecies probiotic supplementation on the severity of core autism symptoms in children with ASD.

How They Measured It

See study for outcome measures

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3

To investigate the effects of Bifidobacterium infantis in effects of a live versus heat-inactivated probiotic bifidobacterium spp in preterm infants: a randomised clinical trial.

2025 ? participants 32 weeks Bifidobacterium infantis (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of Bifidobacterium infantis in effects of a live versus heat-inactivated probiotic bifidobacterium spp in preterm infants: a randomised clinical trial.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

32 weeks

Results

Heat-inactivated probiotics (HPs) may provide an effective alternative to live probiotics (P) by avoiding their risks (eg, probiotic sepsis) while retaining the benefits. We assessed the safety and efficacy of a HP in very preterm (VP: gestation <32 weeks) infants.

How They Measured It

See study for outcome measures

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4

To investigate the effects of Bifidobacterium infantis in safety and tolerance of bifidobacterium longum subsp. infantis ylgb-1496 in toddlers with respiratory symptoms.

2025 ? participants Duration not specified 1496 g
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of Bifidobacterium infantis in safety and tolerance of bifidobacterium longum subsp. infantis ylgb-1496 in toddlers with respiratory symptoms.

Dose

1496 g

Participants

Participants not specified

Duration

Duration not specified

Results

: B. infantis YLGB-1496 demonstrated excellent safety and tolerability in toddlers and effectively reduced the gastrointestinal discomfort associated with respiratory illnesses.

How They Measured It

See study for outcome measures

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5

To investigate the effects of Bifidobacterium infantis in clinical benefits of bifidobacterium infantis ylgb-1496 in modulating gut microbiota and immunity in young children.

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Human Study Mixed

Study Type

Clinical trial

Purpose

To investigate the effects of Bifidobacterium infantis in clinical benefits of bifidobacterium infantis ylgb-1496 in modulating gut microbiota and immunity in young children.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

arly-life gut microbiota is critical for immune development and long-term health, and plays an essential role in the digestion and metabolism of dietary components, including human milk oligosaccharides (HMOs). Probiotic supplementation is a promising strategy to modulate this ecosystem and prevent common childhood infectious illnesses, though strain-specific effects require further investigation.

How They Measured It

See study for outcome measures

Read full study
6

To investigate the effects of Bifidobacterium infantis in bifidobacterium and lactobacillus probiotics and gut dysbiosis in preterm infants: the primal randomized clinical trial.

2024 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of Bifidobacterium infantis in bifidobacterium and lactobacillus probiotics and gut dysbiosis in preterm infants: the primal randomized clinical trial.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

The effects of probiotic interventions on colonization with resistant bacteria and early microbiome development in preterm infants remain to be clarified.

How They Measured It

See study for outcome measures

Read full study
7

To investigate the effects of Bifidobacterium infantis in pre-sleep casein ingestion with probiotic strains improves anaerobic power and lower-body-specific strength and power performance in soccer players.

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of Bifidobacterium infantis in pre-sleep casein ingestion with probiotic strains improves anaerobic power and lower-body-specific strength and power performance in soccer players.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

ers have recently focused on the relationship between probiotic consumption and improved gut microbiota function, enhanced digestion, increased nutrient absorption, and enhanced sports performance. Therefore, the present study investigated the effects of pre-sleep casein intake, coupled with probiotic strains, on soccer players' anaerobic power, lower-body-specific strength, and power performance.

How They Measured It

See study for outcome measures

Read full study
8

To investigate the effects of Bifidobacterium infantis in therapeutic potential of bifidobacterium longum subsp. infantis b8762 on gut and respiratory health in infant.

2025 57 participants 4 weeks 10 CFU
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of Bifidobacterium infantis in therapeutic potential of bifidobacterium longum subsp. infantis b8762 on gut and respiratory health in infant.

Dose

10 CFU

Participants

57 participants

Duration

4 weeks

Results

tokine response, indicating modulation of the immune system. Genomic analysis showed that B8762 harbors various genes for the synthesis of proteins and vitamins crucial for the gut health of children. Both the clinical and genomic findings suggested that B8762 offered a therapeutic effect on gut and respiratory health in children, highlighting its potential in managing common pediatric infections.

How They Measured It

See study for outcome measures

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9

To investigate the effects of Bifidobacterium infantis in feasibility, safety, and impact of the probiotics lactiplantibacillus plantarum and bifidobacterium longum subspecies infantis in papua new guinean in

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Human Study Mixed

Study Type

Clinical trial

Purpose

To investigate the effects of Bifidobacterium infantis in feasibility, safety, and impact of the probiotics lactiplantibacillus plantarum and bifidobacterium longum subspecies infantis in papua new guinean in

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

Childhood mortality in low- or middle-income countries (LMICs) remains a major public health concern, with infections being a leading cause of infant death. Probiotics have shown promise in reducing infection-related morbidity and mortality in preterm infants, but their use in newborns born at or near term in LMICs requires further investigation.

How They Measured It

See study for outcome measures

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Systematic reviews

1

To investigate the effects of Bifidobacterium infantis in probiotics in term infants: clinical impact of infant-type bifidobacteria: a systematic review and meta-analyses.

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of Bifidobacterium infantis in probiotics in term infants: clinical impact of infant-type bifidobacteria: a systematic review and meta-analyses.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

iratory tract infections. However, the evidence is limited by study heterogeneity and a lack of long-term follow-up data. Further high-quality randomized controlled trials with larger sample sizes and standardized outcome measures are needed to clarify both short- and long-term effects of ITB probiotic administration in neonates and infants. This trial was registered at PROSPERO as CRD42024507608.

How They Measured It

See study for outcome measures

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2

To investigate the effects of Bifidobacterium infantis in probability of vertical hiv transmission: a systematic review and meta-regression.

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Review/Other Mixed

Study Type

Systematic review

Purpose

To investigate the effects of Bifidobacterium infantis in probability of vertical hiv transmission: a systematic review and meta-regression.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

stimating paediatric HIV infections with the Joint United Nations Programme on HIV/AIDS supported Spectrum AIDS Impact Module (Spectrum-AIM). Recent innovations in antiretroviral therapy (ART) service delivery models and first-line regimens aimed to reduce VT probabilities. We conducted a systematic review and meta-analysis to estimate VT probabilities by maternal immunologic and treatment status.

How They Measured It

See study for outcome measures

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3

To investigate the effects of Bifidobacterium infantis in the effectiveness of probiotics as an adjunct therapy in patients under mechanical ventilation: an umbrella systematic review and meta-analysis.

2024 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of Bifidobacterium infantis in the effectiveness of probiotics as an adjunct therapy in patients under mechanical ventilation: an umbrella systematic review and meta-analysis.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

, B. salivarius , Pediococcus pentosaceus , Lactococcus raffinolactis , B. infantis , B. bifidum , Streptococcus thermophilus , Ligilactobacillus salivarius , L. lactis , B. lactis , Saccharomyces boulardii , L. rhamnosus GG, L. johnsonii , L. casei , S. faecalis , Clostridium butyricum , Bacillus mesentericus , L. sporogenes , S. boulardii , L. paracasei , B. subtilis , and Enterococcus faecium .

How They Measured It

See study for outcome measures

Read full study
4

To investigate the effects of Bifidobacterium infantis in probability of vertical hiv transmission: a systematic review and meta-regression.

2025 ? participants Duration not specified Bifidobacterium infantis (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of Bifidobacterium infantis in probability of vertical hiv transmission: a systematic review and meta-regression.

Dose

Bifidobacterium infantis (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

arly-life gut microbiota is critical for immune development and long-term health, and plays an essential role in the digestion and metabolism of dietary components, including human milk oligosaccharides (HMOs). Probiotic supplementation is a promising strategy to modulate this ecosystem and prevent common childhood infectious illnesses, though strain-specific effects require further investigation.

How They Measured It

See study for outcome measures

Read full study

Frequently Asked Questions

Common questions about Bifidobacterium infantis research

What does the research say about Bifidobacterium infantis?

There are currently 20 peer-reviewed studies on Bifidobacterium infantis (Bifidobacterium longum subsp. infantis), involving 704 total participants. Research covers IBS Symptom Relief, Infant Microbiome, Anti-inflammatory Effects and 2 more areas. The overall evidence strength is rated as Strong.

How strong is the evidence for Bifidobacterium infantis?

The evidence is currently rated as "Strong Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (16 human studies), and reported outcomes.

What health goals has Bifidobacterium infantis been studied for?

Bifidobacterium infantis has been researched for: IBS Symptom Relief, Infant Microbiome, Anti-inflammatory Effects, Clinical trials, Systematic reviews. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Bifidobacterium infantis based on human trials?

Yes, 16 out of 20 studies are human trials. Human trials carry more weight in our evidence scoring system.