کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6020368 | 1580396 | 2015 | 6 صفحه PDF | دانلود رایگان |
- The influence of the innate immunity on GBM pathology remains unclear.
- We investigated complement activation and progression in glial tumor patients.
- Key-proteins of the alternative and classical pathways were decreased in GBM patients.
- MBL deficiency was less frequent among GBM patients compared to controls.
- Lower frequency of MBL deficiency may suggest a protective effect on tumor initiation.
Inflammation plays a key role in the pathophysiology of Glioblastoma Multiforme (GBM). Here we focus on the contribution of the so far largely ignored complement system.ELISA and immunohistochemistry were combined to assess levels and localization of critical components of the initiation- and effector pathways of the complement cascade in sera and tumor tissue from GBM patients and matched controls.Serum levels of factor-B were decreased in GBM patients whereas C1q levels were increased. C1q and factor-B deposited in the tumor tissue. Deposition of C3 and C5b-9 suggests local complement activation. MBL deficiency, based on serum levels, was significantly less frequent among GBM patients compared to controls (14% vs. 33%). Therefore low levels of MBL may protect against the initiation/progression of GBM.
Journal: Journal of Neuroimmunology - Volume 278, 15 January 2015, Pages 271-276