Abstract
Background
Lactococcus lactis JCM 5805 (LC-Plasma) is a unique lactic acid bacteria (LAB) which activates plasmacytoid dendritic cells (pDC). We aimed to evaluate the effect of LC-Plasma on dendritic cell (DC) activity and subjective indices of upper respiratory tract infections (URTI) and fatigue in athletes under high intensity exercise.
Methods
We conducted a randomized, placebo-controlled, double-blinded trial. Fifty-one male subjects belonging to a university sports club were randomized into placebo (n = 25) and LC-Plasma (n = 26) groups. Individuals ingested placebo capsules containing cornstarch or LC-Plasma capsules containing 100 billion cells of heat-killed LC-Plasma per day for 13 days. During the intervention period, subjects performed high intensity exercise according to their sports club training regime. Blood and saliva sampling were obtained at days 1 and 14, and physical conditions were recorded in a diary. We investigated expression of maturation markers on DCs, muscle damage and stress markers and used student’s t test adjusted by Bonferoni’s method for multiple comparison between groups. These data were presented as mean ± SD. We also investigated cumulative days of symptoms regarding infections and fatigue and used Chi-square test for comparison between groups. These data were presented as cumulative number.
Results
CD86 as maturation marker on pDC was significantly increased in the LC-Plasma group at day 14 (Placebo: 296 ± 70 vs. LC-Plasma: 365 ± 115; Mean Fluorescent Intensity; p = 0.013). Cumulative days of URTI were significantly lower in the LC-Plasma group (Placebo: URTI positive 56, URTI negative 256 vs. LC-Plasma: URTI positive 39, URTI negative 299; days; p = 0.028) and symptoms like sneeze or running nose were significantly lower in the LC-Plasma group (Placebo: Symptom positive 52, Symptom negative 258, vs. LC-Plasma: Symptom positive 36, Symptom negative 301; days; p = 0.032). Moreover, the cumulative days of fatigue were significantly fewer in the LC-Plasma group (Placebo: Symptom positive 128, Symptom negative 182, vs. LC-Plasma: Symptom positive 110, Symptom negative 225; days; p = 0.032). Markers of muscle damage and stress markers were not significantly different between groups.
Conclusion
We consider that heat-killed LC-Plasma supplementation relieves morbidity and symptoms of URTI via activation of pDC and decreases fatigue accumulation during consecutive high intensity exercise in athletes. However, LC-Plasma ingestion did not affect markers of muscle damage and stress.
Trial registration
UMIN-CTR, UMIN000020372. Registered 28 December 2015.
Background
It has been well-known that prolonged high intensity exercise (HIE) increases the risk of upper respiratory tract infections (URTI). URTI are common and account for about 65% of non-injury-related symptoms in athletes [Citation1, Citation2]. It is also known that the increase of URTI by HIE is attributed to a decrease in immunity [Citation3]. Several reports demonstrated that the concentration of salivary secretary immunoglobulin A (sIgA) and natural killer cells, well-known immunocytes against viral and bacterial infections, decreased after prolonged HIE [Citation4–Citation6]. It is understood that immunity and fatigue are closely related, and that chronic fatigue patients are susceptible to virus infections [Citation7]. Therefore, for athletes, not only decrease of immunity but also increase of fatigue is a serious problem.
Dendritic cells (DCs) play pivotal roles in the immune system such as antigen-presentation [Citation8]. DCs are classified into plasmacytoid DC (pDC) and myeloid DC (mDC) based on phenotype and function [Citation9]. pDC are responsible for the antiviral response. When viral infections are detected by pDC via toll-like receptor 7 (TLR7) or TLR9, pDC produce interferon-α (IFN-α) [Citation10] and induce expression of antiviral factors for inhibition of viral replication and spread [Citation11]. It was reported that 70% of URTI morbidity is caused by viral infections [Citation12]. mDC are responsible for the response to bacterial infections, and are activated by bacteria ligands via TLR1, TLR2, and TLR6 [Citation9]. mDC produce IL-10 and IL-12 [Citation13, Citation14]. It was reported that 70% of URTI morbidity is caused by viral infections [Citation12]. Therefore, the study of pDC is more important to improve URTI morbidity. There are a few reports studying the relationship between pDC and single HIE although there is no report regarding changes of pDC function after consecutive HIE [Citation15, Citation16].
Probiotics such as lactic acid bacteria (LAB) are well-known food supplements to improve immune function and decrease URTI symptoms [Citation17–Citation19]. Lactobacillus plantarum, Lactobacillus paracasei Lactobacillus gasseri, Bifidobacterium longum, Bifidobacterium bifidum and Lactobacillus acidophilus supplementation were reported to decrease the risk of URTI in general healthy subjects. It was also reported in athletes that Lactobacillus salivarius improved sIgA concentration [Citation20, Citation21].
Lactococcus lactis JCM 5805 (LC-Plasma, also referred to as Lactococcus lactis strain plasma) has been shown to be a unique LAB which activates pDC in vitro and in vivo [Citation22]. There are several reports regarding the efficacy of LC-Plasma supplementation in healthy subjects. LC-Plasma yogurt intake for 4 weeks activated maturation markers of pDC and intake for 12 weeks reduced the cumulative number of incidence days of influenza-like symptoms [Citation23, Citation24]. In addition, heat-killed LC-Plasma supplementation for 12 weeks reduced the number of incidence days of symptoms related to URTI [Citation25]. However, there is no report regarding the efficacy of LC-Plasma supplementation on pDC activation in athletes under HIE. Moreover, the influence of LC-Plasma intake on fatigue in athletes has never been evaluated. Based on the fact that pDCs are affected by single HIE and that LC-Plasma activates pDC and improves URTI, we hypothesized that ingestion of LC-Plasma would maintain pDC activity and suppress infection morbidity even during consecutive HIE. Moreover, we also hypothesize that LC-Plasma intake is effective for fatigue accumulation of athletes. To this end, we conducted a randomized, placebo-controlled, double-blinded trial to examine the effects of heat-killed LC-Plasma supplementation on maturation markers on DCs, and subjective indices correlating infections and fatigue under HIE. The primary efficacy outcomes were maturation markers (CD86, HLA-DR) on DCs and subjective indices (evaluation of influenza and URTI, and symptom severity including fatigue). Secondary outcomes were markers of muscle damage (creatine phospho kinase (CPK) and lactate dehydrogenase (LDH)) and stress markers (adrenaline and salivary cortisol).
Methods
Subjects
The Consolidated Standards of Trials diagram for this study is shown in Fig. . The required sample size was estimated using data of a previous clinical intervention study regarding LC-Plasma [Citation23]. Based on previous data of maturation markers on pDC, more than 20 subjects in each group would allow detection of differences between groups with a 5% statistical significant level. Initially, 57 healthy male athletes over 20 years of age were recruited between December 2015 and January 2016 from students belonging to sports clubs (track and field, futsal, and football) of the Juntendo University. Informed consent was obtained from 51 subjects (6 subjects declined to participate). No one met the exclusion criteria (subjects with severe chronic disease, steroid treatment, previous history of high risk for exercise, under treatment for pollinosis, and positive against HBV antigen, HCV antibodies, HIV antibodies, or HTLV-1 antibodies, and who could not stop eating functional foods or supplements containing lactic acid bacteria, oligosaccharide and fermented foods). A total of 51 subjects were randomly allocated to the placebo (n = 25) or LC-Plasma (n = 26) groups using a stratified randomization method. No participants dropped out during the intervention period. One subject in the placebo group was excluded from the analysis because of ingestion of steroid drugs included in the exclusion criteria during the intervention period. We analyzed data from 24 subjects in the placebo group and 26 subjects in the LC-Plasma group.
Study design
A randomized, double blind, placebo-controlled trial was conducted with two groups. A stratified randomization method was used to balance the number subjects in the groups. Subjects were randomly assigned to the placebo group or the LC-Plasma group in a 1:1 ratio. Placebo capsules contained cornstarch (Showa Sangyo Co., Ltd., Tokyo, Japan) and LC-Plasma capsules contained approximately 100 billion cells of heat-killed dried powder of LC-Plasma (KYOWA HAKKO BIO CO., Ltd., Tokyo, Japan) and cornstarch. Each subject ingested 1 capsule per day for 13 days between January and February 2016. Neither the study team nor the subjects could distinguish between the placebo and the LC-Plasma capsules, and the capsule codes were stored by a responsible person of allocation until all analyses were finished and the codes were opened after the data set was locked. During the intervention period, subjects exercised according to the training regime of their sports clubs. Subjects filled the records of capsule intake, exercise, meals, and a physical condition questionnaire in the diary every day. We adopted the amount of physical activity as metabolic rate-hour (MET-h) which is globally used index based energy consumption [Citation26]. We calculated MET-h from records of exercise according to a previous report [Citation27].
Blood and saliva sampling
Blood and saliva samples were collected twice, before and after the intervention period (day 1 and day 14) and at the same time of the day (between 08:00 to 09:00 a.m.). Saliva samples were collected using salimetrics oral swabs (Salimetrics LLC, PA, USA) according to the manufacturer’s instructions.
Measurement of blood and saliva samples
CPK and LDH were analyzed using the Japan Society of Clinical Chemistry recommended methods by the SRL, Inc. (Tokyo, Japan). Serum adrenaline concentration was measured using an ELISA kit (Arigo Biolaboratories Corp., Hsinchu City, Taiwan). Salivary cortisol was measured by an immunoassay kit according to the manufacturer’s instructions (Salimetrics LLC).
Preparation of peripheral blood mononuclear cells (PBMCs) by flow cytometry analysis
PBMCs were isolated from whole blood according to a previous report [Citation23]. PBMCs were stained with fluorescent dye conjugated to antibodies. For pDC, anti-Human CD123-FITC (AC145) (Miltenyi Biotec., Bergisch Gladbach, Germany), BDCA4-APC (AD-17F6) (Miltenyi Biotec.), CD86-PE (IT2.2) (eBioscience, San Diego, CA, USA), and HLA-DR-PerCP (L243) (BD Bioscience, NJ, USA) were used. For mDC, anti-human Lineage Cocktail 1-FITC (Lin1) (CD3, CD14, CD16, CD19, CD20, CD56) (MφP9, NCAM16.2, 3G8, L27, SJ25C1, SK7) (BD Bioscience), CD11c-APC (MJ4-27G12) (Miltenyi Biotec.), CD1c-PE-Cy7 (L161) (BioLegend, MS, USA), CD86-PE (IT2.2) (eBioscience), and HLA-DR-PerCP (L243) (BD Bioscience) were used. CD123+BDCA4+ cells were defined as pDC and Lin1−CD1c+CD11c+ cells were identified as mDC. The expression levels of HLA-DR and CD86 were used as maturation markers of pDC and mDC. After staining, cells were analyzed by flow cytometry using FACS Cant II (BD Biosciences). Data were analyzed using the FlowJo software (Treestar, ON, USA).
Measurements of incident days of influenza and URTI, and severity of symptoms
Subjects reported their conditions every day during the intervention period. The daily questionnaire asked about severity of sneeze or running nose, sore throat, cough, physical condition, fatigue, articular pain, chill, lassitude, and muscle pain. The severity of each symptom was scored using 5 grades. Evaluation of influenza and URTI incidence was performed from the severity of symptoms according to a previously reported diagnostic criterion list [Citation25]. Measurements of severity of each symptoms were performed according to a previous report [Citation28].
Statistical analysis
Within group comparisons of blood and saliva samples were performed using paired t test. Between groups comparisons of blood and saliva samples were performed using student’s t test. We used Bonferoni’s method for multiple comparisons and significant p value was set at p < 0.05/3 = 0.016. Effect sizes were calculated by Cohen’s D. Cumulative incidence days of influenza and URTI symptoms, and subjective symptoms severities were compared between groups by the Chi-square test. Significant p value was set at p < 0.05. Data of subject’s background and training records, maturation marker on DCs, muscle damage and stress marker were reported mean ± SD. Data of cumulative day of URTI, URTI symptoms and systemic symptoms were presented as incident number (n).
Results
Background information and training records
Table shows the background information and training records of the study subjects. No significant differences were detected in these parameters between the placebo and the LC-Plasma groups.
Table 1 Characteristics of subjects and training records during intervention
Muscle pain parameters and stress hormone
In order to evaluate the intensity of training during the intervention period, CPK, LDH, adrenaline, and cortisol were measured (Table ). CPK, LDH, and adrenaline were significantly increased at day 14 compared to day 1 in both the placebo and LC-Plasma groups. There were no differences between the placebo and LC-Plasma groups in these indices.
Table 2 Markers of muscle damage and stress at Day 1 and Day 14
Maturation markers on DCs
Expression of CD86 on pDC was significantly increased in the LC-Plasma group compared to the placebo group at day 14 (Fig. ). HLA-DR on pDC was not significantly different between groups at day 14 (Fig. ). CD86 and HLA-DR on mDC did not significantly change between the placebo and LC-Plasma groups at day 14 (Fig. ). A significant decrease of CD86 on mDC was detected in the placebo group after the intervention period (Fig. ).
Fig. 2 Maturation markers on DCs were measured before and after the intervention period. Comparison of (a) CD86 on pDC, (b) HLA-DR on pDC, (c) CD86 on mDC, (d) HLA-DR on mDC between placebo and LC-Plasma groups. The solid line shows the placebo group and the broken line shows the LC-Plasma group. Values are means ± SD. *: Significantly difference between groups (p < 0.016). Effect size was calculated by Cohen’s D as 0.72. †: Significantly difference within Placebo group (p < 0.016). Effect size was calculated by Cohen’s D as − 0.68
![](/cms/asset/2e13bfa2-02cd-43cd-9c3d-1892122d7810/rssn_a_12130057_f0002_oc.png)
Cumulative days of influenza and URTI symptoms
The incidence of influenza and URTI symptoms was evaluated according to previous report [Citation25]. There were no subjects judged as influenza infected. Numbers of subjects of URTI were not significantly difference between the placebo and LC-Plasma groups (Table ). However, cumulative days of URTI positive were significantly lower in the LC-Plasma group compared to the placebo group (Table ).
Table 3 Number of subjects and cumulative days of URTI during intervention period
Severity of subjective symptoms during the intervention period
Tables and shows the frequency of each evaluated symptom. The frequencies of incidence days of subjective symptoms including, sneeze or running nose, physical condition, fatigue, and articular pain were significantly lower in the LC-Plasma group than in the placebo group.
Table 4 Cumulative number of days of URTI symptoms during intervention period
Table 5 Cumulative number of days of systemic symptoms during intervention period
Discussion
LC-Plasma is a unique LAB which activates plasmacytoid dendritic cells (pDC) in healthy subjects. However, efficacy during consecutive HIE have not been evaluated. We conducted human study and researched the effects of LC-Plasma in athletes. The results indicated that LC-Plasma supplementation for 13 days would able to increase maturation marker of pDC (CD86) and decrease cumulative days of URTI symptom. Furthermore, we observed that LC-Plasma ingestion could decrease cumulative days of fatigue. These findings indicated that intake of LC-Plasma would prevent URTI infection via pDC activation and improve fatigue accumulation, suggesting that our hypothesis was acceptable.
There were no significantly differences between the groups in the training records during intervention (Table ). It was reported that exercise for more than 11 h a week is reported to be high intensity and increasing URTI morbidity [Citation29]. Although we did not strictly control exercise, both groups exercised for more than 11 h a week. Therefore, we thought that high intensity exercise was loaded to both groups as the physical condition of subjects became decrease. In addition, CPK and LDH as markers of muscle damage, and adrenaline and cortisol as stress hormones were also no different at day 14 (Table ). These results suggested that exercise stress load between the placebo and LC-Plasma group was comparable in this study.
CPK, LDH and adrenaline were significantly increased at day 14 compared to day 1. Our data showed that exercise during the intervention period was high enough to affect markers of muscle damage and stress hormone. CPK and adrenaline reported to increase after HIE and to be involved in immunity and fatigue [Citation30–Citation32]. We found that maturation markers (CD86 and HLA-DR) on DCs were decreased in the placebo group (Fig. ). These results indicated that DCs are also involved in immuno-reduction under high stress condition such as consecutive HIE.
We showed that CD86 on pDC increased in the LC-Plasma group compared to the placebo group after consecutive HIE. This suggests that LC-Plasma increases pDC maturation in athletes under HIE as in general healthy subjects as reported previously [Citation23].
Cumulative incidence days of URTI and symptom like sneeze or running nose decreased in the LC-Plasma group. Since pDC were reported to play antiviral functions [Citation10] and that 70% of the causes of URTI were viral infections [Citation12], we can conclude that LC-Plasma supplementation relieves URTI morbidity during HIE via pDC activation. In previous reports, LC-Plasma supplementation for more than 4 weeks was effective in general healthy subjects [Citation23, Citation24, Citation28]. We found that LC-Plasma was effective even in a short intervention period of 13 days. Because this study was conducted under high stress conditions, the effect of LC-Plasma supplementation could be confirmed earlier and clearly.
We found that fatigue accumulation was lower in the LC-Plasma group compared to the placebo group. There are no reports regarding probiotics improving fatigue in athletes. Therefore, here we showed for the first time that LAB material such as LC-Plasma supplementation was effective for improving fatigue during consecutive HIE. For people under physically stressful conditions such as athletes, fatigue accumulation is a serious problem [Citation33–Citation35], therefore our finding is valuable for athletes.
Since there was no significant difference in markers of muscle damage and stress in LC-Plasma group compared to Placebo, LC-Plasma might not directly affect recovery through these markers. Although detailed mechanism for fatigue reduction by LC-Plasma is not fully understood, one possibility is autonomic nerves, affected by HIE and related to fatigue [Citation36]. Athletes who develop chronic fatigue or depression due to excessive HIE were reported to have abnormal autonomic nerves [Citation37]. It was also reported that TLR9 knock out mice exhibited changes of autonomic nerve functions (heart rate and pulse interval) and behavior with responsiveness to stress [Citation38]. Considering that LC-Plasma is a ligand of TLR9 [Citation22], LC-Plasma might affect autonomic nerves and accordingly improve fatigue state via TLR9. Further research is necessary in order to confirm the precise mechanism of LC-Plasma regarding fatigue.
There were some limitations regarding the analysis, which may affect the results of this study. The study subjects were composed of only male and university students. Furthermore, even though the exercise load was not different between groups, the training regime was not strictly controlled. Since this study was conducted in 13 days of ingestion which is thought to be relatively short period, the efficacy of LC-Plasma for athletes during long-term ingestion was unknown. More extensive studies with a wide range of subjects or homogeneous exercise load like ergometer exercise or long and high intensive exercise are required to confirm our findings.
Conclusions
In this study, we showed that heat-killed LC-Plasma supplementation relieves URTI morbidity and symptoms during consecutive HIE via activation of pDC. Moreover, LC-Plasma ingestion decreased fatigue accumulation. We suggest that heat-killed LC-Plasma was beneficial to solve problems of athletes such as immune-reduction and increased fatigue.
Authors’ contributions
YK, HN, KS, and HD conceived and designed the experiments. YK, KF, and YI performed the experiments. YK, KF, and YI analyzed the data. YK, TF, TK, and KS wrote the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study protocol was ethically reviewed and approved by the institution review board at Juntendo University (15–057), Tokyo, Japan and carried out in accordance with the principles outlined in the 2002 Declaration of Helsinki of the World Medical Association. This study was registered at the University Hospital Medical Information Network Clinical Trials Registry as UMIN000020372.
Consent for publication
Not applicable.
Competing interests
Y.K., T.F., and T.K. are employees of Kirin Co., Ltd. The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Acknowledgements
We thank Takumi Horiike, Akira Nakamura, Shunsuke Nagato who were supervisor of Juntendo University sports clubs for good partnership in this study. We also thank Dr. Tetsuro Miyazaki, Dr. Tomoyuki Shiozawa, Dr. Shuhei Takahashi, and Dr. Tomoyasu Kadoguchi of Juntendo University and Dr. Osamu Kanauchi, and Dr. Keiji Kondo of Kirin Co., Ltd. for valuable discussions and technical supports.
Funding
This study was funded by Kirin Co., Ltd.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
References
- MoreiraADelgadoLMoreiraPHaahtelaTDoes exercise increase the risk of upper respiratory tract infections?Br Med Bull200990 111 131 https://doi.org/10.1093/bmb/ldp010 19336500
- GleesonMPyneDBRespiratory inflammation and infections in high-performance athletesImmunol Cell Biol201694 2 124 131 https://doi.org/10.1038/icb.2015.100 26568028 1:CAS:528:DC%2BC2MXitVymtbzF
- GleesonMPyneDBSpecial feature for the Olympics: effects of exercise on the immune system: exercise effects on mucosal immunityImmunol Cell Biol200078 5 536 544 https://doi.org/10.1111/j.1440-1711.2000.t01-8-.x 11050537 1:CAS:528:DC%2BD3cXnsFeht78%3D
- SuzuiMKawaiTKimuraHTakedaKYagitaHOkumuraK et al Natural killer cell lytic activity and CD56(dim) and CD56(bright) cell distributions during and after intensive trainingJournal of applied physiology200496 6 2167 2173 https://doi.org/10.1152/japplphysiol.00513.2003 14752119
- GleesonMPyneDBAustinJPLynn FrancisJClancyRLMcDonaldWA et al Epstein-Barr virus reactivation and upper-respiratory illness in elite swimmersMed Sci Sports Exerc200234 3 411 417 https://doi.org/10.1097/00005768-200203000-00005 11880803
- TomasiTBTrudeauFBCzerwinskiDErredgeSImmune parameters in athletes before and after strenuous exerciseJ Clin Immunol19822 3 173 178 https://doi.org/10.1007/BF00915219 6981653 1:STN:280:DyaL3s%2FgslKgtQ%3D%3D
- BansalASBradleyASBishopKNKiani-AlikhanSFordBChronic fatigue syndrome, the immune system and viral infectionBrain Behav Immun201226 1 24 31 https://doi.org/10.1016/j.bbi.2011.06.016 21756995 1:CAS:528:DC%2BC3MXhsFSlu7nO
- WynnTABasophils trump dendritic cells as APCs for T(H)2 responsesNat Immunol200910 7 679 681 https://doi.org/10.1038/ni0709-679 19536189 2756226 1:CAS:528:DC%2BD1MXnsVagsb0%3D
- WimmersFSchreibeltGSkoldAEFigdorCGDe VriesIJParadigm shift in dendritic cell-based immunotherapy: from in vitro generated monocyte-derived DCs to naturally circulating DC subsetsFront Immunol20145 165 https://doi.org/10.3389/fimmu.2014.00165 24782868 3990057 1:CAS:528:DC%2BC2MXht1enurfI
- PiccioliDSammicheliCTavariniSNutiSFrigimelicaEManettiAG et al Human plasmacytoid dendritic cells are unresponsive to bacterial stimulation and require a novel type of cooperation with myeloid dendritic cells for maturationBlood2009113 18 4232 4239 https://doi.org/10.1182/blood-2008-10-186890 19176317 1:CAS:528:DC%2BD1MXlvVGisLY%3D
- SchneiderWMChevillotteMDRiceCMInterferon-stimulated genes: a complex web of host defensesAnnu Rev Immunol201432 513 545 https://doi.org/10.1146/annurev-immunol-032713-120231 24555472 4313732 1:CAS:528:DC%2BC2cXovVemt7c%3D
- MakelaMJPuhakkaTRuuskanenOLeinonenMSaikkuPKimpimakiM et al Viruses and bacteria in the etiology of the common coldJ Clin Microbiol199836 2 539 542 9466772 104573 1:STN:280:DyaK1c7is1anug%3D%3D
- VegliaFGabrilovichDIDendritic cells in cancer: the role revisitedCurr Opin Immunol201745 43 51 https://doi.org/10.1016/j.coi.2017.01.002 28192720 5449252 1:CAS:528:DC%2BC2sXitFeksb8%3D
- HemontCNeelAHeslanMBraudeauCJosienRHuman blood mDC subsets exhibit distinct TLR repertoire and responsivenessJ Leukoc Biol201393 4 599 609 https://doi.org/10.1189/jlb.0912452 23341538 1:CAS:528:DC%2BC3sXlsVyktLc%3D
- NickelTEmslanderISisicZDavidRSchmadererCMarxN et al Modulation of dendritic cells and toll-like receptors by marathon runningEur J Appl Physiol2012112 5 1699 1708 https://doi.org/10.1007/s00421-011-2140-8 21881949 1:CAS:528:DC%2BC38Xls1Sit7k%3D
- LackermairKScherrJWaidhauserGMetheHHosterENiemanDC et al Influence of polyphenol-rich diet on exercise-induced immunomodulation in male endurance athletesApplied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme201742 10 1023 1030 https://doi.org/10.1139/apnm-2017-0063 28591543 1:CAS:528:DC%2BC2sXht1yitLnP
- ClancyRLGleesonMCoxACallisterRDorringtonMD'EsteC et al Reversal in fatigued athletes of a defect in interferon gamma secretion after administration of lactobacillus acidophilusBr J Sports Med200640 4 351 354 https://doi.org/10.1136/bjsm.2005.024364 16556792 2577537 1:STN:280:DC%2BD287mslajuw%3D%3D
- BerggrenALazou AhrenILarssonNOnningGRandomised, double-blind and placebo-controlled study using new probiotic lactobacilli for strengthening the body immune defence against viral infectionsEur J Nutr201150 3 203 210 https://doi.org/10.1007/s00394-010-0127-6 20803023
- de VreseMWinklerPRautenbergPHarderTNoahCLaueC et al Effect of Lactobacillus gasseri PA 16/8, Bifidobacterium longum SP 07/3, B. bifidum MF 20/5 on common cold episodes: a double blind, randomized, controlled trialClinical nutrition200524 4 481 491 https://doi.org/10.1016/j.clnu.2005.02.006 16054520
- GleesonMBishopNCOliveiraMMcCauleyTTaulerPLawrenceCEffects of a lactobacillus salivarius probiotic intervention on infection, cold symptom duration and severity, and mucosal immunity in endurance athletesInt j sport nutr exerc metab201222 4 235 242 https://doi.org/10.1123/ijsnem.22.4.235 22645171 1:CAS:528:DC%2BC38XhtlOgu7bE
- TiollierEChennaouiMGomez-MerinoDDrogouCFilaireEGuezennecCYEffect of a probiotics supplementation on respiratory infections and immune and hormonal parameters during intense military trainingMil Med2007172 9 1006 1011 https://doi.org/10.7205/MILMED.172.9.1006 17937368
- JounaiKIkadoKSugimuraTAnoYBraunJFujiwaraDSpherical lactic acid bacteria activate plasmacytoid dendritic cells immunomodulatory function via TLR9-dependent crosstalk with myeloid dendritic cellsPLoS One20127 4 e32588 https://doi.org/10.1371/journal.pone.0032588 22505996 3323594 1:CAS:528:DC%2BC38XlvFCjtbs%3D
- SugimuraTJounaiKOhshioKTanakaTSuwaMFujiwaraDImmunomodulatory effect of Lactococcus lactis JCM5805 on human plasmacytoid dendritic cellsClinical immunology2013149 3 509 518 https://doi.org/10.1016/j.clim.2013.10.007 24239838 1:CAS:528:DC%2BC3sXhvFeltLnL
- SugimuraTTakahashiHJounaiKOhshioKKanayamaMTazumiK et al Effects of oral intake of plasmacytoid dendritic cells-stimulative lactic acid bacterial strain on pathogenesis of influenza-like illness and immunological response to influenza virusBr J Nutr2015114 5 727 733 https://doi.org/10.1017/S0007114515002408 26234407 1:CAS:528:DC%2BC2MXhsVSntrrF
- ShibataTKanayamaMHaidaMFujimotoSOroguchiTSataK et al Lactococcus lactis JCM5805 activates anti-viral immunity and reduces symptoms of common cold and influenza in healthy adults in a randomized controlled trialJ Funct Foods201624 492 500 https://doi.org/10.1016/j.jff.2016.03.035 1:CAS:528:DC%2BC28XntVCgu7o%3D
- MichalickovaDMinicRDikicNAndjelkovicMKostic-VucicevicMStojmenovicT et al Lactobacillus helveticus Lafti L10 supplementation reduces respiratory infection duration in a cohort of elite athletes: a randomized, double-blind, placebo-controlled trialApplied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme201641 7 782 789 https://doi.org/10.1139/apnm-2015-0541 27363733 1:CAS:528:DC%2BC28XhtFSit7bM
- AinsworthBEHaskellWLHerrmannSDMeckesNBassettDRJrTudor-LockeC et al 2011 compendium of physical activities: a second update of codes and MET valuesMed Sci Sports Exerc201143 8 1575 1581 https://doi.org/10.1249/MSS.0b013e31821ece12 21681120
- FujiiTJounaiKHorieATakahashiHSuzukiHOhshioK et al Effects of heat-killed Lactococcus lactis subsp. lactis JCM 5805 on mucosal and systemic immune parameters, and antiviral reactions to influenza virus in healthy adults; a randomized controlled double-blind studyJournal of Functional Foods201735 513 521 https://doi.org/10.1016/j.jff.2017.06.011 1:CAS:528:DC%2BC2sXhtVKgtrzJ
- GleesonMBishopNOliveiraMTaulerPInfluence of training load on upper respiratory tract infection incidence and antigen-stimulated cytokine productionScand J Med Sci Sports201323 4 451 457 https://doi.org/10.1111/j.1600-0838.2011.01422.x 22151281 1:STN:280:DC%2BC38zosFGjsw%3D%3D
- LeeNKimJHyungGAParkJHKimSJKimHB et al Training effects on immune function in JudoistsAsian journal of sports medicine20156 3 https://doi.org/10.5812/asjsm.24050 26448852 4594140
- Muders K, Pilat C. Effects of Traumeel (Tr14) on Exercise-Induced Muscle Damage Response in Healthy Subjects: A Double-Blind RCT. Mediators Inflamm 2016. doi: https://doi.org/https://doi.org/10.1155/2016/1693918.
- SkurvydasAVerbickasVEimantasNBaranauskieneNCernychMSkrodenieneE et al Psychological and physiological biomarkers of neuromuscular fatigue after two bouts of Sprint interval exerciseFront Psychol20178 2282 https://doi.org/10.3389/fpsyg.2017.02282 29312105 5744043
- RiceSMParkerAGRosenbaumSBaileyAMawrenDPurcellRSport-Related Concussion and Mental Health Outcomes in Elite Athletes: A Systematic ReviewSports medicine201748 2 447 465 https://doi.org/10.1007/s40279-017-0810-3
- MalhotraRKSleep, recovery, and performance in sportsNeurol Clin201735 3 547 557 https://doi.org/10.1016/j.ncl.2017.03.002 28673415
- DeuschleMGotthardtUSchweigerUDettlingMHolsboerFHeuserIHypothalamic-pituitary-adrenocortical dysfunction in elderly, male Marathon runners: feedback sensitivity, stress response, and effects on verbal memoryNeuroendocrinology2017105 2 150 156 https://doi.org/10.1159/000450856 27677093 1:CAS:528:DC%2BC2sXhtlWntrfO
- BellengerCRFullerJTThomsonRLDavisonKRobertsonEYBuckleyJDMonitoring Athletic Training Status Through Autonomic Heart Rate Regulation: A Systematic Review and Meta-AnalysisSports medicine201646 10 1461 1486 https://doi.org/10.1007/s40279-016-0484-2 26888648
- KiviniemiAMTulppoMPHautalaAJVanninenEUusitaloALAltered relationship between R-R interval and R-R interval variability in endurance athletes with overtraining syndromeScand J Med Sci Sports201424 2 e77 e85 https://doi.org/10.1111/sms.12114 24024550 1:STN:280:DC%2BC3sbntFCltQ%3D%3D
- RodriguesFLSilvaLEHottSCBomfimGFda SilvaCAFazanRJr et al Toll-like receptor 9 plays a key role in the autonomic cardiac and baroreflex control of arterial pressureAm j physiol Regul integ com physiol2015308 8 R714 R723 https://doi.org/10.1152/ajpregu.00150.2014 1:CAS:528:DC%2BC2MXnvFKlsbw%3D