Requirement for leptin in the induction and progression of autoimmune encephalomyelitis

被引:272
作者
Matarese, G
Di Giacomo, A
Sanna, V
Lord, GM
Howard, JK
Di Tuoro, A
Bloom, SR
Lechler, RI
Zappacosta, S
Fontana, S
机构
[1] Hammersmith Hosp, Imperial Coll Sch Med, Dept Immunol, London W12 0NN, England
[2] Univ Naples Federico II, Cattedra Immunol, Dipartimento Biol & Patol Cellulare & Mol, Naples, Italy
[3] Univ Naples Federico II, Dipartimento Sci Biomorfol, Naples, Italy
[4] Azienda Osped V Monaldi, Lab Immunol Cellulare, Naples, Italy
[5] CNR, Ctr Endocrinol & Oncol Sperimentale, I-80125 Naples, Italy
[6] Hammersmith Hosp, Imperial Coll Sch Med, Endocrine Unit, London W12 0NN, England
关键词
D O I
10.4049/jimmunol.166.10.5909
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent evidence indicates that leptin modifies T cell immunity, and may provide a key link between nutritional deficiency and immune dysfunction. To study the influence of leptin on autoimmunity, susceptibility to experimental autoimmune encephalomyelitis induced by immunization with a myelin-derived peptide was examined in leptin-deficient, C57BL/6J-ob/ob mice, with or without leptin replacement, and in wild-type controls. Leptin replacement converted disease resistance to susceptibility in the C57BL/6J-ob/ob mice; this was accompanied by a switch from a Th2 to Th1 pattern of cytokine release and consequent reversal of Ig subclass production. Our findings suggest that leptin is required for the induction and maintenance of an effective proinflammatory immune response in the CNS.
引用
收藏
页码:5909 / 5916
页数:8
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