1.Analysis of differential expression of tight junction proteins in cultured oral epithelial cells altered by Porphyromonas gingivalis, Porphyromonas gingivalis lipopolysaccharide, and extracellular adenosine triphosphate.
Wei GUO ; Peng WANG ; Zhong-Hao LIU ; Ping YE
International Journal of Oral Science 2018;10(1):e8-e8
Tight junctions (TJs) are the most apical intercellular junctions of epithelial cells formed by occludin, claudins, junctional adhesion molecules (JAMs), and zonula occludens (ZO). Tight junction proteins can sense the presence of bacteria and regulate the transcription of target genes that encode effectors and regulators of the immune response. The aim of this study was to determine the impact of TJ proteins in response to Porphyromonas gingivalis (P. gingivalis), P. gingivalis lipopolysaccharide (P. gingivalis LPS), and extracellular adenosine triphosphate (ATP) in the oral epithelial cell culture model. Quantified real time-polymerase chain reaction (RT-PCR), immunoblots, and immunostaining were performed to assess the gene and protein expression in TJs. It was found that P. gingivalis infection led to transient upregulation of the genes encoding occludin, claudin-1, and claudin-4 but not JAM-A, claudin-15, or ZO-1, while P. gingivalis LPS increased claudin-1, claudin-15, and ZO-1 and decreased occludin, JAM-A, and claudin-4. Tight junction proteins showed significant upregulation in the above two groups when cells were pretreated with ATP for 3 h. The findings indicated that P. gingivalis induced the host defence responses at an early stage. P. gingivalis LPS exerted a more powerful stimulatory effect on the disruption of the epithelial barrier than P. gingivalis. ATP stimulation enhanced the reaction of TJ proteins to P. gingivalis invasion and LPS destruction of the epithelium.International Journal of Oral Science (2018) 10, e8; doi:10.1038/ijos.2017.51; published online 10 January 2018.
Adenosine Triphosphate
;
pharmacology
;
Cells, Cultured
;
Epithelial Cells
;
cytology
;
Gene Expression
;
Humans
;
Immunoblotting
;
Lipopolysaccharides
;
pharmacology
;
Mouth Mucosa
;
cytology
;
Porphyromonas gingivalis
;
immunology
;
Real-Time Polymerase Chain Reaction
;
Tight Junction Proteins
;
metabolism
;
Up-Regulation
2.IgE Sensitization Patterns to Commonly Consumed Foods Determined by Skin Prick Test in Korean Adults.
Sung Ryeol KIM ; Hye Jung PARK ; Kyung Hee PARK ; Jae Hyun LEE ; Jung Won PARK
Journal of Korean Medical Science 2016;31(8):1197-1201
Offending food allergens can vary with regional preferences in food consumption. In this study, we analysed sensitization rates to commonly consumed foods in Korean adults suspected of having food allergy. One hundred and thirty four subjects underwent a skin prick test (SPT) with 55 food allergens, of which 13 were made by our laboratory and the rest were commercially purchased. Of the 134 patients, 73 (54.5%) were sensitized to one or more food allergens. Sensitization to chrysalis was detected most frequently, at a rate of 25.4%. Sensitization rates to other food allergens were as follows: maize grain (13.4%), shrimp (11.9%), almond (11.1%), wheat flour (8.2%), lobster (8.2%), buckwheat (8.2%), mackerel (5.2%), pollack (5.2%), halibut (4.5%), peanut (4.5%), anchovy (4.4%), squid (3.7%), saury (3.0%), common eel (3.0%), yellow corvina (3.0%), hairtail (2.2%), octopus (2.2%), and others. In addition to well-known food allergens, sensitivity to mackerel, chrysalis, pollack, and halibut, which are popular foods in Korea, was observed at high rates in Korean adults. We suggest that the SPT panel for food allergy in Korea should include these allergens.
Adult
;
Aged
;
Allergens/immunology
;
Animals
;
Asian Continental Ancestry Group
;
Female
;
Flounder/immunology
;
Food Hypersensitivity/*diagnosis
;
Humans
;
Immunoglobulin E/*analysis/immunology
;
Male
;
Middle Aged
;
Mouth/immunology
;
Perciformes/immunology
;
Republic of Korea
;
*Skin Tests
;
Young Adult
3.Expression of vasoactive intestinal peptide in peripheral blood of children with hand, foot and mouth disease.
Jin-Song REN ; Hao-Miao SUN ; Lei ZHANG ; Jing-De LIN ; Cheng WEN ; Dai-Hua FANG
Chinese Journal of Contemporary Pediatrics 2016;18(11):1106-1110
OBJECTIVETo investigate the expression of vasoactive intestinal peptide (VIP) in peripheral blood of children with hand, foot and mouth disease and its significance.
METHODSAccording to the condition of the disease, 86 children with hand, foot and mouth disease were classified into phase 1 group (19 children) and phase 2 group (67 children). ELISA was used to measure the concentrations of plasma VIP, interferon-γ (IFN-γ), and interleukin-4 (IL-4) in peripheral blood. Flow cytometry was used to measure CD3, CD4, and CD8T lymphocyte subsets. RT-PCR was used for qualitative detection of enterovirus 71 (EV71) RNA in stool.
RESULTSCompared with the phase 1 group, the phase 2 group had a significantly higher positive rate of EV71-RNA (P<0.05) and significantly higher serum levels of IgG, IgA, IgM, and C3 (P<0.05). The phase 2 group had significantly lower proportions of peripheral CD3, CD4, and CD8T lymphocyte subsets than the phase 1 group (P<0.05), as well as significantly lower proportion of peripheral B cells and CD4/CD8ratio than the phase 1 group (P<0.05). The phase 2 group also had a significantly lower concentration of VIP in peripheral blood than the phase 1 group (P<0.05). In the 86 children with hand, foot and mouth disease, the concentration of VIP in peripheral blood was positively correlated with the proportion of CD4T lymphocyte subset and CD4/CD8ratio (r=0.533 and 0.532 respectively; P<0.05).
CONCLUSIONSVIP may be an important marker of the severity of hand, foot and mouth disease.
Biomarkers ; CD4-CD8 Ratio ; Child, Preschool ; Female ; Hand, Foot and Mouth Disease ; immunology ; Humans ; Infant ; Interferon-gamma ; blood ; Interleukin-4 ; blood ; Male ; Severity of Illness Index ; Vasoactive Intestinal Peptide ; blood
4.Effect of continuous hemofiltration on inflammatory mediators and hemodynamics in children with severe hand, foot and mouth disease.
Li-Jing CAO ; Wen-Jin GENG ; Mei-Xian XU ; Xi-Min HUO ; Xiao-Dong WANG ; Xiao-Na SHI
Chinese Journal of Contemporary Pediatrics 2016;18(3):219-223
OBJECTIVETo investigate the effect of continuous veno-venous hemofiltration (CVVH) on inflammatory mediators in children with severe hand, foot and mouth disease (HFMD), and to investigate its clinical efficacy.
METHODSA total of 36 children with stage IV HFMD were enrolled and randomly divided into conventional treatment group and CVVH group (n=18 each). The children in the CVVH group were given CVVH for 48 hours in addition to the conventional treatment. The levels of interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-10 (IL-10), tumor necrosis factor-α (TNF-α) and lactic acid in peripheral venous blood, heart rate, blood pressure, and left ventricular ejection fraction were measured before treatment and after 24 and 48 hours of treatment.
RESULTSAfter 24 hours of treatment, the conventional treatment group had a significantly reduced serum IL-2 level (P<0.01), and the CVVH treatment group had significantly reduced serum levels of IL-2, IL-6, IL-10, and TNF-α (P<0.05). After 48 hours of treatment, both groups had significantly reduced serum levels of IL-2, IL-6, IL-10, and TNF-α (P<0.01), and the CVVH group had significantly lower levels of these inflammatory factors than the conventional treatment group (P<0.01). After 48 hours of treatment, heart rate, systolic pressure, and blood lactic acid level were significantly reduced, and left ventricular ejection fraction was significantly increased in both groups, and the CVVH group had significantly greater changes in these indices except systolic pressure than the conventional treatment group (P<0.01).
CONCLUSIONSCVVH can effectively eliminate inflammatory factors, reduce heart rate and venous blood lactic acid, and improve heart function in children with severe HFMD.
Child, Preschool ; Cytokines ; blood ; Female ; Hand, Foot and Mouth Disease ; immunology ; physiopathology ; therapy ; Hemodynamics ; Hemofiltration ; Humans ; Infant ; Inflammation Mediators ; blood ; Male ; Ventricular Function, Left
5.Protein expression profile of mast cells in response to recombinant VP1-VP4 of foot-and-mouth disease virus.
Yan WANG ; Shasha ZHANG ; Lei WANG ; Xuefang LIU ; En ZHANG ; Na LI ; Yunhuan GAO ; Yiming ZHANG ; Limin LI ; Jiaxin WANG
Chinese Journal of Biotechnology 2016;32(9):1194-1203
To reveal the innate immunity of mast cells against recombinant VP1-VP4 protein of foot-and-mouth disease virus (FMDV), mouse peritoneal mast cells (PMCs) were pulsed with recombinant VP1-VP4 protein. The supernatants harvested from PMCs cultures were applied to the high throughput ELISA array. Our results show that the expression levels of CCL19, L-selectin, CCL17, and TNF alpha released from PMCs pulsed with recombinant VP1-VP4 were significantly down-regulated compared with PMCs alone (P<0.001). Surprisingly, in comparison with PMCs alone, the expression levels of CCL19, IL-15, IL-9, G-CSF, and Galectin-1 in PMCs with the mannose receptor (MR) inhibitor were significantly up-regulated (Plt;0.01), and the expression level of IL-10 was also remarkably up-regulated (Plt;0.05). Importantly, the protein expression levels in PMCs treated with MR inhibitor were higher than PMCs pulsed with VP1-VP4, including IL-10, IL-17, CCL20, IL-15, IL-9, L-selectin, CCL17, TNF alpha, and CCL19 (Plt;0.01) as well as CCL21, and G-CSF (Plt;0.05). Differential expression analysis in bioinformatics shows that both L-selectin and CCL17 were recognized as differentially expressed protein molecules (Log2(ratio)≤-1) when compared with PMCs alone. Furthermore, the up-regulation of the expression levels of CCL20, CCL19, L-selectin, and IL-15 in PMCs treated with MR inhibitor was defined as differential expression (Log2(ratio)≥1). These data indicate that PMCs are capable of secreting CCL19, L-selectin, CCL17, and TNF alpha spontaneously and the recombinant VP1-VP4 has an inhibitive potential to PMCs during their performance of innate immune response. Given the protein expression levels from PMCs pre-treated with MR inhibitor were significantly increased, it can be deduced that immunosuppression of FMDV is presumably initiated by the VP1 recognition of MR on mast cells.
Animals
;
Capsid Proteins
;
immunology
;
Cells, Cultured
;
Cytokines
;
immunology
;
Enzyme-Linked Immunosorbent Assay
;
Foot-and-Mouth Disease
;
Foot-and-Mouth Disease Virus
;
Interleukins
;
immunology
;
Mast Cells
;
immunology
;
Mice
;
Proteome
;
immunology
;
Recombinant Proteins
;
immunology
;
Viral Structural Proteins
;
immunology
6.Guan's tongue acupuncture for 20 cases of burning mouth syndrome.
Suna WANG ; Sujuan XIE ; Zuhong WANG
Chinese Acupuncture & Moxibustion 2015;35(7):695-696
Acupuncture Points
;
Acupuncture Therapy
;
Adult
;
Aged
;
Burning Mouth Syndrome
;
therapy
;
Female
;
Humans
;
Male
;
Middle Aged
;
Tongue
;
anatomy & histology
;
immunology
7.Association of the time that elapsed from last vaccination with protective effectiveness against foot-and-mouth disease in small ruminants.
Ehud ELNEKAVE ; Boris EVEN-TOV ; Boris GELMAN ; Beni SHARIR ; Eyal KLEMENT
Journal of Veterinary Science 2015;16(1):87-92
Routine and emergency vaccination of small ruminants against foot-and-mouth disease (FMD) is mandatory in many endemic countries, yet data on the field effectiveness of the vaccines used is scarce. We conducted an investigation of a serotype O FMD outbreak that took place in a sheep and goat pen, and estimated the effectiveness of various routine vaccination statuses. We also evaluated the protection provided by colostrum administration and emergency vaccination. Animals which were routinely vaccinated twice were not clinically affected while disease incidence was observed among animals routinely vaccinated only once (p = 0.004 according to a two-sided Fisher's exact test). In groups vaccinated only once, there was a significant association between the average time that elapsed since last vaccination and the disease incidence (n = 5; Spearman correlation coefficient: r(s) = 1.0, p < 0.01). In addition, non-vaccinated lambs fed colostrum from dams vaccinated more than 2 months before parturition had a mortality rate of 33%. Administration of emergency vaccination 2 days after the occurrence of the index case was the probable reason for the rapid blocking of the FMD spread within 6 days from its onset in the pen.
Animals
;
Colostrum
;
Disease Outbreaks/veterinary
;
Foot-and-Mouth Disease/*prevention & control
;
Goat Diseases/*prevention & control
;
Goats
;
Immunization Schedule
;
Sheep
;
Sheep Diseases/*prevention & control
;
Viral Vaccines/administration & dosage/*immunology
8.Dietary germanium biotite supplementation enhances the induction of antibody responses to foot-and-mouth disease virus vaccine in pigs.
Jin A LEE ; Bock Gie JUNG ; Myunghwan JUNG ; Tae Hoon KIM ; Han Sang YOO ; Bong Joo LEE
Journal of Veterinary Science 2014;15(3):443-447
We evaluated the potential ability of germanium biotite (GB) to stimulate the production of antibodies specific for foot-and-mouth disease virus (FMDV). To this aim, we measured the total FMDV-specific antibody responses and IgM production after vaccination against FMD both experimentally and in the field. GB supplementation with FMDV vaccination stimulated the production of anti-FMDV antibodies, and effectively increased IFN-gamma and TNF-alpha levels. These results suggest that GB may be a novel alternative feed supplement that can serve as a boosting agent and an immunostimulator for increasing the efficacy of FMDV vaccination in pigs.
Adjuvants, Immunologic/therapeutic use
;
Aluminum Silicates/*therapeutic use
;
Animals
;
Antibodies, Viral/*immunology
;
Antibody Formation/drug effects
;
*Dietary Supplements
;
Ferrous Compounds/*therapeutic use
;
Foot-and-Mouth Disease/*immunology/prevention & control
;
Foot-and-Mouth Disease Virus/immunology
;
Germanium/*therapeutic use
;
Swine
;
Swine Diseases/immunology/prevention & control/*virology
9.Advances in reverse genetics-based vaccines of foot and mouth disease.
Bo YANG ; Fan YANG ; Song-Hao WANG ; Yan ZHANG ; Wei-Jun CAO ; Hong YIN ; Hai-Xue ZHENG
Chinese Journal of Virology 2014;30(2):213-220
Reverse-genetic engineering of foot and mouth disease virus (FMDV) can improve the productivity, antigen matching, antigen stability, immune response ability, and biological safety of vaccines, so vaccine candidates with anticipated biological characteristics can be promptly achieved. Negative influence in taming of virulent strains can also be decreased or avoided. Reverse genetics not only make up for deficiencies like limitation of viral nature, low success rate, and time and energy consuming, but also realize more active designing of vaccines. Therefore, reverse genetics is significant in improving integral quality and efficiency of vaccines. In this review, we use FMDV vaccines as an example to summarize improvement in biological characteristics of virulent strains and provide a reference for related researches.
Animals
;
Antibodies, Viral
;
immunology
;
Foot-and-Mouth Disease
;
immunology
;
prevention & control
;
virology
;
Foot-and-Mouth Disease Virus
;
genetics
;
immunology
;
Reverse Genetics
;
Viral Vaccines
;
genetics
;
immunology
10.Oral microbiota and host innate immune response in bisphosphonate-related osteonecrosis of the jaw.
Smruti PUSHALKAR ; Xin LI ; Zoya KURAGO ; Lalitha V RAMANATHAPURAM ; Satoko MATSUMURA ; Kenneth E FLEISHER ; Robert GLICKMAN ; Wenbo YAN ; Yihong LI ; Deepak SAXENA
International Journal of Oral Science 2014;6(4):219-226
Bacterial biofilms have emerged as potential critical triggers in the pathogenesis of bisphosphonate (BP)-related osteonecrosis of the jaw (ONJ) or BRONJ. BRONJ lesions have shown to be heavily colonized by oral bacteria, most of these difficult to cultivate and presents many clinical challenges. The purpose of this study was to characterize the bacterial diversity in BRONJ lesions and to determine host immune response. We examined tissue specimens from three cohorts (n=30); patients with periodontal disease without a history of BP therapy (Control, n=10), patients with periodontal disease having history of BP therapy but without ONJ (BP, n=5) and patients with BRONJ (BRONJ, n=15). Denaturing gradient gel electrophoresis of polymerase chain reaction (PCR)-amplified 16S rRNA gene fragments revealed less bacterial diversity in BRONJ than BP and Control cohorts. Sequence analysis detected six phyla with predominant affiliation to Firmicutes in BRONJ (71.6%), BP (70.3%) and Control (59.1%). Significant differences (P<0.05) in genera were observed, between Control/BP, Control/BRONJ and BP/BRONJ cohorts. Enzyme-linked immunosorbent assay (ELISA) results indicated that the levels of myeloperoxidase were significantly lower, whereas interleukin-6 and tumor necrosis factor-alpha levels were moderately elevated in BRONJ patients as compared to Controls. PCR array showed significant changes in BRONJ patients with downregulation of host genes, such as nucleotide-binding oligomerization domain containing protein 2, and cathepsin G, the key modulators for antibacterial response and upregulation of secretory leukocyte protease inhibitor, proteinase 3 and conserved helix-loop-helix ubiquitous kinase. The results suggest that colonization of unique bacterial communities coupled with deficient innate immune response is likely to impact the pathogenesis of ONJ.
Actinobacteria
;
classification
;
Bacteria
;
classification
;
Bacteroidetes
;
classification
;
Biofilms
;
Bisphosphonate-Associated Osteonecrosis of the Jaw
;
immunology
;
microbiology
;
Bone Density Conservation Agents
;
therapeutic use
;
Cathepsin G
;
analysis
;
Cohort Studies
;
Down-Regulation
;
Female
;
Fusobacteria
;
classification
;
Gram-Negative Bacteria
;
classification
;
Host-Pathogen Interactions
;
immunology
;
Humans
;
I-kappa B Kinase
;
analysis
;
Immunity, Innate
;
immunology
;
Interleukin-6
;
analysis
;
Male
;
Middle Aged
;
Mouth
;
immunology
;
microbiology
;
Myeloblastin
;
analysis
;
antagonists & inhibitors
;
Nod2 Signaling Adaptor Protein
;
analysis
;
Periodontal Diseases
;
microbiology
;
Peroxidase
;
analysis
;
Proteobacteria
;
classification
;
Tumor Necrosis Factor-alpha
;
analysis

Result Analysis
Print
Save
E-mail