2.Screening of Anti-HIV-1 Activity of Natural Product by MTT Assay.
Joo Shil LEE ; Jeong Gu NAM ; Chun KANG ; Hong Rae LEE ; Young Jong LEE ; Yung Oh SHIN
Journal of the Korean Society of Virology 1997;27(1):87-95
Methanol and/or boiling water extraction of 201 natural products and subsequent MTT assay using MT-4 cell line was carried out to screen the anti-HIV-1 activity. Among 97 methanol extracts, 7 extracts from Chrysanthemi Indicium Flos, Magnoliae Cortex Machili Cortex, Reynoutriae Rhizoma, Lithospermi Radix Agastachis Herba, and Chaenomelis Fructus showed anti-HIV-1 activity and their SI value were 2.25 to 5.77. In addition, among 119 boiling water extracts, 10 extracts from Lonicerae Caulis et Foloium, Elsholtziae Herba, Leonuri Herba, Portulacae Herba, Schizonepetae Herba, Curcumae Rhizoma, Amomi Cardamomi Fructus, Cirsii Radix et Herba, Carpesii Herba, and Siegesbeckiae Herba showed anti-HIV-1 activity and their SI value were 1.30 to 7.64. Methanol extracts of above seven natural products were fractionated and the anti-HRs_1 activity of each fraction was examined. Extraction was carried out with hexane, chloroform, butanol, and water to trace active anti-HIV-1 componets. As a result, the water fraction of Magnoliae Cortex, Machili Cortex, Reynoutriae Rhizoma, Agastachis Herba, Chaenomelis Fructus and the butanol fraction of Chrysanthemi Indicium Flos, Reynoutriae Rhizoma showed anti-HIV-1 activity and their SI value were 1.40 to 8.02. We could reach a conclusion that studies to trace the anti-HIV-1 active component of each natural products in further Sractionation and to identify its structure by Infrared spectroscopy, NMR spectroscopy and gel permeation chromatography were needed.
Biological Products
;
Cell Line
;
Chloroform
;
Chromatography, Gel
;
Curcuma
;
Lamiaceae
;
Lithospermum
;
Lonicera
;
Magnetic Resonance Spectroscopy
;
Magnolia
;
Mass Screening*
;
Methanol
;
Portulaca
;
Spectrum Analysis
;
Water
3.The Clinical Features of the Infants Born from Mothers with Genital Ureaplasma urealyticum Colonization.
Ji Young CHANG ; Young Shil PARK ; Gae Shik SHIM ; Chong Woo BAE ; Hyun Joo SEOL
Korean Journal of Perinatology 2010;21(3):288-297
PURPOSE: Regardless of premature rupture of membranes, the genital colonization of Ureaplasma urealyticum (Uu) in pregnant women could transmit vertical infections of their babies and cause neonatal infections, which ultimately result in infections in many other organs. The purpose of this study is to determine clinical influences on the infants born from mothers suffering genital Uu colonization. METHODS: We retrospectively reviewed the data for analysis of the 219 infants born from mothers who had been tested for genital Uu culture (about 470 cases) for past 3 years from Mar. 2006 to Jun. 2009, in East-West Neo Medical Center, Kyunghee University. The neonatal clinical manifestations such as duration of tachypnea, incidence of oxygen therapy, respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), sepsis, jaundice, feeding intolerance, etc. were investigated during gestational period. RESULTS: In case of positive genital Uu culture of mothers, the preterm infants (gestational period <35 weeks) had symptoms of increased heart rate within 6 hours after birth, prolonged tachypnea, short period of antibiotics use, and lower incidence of RDS and hypocalcemia. Durations of oxygen therapy, the methods and durations of positive pressure ventilation and incidences of BPD of preterm infants were not affected by maternal Uu results. The near and full term infants (gestational period > or =35 weeks) from Uu positive mothers showed the increased incidence of jaundice. CONCLUSION: It is hard to say that genital Uu colonization in pregnant women influence the near and full term infants except jaundice. However, the data analysis of the preterm infants from Uu mothers demonstrated increased heart rate within 6 hours after birth, prolonged tachypnea, short period of antibiotics use, lower incidence of RDS and hypocalcemia.
Anti-Bacterial Agents
;
Bronchopulmonary Dysplasia
;
Colon
;
Female
;
Heart Rate
;
Humans
;
Hypocalcemia
;
Incidence
;
Infant
;
Infant, Newborn
;
Infant, Premature
;
Jaundice
;
Membranes
;
Mothers
;
Oxygen
;
Parturition
;
Positive-Pressure Respiration
;
Pregnant Women
;
Respiratory Therapy
;
Retrospective Studies
;
Rupture
;
Sepsis
;
Statistics as Topic
;
Stress, Psychological
;
Tachypnea
;
Ureaplasma
;
Ureaplasma urealyticum
4.Comparison of Real-time PCR Methods and pp65 Antigenemia Assay to Detect Cytomegalovirus Reactivation in Hematopoietic Stem Cell Transplantation.
Seon Young LEE ; Byeong Sun CHOI ; Sung Soon KIM ; Su Mi CHOI ; Wan Shik SHIN ; Joo Shil LEE
Infection and Chemotherapy 2008;40(3):167-169
Human cytomegalovirus (HCMV) is a common human pathogen that causes morbidity and mortality in hematopoietic stem cell transplantation (HSCT) recipients. Early diagnosis of HCMV infection or reactivation, and setting threshold values for effective pre-emptive therapies, are required for appropriate HCMV disease prevention in HSCT recipients. We compared the HCMV infections detected by the two methods, LightCycler-based PCR (LC PCR) and in-house immediate early protein PCR (in-house IE PCR) with the results of a pp65 antigenemia assay as the reference. The sensitivity and specificity for the in-house IE PCR were 79.3% and 72.7%, respectively, and 82.9% and 40.7%, respectively, for the LC PCR. The correlation between the HCMV viral load and pp65 antigenemia in HSCT recipients was r=0.603 with in-house IE PCR and r=0.525 with LC PCR. The discordant results between methods and relatively low (r) values suggest that we need more study to set threshold values according to the using methods with clinical outcome.
Cytomegalovirus
;
Early Diagnosis
;
Hematopoietic Stem Cell Transplantation
;
Hematopoietic Stem Cells
;
Humans
;
Polymerase Chain Reaction
;
Real-Time Polymerase Chain Reaction
;
Sensitivity and Specificity
;
Viral Load
5.Comparison of Real-time PCR Methods and pp65 Antigenemia Assay to Detect Cytomegalovirus Reactivation in Hematopoietic Stem Cell Transplantation.
Seon Young LEE ; Byeong Sun CHOI ; Sung Soon KIM ; Su Mi CHOI ; Wan Shik SHIN ; Joo Shil LEE
Infection and Chemotherapy 2008;40(3):167-169
Human cytomegalovirus (HCMV) is a common human pathogen that causes morbidity and mortality in hematopoietic stem cell transplantation (HSCT) recipients. Early diagnosis of HCMV infection or reactivation, and setting threshold values for effective pre-emptive therapies, are required for appropriate HCMV disease prevention in HSCT recipients. We compared the HCMV infections detected by the two methods, LightCycler-based PCR (LC PCR) and in-house immediate early protein PCR (in-house IE PCR) with the results of a pp65 antigenemia assay as the reference. The sensitivity and specificity for the in-house IE PCR were 79.3% and 72.7%, respectively, and 82.9% and 40.7%, respectively, for the LC PCR. The correlation between the HCMV viral load and pp65 antigenemia in HSCT recipients was r=0.603 with in-house IE PCR and r=0.525 with LC PCR. The discordant results between methods and relatively low (r) values suggest that we need more study to set threshold values according to the using methods with clinical outcome.
Cytomegalovirus
;
Early Diagnosis
;
Hematopoietic Stem Cell Transplantation
;
Hematopoietic Stem Cells
;
Humans
;
Polymerase Chain Reaction
;
Real-Time Polymerase Chain Reaction
;
Sensitivity and Specificity
;
Viral Load
6.Endotoxin Is Not Essential for the Development of Cockroach Induced Allergic Airway Inflammation.
Yoo Seob SHIN ; Jung Ho SOHN ; Joo Young KIM ; Jae Hyun LEE ; Sang Heon CHO ; Soo Jong HONG ; Joo Shil LEE ; Chein Soo HONG ; Jung Won PARK
Yonsei Medical Journal 2012;53(3):593-602
PURPOSE: Cockroach (CR) is an important inhalant allergen and can induce allergic asthma. However, the mechanism by which CR induces airway allergic inflammation and the role of endotoxin in CR extract are not clearly understood in regards to the development of airway inflammation. In this study, we evaluated whether endotoxin is essential to the development of CR induced airway allergic inflammation in mice. MATERIALS AND METHODS: Airway allergic inflammation was induced by intranasal administration of either CR extract, CR with additional endotoxin, or endotoxin depleted CR extract, respectively, in BALB/c wild type mice. CR induced inflammation was also evaluated with toll like receptor-4 (TLR-4) mutant (C3H/HeJ) and wild type (C3H/HeN) mice. RESULTS: Intranasal administration of CR extracts significantly induced airway hyperresponsiveness (AHR), eosinophilic and neutrophilic airway inflammation, as well as goblet cell hyperplasia in a dose-dependent manner. The addition of endotoxin along with CR allergen attenuated eosinophilic inflammation, interleukin (IL)-13 level, and goblet cell hyperplasia of respiratory epithelium; however, it did not affect the development of AHR. Endotoxin depletion in CR extract did not attenuate eosinophilic inflammation and lymphocytosis in BAL fluid, AHR and IL-13 expression in the lungs compared to CR alone. The attenuation of AHR, eosinophilic inflammation, and goblet cell hyperplasia induced by CR extract alone was not different between TLR-4 mutant and the wild type mice. In addition, heat inactivated CR extract administration induced attenuated AHR and eosinophilic inflammation. CONCLUSION: Endotoxin in CR extracts may not be essential to the development of airway inflammation.
Allergens/*immunology
;
Animals
;
Asthma/*chemically induced/*immunology/metabolism
;
Cockroaches/*immunology
;
Endotoxins/*immunology
;
Enzyme-Linked Immunosorbent Assay
;
Female
;
Inflammation/*chemically induced/*immunology/metabolism
;
Interferon-gamma/metabolism
;
Interleukin-13/metabolism
;
Interleukin-5/metabolism
;
Mice
;
Mice, Inbred BALB C
;
Respiratory Hypersensitivity/chemically induced/*immunology
7.Clinical outcomes of hematopoietic stem cell transplantation from HLA-matched parental donor in childhood acute leukemia.
Eun Young CHA ; Moon Hee LEE ; Jae Wook LEE ; Young Joo KWON ; Dae Hyoung LEE ; Young Shil PARK ; Nak Gyun CHUNG ; Dae Chul JEONG ; Bin CHO ; Hack Ki KIM
Korean Journal of Pediatrics 2008;51(1):67-72
PURPOSE: In this study, we retrospectively analyzed the clinical outcomes of patients who underwent allogeneic hematopoietic stem cell transplantation (HSCT) grafted from HLA-matched parents. METHODS: Seven children with acute leukemia (4 acute lymphoblastic leukemia, 3 acute myeloid leukemia) in first complete remission received allogeneic HSCT from their respective parents at the St. Marys Hospital between April, 1999 and October, 2005. The median age of patients at transplantation was 5 years (range, 1-11 years; 2 male, 5 female) and the median age of donors was 35 years (range, 30-41 years; 5 male, 2 female). We investigated the clinical outcomes such as engraftment, acute and chronic graft-versus-host disease (GVHD), transplant-related morbidity and mortality, relapse and survival. RESULTS: Median time from transplantation to last follow-up was 69.5 months (range, 18.8-96.5 months). All patients were successfully engrafted, with a median time of 11 days (range, 10-16 days) and 26 days (range, 13-39 days) for neutrophil and platelet recovery, respectively. Grade II acute GVHD occurred in 3, and grade III acute GVHD in 1 of 7 recipients. Extensive chronic GVHD developed in 2, and limited chronic GVHD in 1 of 7 recipients. Death from transplant-related complications occurred in 1, and relapse occurred in 1 of 7 recipients. Estimated 5-year overall survival was 83+/-15%. CONCLUSION: The clinical outcomes of recipients who underwent HSCT from HLA-matched parents were comparable to those of patients who received HSCT grafted from HLA-matched sibling donors in childhood leukemia. HLA typing of parents, as well as siblings will increase the likelihood of finding an HLA-matched family donor for patients who need HSCT.
Blood Platelets
;
Child
;
Follow-Up Studies
;
Graft vs Host Disease
;
Hematopoietic Stem Cell Transplantation
;
Hematopoietic Stem Cells
;
Histocompatibility Testing
;
Humans
;
Leukemia
;
Male
;
Neutrophils
;
Parents
;
Precursor Cell Lymphoblastic Leukemia-Lymphoma
;
Recurrence
;
Retrospective Studies
;
Siblings
;
Tissue Donors
;
Transplants
8.A case of mediastinal ectopic thyroid presenting with a paratracheal mass.
Eun ROH ; Eun Shil HONG ; Hwa Young AHN ; So Yeon PARK ; Ho Il YOON ; Kyong Soo PARK ; Young Joo PARK
The Korean Journal of Internal Medicine 2013;28(3):361-364
Mediastinal ectopic thyroid is a very rare condition, with few reported cases in the literature and no reported cases in Korea. This report describes an asymptomatic 65-year-old man with a right paratracheal mass compressing the superior vena. Additionally, the epidemiology, clinical manifestation, diagnosis, and management of mediastinal ectopic thyroids are discussed. A mediastinal ectopic thyroid should be considered in the differential diagnosis of all mediastinal masses. Surgical excision is recommended for both the diagnosis and treatment of this condition, because of its potential for malignancy and compression of mediastinal structures. This case demonstrates the clinical importance of mediastinal etopic thyroid.
Aged
;
Choristoma/*diagnosis
;
Humans
;
Incidental Findings
;
Male
;
Mediastinal Diseases/*diagnosis
;
*Thyroid Gland
9.Evaluation of Xerostomia Following Intensity Modulated Radiotherapy (IMRT) for Head and Neck Cancer Patients.
Seok Ho LEE ; Tae Hyun KIM ; Eui Kyu CHIE ; Hyun Shil IM ; En Shil IM ; Jun Sun RYU ; Yoo Seok JUNG ; Sung Yong PARK ; Joo Young KIM ; Hong Ryull PYO ; Kyung Hwan SHIN ; Dae Yong KIM ; Kwan Ho CHO
The Journal of the Korean Society for Therapeutic Radiology and Oncology 2004;22(2):106-114
PURPOSE: This study was done to evaluate xerostomia following intensity modulated radiotherapy for patients with head and neck cancer, and to analyze the correlation between the dosimetric parameters and xerostomia parameters. MATERIALS AND MEHTODS: From February till October 2003, 13 patients with 3 months of follow-up were evaluated for xerostomia after being treated for head and neck cancer with IMRT. Their median age was 57 years (range: 43~77). Xerostomia were assessed with a 4-question xerostomia questionnaire score (XQS) and a test for salivary flow rates (unstimulated and stimulated). The patients were also given a validated LENT SOMA scale (LSC) questionnaire. The evaluations were completed before radiation therapy (pre-RT) and at 1 and, 3 months after radiation therapy (RT). We evaluated xerostomia at pre-RT, 1 and, 3 months after RT. The association between the xerostomia parameters (XQS and LSC) and salivary flow rates (unstimulated and stimulated: USFR and SSFR) was assessed at 1 and 3 months after RT. RESULTS: All 13 patients showed no significant changes in XQS, LSC and Salivary Flow rates. As a result, we couldn`t find out about xerostomia development. Based on the total mean parotid dose, 3,500 cGy, we divided these patients into two groups. The 8 patients (<3,500 cGy) showed no significant changes in XQS, LSC and Salivary Flow rates. However, in 5 patients (> or =3,500 cGy), there was a significant increase in USFR and, SSFR at 3 months after RT, and for the XQS and, LSC at 1 and 3 months after RT. The correlation between XQS and, LSC, and USFR and, SSFR in all patients (13) was significant at 3 months after RT. The correlation had a tendency to the decrease for USFR and, SSFR in proportion to the increase of XQS and, LSC. CONCLUSION: Based on the results of this study, IMRT seem to be an effective treatment to significantly decrease the xerostomia. XQS and, LSC seem to be a effective tool for predicting the xerostomia. A total parotid gland mean dose of <3,500 cGy should be a planning goal if substantial sparing of the gland function is desired. Furthermore, patients should be enrolled in a study to define a more accurate threshold dose for the parotid gland.
Carisoprodol
;
Follow-Up Studies
;
Head and Neck Neoplasms*
;
Head*
;
Humans
;
Parotid Gland
;
Surveys and Questionnaires
;
Radiotherapy*
;
Xerostomia*
10.Erratum: In Vitro Evaluation of Allergen Potencies of Commercial House Dust Mite Sublingual Immunotherapy Reagents.
Kyung Hee PARK ; Mina SON ; Soo Young CHOI ; Hey Jung PARK ; Jae Hyun LEE ; Kyoung Yong JEONG ; Joo Shil LEE ; Jung Won PARK
Allergy, Asthma & Immunology Research 2017;9(2):187-187
Corrections for Table. 1 in page 125 are needed. We apologize for any inconvenience that this may have caused.