Volume 12, Issue 6 pp. 1261-1265
Original Article
Free Access

Changes in interferon receptors on peripheral blood mononuclear cells from patients with chronic hepatitis B being treated with interferon

Dr. Shinya Nakajima

Corresponding Author

Dr. Shinya Nakajima

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

Third Department of Internal Medicine, Osaka City University Medical School, 1-5-7 Asahi-machi, Abeno-ku, Osaka 545, Japan===Search for more papers by this author
Tetsuo Kuroki

Tetsuo Kuroki

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Machiko Shintani

Machiko Shintani

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Osamu Kurai

Osamu Kurai

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Tadashi Takeda

Tadashi Takeda

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Shuhei Nishiguchi

Shuhei Nishiguchi

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Susumu Shiomi

Susumu Shiomi

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Shuichi Seki

Shuichi Seki

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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Kenzo Kobayashi

Kenzo Kobayashi

Third Department of Internal Medicine, Osaka City University Medical School, Osaka 545, Japan

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First published: December 1990
Citations: 31

Abstract

We studied the binding of 125I-labeled human interferon-α to peripheral blood mononuclear cells and the activity of 2′,5′-oligoadenylate synthetase in peripheral blood mononuclear cells obtained from 21 patients with chronic hepatitis B who were treated with human interferon-α or interferon-β. Fourteen patients were given interferon daily for 4 wk. Interferon receptors per cell decreased to about 50% of baseline but increased to baseline by 2 wk after therapy ended. The activity of 2′,5′-oligoadenylate synthetase rose about fivefold during therapy, decreasing to baseline by 1 wk after the end of therapy. The seven other patients were given interferon daily for 2 wk, no interferon for 2 wk and then interferon daily for 2 wk more. During both periods of therapy on this schedule, interferon receptors decreased to about 50% but returned to baseline 1 wk after the interferon was stopped. The activity of 2′,5′-oligoadenylate synthetase increased about fivefold during both the first and second periods of therapy and decreased to baseline 1 wk after interferon was stopped. Close negative correlation existed between the number of interferon receptors and the 2′,5′-oligoadenylate synthetase activity. The results of interferon therapy could not be predicted by either the numbers of interferon receptors before therapy or by the decrease in this number during therapy. (HEPATOLOGY 1990;12:1261–1265).

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