1.A Case of Toxic Epidermal Necrolysis.
Eun Hwa SHIN ; Youn Hong CHOI ; Ju Hong CHA ; Kwang Jun KI ; Kyung Je SUNG
Journal of the Korean Pediatric Society 1988;31(8):1079-1084
No abstract available.
Stevens-Johnson Syndrome*
2.Oral Tolerance Increased the Proportion of CD8+ T Cells in Mouse Intestinal Lamina Propria.
Kyung Ah CHO ; Je Eun CHA ; So Youn WOO
Immune Network 2008;8(2):46-52
BACKGROUND: Oral tolerance is defined by the inhibition of immune responsiveness to a protein previously exposed via the oral route. Protein antigens exposed via the oral route can be absorbed through the mucosal surfaces of the gastrointestinal tract and can make physical contact with immune cells residing in the intestinal lamina propria (LP). However, the mechanisms of oral tolerance and immune regulation in the intestines currently remain to be clearly elucidated. METHODS: In order to determine the effect of oral protein antigen intake (ovalbumin, OVA) on the intestinal LP, we assessed the expression profile of the T cell receptor and the co-receptors on the cells from the intestines of the tolerant and immune mouse groups. RESULTS: We determined that the proportion of OVA-specific B cells and gamma delta T cells had decreased, but the CD8alpha beta and CD8alpha alpha T cells were increased in the LP from the tolerant group. The proportion of CD8+ T cells in the spleen did not evidence any significant differences between treatment groups. CONCLUSION: These results indicate that CD8+ T cells in the intestinal LP may perform a regulatory role following antigen challenge via the oral route.
Animals
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B-Lymphocytes
;
Gastrointestinal Tract
;
Intestines
;
Mice
;
Mucous Membrane
;
Ovalbumin
;
Receptors, Antigen, T-Cell
;
Spleen
;
T-Lymphocytes
3.Endometrial Carcinoma in 46, X, I(X)(q 10)Turner s Syndrome without Hormone Replacement Therapy.
Kyong Bong CHA ; Sang Tak UM ; Eun Ju LEE ; Sang Yun OH ; Chang Soo PARK ; Duk Soo BAE ; Je Ho LEE
Korean Journal of Obstetrics and Gynecology 2000;43(10):1837-1839
No abstract available.
Endometrial Neoplasms*
;
Female
;
Hormone Replacement Therapy*
4.Escherichia coli pap Genes as well as Adenovirus Type 11 and Type 21, and BK Virus were Involved with Severe Urinary Tract Infection in Infants.
Hae Kyung PARK ; So Youn WOO ; Eun Ok LEE ; Je Eun CHA ; Ko Eun LEE ; Haesook PARK ; Seung Joo LEE
Journal of Bacteriology and Virology 2011;41(4):245-254
In infants, urinary tract infections (UTIs) are quite common and primarily caused by bacterial pathogens. However, little research has been conducted regarding the relationship between uropathogenic bacteria, virulent genes, and uropathogenic viruses that might induce UTIs in infants. In this study, we evaluated infants with UTIs to determine the influence of bacterial virulent genes and type of viral infections on clinical aspects. First, we detected 44 cases of bacterial UTI from 600 suspected cases in infants and children. We detected E. coli urovirulence genes (kps, usp, pap, ireA, and cnf), two enteropathogenic E. coli genes (bfpA, and eae) and four S. aureus and S. epidermidis genes (mecA, pvl, bbp, and icaA) in urine samples from infant UTI cases. We also simultaneously detected hematuria-related adenovirus type 11, 21, and BK virus (BKV) in urine samples by PCR. As a result, E. coli was the most prevalent bacteria and in Dimercaptosuccinic acid (DMSA)-positive UTI cases, the uropathogenic E. coli virulence factor pap was significantly high. We found that BKV detection was significantly higher in DMSA-positive UTI infants (89%) compared with 50% of non-UTI (no bacteria detected) cases. These results are indicative of combined multiple bacterial and viral infections and show severe infant pyelonephritis.
Adenoviridae
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Bacteria
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Benzophenones
;
BK Virus
;
Boronic Acids
;
Child
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Enteropathogenic Escherichia coli
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Escherichia
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Escherichia coli
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Humans
;
Infant
;
Polymerase Chain Reaction
;
Pyelonephritis
;
Succimer
;
Urinary Tract
;
Urinary Tract Infections
5.Detection of Virulence Genes of Staphyloccus aureus and Staphylococcus epidermidis Isolated from Suprapubic Urine from Infants with Fever.
Hae Kyung PARK ; So Youn WOO ; Yun Jae JUNG ; Eun Ok LEE ; Je Eun CHA ; Hye Sook PARK ; Seung Joo LEE
Journal of Bacteriology and Virology 2008;38(4):189-196
While methicillin-resistant Staphylococcus aureus (MRSA) isolated from urinary tract infection (UTI) has recently increased in elderly adult urology patients, it has been only rarely reported in infants. Therefore, in this study to understand whether MRSA may be involved in UTI of infants who run fever without other apparent causes, we identified and counted S. aureus and S. epidermidis in suprapubic urine from 750 febrile infants via microbiological methods, and confirmed the counts via multiplex PCR. And we also detected four virulence genes, mecA, PVL, bbp and icaA genes for S. aureus and S. epidermidis via multiplex PCR in the same specimens. S. aureus (28 cases) counts were as follows: >10(4) CFU/ml (3/28), 10(2)~10(3) CFU/ml (1/28) and <10(2)~10(3) CFU/ml (24/28). S. epidermidis (26 cases) counts were as follows: >10(4) CFU/ml (2/26), 10(2)~10(3) CFU/ml (4/26) and 10(2)~10(3) CFU/ml (20/26). S. aureus virulence genes were detected in 26 cases as mecA (16/26, 59.3%), PVL (17/26, 63.0%), bbp (7/26, 26.9%) and icaA (20/26, 76.9%). S. epidermidis virulence genes were detected in 22 cases as mecA (17/22, 81.0%), PVL (15/22, 71.4%), bbp (3/22, 13.6%) and icaA (13/22, 50.1%). Therefore, mecA, PVL and icaA genes of MRSA and MRSE were detected with high positivity in urines from infants with fever. The results demonstrate that community-acquired MRSA or MRSE may be responsible for UTI incidence in febrile infants.
Adenosine
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Adult
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Aged
;
Benzophenones
;
Boronic Acids
;
Fever
;
Humans
;
Incidence
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Infant
;
Methicillin-Resistant Staphylococcus aureus
;
Multiplex Polymerase Chain Reaction
;
Staphylococcus
;
Staphylococcus aureus
;
Staphylococcus epidermidis
;
Urinary Tract Infections
;
Urology
6.Effect on Cell Cycle Progression by N-Myc Knockdown in SK-N-BE(2) Neuroblastoma Cell Line and Cytotoxicity with STI-571 Compound.
Un Young YU ; Je Eun CHA ; Sun Young JU ; Kyung Ah CHO ; Eun Sun YOO ; Kyung Ha RYU ; So Youn WOO
Cancer Research and Treatment 2008;40(1):27-32
PURPOSE: Neuroblastoma is a common tumor in childhood, and generally exhibits heterogeneity and a malignant progression. MYCN expression and amplification profiles frequently correlate with therapeutic prognosis. Although it has been reported that MYCN silencing causes differentiation and apoptosis in human neuroblastoma cells, MYCN expression influences the cytotoxic potential of chemotherapeutic drugs via the deregulation of the cell cycle. STI-571 may constitute a promising therapeutic agent against neuroblastoma, particularly in cases in which c-Kit is expressed preferentially in MYCN-amplified neuroblastoma. MATERIALS AND METHODS: To determine whether STI-571 exerts a synergistic effect on cytotoxicity with MYCN expression, we assessed apoptotic cell death and cell cycle distribution after 72 h of exposure to STI-571 with or with out treatment of SK-N-BE(2) neuroblastoma cells with MYCN siRNA. RESULTS: MYCN siRNA-treated SK-N-BE(2) cells did not affect apoptosis and cells were arrested in G0/G1 phase after STI-571 treatment. CONCLUSIONS: siRNA therapy targeted to MYCN may not be effective when administered in combination with STI-571 treatment in cases of neuroblastoma. Therefore, chemotherapeutic drugs that target S or G2-M phase may prove ineffective when applied to cells arrested in the G0/1 phase as the result of MYCN knockdown and STI-571 treatment.
Apoptosis
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Benzamides
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Cell Cycle
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Cell Death
;
Cell Line
;
Humans
;
Neuroblastoma
;
Piperazines
;
Population Characteristics
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Prognosis
;
Pyrimidines
;
Imatinib Mesylate
;
RNA, Small Interfering
7.Changes of the Video Head Impulse Test Gains by the Directions of Head Rotation at Different Target Distances and Rotation Speeds.
Chan Il SONG ; Yeong Eun KIM ; Eun Hye CHA ; Myung Hoon YOO ; Je Yeon LEE ; Hong Ju PARK
Korean Journal of Otolaryngology - Head and Neck Surgery 2015;58(8):547-551
BACKGROUND AND OBJECTIVES: The conventional instrument for video head impulse test (vHIT) records the movement of the right eye only. The aim of this study was to evaluate the changes in the gain of vHIT results qdue to different directions of head rotation directons at different target distances and rotation speeds. SUBJECTS AND METHOD: Horizontal head impulse was recorded by vHIT in 20 normal subjects. vestibulo-ocular reflex (VOR) gains to the right and left directions were compared at different test conditions. Two different impulses with low (50-150 deg/sec) and high (200-300 deg/sec) peak-head-velocities were tested and the subjects were also instructed to fixate a laser dot on a screen at different distances of 60, 100, and 200 cm. Eye movements were recorded on the right eye. RESULTS: Regardless of the target distances and peak-head-velocities, the VOR gains to the rightward head rotation were significantly greater than those to the leftward head rotation. In more than 85% of normal subjects, vHIT gain to the rightward head rotation was greater than that to the leftward head rotation. Mean gain asymmetries were 2.16-3.33% and the mean interaural vHIT gain differences were 0.04-0.07. CONCLUSION: Regardless of the target distances and peak-head-velocities, the VOR gains to the rightward head rotation were significantly greater than those to the leftward head rotation. Directional asymmetry of VOR gain should be considered when interpreting vHIT results in patients with vestibular disorders.
Eye Movements
;
Head Impulse Test*
;
Head*
;
Humans
;
Reflex, Vestibulo-Ocular
8.Detection of HBV YMDD Mutation by Sequencing Method.
Yong Hak SOHN ; Choong Hwan CHA ; Seongsoo JANG ; Han Joo LEE ; Kwan Je LEE ; Eun Soon SHIN ; Heung Bum OH
The Korean Journal of Laboratory Medicine 2003;23(4):292-297
BACKGROUND: YMDD motif variants of the hepatitis B virus (HBV) emerge in some chronic hepatitis B patients after prolonged lamivudine treatment. HBV DNA breakthrough may be accompanied by the emergence of YMDD variants. The detection of YMDD motif variants will be necessary since Adefovir dipivoxil was recently approved to be an effective treatment for lamivudine-resistant patients. METHODS: Samples were chosen from twenty-one patients who experienced the DNA breakthrough after an undetectable HBV DNA period by HBV DNA hybrid-capture assay. We tested the samples of each stage for detection of YMDD motif variants by a sequencing method using Accu-Typer(TM) HBV YMDD typing Kit (DNA Link, Seoul, Korea) and ABI PRISM 3700 DNA Analyzer. RESULTS: All 17 samples that were collected before treatment had the wild-type YMDD motif. Of 20 samples amplified, which were from the undetectable HBV DNA period, three (15%) samples showed YMDD mutation. After DNA breakthrough, YMDD mutants were detected in 13 (63%) of 21 samples (YIDD 8 cases, YVDD 5 cases). CONCLUSION: We could reconfirmed that YMDD motif variants were remarkably related to the lamivudin resistance. YMDD motif variants; however, were not detected in one-third of the lamivudine resistance. The sequencing method of our study would be useful in providing the neighboring nucleotide information other than the YMDD motif in patients experiencing DNA breakthrough.
DNA
;
Hepatitis B virus
;
Hepatitis B, Chronic
;
Humans
;
Lamivudine
;
Seoul
9.Plasmodium falciparum Cultivation Using the Petri Dish: Revisiting the Effect of the 'Age' of Erythrocytes and the Interval of Medium Change.
Young A KIM ; Je Eun CHA ; Sun Young AHN ; Seung Ho RYU ; Joon Sup YEOM ; Hyo Il LEE ; Chang Gyun KIM ; Ju Young SEOH ; Jae Won PARK
Journal of Korean Medical Science 2007;22(6):1022-1025
Differences in the characteristics of the culture conditions can influence the multiplication rate of Plasmodium falciparum. The Petri dish method is one of the most popular methods of cultivating this parasite. In many previous studies, ideal culture conditions of the Petri dish method were achieved by using erythrocytes collected from blood that had been stored for at least 2 weeks, with daily changes of the medium. In the present study, we studied the multiplication rate of P. falciparum in cultures containing erythrocytes of various ages together with changing the medium at various intervals of time. Our results strongly suggest that the rate of in vitro multiplication of P. falciparum was higher in freshly collected erythrocytes than in aged erythrocytes regardless of the anticoagulant and that when the parasitemia is lower than 8% with a hematocrit of 5%, the medium change interval can be as long as 48 hr without a great reduction in the rate of multiplication.
Animals
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Blood Specimen Collection
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Cell Aging
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Culture Media
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Erythrocytes/*parasitology
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Plasmodium falciparum/*growth & development
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Time Factors
10.Genotype Analysis of Hepatitis B Virus Isolated from Korean Hepatitis Patients.
Choong Hwan CHA ; Yong Hak SOHN ; Seong soo JANG ; Han Joo LEE ; Kwan Je LEE ; Eun Soon SHIN ; Heung Bum OH
The Korean Journal of Laboratory Medicine 2003;23(5):352-356
BACKGROUND: Hepatitis B virus (HBV) is classified into 7 genotypes (A-G) that have distinct geographic distribution. Several studies have suggested that the HBV genotypic differences influence the severity of liver disease and clinical outcomes such that genotype C is associated with more advanced liver diseases and genotype B is associated with the earlier development of hepatocellular carcinoma. With the different genotypes of HBV reported in Shanghai, Taiwan and Japan, wetried to investigate the distribution of the HBV genotype and the utility of HBV genotyping tests in the Korea population. METHODS: A total of 51 HBV DNA positive serum from Korean hepatitis B patients were used for the genotyping. After PCR and sequencing, HBV genotypes were determined by phylogenetic analysis using the NCBI database (www.ncbi.nlm.nih.gov). RESULTS: By phylogenetic analysis in the Pre-S region, all the genotypes of HBV (100%) proved to be C. CONCLUSIONS: All patients in this study had genotype C. This result is consistent with previous studies reporting 96-100% distribution of genotype C in Korea. HBV genotyping in Korea is not informative in predicting individual variation of clinical outcome, so that it is meaningless to genotype HBV in routine laboratory genotyping.
Carcinoma, Hepatocellular
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DNA
;
Genotype*
;
Hepatitis B
;
Hepatitis B virus*
;
Hepatitis*
;
Humans
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Japan
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Korea
;
Liver Diseases
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Polymerase Chain Reaction
;
Taiwan