The appearance of unusual phenotypic cells (CD4(+) Mac-1(+) class II+) in the liver of (NZW x BXSB) F-1 mice is possibly an animal model for autoimmune hepatitis

被引:4
作者
Amoh, Y
Yasumizu, R
Yamamoto, Y
Toki, J
Nishio, N
Adachi, Y
Watanabe, H
Inoue, K
Ikehara, S
机构
[1] KANSAI MED UNIV,DEPT PATHOL 1,MORIGUCHI,OSAKA 570,JAPAN
[2] KANSAI MED UNIV,DEPT INTERNAL MED 3,MORIGUCHI,OSAKA 570,JAPAN
关键词
D O I
10.1016/S0171-2985(97)80055-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The male (NZW x BXSB)F-1 (W/BF1) mouse, a murine model for autoimmune diseases, shows hepatosplenomegaly with lymphoid cell infiltration in the liver by 20 weeks of age. The majority of infiltrating cells are T cells, B cells and plasma cells, as seen in autoimmune hepatitis. Together with the increase in serum glutamate pyruvate transaminase (GPT) levels, anti-dsDNA antibody (Ab) and circulating immune complex (CIC) levels increase with age. These findings are compatible with these of autoimmune hepatitis in humans. In addition, a unique finding in this mouse is the accumulation of CD4(+) Mac-1(+) Class II+ cells in the sinusoidal space. The cells have the capacity to proliferate and differentiate into macrophages in vitro, indicating that they are the precursors oi macrophages. This W/BF1, mouse provides a useful tool for not only analyzing the pathogenesis of autoimmune hepatitis but also establishing a new therapeutic strategy for it. In addition, we discuss the significance of the appearance of abnormal cells in autoimmune-prone mice.
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页码:31 / 43
页数:13
相关论文
共 15 条
[1]   FUNCTIONAL ANALYSES OF B-CELLS IN (NZW X BXSB) F1-MICE [J].
ADACHI, Y ;
INABA, M ;
INABA, K ;
NAGATA, N ;
KOBAYASHI, Y ;
IKEHARA, S .
AUTOIMMUNITY, 1993, 15 (02) :99-105
[2]   (NZW X BXSB)F1 HYBRID - A MODEL OF ACUTE LUPUS AND CORONARY VASCULAR-DISEASE WITH MYOCARDIAL-INFARCTION [J].
HANG, LM ;
IZUI, S ;
DIXON, FJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1981, 154 (01) :216-221
[3]  
HASHIMOTO Y, 1992, J IMMUNOL, V149, P1063
[4]   RATIONALE FOR BONE-MARROW TRANSPLANTATION IN THE TREATMENT OF AUTOIMMUNE-DISEASES [J].
IKEHARA, S ;
GOOD, RA ;
NAKAMURA, T ;
SEKITA, K ;
INOUE, S ;
OO, MM ;
MUSO, E ;
OGAWA, K ;
HAMASHIMA, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (08) :2483-2487
[5]   LONG-TERM OBSERVATIONS OF AUTOIMMUNE-PRONE MICE TREATED FOR AUTOIMMUNE-DISEASE BY ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
IKEHARA, S ;
YASUMIZU, R ;
INABA, M ;
IZUI, S ;
HAYAKAWA, K ;
SEKITA, KI ;
TOKI, J ;
SUGIURA, K ;
IWAI, H ;
NAKAMURA, T ;
MUSO, E ;
HAMASHIMA, Y ;
GOOD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3306-3310
[6]   PREVENTION OF TYPE-I DIABETES IN NONOBESE DIABETIC MICE BY ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
IKEHARA, S ;
OHTSUKI, H ;
GOOD, RA ;
ASAMOTO, H ;
NAKAMURA, T ;
SEKITA, K ;
MUSO, E ;
TOCHINO, Y ;
IDA, T ;
KUZUYA, H ;
IMURA, H ;
HAMASHIMA, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (22) :7743-7747
[7]  
IZUI S, 1980, CLIN IMMUNOL IMMUNOP, V15, P258
[8]   FORMULATION AND APPLICATION OF A NUMERICAL SCORING SYSTEM FOR ASSESSING HISTOLOGICAL ACTIVITY IN ASYMPTOMATIC CHRONIC ACTIVE HEPATITIS [J].
KNODELL, RG ;
ISHAK, KG ;
BLACK, WC ;
CHEN, TS ;
CRAIG, R ;
KAPLOWITZ, N ;
KIERNAN, TW ;
WOLLMAN, J .
HEPATOLOGY, 1981, 1 (05) :431-435
[9]  
MACKAY IR, 1991, AUTOIMMUNE LIVER DIS, P21
[10]   (NZW X BXSB)F1 MOUSE - A NEW ANIMAL-MODEL OF IDIOPATHIC THROMBOCYTOPENIC PURPURA [J].
OYAIZU, N ;
YASUMIZU, R ;
MIYAMAINABA, M ;
NOMURA, S ;
YOSHIDA, H ;
MIYAWAKI, S ;
SHIBATA, Y ;
MITSUOKA, S ;
YASUNAGA, K ;
MORII, S ;
GOOD, RA ;
IKEHARA, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (06) :2017-2022