Manipulating the type 1 vs type 2 balance in type 1 diabetes

被引:27
作者
Christen, U [1 ]
von Herrath, MG [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Dept Dev Immunol, San Diego, CA 92121 USA
关键词
chemokines; cytokines; CXCL10; TNF alpha; LCMV; autoimmunity; inflammation;
D O I
10.1385/IR:30:3:309
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Virus infections cause a strong inflammatory reaction that is dominated by the expression of type 1 cytokines and chemokines. Such an aggressive immune response by the host is necessary to eliminate intracellular pathogens. However, because of this shift in the type 1 vs type 2 balance of the immune response, virus infections are potential candidates for triggering autoimmune diseases, such as type 1 diabetes (T1D), herpes stromal keratitis, or multiple sclerosis (MS). In this review we will focus on the pathogenesis of T1D in a virus-induced transgenic mouse model and discuss possibilities of how an agressive type 1-dominated immune response can be restrained and autoimmunity be abrogated.
引用
收藏
页码:309 / 325
页数:17
相关论文
共 138 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   CXCR3 and its ligand CXCL10 are expressed by inflammatory cells infiltrating lung allografts and mediate chemotaxis of T cells at sites of rejection [J].
Agostini, C ;
Calabrese, F ;
Rea, F ;
Facco, M ;
Tosoni, A ;
Loy, M ;
Binotto, G ;
Valente, M ;
Trentin, L ;
Semenzato, G .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (05) :1703-1711
[3]   CONSEQUENCES OF IN-SITU PRODUCTION OF IL-2 FOR ISLET-CELL DEATH [J].
ALLISON, J ;
OXBROW, L ;
MILLER, JFAP .
INTERNATIONAL IMMUNOLOGY, 1994, 6 (04) :541-549
[4]   GENETIC REQUIREMENTS FOR ACCELERATION OF DIABETES IN NONOBESE DIABETIC MICE EXPRESSING INTERLEUKIN-2 IN ISLET BETA-CELLS [J].
ALLISON, J ;
MCCLIVE, P ;
OXBROW, L ;
BAXTER, A ;
MORAHAN, G ;
MILLER, JFAP .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (10) :2535-2541
[5]   CELLULAR-IMMUNITY TO A DETERMINANT COMMON TO GLUTAMATE-DECARBOXYLASE AND COXSACKIE-VIRUS IN INSULIN-DEPENDENT DIABETES [J].
ATKINSON, MA ;
BOWMAN, MA ;
CAMPBELL, L ;
DARROW, BL ;
KAUFMAN, DL ;
MACLAREN, NK .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :2125-2129
[6]   Human chemokines: An update [J].
Baggiolini, M ;
Dewald, B ;
Moser, B .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :675-705
[7]   Islet-specific expression of IL-10 promotes diabetes in nonobese diabetic mice independent of Fas, perforin, TNF receptor-1, and TNF receptor-2 molecules [J].
Balasa, B ;
Van Gunst, K ;
Jung, N ;
Balakrishna, D ;
Santamaria, P ;
Hanafusa, T ;
Itoh, N ;
Sarvetnick, N .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2841-2849
[8]  
Balasa B, 1998, J IMMUNOL, V161, P4420
[9]   Active suppression of diabetes after oral administration of insulin is determined by antigen dosage [J].
Bergerot, I ;
Fabien, N ;
Mayer, A ;
Thivolet, C .
ORAL TOLERANCE: MECHANISMS AND APPLICATIONS, 1996, 778 :362-367
[10]   Differential expression of chemokine receptors and chemotactic responsiveness of type 1 T helper cells (Th1s) and Th2s [J].
Bonecchi, R ;
Bianchi, G ;
Bordignon, PP ;
D'Ambrosio, D ;
Lang, R ;
Borsatti, A ;
Sozzani, S ;
Allavena, P ;
Gray, PA ;
Mantovani, A ;
Sinigaglia, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (01) :129-134