CERVICAL LYMPHOID-TISSUE BUT NOT THE CENTRAL-NERVOUS-SYSTEM SUPPORTS PROLIFERATION OF VIRUS-SPECIFIC T-LYMPHOCYTES DURING CORONAVIRUS-INDUCED ENCEPHALITIS IN RATS

被引:16
作者
IMRICH, H [1 ]
SCHWENDER, S [1 ]
HEIN, A [1 ]
DORRIES, R [1 ]
机构
[1] UNIV WURZBURG,MED KLIN,ZENT LAB,W-8700 WURZBURG,GERMANY
关键词
VIRAL ENCEPHALITIS; T CELLS; PROLIFERATION; CENTRAL NERVOUS SYSTEM; CERVICAL LYMPH NODES;
D O I
10.1016/0165-5728(94)90066-3
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 CD4(+) T lymphocyte response in the central nervous system (CNS) and cervical lymph nodes (CLNs) of rats with different susceptibility to coronavirus-induced encephalitis was investigated. The majority of CD4(+) T lymphocytes entering the virus-infected CNS in the course of the infection are primed cells that neither proliferate ex vivo nor can be stimulated to proliferation by viral antigens or mitogen in vitro. In contrast, T lymphocytes taken from CLNs of the same animals revealed a strong proliferative response. Restimulation of CLN lymphocytes by viral antigens disclosed a striking difference between the disease-resistant rat strain Brown Norway (BN) and the susceptible Lewis (LEW) strain. Whereas BN lymphocytes responded as early as 5 days post infection, it took more than 11 days until a comparable proliferation was detectable in LEW lymphocytes. From these data we postulate that the majority of T lymphocytes entering the virus-infected brain after sensitisation and expansion in cervical lymph nodes is unresponsive to further proliferation signals and that the kinetics and magnitude of T lymphocyte stimulation in CLNs play an important role in the clinical course of the infection.
引用
收藏
页码:73 / 81
页数:9
相关论文
共 33 条
[1]   HYPOTHESIS - ANTIGEN-SPECIFIC T-CELLS PRIME CENTRAL-NERVOUS-SYSTEM ENDOTHELIUM FOR RECRUITMENT OF NONSPECIFIC INFLAMMATORY CELLS TO EFFECT AUTOIMMUNE DEMYELINATION [J].
CROSS, AH ;
CANNELLA, B ;
BROSNAN, CF ;
RAINE, CS .
JOURNAL OF NEUROIMMUNOLOGY, 1991, 33 (03) :237-244
[2]   CERVICAL LYMPHATICS, THE BLOOD-BRAIN-BARRIER AND THE IMMUNOREACTIVITY OF THE BRAIN - A NEW VIEW [J].
CSERR, HF ;
KNOPF, PM .
IMMUNOLOGY TODAY, 1992, 13 (12) :507-512
[3]  
DOHERTY PC, 1990, IMMUNOL TODAY, V11, P55
[4]  
DORRIES R, 1991, IMMUNOLOGY, V74, P539
[5]   MURINE CORONAVIRUS-INDUCED ENCEPHALOMYELITIDES IN RATS - ANALYSIS OF IMMUNOGLOBULINS AND VIRUS-SPECIFIC ANTIBODIES IN SERUM AND CEREBROSPINAL-FLUID [J].
DORRIES, R ;
WATANABE, R ;
WEGE, H ;
TERMEULEN, V .
JOURNAL OF NEUROIMMUNOLOGY, 1986, 12 (02) :131-142
[6]   ANTIGEN PRESENTATION AND TUMOR-CYTOTOXICITY BY INTERFERON-GAMMA-TREATED MICROGLIAL CELLS [J].
FREI, K ;
SIEPL, C ;
GROSCURTH, P ;
BODMER, S ;
SCHWERDEL, C ;
FONTANA, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (09) :1271-1278
[7]  
Griffin D E, 1992, Semin Immunol, V4, P111
[8]   ROLE OF CERVICAL LYMPH-NODES IN THE SYSTEMIC HUMORAL IMMUNE-RESPONSE TO HUMAN-SERUM ALBUMIN MICROINFUSED INTO RAT CEREBROSPINAL-FLUID [J].
HARLINGBERG, C ;
KNOPF, PM ;
MERRIAM, J ;
CSERR, HF .
JOURNAL OF NEUROIMMUNOLOGY, 1989, 25 (2-3) :185-193
[9]   MICROGLIA ARE THE MAJOR CELL TYPE EXPRESSING MHC CLASS-II IN HUMAN WHITE MATTER [J].
HAYES, GM ;
WOODROOFE, MN ;
CUZNER, ML .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1987, 80 (01) :25-37
[10]   PERIVASCULAR MICROGLIAL CELLS OF THE CNS ARE BONE-MARROW DERIVED AND PRESENT ANTIGEN INVIVO [J].
HICKEY, WF ;
KIMURA, H .
SCIENCE, 1988, 239 (4837) :290-292