Kanzo
Online ISSN : 1881-3593
Print ISSN : 0451-4203
ISSN-L : 0451-4203
Volume 39, Issue 6
Displaying 1-10 of 10 articles from this issue
  • [in Japanese]
    1998 Volume 39 Issue 6 Pages 363-365
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
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  • Naoki HOSOMI, Keiji ARIMA, Kazumi KONO, Kazutaka KUROKOHCHI, Seishiro ...
    1998 Volume 39 Issue 6 Pages 366-373
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
    To detect the anti-liver/kidney microsome tyge 1 antibody (anti-LKM1), a novel enzyme-linked immunosorbent assay (ELISA) system was established utilizing the recombinant CYP2D6 antigen and its efficacy was evaluated. Total 432 sera were tested including 317 from patients with various liver diseases [14 from autoimmune hepatitis (AIH) type II, 218 from chronic viral hepatitis C (CH-C), etc.], 15 from patients without liver diseases and 100 sera from healthy blood donors. By indirect immunofluorescence (IIF), the anti-LKM1 was detected in all 14 sera (100.0%) from AIH type II patients and 7 (3.2%) out of 218 cases of CH-C patients. By ELISA, antibodies from AIH type II patients and CH-C patients that the anti-LKM1 was detected by IIF (CH-C/anti-LKM1+) showed significantly higher reactivity [AIH type II; p<0.0001, CH-C/anti-LKM1+; p<0.0001] . And only 14 cases from AIH type II patients and 7 cases from CH-C/anti-LKM1+ patients were shown to be positive for the anti-LKM1 by ELISA. The reactivity of the anti-LKM1 by ELISA and the IIF titer were also well correlated each other [AIH type II; r=0.883, p<0.001, CH-C/anti-LKM1+; r=0.927, p<0.005]. Furthermore, these results were confirmed by Western blot analysis. All patients positive for the anti-LKM1 by ELISA were also positive by Western blot. These results indicated that the established ELISA system was effective to detect the anti-LKM1 antibody in sera, from the standpoints of simplicity and mass-screening as well as quantitation.
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  • Toshihiko MIZUTA, Toshiya HARA, Noriko FUKUSHIMA, Ikuko WADA, Iwata OZ ...
    1998 Volume 39 Issue 6 Pages 374-378
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
    We studied the efficacy of interferon (IFN) -β and IFN-α combination therapy (β+α group) on virology and hepatic function in patients with chronic hepatitis C, a high viral load (≥104copies/50μl or≥ 1Meq/ml), and genotype 1b. Eight patients received 600MU of IFN-β daily for 9 weeks, followed by 1000 MU of IFN-α three times weekly for 15 weeks. Standard IFN therapy was given in the form of IFN-β to ten patients (β group) and in the form of IFN-α to 16 patients (α group). None of the regimens produced sustained virus eradication. However, serum ALT levels in patients in the β+α group were significantly decreased and the rate of normalization of serum ALT at both 6 and 12 months after the completion of treatment was 75% (6 of 8 patients). By contrast, no decrease in serum ALT levels were observed in either the β group or α group after treatment, and the rates of sustained serum ALT normalization were 10% (1 of 10 patients) and 12.5% (2 of 16 patients), respectively. The platelet number in the patients in the β+α group increased compared with that in patients in the standard-therapy groups. These results suggest that the combination of IFN-β and IFN-α comprised an excellent regimen for improving hepatic function, but provided no additional virological effect over that produced by standard therapy.
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  • The experimental and clinical studies of contrast medium-PEIT (CM-PEIT)
    Toshifumi NEKOHASHI
    1998 Volume 39 Issue 6 Pages 379-389
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
    To evaluate the therapeutic effect of percutaneous ethanol inlection therapy (PEIT) to large hepatocellular carcinomas (HCC) (over 30mm in diameter), we have demonstrated contrast-medium PEIT (CM-PEIT). CM-PEIT is a newly developed methods that HCC nodules are punctured by a needle under ultrasound imaging and inlected with ethanol mixed with water-soluble contrast medium (Iopamidol containing 370mg/ml iodine) (vol/vol: 7/3) (CME). In this study, CM-PEIT was evaluated on experimental and clinical studies.
    In elemental study, ethanol at various concentrations (30%, 50%, 70% and 100%) was injected to DAB-induced rat hepatomas. Histological findings of rat hepatomas following the injection of 70% ethanol were similar to those of rat hepatomas injected 100% ethanol. Completely enhanced rat hepatoma nodules on soft X-p tumorgraphy after 70% CME injection was revealed histologically complete necrosis.
    In clinical study, CM-PEIT was performed to large HCCs and the therapeutic effect was evaluated by CT tumorgraphy and X-p tumorgraphy. The area spreaded into HCC nodules by 70% CME on CT tumorgraphy was the same as that of histologically complete necrosis on surgical resection or autopsy. Completely enhanced large HCC nodules on X-p tumorgraphy after 70% CME injection showed almost histologically complete necrosis.
    These results suggest that CM-PEIT is a new useful method to evaluate the therapeutic effect of PEIT on large HCCs.
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  • Masato TAKAMATSU, Hiroshi YAMAGUCHI, Takeshi HISA
    1998 Volume 39 Issue 6 Pages 390-395
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
  • Satoru MATSUYAMA, Kohji MIYAZAKI, Michito MORI, Kenji KITAHARA
    1998 Volume 39 Issue 6 Pages 396-400
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
  • An autopsy case of hepatocellular carcinoma producing granulocyte colony-stimulating factor
    Shinichiro HORI, Jiro TAKEBAYASHI, Tomoko OKAMOTO, Koujun SETSU, Tomon ...
    1998 Volume 39 Issue 6 Pages 401-405
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    1998 Volume 39 Issue 6 Pages 406-407
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
    Download PDF (354K)
  • [in Japanese], [in Japanese]
    1998 Volume 39 Issue 6 Pages 408-409
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    1998 Volume 39 Issue 6 Pages 410-411
    Published: June 25, 1998
    Released on J-STAGE: November 17, 2009
    JOURNAL FREE ACCESS
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