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急性和慢性肝病的淋巴细胞毒性研究。

Studies on lymphocytotoxicity in acute and chronic liver disease.

作者信息

Warnatz H, Gutmann W, Rösch W, Hommel G

出版信息

Z Immunitatsforsch Immunobiol. 1977 Dec;153(5):435-49.

PMID:602346
Abstract

The cytotoxicity of lymphocytes from patients with chronic active hepatitis, chronic persistent hepatitis, acute hepatitis B and rheumatoid arthritis as well as from normal controls was studied in a microcytotoxicity assay according to COHEN et al. using 125I-iododeoxyuridine labeled embryonal liver cells and Chang cells as target cells. Unfractionated lymphocytes of the peripheral blood from patients with chronic active hepatitis and rheumatoid arthritis showed a high frequency of cytotoxic activity. The lymphocytotoxicity in chronic active hepatitis was significantly increased in comparison to normal controls at the EC/TC of 10:1 and 100:1. Specificity of the cytotoxic reaction to target cells could not be demonstrated. Addition of autologous serum to the cytotoxic assay blocked the lymphocytotoxicity in patients with chronic active hepatitis. A weak potentiating effect on lymphocytotoxicity was observed in patients with hepatitis B after addition of autologous serum. It is discussed that this reaction is due to the presence of HB-antigen in the serum since addition of HB-antigen from other sources increased also the lymphocytotoxicity in hepatitis B patients. This effect was observed neither in HB-antigen positive nor in HB-antigen negative patients with chronic active hepatitis or chronic persistent hepatisis.

摘要

根据科恩等人的方法,采用微量细胞毒性试验,以125I-碘脱氧尿苷标记的胚胎肝细胞和张氏细胞作为靶细胞,研究慢性活动性肝炎、慢性持续性肝炎、急性乙型肝炎和类风湿性关节炎患者以及正常对照者淋巴细胞的细胞毒性。慢性活动性肝炎和类风湿性关节炎患者外周血未分离的淋巴细胞显示出高频率的细胞毒性活性。在效靶比为10:1和100:1时,慢性活动性肝炎患者的淋巴细胞毒性与正常对照相比显著增加。未证实细胞毒性反应对靶细胞具有特异性。在细胞毒性试验中加入自体血清可阻断慢性活动性肝炎患者的淋巴细胞毒性。在乙型肝炎患者中加入自体血清后,观察到对淋巴细胞毒性有微弱的增强作用。有人认为这种反应是由于血清中存在乙肝抗原,因为加入其他来源的乙肝抗原也会增加乙型肝炎患者的淋巴细胞毒性。在慢性活动性肝炎或慢性持续性肝炎的乙肝抗原阳性和阴性患者中均未观察到这种效应。

相似文献

1
Studies on lymphocytotoxicity in acute and chronic liver disease.急性和慢性肝病的淋巴细胞毒性研究。
Z Immunitatsforsch Immunobiol. 1977 Dec;153(5):435-49.
2
In vitro studies on lymphocytotoxicity to synovial cells and Chang cells in rheumatoid arthritis patients and healthy controls.类风湿关节炎患者和健康对照者淋巴细胞对滑膜细胞和Chang细胞细胞毒性的体外研究。
Z Rheumatol. 1979 Mar-Apr;38(3-4):129-37.
3
Immunological studies in patients with chronic active hepatitis. Cytotoxic activity of lymphocytes to autochthonous liver cells grown in tissue culture.慢性活动性肝炎患者的免疫学研究。淋巴细胞对组织培养中生长的自身肝细胞的细胞毒性活性。
Clin Exp Immunol. 1975 Jan;19(1):99-104.
4
Cell-mediated immunity in acute and chronic hepatitis.急性和慢性肝炎中的细胞介导免疫
J Clin Invest. 1975 May;55(5):921-9. doi: 10.1172/JCI108021.
5
Direct and serum-induced lymphocytotoxicity against rabbit hepatocytes in chronic active hepatitis.慢性活动性肝炎中针对兔肝细胞的直接及血清诱导淋巴细胞毒性作用
Boll Ist Sieroter Milan. 1981;60(1):46-51.
6
[Direct and induced lymphocytotoxicity to rabbit hepatocytes in chronic active hepatitis].[慢性活动性肝炎中对兔肝细胞的直接和诱导淋巴细胞毒性]
Arch Sci Med (Torino). 1980 Oct-Dec;137(4):575-7.
7
Lymphocyte cytotoxicity to autologous hepatocytes in HBsAg-negative chronic active hepatitis.乙肝表面抗原阴性的慢性活动性肝炎中淋巴细胞对自体肝细胞的细胞毒性
Clin Exp Immunol. 1979 Oct;38(1):16-21.
8
In-vitro cell-mediated cytotoxicity for autologous liver cells in chronic non-A, non-B hepatitis.慢性非甲非乙型肝炎中自体肝细胞的体外细胞介导细胞毒性
Clin Exp Immunol. 1986 Jan;63(1):147-55.
9
K-cell-mediated antibody-dependent cellular cytotoxicity in chronic active liver disease.慢性活动性肝病中K细胞介导的抗体依赖性细胞毒性作用
Gastroenterology. 1979 Jan;76(1):151-8.
10
Antibody dependent cellular cytotoxicity (ADCC) in acute hepatitis B and in chronic active hepatitis.急性乙型肝炎和慢性活动性肝炎中的抗体依赖性细胞毒性(ADCC)
Clin Exp Immunol. 1978 Aug;33(2):211-6.

引用本文的文献

1
Studies on immunoregulatory mechanisms in acute and chronic hepatitis B.急慢性乙型肝炎免疫调节机制的研究
Clin Exp Immunol. 1983 May;52(2):250-8.
2
Antibody-dependent cell-mediated cytotoxicity (ADCC) and cell-mediated cytotoxicity (CMC) to HBsAg-coated target cells in patients with hepatitis B and chronic hepatitis (CAH).乙型肝炎和慢性活动性肝炎(CAH)患者对乙肝表面抗原包被的靶细胞的抗体依赖性细胞介导的细胞毒性(ADCC)和细胞介导的细胞毒性(CMC)
Clin Exp Immunol. 1979 Jan;35(1):133-40.