Otros Nombres
Bacillus aBacillus casei aBacterium casei aCaseobacterium vulgareLacticaseibacillus caseiLactobacillus casei subsp. caseiLactobacterium caseiStreptobacterium casei
Lacticaseibacillus casei is an organism that belongs to the largest genus in the family Lactobacillaceae, a lactic acid bacterium (LAB), previously classified as Lactobacillus casei. The species is still widely referenced in the literature under its former name Lactobacillus casei, and the two names are used interchangeably in commercial, regulatory, and scientific contexts. Its full taxonomic classification is: Domain: Bacteria; Phylum: Bacillota (Firmicutes); Class: Bacilli; Order: Lactobacillales; Family: Lactobacillaceae; Genus: Lacticaseibacillus; Species: L. casei.
Its species epithet derives from the Latin word casei, meaning "of cheese," a nod to its frequent appearance in fermented milk products. Individual strains are denoted by strain codes (e.g., Shirota, DN-114 001, ATCC 334) and must be considered separately for efficacy and safety. Alternative names include Lactobacillus casei (legacy name), Lacticaseibacillus casei, and commercial designations such as L. casei Shirota or L. casei DN-114 001.
Lactobacilli are Gram-positive, rod-shaped, facultatively anaerobic or microaerophilic, non-spore-forming, acid-tolerant, and catalase-negative bacteria with DNA G+C content that is usually less than 50 mol%. Members of the L. casei group are facultatively heterofermentative, have 45–47 mol% DNA G+C content, and have identical peptidoglycan types (L-Lys-D-Asp). The species is a non-sporing, rod-shaped, Gram-positive microorganism that can be found within the reproductive and digestive tract of the human body.
The Lactobacillus casei group (LCG), composed of the closely related Lactobacillus casei, Lactobacillus paracasei, and Lactobacillus rhamnosus, are some of the most widely researched and applied probiotic species of lactobacilli. The three species have been extensively studied, classified, and reclassified due to their health-promoting properties. Historically, appeals were put forward to the International Committee on Systematic Bacteriology (ICSB) to modify the L. casei group; the status of the nomenclature in this group has been somewhat contested since 1989, with classification wavering between L. casei and L. paracasei. Although this group comprises many commercially valuable strains, its taxonomic status has long been contentious, because methods with inadequate taxonomic resolution have been used, leading to species being mislabeled in products, publications, and some publicly available DNA sequences.
Because of its aciduric nature, L. casei is found in many fermented foods of both plant (e.g., fermented vegetables, sourdough, wine) and animal (e.g., dairy products, cured meat, and fermented sausages) origin. Lactobacillus spp. are part of the microbiota of humans and animals, where they colonize the gastrointestinal tract (GIT) and the urogenital tract. They are also found in a variety of food products from fruits and vegetables to a range of naturally fermented products. These strains, which are frequently used in the fermentation of foods like cheese and yogurts, have been grown and studied. L. casei is found in cheddar cheese, with L. casei and L. rhamnosus recognized as the predominant species in cheddar manufactured in Australia and New Zealand.
The use of fermented foods reflects an intimate relationship between humans and microorganisms, and lactobacilli in particular, stretching back over 8,000 years. People around the world have developed a huge variety of fermented foods from the milk of cows, goats, camels, buffalos, and other animals, or from equivalent plant material such as soybean and maize. Differences in fermentation technologies and microbial environments led to different tastes, forms, and textures. Fermented foods are often intimately bound up with civilization, customs, culture, social relationships, and in some cases beliefs or religion.
The LCG have long been used in fermentations whether as adjunct or starter cultures. Fermentation was originally based on conversion of carbohydrate into organic acids, mostly lactic acid, intended to preserve nutrient in milk, but then it developed into other capabilities associated with health benefit. Lactobacillus strains, which are well-known for enhancing gut flora, are abundant as probiotics in fermented foods including kimchi, sauerkraut, koumiss, yogurt, kurut, cheese, kefir, and kombucha.
Lactobacillus casei has a story that begins in the world of traditional dairy. Scientists first discovered it in cheese in the early 1900s, and in 1971 Hansen and Lessel officially recognized it as a species. The genus Lactobacillus was first formally described by Beijerinck in 1901. In 1919, Orla-Jensen divided it into three subgenera — Thermobacterium, Streptobacterium, and Betabacterium — according to their optimal growth temperature and hexose fermentation pathway.
The traditional applications of L. casei-bearing fermented foods were empirical in character. Fermented dairy and vegetable foods containing L. casei-like organisms have been consumed for centuries for their preservative and sensory properties and traditional association with digestive health (fermented milks, cheeses, pickles). Traditional claims were empirical: improved digestion, preserved foods, and general well-being. A landmark development in the deliberate use of a defined L. casei strain was the commercialization of the Shirota strain by Japanese scientist Minoru Shirota beginning in the 1930s, leading to the Yakult product. The long history of use of Lactobacillus spp. in fermented products has led to their recognition as GRAS (generally recognized as safe) by the US Food and Drug Authority (FDA), and earned them a place on the QPS (qualified presumption of safety) list assembled by the European Food Safety Authority (EFSA).
Unlike a botanical herb with isolable phytochemical constituents, L. casei as a living microorganism exerts its effects through an array of structural and secreted components, metabolites, and the consequences of its colonization and metabolic activity within the host gut. The principal bioactive entities are described below.
It is well documented that bacterial cell surface components and structures are critical factors for host-microbe interaction, immune modulation, and symbiosis. Toll-like receptors (TLRs) expressed on mammalian epithelial and immune cells act as pattern recognition receptors, which are individually responsible for a variety of different bacterial components, such as peptidoglycan (PG), lipoteichoic acid (LTA), and wall teichoic acid (WTA) from Gram-positive bacteria, as well as flagella, lipoproteins, and nucleic acids.
Among the principal bioactive entities identified are Microbe-Associated Molecular Patterns (MAMPs), such as lipoteichoic acid (LTA), peptidoglycan (PGN), exopolysaccharide (EPS), and surface proteins. These molecules are recognized by pattern recognition receptors (PRRs) expressed on epithelial immune cells, including Toll-like receptors (TLRs) and NOD-like receptors (e.g., NOD2). Signal transduction predominantly occurs via the MyD88-dependent pathway, activating NF-κB and MAPKs such as ERK, JNK, and p38, concurrently contributing to the regulation of cytokine production, dendritic cell (DC) activation, and the balance of Th1, Th2, Th17, and Treg lymphocytes.
When fractionated subcellular fractions of Lactobacillus casei were tested for NF-κB activation and TNF-α production in macrophage cell lines, the activity was found to be as follows: protoplast > cell wall ≫ polysaccharide-peptidoglycan complex. Both crude extracts and purified lipoteichoic acids (LTAs) from L. casei significantly induced TNF-α secretion from macrophage cells and splenocytes in a TLR2-dependent manner.
MAMPs such as peptidoglycan (PGN), lipoteichoic acid (LTA), and exopolysaccharides (EPSs) interact with pattern recognition receptors like Toll-like receptors, initiating immune-signaling cascades that regulate cytokine production and inflammation. Lactobacilli-derived MAMPs exhibit dual immunomodulatory effects: they can enhance pro-inflammatory responses (e.g., IL-1β, IL-6, and TNF-α) under inflammatory contexts, while enhancing regulatory pathways via IL-10 and regulatory T-cell (Treg) induction in anti-inflammatory settings.
Protective effects on the intestinal epithelium have been ascribed to P40 and P75, two well-characterized cell wall muramidases present in the culture supernatant of strains belonging to the taxon Lactobacillus casei/paracasei/rhamnosus. Lactobacillus casei BL23 extracellular vesicles (EVs) contain lipoteichoic acid (LTA), and all detected P40 and most of P75 were associated to EVs and possibly located at their external surface.
By producing lactic acid and other metabolites, L. casei can alter luminal pH, which affects enzyme activity and nutrient absorption. Fermentation of dietary fiber and other substrates by L. casei and its interactions with the gut microbiota also contribute to shifts in short-chain fatty acid (SCFA) profiles, which are relevant to gut motility, epithelial energy metabolism, and systemic immune tone.
Some L. casei strains upregulate tight junction proteins in epithelial cells, which can support barrier integrity and reduce translocation of microbial products. Some Lactobacillus strains present probiotic properties through maintaining the micro-ecological balance via different mechanisms, such as mucosal barrier function and barrier immunity. Notably, not only living cells but also Lactobacillus derivatives (postbiotics: soluble secreted products; and para-probiotics: cell structural components) may exert antipathogenic effects and beneficial functions for the gut mucosal barrier.
At the mucosal surface, L. casei can interact with dendritic cells, epithelial pattern-recognition receptors, and secretory immune components. These interactions can lead to modulation of cytokine production, enhancement of secretory IgA, and changes in local T-cell responses. Some Lactobacillus strains present probiotic properties through maintaining the micro-ecological balance via mechanisms that include mucosal barrier function and barrier immunity, and even address some neurological issues by microbiota–gut–brain/liver/lung axis communication.
A recent study found that the immune response in the small intestine induced by L. casei could extend to the systemic immune system. At the same time, the activating of macrophages and stimulating of the production of pro-inflammatory cytokines interferon-γ and TNF occurred. An underlying immunoregulatory mechanism of lactobacilli is that toll-like receptors (TLRs) binding to Lactobacilli activate NF-κB to induce specific gene expressions.
L. casei Shirota (LcS) is able to promote innate immunity by increasing NK cell activity, and it improves inflammatory status by increasing the IL-10/IL-12 ratio. Furthermore, LcS has been described to enhance the activity of cytotoxic T lymphocytes (CD8+ T cells) via induction of pro-inflammatory cytokines. In vitro studies with human peripheral blood mononuclear cells suggest that LcS stimulates monocytes/macrophages to produce IL-12 and augments NK cell activity.
Probiotics may exclude or inhibit the growth of certain pathogens; they may improve gut barrier function; and they can modulate mucosal and/or systemic immune response or metabolic functions. The LCG must be capable of surviving a number of stress conditions if they are to be used in industry, including oxidative stress, osmotic stress, cold stress, acid stress, and long-term storage. In addition to their need to tolerate these conditions in food processing, live strains must be able to survive passage through the GIT if intended for health-promoting purposes.
LcS has been reported to exhibit various beneficial effects on gastrointestinal function and disorders, including prevention of diarrhea, improved bowel movements, and alleviating colitis symptoms, as well as immunomodulatory properties.
A number of randomized controlled trials have examined L. casei for the prevention or treatment of antibiotic-associated diarrhea. In one randomized double-blind clinical trial, a group of hospitalized patients who contracted diarrhea during or after 7 days of antibiotic suspension were randomized to receive probiotics (Lactobacillus casei and Bifidobacterium breve) or placebo three times a day. Seventy patients were studied. The average duration of diarrhea among those who were healed was 4.87 ± 2.13 days in the probiotic group and 4.52 ± 2.55 days in the control (p = 0.36). Four (11.4%) patients in the probiotic group and ten (28.6%) in the placebo group were not cured (p = 0.13). While a trend was observed, the difference did not reach statistical significance in this study, highlighting the heterogeneity of outcomes in this area. In a meta-analysis involving 707 patients from 0 to 18 years of age in six studies, doses between 5.5 and 40 × 10⁹ CFU/day of probiotics from different species or strains were studied.
Two weeks of consecutive ingestion of 65 mL/day of beverages containing 6.5 × 10⁹ CFU/mL Lactobacillus casei strain Shirota (LcS) led to a significant decline in the occurrence of hard and lumpy stool in constipated adults.
In a study investigating the effects of LcS on constipated patients, 16 constipated patients and 22 non-constipated participants were recruited. The subjects consumed 100 mL of an LcS beverage (10⁸ CFU/mL) per day for 28 days. Fecal non-volatile metabolites were determined by GC/MS. In constipated patients, LcS intervention significantly improved defecation frequency (from 4.81 to 7.81 times per week, p < 0.05), stool consistency (from 2.52 to 3.68, p < 0.05), and constipation-related symptoms. A total of 14 non-volatile fecal metabolites were obtained as potential constipation-related metabolites regulated by LcS.
A separate randomized, double-blind, placebo-controlled trial examined LcS in constipated patients with depression. Subjects consumed 100 mL of a LcS beverage (10⁸ CFU/mL) or placebo every day for 9 weeks. After ingesting beverages for this period, no significant differences in total patient constipation-symptom scores were observed in the LcS group compared with the placebo group overall. However, symptoms related to rectal tearing and the stool symptom subscale were more alleviated in the LcS group than in the placebo group. The daily consumption of LcS for 9 weeks appeared to relieve constipation and improve potentially depressive symptoms in patients with depression, and significantly decrease IL-6 levels. The evidence for LcS in constipation is encouraging but mixed across trials, with the most consistent finding being improvement in stool consistency rather than complete symptom resolution.
Meta-analyses point to a modest but significant effect of probiotics on symptoms in irritable bowel syndrome (IBS). A randomized, double-blind, placebo-controlled intervention study was conducted to assess the effect of the probiotic Lactobacillus casei Shirota (LcS) on symptoms and quality of life in IBS patients. IBS patients (Rome II criteria) between 18 and 65 years of age were included. The study consisted of an 8-week intervention period in which participants received probiotic (LcS) or placebo twice daily, followed by an 8-week follow-up period. The primary outcome was a decrease of at least 30% in a composite mean symptom score (MSS) at week 8. After probiotic treatment with LcS, no improvement of 30% in MSS was observed after 8 weeks. This negative result is consistent with a broader finding: in the field of IBS, an RCT with L. casei Shirota also failed to show significant improvement in IBS. Overall, more consistent evidence is needed regarding the efficacy and safety of probiotics for the treatment of patients with IBS. Evidence for LcS in IBS must currently be characterized as weak and inconsistent.
A study found that the scores for "abdominal discomfort and pain" as well as for "indigestion" and "diarrhea" increased at 1–2 weeks before examination in the placebo group, and that the daily consumption of L. casei strain Shirota resulted in a tendency toward improvement in "abdominal discomfort and pain" and a significant improvement of "indigestion" in medical students exposed to academic stress. This finding, from a clinical study of healthy medical students, is preliminary but suggests a plausible role for LcS in stress-modulated gut symptoms.
A prospective randomized controlled study examined the impact of daily LcS fermented milk (LcS-FM) on upper respiratory tract infections (URTIs) in healthy middle-aged office workers. The incidence of URTIs during the intervention period was significantly lower in the LcS-FM group than in the control milk group (22.4 vs. 53.2%, P = 0.002). The time-to-event analysis showed a significantly higher URTI-free rate in the LcS-FM group. The cumulative number of URTI episodes and cumulative days with URTI symptoms per person was lower in the LcS-FM group, and the duration per episode was shorter. Inhibition of both reductions in NK cell activity and increases in salivary cortisol levels was observed in the LcS-FM group. The results suggest that daily intake of fermented milk with LcS may reduce the risk of URTIs in healthy middle-aged office workers, probably through modulation of the immune system.
A separate human study investigated immune responses in healthy adults consuming a probiotic drink containing LcS. Daily ingestion of a probiotic drink containing LcS (1.3 × 10¹⁰ live cells) by healthy adults was investigated over a period including 4 weeks of LcS intake, 6 weeks of discontinuation, and a final 4 weeks of LcS. There was a significant increase in expression of the T cell activation marker CD3+CD69+ and a significant increase in the NK cell marker CD3+CD16/56+. Expression of the NK cell activation marker CD16/56+CD69+ in ex vivo unstimulated blood cells was 62% higher at week 10 and 74% higher at week 14. This study also found that LcS-FM inhibited increases in the levels of the stress hormone cortisol, which has the ability to decrease NK cell activity. While these human immunological data are encouraging, the mechanistic link between NK cell changes and actual infection outcomes requires further investigation. The URTI reduction findings are promising but based on a limited number of trials.
In clinical trials, several strains of Lactobacillus and Bifidobacterium have shown therapeutic effects on IBD. Lactobacillus casei, one of the most widely used probiotics, has been reported to alleviate multiple diseases. However, the effects of this species on intestinal diseases are strain-specific. The physiological characteristics of 29 L. casei strains were determined, including gastrointestinal transit tolerance, oligosaccharide fermentation, HT-29 cell adhesion, generation time, exopolysaccharide production, acetic acid production, and conjugated linoleic acid synthesis. The effects of five candidate strains on mice with induced colitis were evaluated. The results showed that only Lactobacillus casei M2S01 effectively relieved colitis; this strain recovered body weight, restored disease activity index score, and promoted anti-inflammatory cytokine expression. Much of the evidence in IBD for L. casei specifically remains in animal models; robust human clinical trials demonstrating efficacy in Crohn's disease or ulcerative colitis are limited.
Lysate of probiotic bacterium L. casei DN-114 001 was investigated for its ability to decrease the severity of intestinal inflammation in a murine model of IBD. The preventive effect of oral administration of Lc significantly reduced the severity of acute dextran sulfate sodium (DSS) colitis in BALB/c mice. This is preclinical evidence and cannot be directly extrapolated to human clinical outcomes.
A prospective clinical study in hospitalized patients examined the effect of twice-daily LcS administration during acute gastroenteritis. L. casei Shirota administration twice a day had positive effects on the reduction of bowel movements, improvement of kidney function, and inflammation compared to the control group. The authors suggested that additional LcS administration might be considered in patients with acute gastroenteritis who present with high inflammation markers and/or acute impaired kidney function. Treatment with LcS resulted in a significant decrease of CRP on days five, six, and seven. Leukocyte counts decreased in all groups, with the effect significantly higher in the LcS group receiving antibiotics on day three. This evidence is from a single prospective study and requires replication.
Lacticaseibacillus casei (formerly Lactobacillus casei) is a Gram-positive, non-spore-forming lactic acid bacterium commonly used as a food-grade probiotic; typical daily doses in clinical studies range from 1 × 10⁸ to 1 × 10¹⁰ CFU.
The following doses have been reported in published human studies:
Commercially, L. casei is used in fermenting dairy products and in its application as a probiotic. Dosage forms encountered in research include fermented milk beverages, capsules, and food-incorporated preparations. Well-known probiotic strains such as L. casei ATCC 393 have been successfully used as starter or adjunct cultures in the production of dairy products and dry-fermented sausages, especially in cheese production. Supplement capsule products standardized to defined CFU counts are also widely used but dose ranges in capsule-based human studies vary considerably across the literature.
In immunocompetent adults, L. casei is generally safe; common adverse events are mild GI symptoms — bloating (~5–20%) and transient flatulence. The long history of use in fermented products has led to their recognition as GRAS by the US FDA, and they hold a place on the QPS list assembled by EFSA.
A few recent cases of bacteremia and/or sepsis associated with lactobacilli have been reported in patients with different underlying diseases such as ulcerative colitis, suggesting that extensive damage of the colonic mucous membrane increases the risk of bacteremia. Other cases of bacteremia involve HIV-infected populations or other immunocompromised patients. Three cases of L. casei sepsis were described in a pediatric intensive care unit — two with congenital heart disease and the third with a cervical spinal cord injury.
At least eight cases of bacteremia associated with lactobacilli have been reported, including Lactobacillus acidophilus, Lactobacillus casei, and Lactobacillus GG. In general, Lactobacillus endocarditis is a rare condition that affects individuals with underlying heart conditions, such as a heart valve abnormality or artificial heart valve. These individuals have an increased risk of developing bacterial infections in the heart, including Lactobacillus endocarditis.
A published case report documents a rare case of Lactobacillus casei endocarditis in a 71-year-old female, immunocompromised due to chronic steroid intake, who presented with a productive cough and low-grade fever. Blood cultures grew L. casei resistant to vancomycin and meropenem. Transesophageal echocardiography showed mitral and aortic vegetations; valve replacement was done after successfully removing vegetations.
The FDA suggested immunosuppression, structural heart disease, inpatient status, pregnancy, and potential for translocation of probiotic across the bowel wall as conditions potentially associated with at-risk adverse events in probiotic clinical trials. Increasing reports on Lactobacillus bacteremia-associated morbidity and mortality in immunocompromised patients have raised safety concerns about its use in this group.
Antibiotics can inactivate bacterial probiotics; separation of doses by 2–3 hours is recommended to improve co-administration effectiveness. This is particularly relevant since L. casei is frequently studied in the context of antibiotic-associated diarrhea, where probiotic and antibiotic are co-administered.
The scientific information available supports the hypothesis of the existence of a gut resistance gene pool and the possible transferability of antibiotic resistance genes. Reports on possible in vivo transfer are very scarce, although they are needed. Some empirical concerns regarding the safety of probiotics are the occurrence of disease, adverse metabolic effects on the gastrointestinal tract, and gene transfer events. Safety issues include the antimicrobial resistance of the lactobacilli, the convenience of making proper identification of these bacteria, and recent risk reports on probiotic lactobacilli in certain risk groups, mainly immunocompromised patients and patients with short gut syndrome or undergoing cardiac surgery.
Although the L. casei group comprises many commercially valuable strains, its taxonomic status has long been contentious, and methods with inadequate taxonomic resolution have been used, leading to species being mislabeled in products, publications, and some publicly available DNA sequences. This means that products labeled as containing L. casei may not always contain the strain implied, underscoring the importance of strain-level verification in evaluating both commercial products and clinical evidence.
Condiciones de salud que Lactobacillus casei puede ayudar a apoyar.
Lactobacillus casei strains have been studied in IBS clinical trials and appear in combination probiotic preparations with demonstrated efficacy for IBS symptom relief. A double-blind RCT using a combination including L. casei LBC80R improved IBS symptoms and quality of life. NIH ODS meta-analyses include L. casei among studied IBS probiotics.
L. casei has been evaluated in an RCT in preschool children with allergic asthma and/or rhinitis; while asthma outcomes were not significantly improved, the study provided clinical evidence of investigation in respiratory allergic conditions. L. casei Shirota inhibits IgE production in animal models and shifts Th1/Th2 immune balance, providing a mechanistic basis for potential benefit in respiratory allergy.
L. casei 01 has demonstrated clinical benefit in rheumatoid arthritis—an autoimmune joint disease—in a double-blind RCT, reducing disease activity scores and inflammatory cytokines. Broader preclinical evidence shows L. casei modulates Th1/Th17/Treg immune balance relevant to autoimmunity. The anti-inflammatory cytokine IL-10 was specifically increased by L. casei in the RA trial.
L. casei-containing probiotic formulas have been included in multi-strain intervention studies showing blood pressure regulation in at-risk populations, particularly in pre-diabetic and metabolic syndrome contexts. Mechanistically, gut microbiota modulation by L. casei may influence ACE inhibitor peptide production and systemic inflammation relevant to blood pressure regulation.
L. casei LC2W was evaluated in a 2024 RCT in subjects at high risk of metabolic syndrome for effects on glucose metabolism. Broader meta-analyses of Lactobacillus supplementation in overweight/obese adults report modest glycemic improvements. Mechanistically, L. casei modulates gut microbiota composition and SCFA production relevant to glucose homeostasis.
Lactobacillus casei has been studied in combination with L. rhamnosus strains in children with atopic dermatitis and cow's milk protein allergy, showing superiority over placebo in improving SCORAD severity in a 2021 multicenter RCT. It also appears in probiotic pediatric asthma management trials. Its mechanism involves immune modulation through cytokine shifts and gut microbiota restoration. Evidence is strain-specific and generally positive in allergic-sensitized children.
Lactobacillus casei has been evaluated in clinical trials for preventing and treating diarrhea in children attending day care centers. A landmark study found that supplementation with L. casei (strain DN-114 001) in milk ferment significantly reduced acute diarrhea in children in day care. It is among the probiotic strains recognized in pediatric GI literature.
L. casei Shirota has been investigated in children for immune modulation and reduction of respiratory infections. An RCT of 518 children showed that L. casei Shirota as adjunct to antibiotic therapy significantly reduced treatment failure rates in fast breathing pneumonia. L. casei is also known to enhance macrophage, NK cell, and sIgA activity, supporting innate and adaptive immune responses in pediatric populations.
L. casei and L. paracasei have documented bile salt hydrolase (BSH) activity in vitro providing a mechanistic basis for cholesterol reduction. Combination probiotic trials including L. casei have shown improved lipid profiles. L. casei Shirota has been studied in metabolic syndrome for effects including on cholesterol metabolism via improved gut permeability and reduced LPS-driven dyslipidemia.
Multiple clinical trials of L. casei across different inflammatory conditions (RA, metabolic syndrome, respiratory infection) have documented reductions in inflammatory biomarkers including hs-CRP, TNF-α, and IL-12. L. casei Shirota has been specifically investigated for improving intestinal permeability in metabolic syndrome, reducing LPS translocation that drives systemic inflammatory signaling. The evidence is distributed across conditions rather than a single chronic inflammation trial.
L. casei Shirota specifically has been studied in RCTs for common cold and flu. Fermented milk with L. casei Shirota reduced incidence of cold/flu symptoms in healthy medical students under examination stress. A placebo-controlled trial in endurance athletes tested L. casei Shirota for common cold infection and herpes virus antibodies, providing evidence of immunological effect in a physically stressed population.
Lactobacillus casei is among the Lactobacillus strains investigated in multi-strain probiotic trials for ulcerative colitis. It is included in multi-strain synbiotic formulations demonstrating anti-pathogenic and gut microbiota-modulating activity relevant to colitis management.
Lactobacillus casei (including L. casei Shirota) is a probiotic included in constipation RCTs. A 2022 systematic review (30 RCTs) specifically assessed L. casei Shirota in chronic constipation; while the overall probiotic effect was significant, L. casei Shirota did not achieve significant individual effect on stool frequency in isolated subgroup analysis. It is included in multi-strain formulations with demonstrated constipation efficacy.
As atopic dermatitis (AD) and eczema share the same clinical entity (atopic eczema/dermatitis syndrome), the evidence for L. casei in dermatitis is the same body of RCT literature. L. casei strains have been tested in multicenter double-blind RCTs in children with AD, with SCORAD-assessed improvement noted in probiotic groups. Mechanistic work indicates modulation of Th1/IL-10 responses and suppression of pro-allergic cytokines.
L. casei (notably strain GG/LGG) has been studied in multiple RCTs for reducing the duration and severity of acute infectious diarrhea, particularly rotavirus-associated diarrhea in children. Evidence also exists for reducing antibiotic-associated diarrhea (AAD) risk, though results are strain- and dose-dependent. Mechanistically, the organism restores lactic-acid-producing flora, competes with pathogens, and enhances mucosal IgA. Benefits are most robust for viral gastroenteritis in developed-country settings.
Lactobacillus casei is one of the best-studied specific probiotic strains in diverticular disease, featured in multiple dedicated RCTs. Two Tursi et al. prospective randomized open-label studies demonstrated that L. casei reduced recurrence of symptomatic uncomplicated diverticular disease and was most effective when combined with mesalazine for long-term remission maintenance up to 24 months.
Clinical RCTs have examined L. casei and closely related strains for atopic eczema/dermatitis syndrome (AEDS), particularly in infants and young children. A multicenter Polish RCT used a mixture of L. casei ŁOCK 0900, L. casei ŁOCK 0908, and L. paracasei ŁOCK 0919 in 60 children under 24 months with atopic eczema and cow's milk protein allergy, finding improvements in SCORAD index. Proposed mechanisms include Th1/Treg immune skewing and reduction of pro-allergic IL-5.
Lactobacillus casei strains have been studied in combination with L. rhamnosus in RCTs for food allergy and atopic dermatitis. A multicenter double-blind placebo-controlled trial found the L. rhamnosus/L. casei combination superior to placebo in reducing atopic dermatitis severity in children with cow's milk protein allergy. L. casei modulates gut barrier integrity and Th2 immune responses relevant to food sensitivities.
Lactobacillus casei has demonstrated efficacy as an adjunct probiotic in H. pylori eradication and is identified in authoritative reviews as one of the probiotic strains that can effectively reduce H. pylori infection associated with chronic gastritis. Multiple systematic reviews and meta-analyses support its use alongside standard therapies.
Lactobacillus casei (now Lacticaseibacillus casei) is a clinically well-evidenced probiotic that modulates gut microbiota composition, reduces diarrhea, and improves microbial diversity. The Shirota strain (Yakult) is the most studied, with published RCTs confirming gut microbiome-modulating effects across multiple populations.
Lactobacillus casei has been studied in probiotic formulations demonstrating cognitive improvement in Alzheimer's disease patients. It is a component of multi-strain psychobiotic formulations and contributes to gut-brain axis modulation through SCFA production, gut barrier support, and immunomodulation relevant to neuropsychiatric conditions.
Lactobacillus casei has been evaluated in clinical trials for IBS with mixed evidence depending on strain. A 2025 strain-specific meta-analysis found L. casei Shirota did not demonstrate meta-analytic IBS efficacy despite some positive individual trials. The broader genus shows benefit and L. casei is included in British Society of Gastroenterology recognition of Lactobacillus for IBS.
Lactobacillus casei has demonstrated clinical utility in UC in multiple RCTs, both as a standalone probiotic and in combination products. It has been shown to maintain remission in UC, improve intestinal barrier function, and reduce mucosal inflammatory markers including TNF-α and IL-6.
L. casei strains have been studied in metabolic syndrome and obesity contexts for their effects on insulin resistance markers. The 2024 LC2W RCT examined insulin-related endpoints in high-risk MetS subjects. Mechanisms involving SCFA production, GLP-1 modulation, and reduction of LPS-driven insulin resistance provide a plausible biological rationale supported by emerging clinical data.
Lactobacillus casei Shirota, administered with Bifidobacterium breve Yakult for one month, produced significant and sustained improvement in symptom severity scores and hydrogen gas production in lactose-intolerant patients, with benefits persisting for 3 months after cessation. A meta-analysis combination trial also demonstrated reductions in LI symptoms.
Lactobacillus casei is a probiotic strain consistently included in systematic reviews of probiotics that restore intestinal barrier function. It appears in multi-strain formulations that have demonstrated reduced intestinal permeability in IBS and other GI conditions. Clinical patent literature for gut permeability treatment specifically lists L. casei as an effective human-derived probiotic species.
L. casei Shirota has been studied in metabolic syndrome patients for intestinal permeability improvement, and L. casei LC2W was evaluated in a 2024 double-blind RCT in high-risk metabolic syndrome subjects for effects on glucose metabolism and gut microbiota. Evidence spans lipid profiles, glycemic control, and gut barrier function in this population, though individual trials are often small.
Lactobacillus casei has been studied for oral microbiome effects including inhibition of S. mutans and reduction of caries risk in children. It is included in critical appraisals of oral probiotics and has in vitro and clinical evidence supporting oral health benefits.
Lactobacillus casei is among the Lactobacillus strains explicitly listed in major systematic reviews as a constituent of evidence-based probiotic regimens studied in PCOS RCTs, which have shown improvements in metabolic, hormonal, and inflammatory parameters.
L. casei 01 has been tested in a randomized double-blind clinical trial in female RA patients, showing reductions in DAS28 score, tender/swollen joint counts, hs-CRP, and pro-inflammatory cytokines including TNF-α and IL-12. The strain (10⁸ CFU/day for 8 weeks) also increased anti-inflammatory IL-10. Animal model data with collagen-induced arthritis further supports a mechanistic role for L. casei in reducing synovial inflammation.
A randomized, prospective, double-blind trial of 187 preschool children with allergic asthma and/or rhinitis evaluated 12 months of L. casei fermented milk (10⁸ cfu/mL). While no statistically significant difference was found for asthmatic episodes, rhinitis-related outcomes were explored. Mechanistically, L. casei modulates IgE production and Th1/Th2 balance relevant to seasonal allergies.
Lactobacillus casei Shirota was assessed in a 16-week RDBPCT of 60 SAR adults, showing favorable immunological changes at the nasal mucosa following allergen challenge. It is one of the probiotic strains within the dataset of the 2016 meta-analysis of 22 RDBPCTs demonstrating significant AR symptom benefit for probiotics.
L. casei Shirota has been tested in an RCT model of examination stress in healthy medical students and shown to reduce cold/flu symptoms and abdominal symptoms triggered by stress. Broader psychobiotic research implicates L. casei in the gut-brain axis modulation of the HPA axis and cortisol responses. L. casei and its supplement have been shown to alleviate stress-induced depression and anxiety in mouse CUMS models via BDNF-TrkB pathways.
L. casei Shirota inhibits Helicobacter pylori—the primary cause of gastric and duodenal ulcers—in both in vitro assays and in vivo mouse models, including activity against nine clinical H. pylori isolates. In vitro, viable L. casei cells showed direct anti-H. pylori activity and profound inhibition of urease activity. Evidence in humans is primarily indirect (as adjunct to H. pylori eradication therapy).
L. casei Shirota has been evaluated in RCTs for reducing the incidence and duration of upper respiratory tract infections (URTIs) in adults and children. A published RCT in healthy middle-aged office workers found that daily fermented milk with L. casei Shirota reduced URTI incidence and duration. A multi-strain formulation including L. casei 431 reduced URTI incidence in susceptible adults via increased IFN-γ and sIgA.
Lactobacillus casei is a member of the vaginal Döderlein flora with documented urinary tract relevance. Early animal studies showed indigenous L. casei strains could prevent UTI in rats. More recently, oral probiotic containing L. casei BGP93 combined with L. acidophilus and Bifidobacterium animalis was shown to improve UTI treatment outcomes when combined with antibiotics compared to antibiotics alone. European urological guidelines list L. casei strain Shirota among recommended probiotics for recurrent UTI prevention.
L. casei Shirota administration before or after initial challenge has been shown to dramatically inhibit E. coli growth in a murine model of urinary tract infection. The strain is among those studied for UTI prevention through competitive exclusion and immune modulation. Clinical human evidence specific to L. casei for UTI is limited but the preclinical data is documented in peer-reviewed literature.
L. casei Shirota has been documented to dramatically inhibit uropathogenic E. coli in murine UTI models when administered orally. This preclinical evidence, published in a peer-reviewed ASM journal, establishes a scientific basis for L. casei's UTI-protective properties via competitive exclusion and immune modulation pathways.
L. casei Shirota has demonstrated in vitro inhibitory activity against Candida species causing vulvovaginal candidiasis, including antifungal-resistant isolates. It has also been studied in the context of antibiotic-therapy-induced vaginal dysbacteriosis alongside H. pylori treatment. The genus Lactobacillus is the dominant healthy vaginal flora, and strains like L. casei can acidify the vaginal environment.
L. casei Shirota has been studied for its role in modulating antiviral immune responses, including NK cell activity and secretory IgA production. RCT data from respiratory infection trials in office workers, athletes, and students provide clinical evidence for enhanced viral immunity. The strain has also been studied for modulating vaccine antibody responses.
Sistemas corporales que Lactobacillus casei puede ayudar a apoyar.