Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Eu Kyoung Lee is active.

Publication


Featured researches published by Eu Kyoung Lee.


Asia Pacific Allergy | 2015

Immunoglobulin E to allergen components of house dust mite in Korean children with allergic disease

Hwan Soo Kim; Sung Hee Kang; Sulmui Won; Eu Kyoung Lee; Yoon Hong Chun; Jong-Seo Yoon; Hyun Hee Kim; Jin Tack Kim

Background House dust mites (HDMs) are important sources of indoor allergens. Seventeen components have been identified from Dermatophagoides pteronyssinus (Der p). Objective Our aim was to define the prevalence of specific IgE to components of Der p in Korea and investigate the clinical features of them in children with allergic disease. Methods We performed a prospective evaluation of 80 HDM sensitized patients with history of allergic rhinitis (AR), atopic dermatitis (AD), asthma and urticaria (UC). Patients underwent ImmunoCAP for total IgE, Der p, Der f, Der p 1, Der p 2, and Der p 10. Results Seventy-nine patients had detectable serum IgE to Der p, 80 patients were sensitized to Der f, 66 patients were sensitized to Der p 1, 63 patients to Der p 2, and 7 patients were sensitized to Der p 10. Der p 1 specific IgE was significantly lower in the UC group compared with the AD and AR group. Total IgE was significantly higher in the Der p 10 sensitized group. Der p 10 serum IgE level was highly correlated with crab and shrimp specific IgE. There was a significant positive correlation between total IgE and specific IgE to Der p and its components and Der f. Conclusion Sensitization to HDM and its components in Korea is similar to previous studies from temperate climate. The determination of Der p 1, Der p 2, and Der p 10 specific IgE helps in obtaining additional information in regards to allergic disease.


Korean Journal of Pediatrics | 2013

The effect of rhinovirus on airway inflammation in a murine asthma model.

Eugene Kim; Huisu Lee; Hyun Sook Kim; Sulmui Won; Eu Kyoung Lee; Hwan Soo Kim; Kyongwon Bang; Yoon Hong Chun; Jong-Seo Yoon; Hyun Hee Kim; Jin Tack Kim; Joon Sung Lee

Purpose The aim of the present study was to investigate the differences in lower airway inflammatory immune responses, including cellular responses and responses in terms of inflammatory mediators in bronchoalveolar lavage fluid (BALF) and the airway, to rhinovirus (RV) infection on asthma exacerbation by comparing a control and a murine asthma model, with or without RV infection. Methods BALB/c mice were intraperitoneally injected with a crude extract of Dermatophagoides farinae (Df) or phosphate buffered saline (PBS) and were subsequently intranasally treated with a crude extract of Df or PBS. Airway responsiveness and cell infiltration, differential cell counts in BALF, and cytokine and chemokine concentrations in BALF were measured 24 hours after intranasal RV1B infection. Results RV infection increased the enhanced pause (Penh) in both the Df sensitized and challenged mice (Df mice) and PBS-treated mice (PBS mice) (P<0.05). Airway eosinophil infiltration increased in Df mice after RV infection (P<0.05). The levels of interleukin (IL) 13, tumor necrosis factor alpha, and regulated on activation, normal T cells expressed and secreted (RANTES) increased in response to RV infection in Df mice, but not in PBS mice (P<0.05). The level of IL-10 significantly decreased following RV infection in Df mice (P<0.05). Conclusion Our findings suggest that the augmented induction of proinflammatory cytokines, Th2 cytokines, and chemokines that mediate an eosinophil response and the decreased induction of regulatory cytokines after RV infection may be important manifestations leading to airway inflammation with eosinophil infiltration and changes in airway responsiveness in the asthma model.


Pediatric Pulmonology | 2016

Pentraxin 3 as a clinical marker in children with lower respiratory tract infection

Hwan Soo Kim; Sulmui Won; Eu Kyoung Lee; Yoon Hong Chun; Jong-Seo Yoon; Hyun Hee Kim; Jin Tack Kim

Pentraxin 3 (PTX‐3) is an acute‐phase protein that increases in the plasma during inflammation.


Iranian Journal of Pediatrics | 2015

The Early Intestinal Microbiota of Healthy Korean Newborns

Eu Kyoung Lee; Young Tae Ahn; Chul-Sung Huh; Hwan Soo Kim; Eugene Kim; Yoon Hong Chun; Jong-Seo Yoon; Hyun Hee Kim; Jin Tack Kim

Background: The microflora hypothesis may be the underlying explanation for the growth of inflammatory disease. In addition to many known affecting factors, knowing the gut microbiota of healthy newborns can help to understand the gut immunity and modulate it. Objectives: This study examined the microbiota of healthy newborns from urban regions. Patients and Methods: We enrolled 128 full-term newborns, born at Seoul St. Mary and St. Paul hospital from January 2009 to February 2010. All 143 samples of feces were cultivated in six culture plates to determine the amounts of total bacteria, anaerobes, gram-positive bacteria, coliforms, lactobacilli, and bifidobacteria. The samples were evaluated with a bivariate correlation between coliforms and lactobacilli. Terminal restriction fragment length polymorphism (T-RFLP) analysis with HhaI and MspI and a clustering analysis were performed for determination of diversity. Results: Bacteria were cultured in 61.5% of feces in the following order: anaerobes, gram-positive bacteria, lactobacilli, coliform, and bifidobacteria. The growth of total bacteria and lactobacilli increased in feces defecated after 24 hours of birth (P < 0.001, P = 0.008) and anaerobes decreased (P = 0.003). A negative correlation between the growth of lactobacilli and coliforms was found (r = -463, P < 0.001). Conclusions: This study confirms that bacterial colonization of healthy newborns born in cities is non-sterile, but has early diversification and inter-individuality.


Annals of Saudi Medicine | 2015

Eosinophil-related markers and total immunoglobulin E as a predictive marker for antibiotic response in chronic rhinosinusitis.

Youn Ho Shin; Hwan Soo Kim; Eu Kyoung Lee; Young Joo Kim; H. J. Lee; Pil-Sang Jang; Young Hoon Kim; Yoon Hong Chun; Jong-Seo Yoon; Hyun Hee Kim; Young-Yull Koh; Jin Tack Kim

BACKGROUND AND OBJECTIVES Chronic rhinosinusitis (CRS) is a commonly diagnosed disease that has a significant impact on a child’s quality of life. However, no useful biomarker is available to identify antibiotic-responsive CRS. We determined the significance of eosinophil-related markers and total IgE levels in childhood CRS with regard to antibiotic response. DESIGN AND SETTING This was a case-control study of patients admitted to Uijeongbu St. Mary’s Hospital between November 2010 and November 2011 and diagnosed with CRS. PATIENTS AND METHODS In this analytical cross-sectional study, we identified children whose symptoms and radiologic abnormalities did not resolve after 12 weeks despite appropriate antibiotics (non-responder CRS group), children whose symptoms and radiologic abnormalities resolved after 12 weeks with appropriate antibiotics (responder CRS group), and healthy controls selected from clinic patients. Skin prick tests were performed along with serum total IgE, total eosinophil count (TEC), serum eosinophil cationic protein (ECP) level, and ImmunoCAP analysis for common allergens. RESULTS This study included 36 responders, 22 nonresponders and 22 healthy controls. The prevalence of allergic diseases, atopy, and a family history of allergic diseases were significantly higher in the non-responder group than in the responder and control groups. TEC, ECP, and total IgE levels were significantly higher in the non-responder group than in the responder and control groups (all P<.05). Multiple linear regression analysis showed that no response to appropriate antibiotics and TEC was positively associated with ECP concentration. CONCLUSION These findings suggest that there is a high prevalence of allergic diseases in the non-responder group, that the TEC and ECP levels in the non-responder group are significantly higher than those in the responder group and controls, and that no response to antibiotics may be due to eosinophilic inflammation. The measurement of serum ECP may be useful in monitoring the progress of childhood CRS with regard to antibiotic response.


Clinical and Experimental Otorhinolaryngology | 2017

Effect of Proparacaine in a Mouse Model of Allergic Rhinitis

Hwan Soo Kim; Sulmui Won; Eu Kyoung Lee; Yoon Hong Chun; Jong-Seo Yoon; Jin Tack Kim; Hyun Hee Kim

Objectives Lidocaine, a local anaesthetic is a treatment option in uncontrolled asthma due to its immunomodulatory effects. In the present study, proparacaine (PPC), a derivative of lidocaine was examined for its therapeutic application in a mouse model of allergic rhinitis. Methods The mice were grouped into 4 groups: control group, allergic rhinitis (AR) group, ciclesonide (CIC) group, and PPC group. Nasal symptom scores, eosinophil counts, goblet cell counts, and mast cells counts in the nasal mucosa were measured. Serum ovalbumin (OVA)-specific immunoglobulin (Ig) E, OVA-specific IgG1, OVA-specific IgG2a, interleukin (IL)-4, IL-5, and cortisol levels were measured. Results Intranasal administration of PPC significantly decreased nasal symptoms, number of eosinophils, goblet cells, and mast cells in the lamina propria of the nasal mucosa. Serum OVA-specific IgE, OVA-specific IgG1, OVA-specific IgG2a was significantly higher in the AR compared with the control group. Serum level of IL-4 was significantly lower in the CIC group and PPC group in comparison with AR group. Serum IL-5 showed no significant difference among all groups. No significant difference in serum cortisol levels was observed among the 4 groups. Conclusion PPC appears to have a therapeutic potential in treatment of allergic rhinitis in a mouse model by reducing eosinophil, goblet cell, and mast cell infiltration in the nasal mucosa.


Korean Journal of Pediatrics | 2013

A case of familial X-linked thrombocytopenia with a novel WAS gene mutation

Eu Kyoung Lee; Yeun-Joo Eem; Nack Gyun Chung; Myung Shin Kim; Dae Chul Jeong

Wiskott-Aldrich syndrome (WAS) is an inherited X-linked disorder. The WAS gene is located on the X chromosome and undergoes mutations, which affect various domains of the WAS protein, resulting in recurrent infection, eczema, and thrombocytopenia. However, the clinical features and severity of the disease vary according to the type of mutations in the WAS gene. Here, we describe the case of a 4-year-old boy with a history of marked thrombocytopenia since birth, who presented with recurrent herpes simplex infection and late onset of eczema. Examination of his family history revealed that older brother, who died from intracranial hemorrhage, had chronic idiopathic thrombocytopenia. Therefore, we proceeded with genetic analysis and found a new deletion mutation in the WAS gene: c.858delC (p.ser287Leufs*21) as a hemizygous form.


Allergy, Asthma & Respiratory Disease | 2014

Outcome of acute respiratory distress syndrome in children: a single center study

Sung Shil Kang; Ra Mee Pae; Eu Kyoung Lee; Kyung Won Bang; Hwan Soo Kim; Yoon Hong Chun; Jong-Seo Yoon; Hyun Hee Kim; Jin Tack Kim; Joon Sung Lee


The Journal of Allergy and Clinical Immunology | 2015

Immunoglobulin E to Allergen Components of House Dust Mite in Children with Allergic Disease

Jong-Seo Yoon; Sulmui Won; Eu Kyoung Lee; Hwan Soo Kim; Yoon Hong Chun; Hyun Hee Kim; Jin-Tack Kim


Journal of Pediatric infectious diseases | 2014

Congenital Syphilis: An Uncommon Cause of Gross Hematuria, Skin Rash, and Pneumonia

Sun Hee Shim; Ju Young Kim; Eu Kyoung Lee; Kyongwon Bang; Kyoung Soon Cho; Juyoung Lee; Jin Soon Suh; Joong Hyun Bin; Hyun Hee Kim; Won Bae Lee

Collaboration


Dive into the Eu Kyoung Lee's collaboration.

Top Co-Authors

Avatar

Hyun Hee Kim

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Hwan Soo Kim

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Jong-Seo Yoon

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Yoon Hong Chun

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Jin Tack Kim

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Sulmui Won

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Joon Sung Lee

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Eugene Kim

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Jin-Tack Kim

Catholic University of Korea

View shared research outputs
Top Co-Authors

Avatar

Kyongwon Bang

Catholic University of Korea

View shared research outputs
Researchain Logo
Decentralizing Knowledge