198 Effect of Saccharomyces Cerevisiae Fermentate on Immune Cell Function Following Prolonged Head Elevation in 2-year-old Horses in Training

2021 ◽  
Vol 99 (Supplement_3) ◽  
pp. 106-107
Author(s):  
Melissa Tench ◽  
Jillian M Bobel ◽  
Cinthya Bazurto ◽  
Tayler L Hansen ◽  
Nicolet Kirk ◽  
...  

Abstract Horses are often restricted from lowering their heads while being transported, which prevents nasal drainage and triggers upper respiratory tract inflammation. Based on positive outcomes in other species, we hypothesized Saccharomyces cerevisiae fermentate (SCF) would modify this immune response in horses. Two-year-old Quarter Horses (mean ± SEM; initial age 22 ± 0.3 mo and BW 439 ± 3 kg) were randomly assigned to receive SCF (Diamond V, Cedar Rapids, IA; 21 g/d; n = 10) or no supplement (CON; n = 10) added to their diet (60% hay, 40% concentrate) for 60 d. Horses were exercised 4 d/wk for 30–45 min/d at light to moderate intensity. On d 57 horses were tethered with their heads elevated 35 cm above wither height for 12 h to mimic long-distance transport. Whole blood samples were obtained before and up to 72 h after stress induction to evaluate immune cell function. Data were compared using mixed model ANOVA with repeated measures. Serum cortisol (P < 0.01) and blood leukocytes (P < 0.05) were greater after head elevation. Lymphocyte proliferation in response to lipopolysaccharide was lower (P < 0.01) following head elevation but did not differ by treatment. Lymphocyte proliferation in response to concanavalin A exhibited a time × treatment effect (P = 0.05) where it decreased in CON horses after head elevation (P < 0.05) but was unchanged in SCF horses. Neutrophil phagocytosis of Streptococcus equi (a respiratory pathogen) was temporarily reduced (P < 0.05) after head elevation in both treatments. A time × treatment effect (P = 0.05) was observed for phagocytosis-induced oxidative burst, where it increased in SCF (P < 0.01) but did not change in CON horses. These data indicate SCF modified peripheral immune cell activity following a localized mucosal stressor. Whether these responses improve resistance to opportunistic pathogens following transport needs to be determined.

2021 ◽  
Vol 80 (Suppl 1) ◽  
pp. 8.1-8
Author(s):  
G. Robinson ◽  
K. Waddington ◽  
J. Peng ◽  
A. Radziszewska ◽  
H. Peckham ◽  
...  

Background:Males and females have altered immune responses resulting in variation in autoimmune and cardiovascular disease risk (CVR). Recently, these differences have played a role in the inflammatory response to COVID-19. Sex differences exist in the frequency and activity of immune-cell subsets but mechanisms underlying sexual dimorphism remain unknown. Juvenile-onset systemic lupus erythematosus (JSLE) is an autoimmune disorder that commonly emerges during puberty, has a strong female prevalence (female:male ratio, 4.5:1) and results in an increased CVR. JSLE is characterised by chronic inflammation and dyslipidaemia, where cardiovascular disease is a leading cause of mortality for patients. Our previous work identified a link between immune cell function and lipid metabolism in adult-onset SLE. We hypothesised that sex hormones could influence both lipid metabolism and immune cell function and this could determine sex-specific susceptibility to JSLE and associated CVR.Objectives:We investigated the role of sex hormones in modifying systemic lipid metabolism and inflammation.Methods:Nuclear magnetic resonance spectroscopy based serum metabolomics measuring over 130 lipoproteins (14-subsets with lipid compositions), flow cytometry measuring immune-cells, and RNA-sequencing were used to assess the metabolic and immune profile in young, pre/post-pubertal males (n=10/17) and females (n=10/23) and in individuals with gender-dysphoria (GD) under cross-hormone treatment (trans-male/female, n=26/25). This analysis was also performed on a cohort of post-pubertal male (n=12) and female (n=23) JSLE patients. Data was analysed by logistic regression, balanced random forest machine learning (BRF-ML), differential gene expression (DEG) and pathway analysis.Results:Post-pubertal males had significantly reduced cardio-protective high-density lipoprotein (HDL) subsets (p<0.0001) and increased cardio-pathogenic very-low-density lipoprotein subsets (p<0.0001) compared to females. These differences were not observed pre-puberty and were reversed significantly by cross-hormone treatment in GD individuals, suggesting that sex hormones regulate lipid metabolism in-vivo.BRF-ML (28 immune-cell subsets) identified an increased frequency of anti-inflammatory regulatory T-cells (Tregs) in post-pubertal males compared to females (p=0.0097). These Tregs were also more suppressive in males compared to females. Differences in Treg frequency were seen pre-puberty and were not altered by sex hormone treatment in GD individuals. However, Treg DEGs and functional transcriptomic pathways altered between post-pubertal males and females, including those involved in inflammatory signalling, overlapped with those altered by hormones in GD, suggesting hormones may also drive Treg functional changes. In addition, HDL metabolites modified by hormones showed differential associations with Treg phenotypes between post-pubertal males and females.Strikingly, sex differences in lipoproteins and Tregs were lost in JSLE, suggesting hormone signalling could be dysregulated in the pathogenesis of autoimmunity and could increase CVR for patients.Conclusion:Sex hormones drive altered lipoprotein metabolism and functional transcriptomic pathways in Tregs. Males have a lipoprotein profile associated with increased CVR, but a more anti-inflammatory immune profile compared to females. Together, this could explain sex differences in inflammatory disease susceptibilities and inform future sex-specific therapeutic strategies for the management of both JSLE and CVR.Acknowledgements:Lupus UKRosetrees TrustVersus ArthritisNIHR UCLH Biomedical Research CentreDisclosure of Interests:None declared


2021 ◽  
Vol 40 (4) ◽  
pp. S232-S233
Author(s):  
S.D. Maidman ◽  
C. Gidea ◽  
A. Reyentovich ◽  
S. Rao ◽  
T. Saraon ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Philip Newsholme

AbstractVarious nutrients can change cell structure, cellular metabolism, and cell function which is particularly important for cells of the immune system as nutrient availability is associated with the activation and function of diverse immune subsets. The most important nutrients for immune cell function and fate appear to be glucose, amino acids, fatty acids, and vitamin D. This perspective will describe recently published information describing the mechanism of action of prominent nutritional intervention agents where evidence exists as to their action and potency.


2014 ◽  
Vol 28 (2) ◽  
pp. 229-235 ◽  
Author(s):  
Laura J. Wozniak ◽  
Robert S. Venick ◽  
Sherilyn Gordon Burroughs ◽  
Khiet D. Ngo ◽  
John P. Duffy ◽  
...  

1995 ◽  
Vol 209 (4) ◽  
pp. 369-375 ◽  
Author(s):  
M. Roy ◽  
L. Kiremidjian-Schumacher ◽  
H. I. Wishe ◽  
M. W. Cohen ◽  
G. Stotzky

2015 ◽  
Vol 9 (4) ◽  
pp. 974-985 ◽  
Author(s):  
R Brauer ◽  
J Tureckova ◽  
I Kanchev ◽  
M Khoylou ◽  
J Skarda ◽  
...  

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