Skip to main content

Effect of probiotic fermented dairy products on incidence of respiratory tract infections: a systematic review and meta-analysis of randomized clinical trials

Abstract

Background

Previous studies have suggested that the consumption of probiotic fermented dairy products (PFDP) may have a protective effect on respiratory tract infections (RTIs). However, the results of studies are inconclusive. We aimed to systematically investigate the effect of PFDP on RTIs by performing a meta-analysis of randomized controlled trials (RCTs).

Methods

PubMed and Scopus databases were systematically searched up to October 2020 to identify eligible RCTs. Meta-analysis outcomes were risk of incidence of upper (URTIs ) and lower (LRTIs ) respiratory tract infections. A random-effects model was used to pool the relative risks (RR) and corresponding 95 % confidence intervals (CI) for outcomes following conception of PFDP.

Results

A total of 22 RCTs, with a total sample size of 10,190 participants, were included in this meta-analysis. Compared with placebo, consumption of PFDP had a significant protective effect against RTIs in the overall analysis (RR = 0.81, 95 %CI: 0.74 to 0.89) and in children (RR = 0.82, 95 %CI: 0.73 to 0.93), adults (RR = 0.81, 95 %CI: 0.66 to 1.00), and elderly population (RR = 0.78, 95 %CI: 0.61 to 0.98). The significant decreased risk of RTIs was also observed for URTIs (RR = 0.83, 95 %CI: 0.73 to 0.93), while, this effect was marginal for LRTIs (RR = 0.78, 95 %CI: 0.60 to 1.01, P = 0.06). The disease-specific analysis showed that PFDP have a protective effect on pneumonia (RR = 0.76, 95 %CI: 0.61 to 0.95) and common cold (RR = 0.68, 95 %CI: 0.49 to 0.96).

Conclusions

Consumption of PFDP is a potential dietary approach for the prevention of RTIs.

Peer Review reports

Research highlights

  • Consumption of PFDP had a significant protective effect against RTIs in all age groups.

  • PFDP had a protective effect on pneumonia and common cold.

  • The protective effect of PFDP was modified by probiotic genus and type of dairy product used for intervention.

Background

Acute respiratory infections (RTI, including upper RTI (URTI), e.g., cold, and lower RTI (LRTI), e.g., pneumonia and bronchitis, are a pervasive public health problem in all developed and developing countries, leading to nearly four million deaths annually, with more than 60 deaths per 100,000 population [1]. ARIs are a main public health problem worldwide and contribute to increased morbidity and mortality, as they result in a large number of outpatient visits, hospital admissions, and the widespread administration of antibiotics [2]. These diseases affect all age groups every year and put a heavy burden on the world’s health and economic systems. More than 200 types of viruses have been identified as causing respiratory diseases [3, 4]. As well as, 90 % of deaths because of respiratory infections are reported to happen in patients over 65 years of age [5]. Young children are more likely to get this respiratory infection than adults or children [6, 7]. In most cases, the diseases of the upper respiratory tract are mild to moderate and mostly self-limiting. However, LRTIs-induced pneumonia can be predominantly fatal in children and the elderly or in immunocompromised individuals [4, 8].

The health benefits of fermented milk and dairy products have long been known. The health benefits of dairy products are the consequence of the biologically active ingredients existing in native milk and are also produced in fermented or sour milk products produced by the action of probiotic bacteria [9]. Probiotics have been used as an adjunct to reduce the risks of widespread use of antibiotics such as diarrhea and to prevent infections, including respiratory infections [10]. One reason that probiotics are considered to be the main and important components of the diet to reduce the risk of infectious diseases is due to their functional role in the gastrointestinal tract and intestinal epithelium, as well as their relationship with the function of the immune system and intestinal mucosa [11, 12]. Probiotics are living microorganisms that, if administered in sufficient doses, provide health benefits to the host [13].

Studies show that functional foods from fermented cow’s milk with probiotic strains can well prevent infectious diseases, but the data are still inconsistent [14,15,16,17,18,19]. Prevention or control of infectious diseases is one of the most promising health benefits of probiotics [20,21,22]. The useful effects of lactic acid bacteria and cultured milk products have been ascribed to their capability to suppress the growth of pathogens instantly or via the genesis of antibacterial agents [23]. The results of several studies have shown that some probiotics are effective against infections of the gastrointestinal tract and respiratory tract [24]. Furthermore, it has been demonstrated that probiotics have an essential role in extenuating the rate of ARI episodes and antibiotic use [25]. Nonetheless, there are little well-designed individual interventional studies, with contradictory findings, assessing the clinical effects of dairy, mostly for yogurt and milk, supplemented with chosen probiotics against acute RTI.

Considering the potential of probiotic products and the importance of medical nutrition therapy of respiratory tract infections, the current meta-analysis of recently conducted randomized controlled trials (RCTs) aimed to assess the effect of fermented dairy products by probiotics on incidence of respiratory tract infections in children, adults, and elderly.

Main text

Methods

Search strategy

We followed PRISMA guidelines (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) in the design and reporting of the methods for this systematic review [1]. PubMed and Scopus online databases were searched from inception to October 2020 for RCTs examining the effect of probiotic fermented dairy products on incidence of respiratory tract infections. A different combination of keywords was searched (Supplemental file 1). Where possible, Medical Subject Headings in addition to free-text search terms were used in the search. The search results were limited to English-language publications. In addition, we checked references of retrieved eligible papers and previous review articles in this area to make sure we found all relevant articles.

Screening and study selection

First, electronic and manual search results were exported to EndNote software, version X8 (Thomson Reuters) and duplicate publications were eliminated. Selection of eligible controlled trials was carried out independently by two investigators (SA & PJ). Any discrepancies were resolved by consensus. The researchers first assessed the titles and abstracts of studies obtained through preliminary searches, then, independently reviewed the full text of remaining publications.

Eligibility criteria

The PICO for this Meta-analysis and systematic review include: P: People diagnosed with an acute RTI, I: Consuming probiotic fermented dairy products (PFDP), C: Not consuming PFDP, O: Risk of incidence of URTIs or LRTIs. Also, articles were included for analysis if they conformed to the following criteria: (1) were RCT in design; (2) provided original data on the effect of probiotic fermented dairy products on incidence of respiratory tract infections; (3) were published in English; (4) done on human subjects; (5) had full text available, and (6) provided a comparison group. Trials that did not meet our inclusion criteria were excluded, and the remaining studies were selected for further analysis.

Data extraction

Data extraction was performed by two investigators, independently (SA and PJ) using a standardized data extraction sheet. Subsequently, full texts studies were assessed, and disagreements were resolved through discussion with a third independent researcher (BR). The following information was extracted: first author’s name, publication year, country/geographic location, study design including whether parallel or cross-over, target population, mean age, gender, number of participants, study duration, type and dosage of PFDP, relative risks (RR) and 95 % confidence interval (CI) of RTIs.

Quality assessment of studies

Two reviewers (MD & AD) independently assessed the quality of each study according to the Cochrane risk of bias [2], which is composed of the following criteria: random sequence generation, allocation concealment, blinding, and clarification of failures (imperfect outcome data), selective outcome reporting and other biases. According to the Cochrane guideline handbook, the words “yes,” “no,” and “unclear” corresponded to low, high, and unknown risk of bias, respectively. According to the mentioned domains, the overall quality of study was considered as good (low risk for all items), fair (low risk more than three items), and poor (low risk for 3 or fewer items).

Data synthesis and analysis

All analyses were performed using STATA software version 12 (STATA corp, College Station, TX, USA). Due to the fact that selected RCTs were carried out in different settings, a random-effects model was used to pool the RR and 95 %CI for outcomes following consumption of PFDP. Heterogeneity was examined using the I-squared (I2) index. An I2 value > 50 % was considered to indicate substantial heterogeneity between trials [4]. To explore the source of heterogeneity, in addition to the general analysis, we performed subgroup analyses by studied population, probiotic genus used in dairy products, type of dairy product, and type of RTI. Meta-regression analysis was also carried out to explore the effect of the duration of supplementation and age of participants of pooled estimates. The presence of publication bias was tested using the Egger’s regression asymmetry test and P < 0.05 was considered statistically significant, except where otherwise specified.

Results

Study characteristics

A total of 239 articles were identified through the systematic literature search of databases. After excluding 26 duplicate studies and removing 168 irrelevant publications based on titles/abstracts, 45 studies went under full-text screening. Of which, 23 paper were excluded based on the inclusion criteria because they used baby formula supplemented with probiotics as intervention, were on allergic respiratory diseases, were republished studies, did not report sufficient extractable data, or had irrelevant intervention or outcome. Finally, 22 clinical trials with 33 datasets [14, 26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46], with a total sample size of 10,190 subjects were included in this meta-analysis. The flow diagram of study selection is presented in Fig. 1. Some studies reported multiple results; we extracted all suitable data for such studies. For instance, the study by Agustina et al. [26] contained two interventions, a group received fermented milk with Lactobacillus casei CRL431 and another group received fermented milk with Lactobacillus reuteri DSM17938, which both were included. The study by Makino et al. [38] included two separate studies and both were eligible for our meta-analysis. Moreover, some studies reported results for different respiratory tract infections (RTIs) separately, which all effect sizes were included. Data on total RTIs, lower respiratory tract infections (LRTIs), and upper respiratory tract infections (URTIs) were reported in 5 studies with 6 data sets [26, 33, 36, 37, 45], 9 studies with 10 data sets [14, 29,30,31,32, 40, 42, 43, 46], and 14 studies with 17 data sets [14, 27,28,29, 31, 32, 34, 35, 38,39,40,41, 44, 46], respectively. Among the included studies, there were 10 studies with 17 data sets on children [14, 26, 27, 31,32,33, 36, 37, 40, 43] and 6 studies with 8 data sets for each adult [29, 34, 35, 39, 42, 44], and elderly population [28, 30, 38, 41, 45, 46]. The probiotic genus used in fermented dairy products was Lactobacillus in 20 studies [14, 26,27,28,29,30,31,32,33,34,35,36,37,38, 40,41,42, 44,45,46] and Bifidobacterium in 2 studies [39, 43]. Furthermore, the fermented dairy products used as intervention was milk in 14 studies with 21 data sets [26,27,28, 30,31,32,33,34, 36, 37, 40, 43,44,45], yogurt in 4 studies with 5 data sets [35, 38, 39, 41], and a dairy drink in 4 studies with 7 data sets [14, 29, 42, 46]. Concerning study design, all studies were parallel RCT, except for the study by Meng et al.[39], which had a crossover design. The sample size of the included studies ranged from 52 to 1104 participants and follow-up period was between 1 and 12 months. Based on the Cochrane scale, all included studies received scored as moderated to high quality. Other characteristics of the analyzed publications are reported in Table 1.

Fig. 1
figure 1

Flow diagram of the study

Table 1 Study characteristics

Quantitative analysis

Overall and stratified analysis by studied population for the effect of probiotic fermented dairy products (PFDP) on RTIs is presented in Fig. 2. When all studies were pooled, it was found that, compared with placebo, consumption of PFDP has a significant protective effect against RTIs in the overall analysis (RR = 0.81, 95 %CI: 0.74 to 0.89) and in children (RR = 0.82, 95 %CI: 0.73 to 0.93), adults (RR = 0.81, 95 %CI: 0.66 to 1.00), and elderly population (RR = 0.78, 95 %CI: 0.61 to 0.98), with a significant heterogeneity across studies (I2 = 54.8 %, P < 0.001). The significant decreased risk of RTIs was also observed for URTIs (RR = 0.83, 95 %CI: 0.73 to 0.93), while, this association was marginal for LRTIs (RR = 0.78, 95 %CI: 0.60 to 1.01, P = 0.06). In the subgroup analysis, the significant impact of PFDP on RTIs was modified by probiotic genus and type of dairy product used for intervention; while, PFDP consumption had a protective effect on RTIs when Lactobacillus and milk were used as probiotic and fermented dairy product, respectively, but no significant effect was found in studies which administered Bifidobacterium and dairy drink or yogurt (Table 2).

Fig. 2
figure 2

Meta-analysis for the effect of fermented probiotic dairy products on respiratory tract infections stratified by studied population

Table 2 Subgroup analyses for the effect of probiotic dairy products on respiratory tract infections

Fermented probiotic dairy products and specific respiratory tract infections

Meta-analysis for the effect of PFDP on specific respiratory tract infections showed that the consumption of PFDP has a protective effect on pneumonia (RR = 0.76, 95 %CI: 0.61 to 0.95) and common cold (RR = 0.68, 95 %CI: 0.49 to 0.96). PFDP had no significant effect on other RTIs (Fig. 3).

Fig. 3
figure 3

Meta-analysis for the effect of fermented probiotic dairy products on specific respiratory tract infections

Meta-regression, sensitivity analysis, and publication bias

Meta-regression analysis showed that the effect of PFDP on RTIs was not modified by the duration of supplementation and age of participants (Fig. 4). There was a significant evidence for possible publication bias based on funnel plots asymmetry and Egger’s linear regression test (t = − 3.02, P = 0.005) (Fig. 5). In the sensitivity analysis by removing one study at a time and reanalyzing other studies, the polled effect size ranged from (RR = 0.79, 95 %CI: 0.72 to 0.88) to (RR = 0.83, 95 %CI: 0.76 to 0.91) and no single study significantly affected the pooled effect estimate, showing the reliability of the findings.

Fig. 4
figure 4

Meta-regression analysis for the effect of fermented probiotic dairy products on respiratory tract infections based on follow-up duration (A) and age of participants (B)

Fig. 5
figure 5

Funnel plot for publication bias in studies investigating the effect of fermented probiotic dairy products on respiratory tract infections

Discussion

During the past years, numerous investigations have evaluated the potential role of fermented probiotic dairy products against RTIs. Notwithstanding, these studies yielded inconclusive findings. Differences in the experimental design, lower sample sizes, and bacterial strains used in the preparation of the fermented products might be the underlying cause of such conflicting results. To resolve the problem of inconsistency by abrogating the limiting issues present in the individual studies we conducted the current meta-analysis which is the most up-to-date study that contained a significantly higher frequency of studies and individuals in the intervention/placebo groups, and indicated beneficial effects of FPDPs supplementation in reducing the risk of RTIs. Accordingly, overall and stratified analysis highlighted decreased risk of RTIs in overall population, all age subgroup, dairy products fermented with Lactobacillus and those who consume fermented probiotic milk, but not diary drink and yogurt.

Probiotics are defined as “beneficial live microorganisms which its administration in optimal amount confer a health benefit to the user”. The boosting effects of probiotics on the function of gastrointestinal and respiratory systems have been proposed by several studies performed on humans and animals [47, 48]. However, the observed beneficial effects are bacterial strain dependent. It is highlighted that lactobacillus casei resistant to gastric acid and bile. In this regard, several studies have shown that lactobacillus-containing products reach the lower digestive tract without losing its activity, and after localization balance the intestinal flora by promotion of immune cells that are produced in the lower intestinal tract. These cells might migrate to other mucosal sites and contribute in protection against pathogens [49,50,51].

So far, several mechanisms have been suggested on the effectiveness of probiotics to promote immune system. Firstly, Lactobacillus cause an anti-inflammatory impact by reduction of Interleukin-12 (IL-12) and stimulation of Interleukin-10 (IL-10) [52]. From immunological point of view, IL-10 derived from CD4 + T-helper type 2. This cytokine identified as potent inhibitor of monocyte/macrophage function and suppress the production of many pro-inflammatory cytokines [53]. Secondly, probiotics present an immunostimulatory effect which resulted in activation of innate and acquired immunity cells and subsequently production of innate and acquired immunity peptides. Paneth cells, neutrophils, and epithelial cells are among activated cells which produce antimicrobial peptides (AMPs) like lysozyme, lactoferrin, defensins and defend the body against pathogens [54, 55]. Moreover, secretory immunoglobulin A (IgA) which is a functional acquired immunity peptides defenses against pathogens either by immune exclusion or neutralization mechanism [56]. Studies have shown that probiotics induce AMPs, IgA, and IgG, resulting in an augmentation of immune system against infections [57, 58]. In confirm of the aforementioned theoretical facts, Reale et al. showed that probiotic intake can restore natural killer (NK) cell activity, member of innate immunity cells, which strengthen the host’s immune defense and induce a quick recovery by shortening the duration of infection [59, 60]. As our results show, consumption of FPDPs significantly decreased risk of RTIs in all age groups which can be a promising finding supported by potential biological mechanisms. Reduction of RTIs by FPDPs is highly important is it is accompanied by a reduction in medication use, working and school days loss, and social burden. It should be considered that the non-significant effect of studies which administered Bifidobacterium and dairy drink or yogurt on RTIs is due to small number of analyzed studies in these subgroups, which is important to be interpreted with a high caution.

Our meta-analysis was not bereft of limitations and caveats. First, we searched only English-written papers, which may raise the possibility of omission of potentially valuable studies and cause publication bias. Second, we observed a significant heterogeneity among the studies that might stem largely from, ethnicity of participants, year of publication, age, clinical heterogeneity, unreported and unknown study characteristics and many other factors which we are not able to attenuate their impact on final analysis. Therefore, for finding any sources of heterogeneity and attenuating their effects, we conducted subgroup analysis and weighted meta-regression. Collectively, the results of meta-regression showed that duration of supplementation and age of participants were not the expected source of heterogeneity, but probiotic genus and type of dairy product used for intervention were found as sources of observed heterogeneity. However, to deal with statistical heterogeneity, a random-effects model was applied for analyzes, which typically produces more conservative estimates of the significance of a result (a wider confidence interval), as it gives proportionately higher weights to smaller studies and lower weights to larger studies than fixed effect analysis.

Conclusions

Considering all the facts, this was the first comprehensive systematic review and meta-analysis of the effect of probiotic dairy products on respiratory tract infections, by including 22 clinical trials with 33 datasets. Our analysis indicated protection effect of FPDPs against RTIs in all age subgroup.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

PFDP:

Probiotic fermented dairy products

RTIs:

Respiratory tract infections

RCTs:

Randomized controlled trials

URTIs:

Upper respiratory tract infections

LRTIs:

Lower respiratory tract infections

RR:

Relative risks

CI:

Confidence intervals

IL-12:

Interleukin-12

IL-10:

Interleukin-10

AMPs:

Antimicrobial peptides

IgA:

Immunoglobulin A

IgG:

Immunoglobulin G

NK:

Natural killer

References

  1. Organization WH. World health report 2004 statistical annex. Geneva: WHO; 2004.

    Google Scholar 

  2. Mulholland K. Global burden of acute respiratory infections in children: implications for interventions. Pediatr Pulmonol. 2003;36(6):469–74.

    Article  PubMed  Google Scholar 

  3. Heikkinen T, Järvinen A. The common cold. The Lancet. 2003;361(9351):51–9.

    Article  Google Scholar 

  4. Jain S. Epidemiology of viral pneumonia. Clin Chest Med. 2017;38(1):1–9.

    Article  PubMed  Google Scholar 

  5. Mouton CP, Bazaldua OV, Pierce B, Espino DV. Common infections in older adults. Am Family Phys. 2001;63(2):257.

    CAS  Google Scholar 

  6. Chonmaitree T, Revai K, Grady JJ, Clos A, Patel JA, Nair S, et al. Viral upper respiratory tract infection and otitis media complication in young children. Clin Infect Dis. 2008;46(6):815–23.

    Article  PubMed  Google Scholar 

  7. von Linstow ML, Holst KK, Larsen K, Koch A, Andersen PK, Høgh B. Acute respiratory symptoms and general illness during the first year of life: A population-based birth cohort study. Pediatr Pulmonol. 2008;43(6):584–93.

    Article  Google Scholar 

  8. Lehtoranta L, Latvala S, Lehtinen MJ. Role of Probiotics in Stimulating the Immune System in Viral Respiratory Tract Infections: a Narrative Review. Nutrients. 2020;12(10):3163.

    Article  PubMed Central  Google Scholar 

  9. Ebringer L, Ferenčík M, Krajčovič J. Beneficial health effects of milk and fermented dairy products. Folia Microbiol. 2008;53(5):378–94.

    Article  CAS  Google Scholar 

  10. Kekkonen RA, Vasankari TJ, Vuorimaa T, Haahtela T, Julkunen I, Korpela R. The effect of probiotics on respiratory infections and gastrointestinal symptoms during training in marathon runners. Int J Sport Nutr Exerc Metab. 2007;17(4):352–63.

    Article  PubMed  Google Scholar 

  11. Wannmacher L. Evidências sobre uso de antibacterianos nas infecções respiratórias altas. Organização Pan-Americana da Saúde/Organização Mundial da Saúde-Brasil. Uso racional de medicamentos. 2006;4(1).

  12. Rijkers GT, Bengmark S, Enck P, Haller D, Herz U, Kalliomaki M, et al. Guidance for substantiating the evidence for beneficial effects of probiotics: current status and recommendations for future research. J Nutr. 2010;140(3):671S-6S.

    Article  PubMed  CAS  Google Scholar 

  13. Hotel AC, Cordoba A. Health and nutritional properties of probiotics in food including powder milk with live lactic acid bacteria. Prevention. 2001;5(1):1-10.

  14. Merenstein D, Murphy M, Fokar A, Hernandez RK, Park H, Nsouli H, et al. Use of a fermented dairy probiotic drink containing Lactobacillus casei (DN-114 001) to decrease the rate of illness in kids: the DRINK study A patient-oriented, double-blind, cluster-randomized, placebo-controlled, clinical trial. Eur J Clin Nutr. 2010;64(7):669–77.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Brunser O, Araya M, Espinoza J, Guesry P, Secretin M, Pacheco I. Effect of an Acidified Milk on Diarrhoea and the Carrier State in Infants of Low Socio-Economic Stratum. Acta Paediatr. 1989;78(2):259–64.

    Article  CAS  Google Scholar 

  16. Campeotto F, Suau A, Kapel N, Magne F, Viallon V, Ferraris L, et al. A fermented formula in pre-term infants: clinical tolerance, gut microbiota, down-regulation of faecal calprotectin and up-regulation of faecal secretory IgA. Br J Nutr. 2011;105(12):1843–51.

    Article  CAS  PubMed  Google Scholar 

  17. Nagata S, Asahara T, Ohta T, Yamada T, Kondo S, Bian L, et al. Effect of the continuous intake of probiotic-fermented milk containing Lactobacillus casei strain Shirota on fever in a mass outbreak of norovirus gastroenteritis and the faecal microflora in a health service facility for the aged. Br J Nutr. 2011;106(4):549–56.

    Article  CAS  PubMed  Google Scholar 

  18. Thibault H, Aubert-Jacquin C, Goulet O. Effects of long-term consumption of a fermented infant formula (with Bifidobacterium breve c50 and Streptococcus thermophilus 065) on acute diarrhea in healthy infants. J Pediatr Gastroenterol Nutr. 2004;39(2):147–52.

    Article  CAS  PubMed  Google Scholar 

  19. Mullié C, Yazourh A, Thibault H, Odou M-F, Singer E, Kalach N, et al. Increased poliovirus-specific intestinal antibody response coincides with promotion of Bifidobacterium longum-infantis and Bifidobacterium breve in infants: a randomized, double-blind, placebo-controlled trial. Pediatr Res. 2004;56(5):791–5.

    Article  PubMed  CAS  Google Scholar 

  20. Nomoto K. Prevention of infections by probiotics. J Biosci Bioengineer. 2005;100(6):583–92.

    Article  CAS  Google Scholar 

  21. Alvarez-Olmos MI, Oberhelman RA. Probiotic agents and infectious diseases: a modern perspective on a traditional therapy. Clin Infect Dis. 2001;32(11):1567–76.

    Article  CAS  PubMed  Google Scholar 

  22. Jafar-Abadi MA, Dehghani A, Khalili L, Barzegar A, Mesrizad M, Hassanalilou T. A Meta-analysis of Randomized Controlled Trials of the Effect of Probi-otic Food or Supplement on Glycemic Response and Body Mass Index in Patients with Type 2 Diabetes, Updating the Evidence. Curr Diabetes Rev. 2020;17(3):356-364.

  23. Panesar PS, Kaur G, Panesar R, Bera MB. Synbiotics: potential dietary supplements in functional foods. Berkshire: IFIS; 2009.

    Google Scholar 

  24. King S, Glanville J, Sanders ME, Fitzgerald A, Varley D. Effectiveness of probiotics on the duration of illness in healthy children and adults who develop common acute respiratory infectious conditions: a systematic review and meta-analysis. Br J Nutr. 2014;112(1):41–54.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Amaral MA, Guedes GHBF, Epifanio M, Wagner MB, Jones MH, Mattiello R. Network meta-analysis of probiotics to prevent respiratory infections in children and adolescents. Pediatr Pulmonol. 2017;52(6):833–43.

    Article  PubMed  Google Scholar 

  26. Agustina R, Kok FJ, Van De Rest O, Fahmida U, Firmansyah A, Lukito W, et al. Randomized trial of probiotics and calcium on diarrhea and respiratory tract infections in Indonesian children. Pediatrics. 2012;129(5):e1155-e64.

    Article  Google Scholar 

  27. Corsello G, Carta M, Marinello R, Picca M, De Marco G, Micillo M, et al. Preventive effect of cow’s milk fermented with Lactobacillus paracasei CBA L74 on common infectious diseases in children: A multicenter randomized controlled trial. Nutrients. 2017;9(7):669.

    Article  PubMed Central  CAS  Google Scholar 

  28. Fujita R, Iimuro S, Shinozaki T, Sakamaki K, Uemura Y, Takeuchi A, et al. Decreased duration of acute upper respiratory tract infections with daily intake of fermented milk: a multicenter, double-blinded, randomized comparative study in users of day care facilities for the elderly population. Am J Infect Control. 2013;41(12):1231–5.

    Article  PubMed  Google Scholar 

  29. Guillemard E, Tanguy J, Flavigny AL, de la Motte S, Schrezenmeir J. Effects of consumption of a fermented dairy product containing the probiotic Lactobacillus casei DN-114 001 on common respiratory and gastrointestinal infections in shift workers in a randomized controlled trial. J Am Coll Nutr. 2010;29(5):455–68.

    Article  PubMed  Google Scholar 

  30. Guo C, Lei M, Wang Y, Hua L, Xue S, Yu D, et al. Oral Administration of Probiotic Lactobacillus Casei Shirota Decreases Pneumonia and Increases Pulmonary Functions after Single Rib Fracture: A Randomized Double-Blind, Placebo‐Controlled Clinical Trial. J Food Sci. 2018;83(8):2222–6.

    Article  CAS  PubMed  Google Scholar 

  31. Hatakka K, Savilahti E, Pönkä A, Meurman JH, Poussa T, Näse L, et al. Effect of long term consumption of probiotic milk on infections in children attending day care centres: double blind, randomised trial. BMJ. 2001;322(7298):1327.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Hojsak I, Abdović S, Szajewska H, Milošević M, Krznarić Ž, Kolaček S. Lactobacillus GG in the prevention of nosocomial gastrointestinal and respiratory tract infections. Pediatrics. 2010;125(5):e1171-e7.

    Article  Google Scholar 

  33. Hojsak I, Snovak N, Abdović S, Szajewska H, Mišak Z, Kolaček S. Lactobacillus GG in the prevention of gastrointestinal and respiratory tract infections in children who attend day care centers: a randomized, double-blind, placebo-controlled trial. Clin Nutr. 2010;29(3):312–6.

    Article  PubMed  Google Scholar 

  34. Jespersen L, Tarnow I, Eskesen D, Morberg CM, Michelsen B, Bügel S, et al. Effect of Lactobacillus paracasei subsp. paracasei, L. casei 431 on immune response to influenza vaccination and upper respiratory tract infections in healthy adult volunteers: a randomized, double-blind, placebo-controlled, parallel-group study. Am J Clin Nutr. 2015;101(6):1188–96.

    Article  CAS  PubMed  Google Scholar 

  35. Kinoshita T, Maruyama K, Suyama K, Nishijima M, Akamatsu K, Jogamoto A, et al. The effects of OLL1073R-1 yogurt intake on influenza incidence and immunological markers among women healthcare workers: a randomized controlled trial. Food Funct. 2019;10(12):8129–36.

    Article  CAS  PubMed  Google Scholar 

  36. Kumpu M, Kekkonen R, Kautiainen H, Järvenpää S, Kristo A, Huovinen P, et al. Milk containing probiotic Lactobacillus rhamnosus GG and respiratory illness in children: a randomized, double-blind, placebo-controlled trial. Eur J Clin Nutr. 2012;66(9):1020–3.

    Article  CAS  PubMed  Google Scholar 

  37. Mai TT, Thu PT, Hang HT, Trang TT, Yui S, Shigehisa A, Tien VT, Dung TV, Nga PB, Hung NT. Efficacy of probiotics on digestive disorders and acute respiratory infections: a controlled clinical trial in young Vietnamese children. Eur J Clin Nutr. 2021;75(3):513-520.

  38. Makino S, Ikegami S, Kume A, Horiuchi H, Sasaki H, Orii N. Reducing the risk of infection in the elderly by dietary intake of yoghurt fermented with Lactobacillus delbrueckii ssp. bulgaricus OLL1073R-1. Br J Nutr. 2010;104(7):998–1006.

    Article  CAS  PubMed  Google Scholar 

  39. Meng H, Lee Y, Ba Z, Peng J, Lin J, Boyer AS, et al. Consumption of Bifidobacterium animalis subsp. lactis BB-12 impacts upper respiratory tract infection and the function of NK and T cells in healthy adults. Mol Nutr Food Res. 2016;60(5):1161–71.

    Article  CAS  PubMed  Google Scholar 

  40. Prodeus A, Niborski V, Schrezenmeir J, Gorelov A, Shcherbina A, Rumyantsev A. Fermented milk consumption and common infections in children attending day-care centers: a randomized trial. J Pediatr Gastroenterol Nutr. 2016;63(5):534.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Pu F, Guo Y, Li M, Zhu H, Wang S, Shen X, et al. Yogurt supplemented with probiotics can protect the healthy elderly from respiratory infections: a randomized controlled open-label trial. Clin Interv Aging. 2017;12:1223.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Rongrungruang Y, Krajangwittaya D, Pholtawornkulchai K, Tiengrim S, Thamlikitkul V. Randomized controlled study of probiotics containing Lactobacillus casei (Shirota strain) for prevention of ventilator-associated pneumonia. J Med Assoc Thai. 2015;98(3):253–9.

    Google Scholar 

  43. Sazawal S, Dhingra U, Hiremath G, Sarkar A, Dhingra P, Dutta A, et al. Prebiotic and probiotic fortified milk in prevention of morbidities among children: community-based, randomized, double-blind, controlled trial. PloS one. 2010;5(8):e12164.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  44. Shida K, Sato T, Iizuka R, Hoshi R, Watanabe O, Igarashi T, et al. Daily intake of fermented milk with Lactobacillus casei strain Shirota reduces the incidence and duration of upper respiratory tract infections in healthy middle-aged office workers. Eur J Nutr. 2017;56(1):45–53.

    Article  CAS  PubMed  Google Scholar 

  45. Van Puyenbroeck K, Hens N, Coenen S, Michiels B, Beunckens C, Molenberghs G, et al. Efficacy of daily intake of Lactobacillus casei Shirota on respiratory symptoms and influenza vaccination immune response: a randomized, double-blind, placebo-controlled trial in healthy elderly nursing home residents. Am J Clin Nutr. 2012;95(5):1165–71.

    Article  PubMed  CAS  Google Scholar 

  46. Guillemard E, Tondu F, Lacoin F, Schrezenmeir J. Consumption of a fermented dairy product containing the probiotic Lactobacillus casei DN-114 001 reduces the duration of respiratory infections in the elderly in a randomised controlled trial. Br J Nutr. 2010;103(1):58–68.

    Article  CAS  PubMed  Google Scholar 

  47. Rijkers GT, Bengmark S, Enck P, Haller D, Herz U, Kalliomaki M, Kudo S, Lenoir-Wijnkoop I, Mercenier A, Myllyluoma E, Rabot S. Guidance for substantiating the evidence for beneficial effects of probiotics: current status and recommendations for future research. J Nutr. 2010;140(3):671S-6S.

  48. Pineiro M, Stanton CJTJon. Probiotic bacteria: legislative framework—requirements to evidence basis. J Nutr. 2007;137(3):850S-3S.

  49. Nanno M, Kato I, Kobayashi T, Shida KJIjoi, pharmacology. Biological effects of probiotics: what impact does Lactobacillus casei shirota have on us? Int J Immunopathol Pharmacol. 2011;24(1 Suppl):45S-50S.

  50. Dong H, Rowland I, Yaqoob PJBJoN. Comparative effects of six probiotic strains on immune function in vitro. Br J Nutr. 2012;108(3):459-70.

  51. Curto AL, Pitino I, Mandalari G, Dainty JR, Faulks RM, Wickham MSJJFm. Survival of probiotic lactobacilli in the upper gastrointestinal tract using an in vitro gastric model of digestion. Food Microbiol. 2011;28(7):1359-66.

  52. Zagato E, Mileti E, Massimiliano L, Fasano F, Budelli A, Penna G, et al. Lactobacillus paracasei CBA L74 metabolic products and fermented milk for infant formula have anti-inflammatory activity on dendritic cells in vitro and protective effects against colitis and an enteric pathogen in vivo. PLoS One. 2014;9(2):e87615.

  53. Chung FJMoi. Anti-inflammatory cytokines in asthma and allergy: interleukin-10, interleukin-12, interferon-γ. Mediators Inflamm. 2001;10(2):51-59.

  54. Diamond G, Beckloff N, Weinberg A, Kisich KOJCpd. The roles of antimicrobial peptides in innate host defense. Curr Pharm Des. 2009;15(21):2377-92.

  55. Ganz TJTJoci. Antimicrobial polypeptides in host defense of the respiratory tract. J Clin Invest. 2002;109(6):693-7.

  56. Kato LM, Kawamoto S, Maruya M, Fagarasan SJI, biology c. Gut TFH and IgA: key players for regulation of bacterial communities and immune homeostasis. Immunol Cell Biol. 2014;92(1):49-56.

  57. Trebichavský I, Šplíchal I. Probiotics manipulate host cytokine response and induce antimicrobial peptides. Folia Microbiol. 2006;51(5):507–10.

    Article  Google Scholar 

  58. Alberda C, Gramlich L, Meddings J, Field C, McCargar L, Kutsogiannis D, et al. Effects of probiotic therapy in critically ill patients: a randomized, double-blind, placebo-controlled trial. Am J Clin Nutr. 2007;85(3):816–23.

    Article  CAS  PubMed  Google Scholar 

  59. Reale M, Boscolo P, Bellante V, Tarantelli C, Di Nicola M, Forcella L, et al. Daily intake of Lactobacillus casei Shirota increases natural killer cell activity in smokers. Br J Nutr. 2012;108(2):308-14.

  60. Dong H, Rowland I, Tuohy K, Thomas L, Yaqoob PJC, Immunology E. Selective effects of Lactobacillus casei Shirota on T cell activation, natural killer cell activity and cytokine production. Clin Exp Immunol. 2010;161(2):378-88.

Download references

Acknowledgements

Not Applicable.

Funding

None.

Author information

Authors and Affiliations

Authors

Contributions

SA & PJ, MD, and AD contributed to conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Validation, and Visualization. KR and BR contributed to writing the manuscript. SA contributed to Data analysis, Supervision, Validation, Writing - review & editing. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Shahab Alizadeh.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplemental file 1.

Search strategy of the study. Supplemental Table 1. Sensitivity analysis by removing one study at a time and reanalyzing other studies

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Rashidi, K., Razi, B., Darand, M. et al. Effect of probiotic fermented dairy products on incidence of respiratory tract infections: a systematic review and meta-analysis of randomized clinical trials. Nutr J 20, 61 (2021). https://doi.org/10.1186/s12937-021-00718-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12937-021-00718-0

Keywords