Tumor necrosis factor α stimulates expression of adenovirus early region 3 proteins: implications for viral persistence
Korner, Heinrich, Fritzsche, Ulrike, and Burgert, Hans-Gerhard (1992) Tumor necrosis factor α stimulates expression of adenovirus early region 3 proteins: implications for viral persistence. Proceedings of the National Academy of Sciences of the United States of America, 89 (24). pp. 11857-11861.
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Human adenovirus (Ad) can cause persistent infections in humans. Early region 3 (E3) of the virus appears to be implicated in this phenomenon. This transcription unit encodes proteins that interfere in various ways with host cell functions, including (i) cell-surface expression of histocompat- ibility class I antigens (HLA), (ih) cell-surface expression of the epidermal growth factor receptor (EGF-R), and (iii) the bio- logical activity of tumor necrosis factor a (TNF-a). We trans- fected the human cell line 293 with the entire E3 region of Ad2 and investigated the influence of the cytokines TNF-a and interferon y (IFN-y) on cell-surface expression of HLA class I and the EGF-R. Whereas IFN-y treatment induced expression of HLA to some extent but not that of the EGF-R, TNF-a treatment augmented the reduction of these cell-surface mol- ecules. Subsequent studies on the mechanism of this effect showed a TNF-a-dependent upregulation of E3 protein (E3/19K) and mRNA. The significance of this phenomenon was confirmed in infection experiments. A dramatic increase in the amount of E3/19K, even after short induction with low doses of TNF-o! could be demonstrated. The study provides evidence for an interaction between the immune system and Ad in which the virus takes advantage of an immune mediator to escape immunosurveillance of the host.
|Item Type:||Article (Refereed Research - C1)|
|Date Deposited:||07 Nov 2010 22:40|
|FoR Codes:||11 MEDICAL AND HEALTH SCIENCES > 1107 Immunology > 110709 Tumour Immunology @ 100%|
|SEO Codes:||97 EXPANDING KNOWLEDGE > 970111 Expanding Knowledge in the Medical and Health Sciences @ 100%|