QUANTITATION AND TYPING OF SERUM HEPATITIS-C VIRUS-RNA IN PATIENTS WITH CHRONIC HEPATITIS-C TREATED WITH INTERFERON-BETA

被引:38
作者
KOBAYASHI, Y [1 ]
WATANABE, S [1 ]
KONISHI, M [1 ]
YOKOI, M [1 ]
KAKEHASHI, R [1 ]
KAITO, M [1 ]
KONDO, M [1 ]
HAYASHI, Y [1 ]
JOMORI, T [1 ]
SUZUKI, S [1 ]
机构
[1] SANWA KAGAKU KENKYUSHO CO LTD,DIV BIOTECHNOL,MIE 51104,JAPAN
关键词
D O I
10.1016/0270-9139(93)90218-C
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We quantified serum hepatitis C virus RNA titers and determined hepatitis C virus subtypes in chronic hepatitis C patients treated with interferon-beta to investigate relationships among serum ALT response, serum hepatitis C virus titer and hepatitis C virus subtype. Of 146 chronic hepatitis C patients who received interferon-beta therapy, 24 patients with sustained serum ALT normalization (complete responders) and 26 patients without serum ALT normalization (nonresponders) were randomly selected. Detection, typing and quantitation of hepatitis C virus were performed by means of the ''single-tube'' polymerase chain reaction method. Of the 24 complete responders, 21 (87.5%) became negative for hepatitis C virus RNA, whereas 21 (80.8%) of the 26 nonresponders remained positive. Hepatitis C virus infections with types I, II, III, IV, II + III and III + IV occurred in 0 (0%), 22 (51.2%), 10 (23.3%), 1 (2.3%), 7 (16.5%) and 3 (7.9%) patients, respectively. The mean pretreatment hepatitis C virus RNA titer of complete responders (0.4 +/- 2.0 x 10(4) CID50/ml) was significantly lower than that of nonresponders (3.8 +/- 4.5 x 10(4) CID50/ml) (p < 0.01). Regardless of HCV subtype, patients with more than 10(4) CID50/ml of HCV did not show serum ALT normalization, whereas complete serum ALT response was seen in most cases with less than 10(2) CID50/ml HCV. These results show that mixed infections with different hepatitis C virus subtypes appear to be more common than previously reported and that the pretreatment serum level of hepatitis C virus RNA is a more important predictor of outcome of interferon therapy than is virus genotype.
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页码:1319 / 1325
页数:7
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共 27 条
  • [1] CHARLES ES, 1982, J BIOL CHEM, V257, P11791
  • [2] CHAYAMA K, 1991, HEPATOLOGY, V13, P1040
  • [3] ISOLATION OF A CDNA CLONE DERIVED FROM A BLOOD-BORNE NON-A, NON-B VIRAL-HEPATITIS GENOME
    CHOO, QL
    KUO, G
    WEINER, AJ
    OVERBY, LR
    BRADLEY, DW
    HOUGHTON, M
    [J]. SCIENCE, 1989, 244 (4902) : 359 - 362
  • [4] HEPATITIS-C VIRUS - THE MAJOR CAUSATIVE AGENT OF VIRAL NON-A, NON-B HEPATITIS
    CHOO, QL
    WEINER, AJ
    OVERBY, LR
    KUO, G
    HOUGHTON, M
    BRADLEY, DW
    [J]. BRITISH MEDICAL BULLETIN, 1990, 46 (02) : 423 - 441
  • [5] DEGROOTE J, 1968, LANCET, V2, P626
  • [6] RECOMBINANT INTERFERON-ALFA THERAPY FOR CHRONIC HEPATITIS-C - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL
    DIBISCEGLIE, AM
    MARTIN, P
    KASSIANIDES, C
    LISKERMELMAN, M
    MURRAY, L
    WAGGONER, J
    GOODMAN, Z
    BANKS, SM
    HOOFNAGLE, JH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (22) : 1506 - 1510
  • [7] TREATMENT OF CHRONIC NON-A,NON-B HEPATITIS WITH RECOMBINANT HUMAN ALPHA-INTERFERON - A PRELIMINARY-REPORT
    HOOFNAGLE, JH
    MULLEN, KD
    JONES, DB
    RUSTGI, V
    DIBISCEGLIE, A
    PETERS, M
    WAGGONER, JG
    PARK, Y
    JONES, EA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (25) : 1575 - 1578
  • [8] HOOFNAGLE JH, 1989, TRANSFUSION, V2, P215
  • [9] MOLECULAR-BIOLOGY OF THE HEPATITIS-C VIRUSES - IMPLICATIONS FOR DIAGNOSIS, DEVELOPMENT AND CONTROL OF VIRAL DISEASE
    HOUGHTON, M
    WEINER, A
    HAN, J
    KUO, G
    CHOO, QL
    [J]. HEPATOLOGY, 1991, 14 (02) : 381 - 388
  • [10] QUANTITATION OF HEPATITIS-C VIRUS-RNA BY COMPETITIVE POLYMERASE CHAIN-REACTION
    KANEKO, S
    MURAKAMI, S
    UNOURA, M
    KOBAYASHI, K
    [J]. JOURNAL OF MEDICAL VIROLOGY, 1992, 37 (04) : 278 - 282