1.Diagnostic Immunology.
Journal of the Korean Medical Association 1997;40(2):203-209
No abstract available.
Allergy and Immunology*
2.ANCA : The Marker Antibody of Vasculitis.
Journal of the Korean Medical Association 1997;40(3):344-350
No abstract available.
Antibodies, Antineutrophil Cytoplasmic*
;
Vasculitis*
3.Clinical Significance of Membrane CD22 in B-lineage Acute Lymphoblastic Leukemia.
Korean Journal of Clinical Pathology 1999;19(3):337-341
BACKGROUND: CD22 is a glycoprotein expressed on the surface of normal mature B cells and in the cytoplasm of normal B cell precursors. Cytoplasmic CD22 (cCD22) has been proposed as a immunologic marker for the diagnosis of B-lineage acute lymphoblastic leukemia (ALL) while membrane CD22 (mCD22) has been used as the marker for chronic lymphocytic leukemia, B-lineage lymphoma, and hairly cell leukemia, and mCD22 has not been routinely used for the diagnosis and subgrouping of ALL. The purpose of this study was to examine the expression of mCD22 in B-lineage ALL and its clinical significance. METHODS: From 1992 to April, 1998, the leukemic cells of 64 patients newly diagnosed as B-lineage ALL by immunophenotyping were analyzed by the direct immunofluorescence method using monoclonal antibodies including mCD22. RESULTS: mCD22 was positive in 53% (34/64) of all patients, 50% (21/42) of children and 59% (13/22) of adults. According to the immunologic classification, mCD22 was positive in 44% (4/9) of group II, 53% (19/36) of group III, 69% (11/16) of group IV, but negative in 3 cases of group V and VI. The complete remission rate of the mCD22 negative group in group III was significantly higher than that of the mCD22 positive group (P=0.008). There were significant differences in survival rates between the mCD22 positive group and the mCD22 negative group in group II, III and IV (P=0.046) and the above observed significant difference was seen when group III was separately tested (P=0.014). CONCLUSIONS: Our study demonstrated that the expression of mCD22 may be a poor prognostic factor in B-lineage ALL and that mCD22 shall be clinically used as a prognostic marker especially in group III, which is most common among the subgroups of B-lineage ALL.
Adult
;
Antibodies, Monoclonal
;
B-Lymphocytes
;
Biomarkers
;
Child
;
Classification
;
Cytoplasm
;
Diagnosis
;
Fluorescent Antibody Technique, Direct
;
Glycoproteins
;
Humans
;
Immunophenotyping
;
Leukemia
;
Leukemia, Lymphocytic, Chronic, B-Cell
;
Lymphoma
;
Membranes*
;
Precursor Cell Lymphoblastic Leukemia-Lymphoma*
;
Prognosis
;
Survival Rate
4.Prevalence of Hepatitis C Antibody in Patients with Cryoglobulinemia.
Korean Journal of Clinical Pathology 1997;17(6):1100-1108
BACKGROUND: Mixed cryoglobulinemia occurs predominantly in association with chronic liver diseases, infections, autoimmune diseases, and malignancies. Mixed cryoglobulinemia has been classified as essential if no primary disease is identified. Recently, mixed cryoglobulinemia has been reported in cases of hepatitis C virus(HCV) infection in foreign countries, but there have been few reports on the subject In our country. The aim of this study was to assess the prevalence and clinical features of HCV infection in patients with cryoglobuline mia in Korea. METHODS: Eighty-five patients with detectable serum cryoglobulin were studied between June 1996 and January 1997 at Hanyang university Hospital. Anti-HCV antibodies (Ab) were tested In all patients by particle agglutination method (ASAN HCV. PA Kit) and confirming a positive results, were tested by the microparticle enzyme immunoassay method (IMx, Abbott). Medical records were analyzed retrospectively to compare the clinical features between anti-HCV Ab positive and anti-HCV Ab negative patients. RESULTS: Anti-HCV antibodies were found in 12 out of 85 (about 14%) patients with cryoglobulinemia. Six of these patients were diagnosed as rheumatoid arthritis and 4 as osteoarthritis, and 2 as fibromyalgia syndrome. Nine of the 12 patients had no remarkable abnormalities in their liver function test results and there were no statistical differences between anti-HCV _Lb positive and negative groups. There were no meaningful differences between the two groups in immunologic data such as rheumatoid factor, C reactive protein, antinuclear antibody, and antiperinuclear factor. CONCLUSIONS: We found the association of HCV infection and cryglobulin in Korean patients with cryoglobulinemia and recommend routine anti-HCV Ab testing in patients with cryoglobulinemia even if they have normal liver function test results.
Agglutination
;
Antibodies, Antinuclear
;
Arthritis, Rheumatoid
;
Autoimmune Diseases
;
C-Reactive Protein
;
Cryoglobulinemia*
;
Fibromyalgia
;
Hepatitis C Antibodies
;
Hepatitis C*
;
Hepatitis*
;
Humans
;
Immunoenzyme Techniques
;
Korea
;
Liver Diseases
;
Liver Function Tests
;
Medical Records
;
Osteoarthritis
;
Prevalence*
;
Retrospective Studies
;
Rheumatoid Factor
5.A case of Ay phenotype family.
Sang Gyung KIM ; Think You KIM ; Choon Won KIM
Korean Journal of Clinical Pathology 1991;11(1):221-224
No abstract available.
Humans
;
Phenotype*
6.Is the LE Cell Test Necessary?.
Jung Uk SIR ; Hye Rim LEE ; Think You KIM
Korean Journal of Clinical Pathology 1997;17(5):805-811
BACKGROUND: Before the introduction of the antinuclear antibody test (ANA), the lupus erythematosus (LE) cell test was a useful diagnostic test for systemic lupus erythematosus(SLE) But, the ANA test has replaced the LE cell test in virtually all laboratories as the current routine test for SLE. However, because the LE cell test is still performed in some laboratories, the authors compared the LE cell test with the ANA test to reevaluate the LE cell test. METHODS: A total of 522 cases were evaluated from Aug. 1990 to Aug. 1994. In these cases, the LE cell test and the ANA test were performed simultaneously, and the results were compared. The authors defined the 'True LE Phenomenon' as only when the LE cell test results agreed with the anti-histone antibody pattern of the ANA test. RESULTS: Of the total 522 cases, 56 cases(10.7%) were SLE. The LE cell test was positive in 22 cases(39.3%) and the ANA test in 56 cases(100%). The LE cell test produced 6(27%) false positive cases and 3 (8.8%) false negative cases. Therefore, the sensitivity of the LE cell test that was verified by the ANA test was only 28.6%. On the other hand, the sensitivity of the ANA test was 100%. In 2 cases, the LE cell results were different in repetitive tests although the ANA results were the same. In 2 other cases, it was impossible to interprete the results of the LE cell test because of severe leukopenia. CONCLUSIONS: The authors concluded that the LE cell test showed markedly low sensitivity and a high false positive and false negative rates for SLE, and that the LE cell test was difficult to perform and interpret accurately due to numerous interfering factors. Therefore, for accurate diagnosis of SLE, the LE cell test must be replaced by more definitive and quantitative immunologic tests in all laboratories such as the ANA test.
Antibodies, Antinuclear
;
Diagnosis
;
Diagnostic Tests, Routine
;
Hand
;
Immunologic Tests
;
Leukopenia
;
Neutrophils*
7.Is the LE Cell Test Necessary?.
Jung Uk SIR ; Hye Rim LEE ; Think You KIM
Korean Journal of Clinical Pathology 1997;17(5):805-811
BACKGROUND: Before the introduction of the antinuclear antibody test (ANA), the lupus erythematosus (LE) cell test was a useful diagnostic test for systemic lupus erythematosus(SLE) But, the ANA test has replaced the LE cell test in virtually all laboratories as the current routine test for SLE. However, because the LE cell test is still performed in some laboratories, the authors compared the LE cell test with the ANA test to reevaluate the LE cell test. METHODS: A total of 522 cases were evaluated from Aug. 1990 to Aug. 1994. In these cases, the LE cell test and the ANA test were performed simultaneously, and the results were compared. The authors defined the 'True LE Phenomenon' as only when the LE cell test results agreed with the anti-histone antibody pattern of the ANA test. RESULTS: Of the total 522 cases, 56 cases(10.7%) were SLE. The LE cell test was positive in 22 cases(39.3%) and the ANA test in 56 cases(100%). The LE cell test produced 6(27%) false positive cases and 3 (8.8%) false negative cases. Therefore, the sensitivity of the LE cell test that was verified by the ANA test was only 28.6%. On the other hand, the sensitivity of the ANA test was 100%. In 2 cases, the LE cell results were different in repetitive tests although the ANA results were the same. In 2 other cases, it was impossible to interprete the results of the LE cell test because of severe leukopenia. CONCLUSIONS: The authors concluded that the LE cell test showed markedly low sensitivity and a high false positive and false negative rates for SLE, and that the LE cell test was difficult to perform and interpret accurately due to numerous interfering factors. Therefore, for accurate diagnosis of SLE, the LE cell test must be replaced by more definitive and quantitative immunologic tests in all laboratories such as the ANA test.
Antibodies, Antinuclear
;
Diagnosis
;
Diagnostic Tests, Routine
;
Hand
;
Immunologic Tests
;
Leukopenia
;
Neutrophils*
8.A case of microgranular acute promyelocytic leukemia with positive reaction of nonspecific esterase.
Yiel Hea SEO ; Wha Soon CHUNG ; Think You KIM
Korean Journal of Hematology 1991;26(2):435-439
No abstract available.
Carboxylesterase*
;
Leukemia, Promyelocytic, Acute*
9.The incidences of autoantibodies after in vivo administration of interferon-gamma.
Myung Shik LEE ; Seong Hoe PARK ; Yong Seong KIM ; Noe Kyeong KIM ; Think You KIM
Journal of Korean Society of Endocrinology 1991;6(3):227-231
No abstract available.
Autoantibodies*
;
Incidence*
;
Interferon-gamma*
10.A Survey of the Self-contribution Rate of Manuscripts Published in the Korean Journal of Blood Transfusion using Internal Impact Score.
Korean Journal of Blood Transfusion 2007;18(2):105-110
BACKGROUND: The authors produced a new citation index of the Korean Journal of Blood Transfusion (KJBT). The index, which was developed to determine the internal impact score (IIS), could examine contributions to the KJBT according to the manuscript, author and institute. METHODS: For manuscripts published in the KJBT from Volume 1 No. 1 in 1990 to Volume 17 No. 1 in 2006, a database of the journals and their references was constructed, and an index was created. The citation index was analyzed using three indicators, the internal impact score for the manuscript (IIS-M), internal impact score for the author (IIS-A) and the internal impact score for the institute (IIS-I). RESULTS: The total number of references cited in the manuscripts was 5,392. Of these references, 498 (9.2%) were published in the KJBT. The mean IIS-M of all manuscripts cited was 0.97. The total number of authors who participated in the cited manuscripts was 351. The highest IIS-A score, which was calculated in consideration of each author's participation and the weight of the manuscript, was 203.26. The number of institutes that had produced the cited manuscripts was 35. The highest IIS-I score, which was calculated in consideration of each organization's participation and the weight of manuscripts, was 187.45. CONCLUSION: If the indicators developed by the authors are used as tools to analyze the citation indices of the journals, they can quantify the contribution of the manuscripts, authors and institutes to each journal, and promote the development of academic journals based on the quantified contribution.
Academies and Institutes
;
Blood Transfusion*