Skip to main content

Table 3 Studies of dairy proteins on incidence, duration, and severity of acute infections (N=7)

From: The effect of bovine dairy products and their components on the incidence and natural history of infection: a systematic literature review

Author (Year)

Exposure(s) being studied

Study population

Dairy intervention details

Infectious disease

Measures of infection risk

Duration and/or severity of infection or symptoms

N

Age, gender and health status

Kaido et al. (2012) [43]

Hydrolyzed whey peptide

Exp: 40

Control: 36

Adults, post-liver transplant

Exp: Immune-modulating diet enriched with hydrolyzed whey peptide started within the first 24 h after surgery through a jejunostomy tube infused at 20-40 ml/h for 10-14 days

Control: Conventional diet started within the first 24 h after surgery through a jejunostomy tube infused at 20-40 ml/h for 10-14 days

Clinically verified bacteremia

Proportion with bacteremia: SS decrease (p=0.002) exp. vs. control

In-hospital death due to infection: Differences NSS (p=0.145) exp. vs. control

NR

Vitetta et al. (2013) [44]

Bovine lactoferrin/whey protein Ig-rich fraction

Exp: 53

Control: 52

Adults, at least 3 cold events in the past 6 months

Exp: Two 300 mg capsules (containing 200 mg of lactoferrin and 100 mg of IgF) daily for 90 days

Control: Two 300 mg capsules (calcium phosphate) daily for 90 days

Common cold based on self-report of symptoms

Mean cold events 1-90 days:

SS decrease (p <0.001) exp. vs. control

Mean cold events 1-45 days:

SS decrease (p <0.001) exp. vs. control

Mean cold events 46-90 days: SS decrease (p <0.001) exp. vs. control

Total number of symptoms associated with a cold 1-90 days: SS decrease (p < 0.05) exp. vs. control

Median days ill at first follow-up (day 45): Difference NSS (p=0.10) exp. vs. control

Median days ill at second follow-up (day 90): Difference NSS (p=0.49) exp. vs. control

Median cold event severity at first follow-up (day 45): Difference NSS (p=0.76) exp. vs. control

Median cold event severity at second follow-up (day 90): Difference NSS (p=0.08) exp. vs. control

King et al. (2007) [46]

Bovine lactoferrin

Exp: 26

Control: 26

Infants ≤4 weeks of age, healthy

Exp: Similac iron formula with 850 mg/L bovine lactoferrin for 12 months

Control: Regular cow milk based Similac iron formula (102 mg/L bovine lactoferrin) for 12 months

Clinically confirmed URTI, AOM, LRTI

Mean episodes/infant-year:

Differences NSS (p-vales not reported) exp. vs. control for URTI, AOM, and other illnesses

Mean episodes/infant-year, LRTI: SS decrease (p<0.05) exp. vs. control

Mean duration (days): Differences NSS (p-values not reported) for URTI, AOM, LRTI, and other illnesses

Kaur and Gathwala (2015) [47]

Bovine lactoferrin

Exp: 63

Control: 67

Infants, low birth weight and hospitalized

Exp: 100-250 mg bovine lactoferrin (based on weight) dissolved in milk daily from 1st to 28th day of life

Control: Placebo (Glucon D) dissolved in milk daily from 1st to 28th day of life

Clinically confirmed late-onset sepsis

RR of culture-proven sepsis: RR=0.211(95% CI=0.044–1.019) exp. vs. control (p=0.036)

RR of bacterial sepsis: RR=0.242 (95% CI=0.049–1.186) (p= 0.061)

RR of probable sepsis: RR=0.257 (95% CI=0.08-0.828) exp. vs. control (p=0.016)

RR of any sepsis: RR=0.201 (95% CI=0.076-0.537) exp. vs. control (p=0.001)

Sepsis-attributable mortality:

SS decrease (p=0.027) exp. vs. control

NR

Akin et al. (2014) [48]

Bovine lactoferrin

Exp 1: 25

Control 1: 22

Infants, preterm and/or very low birth weight and hospitalized

Exp 1: 200 mg lactoferrin daily, after the baby reached 20 mL/kg/d feeding volume and continued throughout the hospitalization period

Control 1: 2 ml saline once a day, after the baby reached 20 mL/kg/d feeding volume and continued throughout the hospitalization period

Clinically confirmed sepsis

Number of patients with sepsis: Difference NSS (p=0.572) exp. vs. control

Number of sepsis attacks per 1,000 patient days: SS decrease (p=0.007) exp. vs. control

NR

Manzoni et al. (2009) [49]

Bovine lactoferrin and Lactobacillus rhamnosus GG

Exp 1: 153

Exp 2: 151

Control: 168

Infants, very low birth weight and hospitalized

Exp 1: 100 mg lactoferrin daily from birth to 30th day of life

Exp 2: 100 mg lactoferrin and Lactobacillus rhamnosus GG daily from birth to 30th day of life

Control: Placebo daily from birth to 30th day of life

Clinically confirmed late-onset sepsis

RR of late-onset sepsis: RR=0.34 (95% CI=0.17-0.70) exp 1 vs. control

RR of late-onset sepsis:

RR=0.27 (95% CI=0.12-0.60) exp 2 vs. control

Mortality attributable to sepsis: exp 1 vs. control, p=0.008

Mortality attributable to sepsis: RR=0.14 (0.02-1.09) exp 2 vs. control, p=0.04

Multivariable logistic regression: OR=0.32 (95% CI=0.14-0.77) exp 1 vs. control

OR=0.21 (0.08-0.55) exp 2 vs. control

NR

Oda et al. (2021) [45]

Bovine lactoferrin

Exp 1: 103

Exp 2: 103

Control: 104

Adults, healthy

Exp 1: 200 mg lactoferrin daily for 12 weeks

Exp 2: 600 mg lactoferrin daily for 12 weeks

Control: Placebo tablets daily for 12 weeks

Clinically confirmed infectious diseases, including summer colds, gastroenteritis, colds sores and styes

Prevalence of infectious diseases: Difference NSS (p=0.203) exp 1 vs. control

Difference NSS (p=0.240) exp 2 vs. control

p-trend= 0.240

Prevalence of summer colds: Difference NSS (p=0.488) exp 1 vs. control

Difference NSS (p=0.571) exp 2 vs. control

p-trend= 0.571

Median number of episodes, total infectious diseases: Difference NSS (p=0.348) exp 1 vs. control

Difference NSS (p=0.673) exp 2 vs. control

p-trend= 0.612

Median number of episodes, summer colds:

Difference NSS (p=0.857) exp 1 vs. control

Difference NSS (p=0.804) exp 2 vs. control

p-trend= 0.832

Prevalence of summer cold symptoms: Differences NSS (p=0.170, 0.243, 0.895, 0.401, 0.685, 0.305 and 0.571, respectively) for sore throat, cough, nasal secretion, nasal congestion, headache, chills, and fatigue

Median duration, total infectious diseases: SS decrease (p=0.045) exp 1 vs. control

SS decrease (p=0.010) exp 2 vs. control

p-trend=0.011

Median duration, summer cold: Difference NSS (p=0.204) exp 1 vs. control

SS decrease (p=0.036) exp 2 vs. control

p-trend= 0.060

Median duration of cold sores, gastroenteritis, styes: Differences NSS (p-values not reported) exp 1 and 2 vs. control

Median duration of summer cold symptoms: Differences NSS (p=0.096, 0.196, 0.283, 0.884, 0.657, 0.599, and 0.095, respectively) for sore throat, cough, nasal secretion, nasal congestion, headache, chills, and fatigue

Number of medications, total infectious diseases: Difference NSS (p=0.561) exp 1 vs. control

Difference NSS (p=0.910) exp 2 vs. control

p-trend=0.873

Number of medications, summer colds: Difference NSS (p=0.736) exp 1 vs. control

Difference NSS (p=0.895) exp 2 vs. control

p-trend=0.913

Median duration of medication, total infectious diseases: Difference NSS (p=0.352) exp 1 vs. control

Difference NSS (p=0.120) exp 2 vs. control

p-trend=0.085

Median duration of medication, summer colds:

Difference NSS (p=0.460) exp 1 vs. control

Difference NSS (p=0.082) exp 2 vs. control

p-trend=0.053

  1. AOM acute otitis media, CID common infectious disease, EN enteral nutrition, ENT ear, nose and throat, GITI gastrointestinal tract infection, IRR incidence rate ratio, ITT intent-to-treat, LRTI lower respiratory tract infection, NSS not statistically significant, OR odds ratio, PPA per protocol analysis, RTI respiratory tract infection, SS statistically significant, URTI upper respiratory tract infection
  2. Statistical comparisons that were significant at the p=0.05 level are bolded