DETECTION OF CYTOKINE MESSENGER-RNA IN THE BRAINS OF MICE WITH TOXOPLASMIC ENCEPHALITIS

被引:38
作者
HUNTER, CA
ROBERTS, CW
MURRAY, M
ALEXANDER, J
机构
[1] UNIV STRATHCLYDE, TODD CTR, DEPT IMMUNOL, GLASGOW G4 0NR, SCOTLAND
[2] UNIV GLASGOW, DEPT VET MED, GLASGOW G61 1QH, SCOTLAND
关键词
TOXOPLASMA-GONDII; MENINGOENCEPHALITIS; CYTOKINE; ASTROCYTE;
D O I
10.1111/j.1365-3024.1992.tb00015.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
C57B1/10 ScSn mice infected with Toxoplasma gondii developed a meningoencephalitis, characterized by areas of tissue destruction and cellular infiltration including foci of neutrophils. Large numbers of cyst stages were found throughout the brain but were not always associated with inflammation. The use of immunocytochemistry to detect glial fibrillary acidic protein, an astrocyte specific marker, showed a widespread astrocyte activation. This was particularly prominent in areas of intense inflammation but cysts were negative for glial fibrillary acidic protein, indicating that astrocytes were not host cells for the bradyzoites. The use of the polymerase chain reaction to assist in the amplification of total brain RNA allowed the characterization of the cytokines being produced locally within the brains of infected animals. Beta- actin transcripts were detected in all of the uninfected and infected mice. In only one of the seven uninfected control mice were other transcripts found. Transcripts for tumour necrosis factor-alpha, interleukin-1-alpha and beta, interleukin-6, macrophage inflammatory protein-1 and interferon-gamma as well as the CD4 marker were detected in all of the infected mice. However, transcripts for IL-2 and IL-4 were not present. Several of the cytokines present are capable of initiating meningeal inflammation and may play a role in the immunopathogensis of toxoplasmic encephalitis.
引用
收藏
页码:405 / 413
页数:9
相关论文
共 41 条
[21]   TOXOPLASMIC ENCEPHALITIS [J].
LUFT, BJ ;
REMINGTON, JS .
JOURNAL OF INFECTIOUS DISEASES, 1988, 157 (01) :1-6
[22]   CYTOKINES AS COMMUNICATION SIGNALS BETWEEN LEUKOCYTES AND ENDOTHELIAL-CELLS [J].
MANTOVANI, A ;
DEJANA, E .
IMMUNOLOGY TODAY, 1989, 10 (11) :370-375
[23]   EFFECT OF MURINE INTERFERON GAMMA ON MURINE TOXOPLASMOSIS [J].
MCCABE, RE ;
LUFT, BJ ;
REMINGTON, JS .
JOURNAL OF INFECTIOUS DISEASES, 1984, 150 (06) :961-962
[24]  
MCLEOD R, 1989, J IMMUNOL, V143, P3031
[25]  
MOSMANN TR, 1991, IMMUNOL TODAY, V12, P49
[26]   CD8+ T-CELLS ARE THE MAJOR LYMPHOCYTE SUBPOPULATION INVOLVED IN THE PROTECTIVE IMMUNE-RESPONSE TO TOXOPLASMA-GONDII IN MICE [J].
PARKER, SJ ;
ROBERTS, CW ;
ALEXANDER, J .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1991, 84 (02) :207-212
[27]   MODULATION OF CD4 ANTIGEN ON MACROPHAGES AND MICROGLIA IN RAT-BRAIN [J].
PERRY, VH ;
GORDON, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (04) :1138-1143
[28]   INTRATHECAL PRODUCTION OF ANTIBODIES AGAINST TOXOPLASMA-GONDII IN PATIENTS WITH TOXOPLASMIC ENCEPHALITIS AND THE ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS) [J].
POTASMAN, I ;
RESNICK, L ;
LUFT, BJ ;
REMINGTON, JS .
ANNALS OF INTERNAL MEDICINE, 1988, 108 (01) :49-51
[29]   TUMOR NECROSIS FACTOR-ALPHA CACHECTIN AND INTERLEUKIN-1-BETA INITIATE MENINGEAL INFLAMMATION [J].
RAMILO, O ;
SAEZLLORENS, X ;
MERTSOLA, J ;
JAFARI, H ;
OLSEN, KD ;
HANSEN, EJ ;
YOSHINAGA, M ;
OHKAWARA, S ;
NARIUCHI, H ;
MCCRACKEN, GH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (02) :497-507
[30]  
ROBBINS DS, 1987, J IMMUNOL, V139, P2593