1.Research progress on role of chemokine receptor CCR3 signaling in allergic airway diseases.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2012;26(23):1099-1101
Allergic airway diseases have been identified as chronic inflammatory diseases of respiratory membranes, characterized by infiltration of many inflammatory cells, especially eosinophils. The expression of CCR3 is abundant on the cell surface of eosinophils. Increased accumulation of CCR3-driven inflammatory cells is thought to favor the development of allergy. In this review, we survey the properties of CCR3 and its ligands and highlight the roles of CCR3 signaling in allergic airway diseases.
Animals
;
Humans
;
Hypersensitivity
;
metabolism
;
Receptors, CCR3
;
metabolism
;
Respiratory System
;
metabolism
;
Signal Transduction
2.IgE binding patterns to German cockroach whole body extract in Korean atopic asthmatic children.
Soo Young LEE ; Dong Soo LEE ; Kyu Earn KIM ; Byung Joo JEAUNG ; Ki You LEE
Yonsei Medical Journal 1998;39(5):409-416
It is widely known that the cockroach is an inhalant allergen in atopic asthma and allergic rhinitis. Even though Bla g I and Bla g II are considered as the major allergens, several relatively high-molecular weight (MW) cockroach allergens have also been recently identified by IgE-immunoblot in western countries. However, the environmental control and diagnostic tests mainly focussed on Bla g I and Bla g II. Furthermore there is no data about major IgE-binding cockroach antigens in Korea. We performed this study to identify the major German cockroach allergens in Korean atopic children. By the results of allergy skin tests, 14 children with atopic asthma (9 were cockroach-sensitive and 5 were cockroach-nonsensitive atopics) were enrolled in this study. We conducted IgE immunoblot and autoradiographic analysis using Yonsei-extract of German cockroach antigen produced in our laboratory, individual sera from 9 cockroach- sensitive children, and the pooled sera of 5 house-dust-mites-only-sensitive children. We performed an allergic skin test to cockroach mix, and a radioallergosorbent test (RAST) using German cockroach crude extract on all subjects. German cockroach-specific IgE was detected in 6 out of 9 subjects by RAST. We identified at least 15 IgE-binding protein bands, and among them, the components of MWs of 76, 64, 50, 38, and <14 kilodaltons (kDa) were the major German cockroach allergens in study subjects. Therefore, Bla g I (25-30 kDa) and Bla g II (36 kDa) could not be the absolute indicators of German cockroach sensitization and parameters of environmental control.
Adolescence
;
Allergens/analysis
;
Animal
;
Asthma/metabolism*
;
Asthma/immunology
;
Asthma/complications
;
Child
;
Child, Preschool
;
Cockroaches/immunology
;
Cockroaches/chemistry*
;
Female
;
Human
;
Hypersensitivity/metabolism*
;
Hypersensitivity/immunology
;
Hypersensitivity/complications
;
IgE/metabolism*
;
Korea
;
Male
;
Tissue Extracts/metabolism*
4.Platelet Additive Solutions.
Jin Hyuk YANG ; So Yong KWON ; Juyeon LEE ; Yong Hun JEE ; Myunghan KIM
Korean Journal of Blood Transfusion 2013;24(3):207-216
Storage of platelet concentrates in platelet additive solution (PAS) with plasma removal has many advantages, including reduction of allergic reactions, contributing to the available plasma pool for fractionation or transfusion, and employment of pathogen reduction technology. In order to decrease platelet activation for improvement of in vivo viability, PAS should be designed for optimization of aerobic metabolism using compounds such as glucose, acetate, citrate, phosphate, and electrolytes. After a thorough discussion, particularly on the efficacy and regulations, use of the buffy coat method as well as application of a new generation of PAS may likely be the future direction of platelet storage in Korea.
Blood Platelets*
;
Citric Acid
;
Electrolytes
;
Employment
;
Glucose
;
Hypersensitivity
;
Korea
;
Metabolism
;
Plasma
;
Platelet Activation
;
Social Control, Formal
5.The role of vitamin D in allergic rhinitis
Asia Pacific Allergy 2017;7(2):65-73
Recent studies suggest that vitamin D is related to allergic rhinitis (AR). In this review, we first discuss the physiology and metabolism of vitamin D, then we review the function of vitamin D in the immune system, and above all, we highlight the current research regarding the role of vitamin D in AR. Finally, we find that there are both experimental and clinical studies showing that vitamin D is associated with AR, although the results are not consistent and even conflicting. Evidences from those clinical studies show a slightly tendency that serum vitamin D level might be inversely associated with the risk of AR. Meanwhile, it seems that gender and age may influence the relationship between vitamin D and AR. However, because of the heterogeneity in defining AR, differences in study design and so on, all these findings need to be confirmed by further studies. Additional clinical studies as well as experimental research are needed to better understand how vitamin D influences AR.
Hypersensitivity
;
Immune System
;
Metabolism
;
Physiology
;
Population Characteristics
;
Rhinitis, Allergic
;
Vitamin D
;
Vitamins
6.Major house dust mite allergen, Der p I, activates phospholipase D in human peripheral blood mononuclear cells from allergic patients: involvement of protein kinase C.
Jae Won OH ; Jong Hoon KIM ; Ki Sung LEE ; Joong Soo HAN
Experimental & Molecular Medicine 2000;32(2):67-71
The major house-dust-mite allergen, Der p I, stimulates the phospholipase D (PLD) in peripheral blood mononuclear cells (PBMC) from allergic patients with maximal responses after 30 min exposure. At 30 min, Der p I stimulated PLD activity by 1.4-fold in mild, 1.6-fold in moderate and 2-fold in severe allergic patients over control values (p < 0.05). When the cells were pretreated for 24 h with phorbol myristate acetate to down-regulate protein kinase C (PKC), PLD stimulation by Der p I was largely abolished. These results indicate that in PBMC from allergic patients, Der p I can stimulate PLD activity, and that PKC activation is involved in this stimulation.
Adult
;
Allergens/metabolism*
;
Allergens/immunology
;
Animal
;
Down-Regulation (Physiology)
;
Glycoproteins/metabolism*
;
Glycoproteins/immunology
;
Human
;
Hypersensitivity/metabolism
;
Hypersensitivity/immunology
;
Hypersensitivity/blood
;
IgE/blood
;
In Vitro
;
Leukocytes, Mononuclear/metabolism
;
Leukocytes, Mononuclear/immunology
;
Mites/metabolism
;
Mites/immunology
;
Phospholipase D/metabolism*
;
Phospholipase D/immunology
;
Protein Kinase C/metabolism*
;
Skin Tests
;
Tetradecanoylphorbol Acetate/pharmacology
7.Effect of cetirizine hydrochloride on the expression of substance P in IgE-mediated triphasic cutaneous reaction.
Ji-Yong LIU ; Jin-Hong HU ; Quan-Gang ZHU ; Feng-Qian LI ; Hua-Jun SUN
Acta Pharmaceutica Sinica 2005;40(7):649-653
AIMTo investigate the effect of cetirizine hydrochloride on the expression of neuropeptide substance P (SP) in IgE-dependent triphasic cutaneous reaction induced by dinitrofluorobenzene (DNFB) in the ears of BALB/c mice.
METHODSBALB/c mice were passively sensitized by intravenous infection of anti-DNP IgE monoclonal antibody 24 h before DNFB challenge. Skin reaction was elicited by applying DNFB to both sides of each ear of sensitized mice. Mice were treated with cetirizine (1 and 10 mg x kg)-1), ig). The ears were removed for pathohistological examination and immunohistochemical staining of SP at different designated times after challenge. The contents of SP in the skin of mouse ear were determined by radioimmunoassay (RIA).
RESULTSThe mice exhibited a triphasic cutaneous reaction with an immediate-phase response (IPR) at 1 h, a late-phase response (LPR) at 24 h and a very late-phase response (vLPR) at 7 days after challenge with DNFB. The expression of SP in different phases increased gradually. Cetirizine (1 and 10 mg x kg(-1)) was shown to significantly inhibit the ear swellings induced by the IPR (P < 0.01), while no obvious effect on the vLPR. The SP contents in ear skin of triphasic cutaneous reaction were decreased by cetirizine.
CONCLUSIONSP is considered to be involved in the pathogenesis of allergic dermatitis. Cetirizine hydrochloride can inhibit the expression of SP in IgE-dependent triphasic cutaneous reaction. It might be part of the mechanisms of anti-anaphylaxis of cetirizine.
Animals ; Anti-Allergic Agents ; pharmacology ; Cetirizine ; pharmacology ; Dose-Response Relationship, Drug ; Ear ; Edema ; metabolism ; Female ; Hypersensitivity, Delayed ; metabolism ; Hypersensitivity, Immediate ; metabolism ; Immunoglobulin E ; immunology ; Mice ; Mice, Inbred BALB C ; Passive Cutaneous Anaphylaxis ; drug effects ; Substance P ; metabolism
8.Recognition of self and altered self by T cells in autoimmunity and allergy.
Lei YIN ; Shaodong DAI ; Gina CLAYTON ; Wei GAO ; Yang WANG ; John KAPPLER ; Philippa MARRACK
Protein & Cell 2013;4(1):8-16
T cell recognition of foreign peptide antigen and tolerance to self peptides is key to the proper function of the immune system. Usually, in the thymus T cells that recognize self MHC + self peptides are deleted and those with the potential to recognize self MHC + foreign peptides are selected to mature. However there are exceptions to these rules. Autoimmunity and allergy are two of the most common immune diseases that can be related to recognition of self. Many genes work together to lead to autoimmunity. Of those, particular MHC alleles are the most strongly associated, reflecting the key importance of MHC presentation of self peptides in autoimmunity. T cells specific for combinations of self MHC and self peptides may escape thymus deletion, and thus be able to drive autoimmunity, for several reasons: the relevant self peptide may be presented at low abundance in the thymus but at high level in particular peripheral tissues; the relevant self peptide may bind to MHC in an unusual register, not present in the thymus but apparent elsewhere; finally the relevant self peptide may be post translationally modified in a tissue specific fashion. In some types of allergy, the peptide + MHC combination may also be fully derived from self. However the combination in question may be modified by the presence of other ligands, such as small drug molecules or metal ions. Thus these types of allergies may act like the post translationally modified peptides involved some types of autoimmunity.
Animals
;
Autoantigens
;
immunology
;
Autoimmunity
;
HLA Antigens
;
immunology
;
Humans
;
Hypersensitivity
;
immunology
;
Receptors, Antigen, T-Cell
;
metabolism
;
T-Lymphocytes
;
immunology
;
metabolism
9.Prevalence of Soy Protein Hypersensitivity in Cow's Milk Protein-Sensitive Children in Korea.
Kang Mo AHN ; Young Shin HAN ; Seung Yeon NAM ; Hwa Young PARK ; Mee Yong SHIN ; Sang Il LEE
Journal of Korean Medical Science 2003;18(4):473-477
This study was aimed to evaluate the prevalence of soy protein hypersensitivity in cow's milk protein-sensitive children in Korea. A total of 1,363 patients with atopic dermatitis, urticaria, enterocolitis syndrome, bronchial asthma or allergic rhinitis were recruited. First, we estimated the prevalence of sensitization to soy in children sensitized to cow's milk. Specific IgE levels > 0.7 kU/L by CAP assay were considered positive. Next, the prevalence of soy allergy in cow's milk allergy (CMA) patients was investigated. Those children whose parents agreed to participate the open challenge test with soy had a convincing history of allergic reactions elicited by cow's milk and these symptoms were relieved by elimination. All of them had negative soy-specific IgE. Patients with positive soy-specific IgE accounted for 18.3% of 224 children sensitized to cow's milk protein. The prevalence of sensitization to soy decreased with age (36.8% in the first year of life, 16.4% in the second year, and 13.7% in the third year). Of 21 CMA patients, 42.9% (n=9) were determined to have soy allergy (mean age 10.3 months). Our results suggest that soy protein formula should be carefully used as a substitute for cow's milk in CMA patients, especially during infancy.
Adolescent
;
Age Factors
;
Allergens
;
Asthma/immunology
;
Child
;
Child, Preschool
;
Dermatitis, Atopic/immunology
;
Enterocolitis/immunology
;
Female
;
Food Hypersensitivity/*epidemiology/immunology
;
Human
;
Hypersensitivity
;
Immunoglobulin E/blood/metabolism
;
Infant
;
Korea
;
Male
;
Milk Hypersensitivity/*epidemiology/immunology
;
Prevalence
;
Rhinitis/immunology
;
Soybean Proteins/*chemistry
;
Urticaria/immunology
10.Allergens-induced sensitization alters airway epithelial adhesion molecules expression in mice.
Dan ZENG ; Mei-Ling TAN ; Yang XIANG ; Xiao-Qun QIN ; Li-Ming ZHU ; Ai-Guo DAI
Acta Physiologica Sinica 2015;67(6):596-602
To explore the relationship between the epithelial adhesion molecules and immune responses of airway epithelium, we observed the expression of integrin β4 and intercellular adhesion molecule-1 (ICAM-1) in the mice airway epithelium after sensitization with allergens. BALB/c mice were sensitized with intraperitoneal injection of ovalbumin (OVA) or house dust mite (HDM) and then developed airway hyper-responsiveness as determined by barometric whole-body plethysmography. Both OVA and HDM sensitization led to increases of the number of peripheral leukocytes as well as inflammatory cells infiltration in lungs. OVA sensitized mice showed more severe inflammatory cells infiltration than HDM sensitized mice. Immunohistochemistry analysis of mice lung tissues revealed that sensitization with both allergens also led to a decrease of integrin β4 expression and an increase of ICAM-1 expression in airway epithelia. OVA sensitized mice showed a more significant increase of ICAM-1 expression compared with HDM sensitized mice. siRNA mediated silencing of integrin β4 gene in 16HBE cells resulted in an up-regulation of ICAM-1 expression. Our results indicate a possible role of airway epithelial adhesion molecules in allergen-induced airway immune responses.
Allergens
;
pharmacology
;
Animals
;
Integrin beta4
;
metabolism
;
Intercellular Adhesion Molecule-1
;
metabolism
;
Lung
;
metabolism
;
physiopathology
;
Mice
;
Mice, Inbred BALB C
;
Ovalbumin
;
Pyroglyphidae
;
Respiratory Hypersensitivity
;
metabolism