The role of IL‐28, IFN‐γ, and TNF‐α in predicting response to pegylated interferon/ribavirin in chronic HCV patients. Issue 1 (6th August 2014)
- Record Type:
- Journal Article
- Title:
- The role of IL‐28, IFN‐γ, and TNF‐α in predicting response to pegylated interferon/ribavirin in chronic HCV patients. Issue 1 (6th August 2014)
- Main Title:
- The role of IL‐28, IFN‐γ, and TNF‐α in predicting response to pegylated interferon/ribavirin in chronic HCV patients
- Authors:
- Abdou, Asmaa Gaber
Asaad, Nancy Youssef
Ehsan, Nermin
Eltahmody, Mohammad
El‐Sabaawy, Maha Mohamed
Elkholy, Shimaa
Elnaidany, Nada Farag - Abstract:
- <abstract abstract-type="main" id="apm12301-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The primary goal of HCV therapy is to achieve a sustained virological response (SVR). Many host and viral factors influence the treatment response. Cytokines play an important role in the defense against viral infections, where successful treatment of hepatitis C depends on a complex balance between pro‐ and anti‐inflammatory responses. In the present study, we investigated the relationship between the presence and percentage of some cytokines (IL‐28, IFN‐γ, and TNF‐α) regarding different clinicopathological parameters including response to therapy in chronic HCV patients using immunohistochemical technique. This study was carried out on 64 chronic HCV patients (34 responders and 30 non‐responders). Of cases, 54% showed IL‐28 expression, which was associated with low AST (p = 0.002) and low HAI score (p = 0.006). Of cases, 67 and 45% showed IFN‐γ and TNF‐α expression, respectively, where the median percentage of TNF‐α expression was higher in grade II spotty necrosis compared to grade I. Some inflammatory cytokines expressed by intrahepatic inflammatory cells in chronic HCV patients promote inflammation and injury (pro‐inflammatory) such as TNF‐α. Other cytokines aid in resolving inflammation and injury (anti‐inflammatory) such as IL‐28. The balance between these cytokines will determine the degree of inflammatory state. None of the investigated cytokines proved<abstract abstract-type="main" id="apm12301-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The primary goal of HCV therapy is to achieve a sustained virological response (SVR). Many host and viral factors influence the treatment response. Cytokines play an important role in the defense against viral infections, where successful treatment of hepatitis C depends on a complex balance between pro‐ and anti‐inflammatory responses. In the present study, we investigated the relationship between the presence and percentage of some cytokines (IL‐28, IFN‐γ, and TNF‐α) regarding different clinicopathological parameters including response to therapy in chronic HCV patients using immunohistochemical technique. This study was carried out on 64 chronic HCV patients (34 responders and 30 non‐responders). Of cases, 54% showed IL‐28 expression, which was associated with low AST (p = 0.002) and low HAI score (p = 0.006). Of cases, 67 and 45% showed IFN‐γ and TNF‐α expression, respectively, where the median percentage of TNF‐α expression was higher in grade II spotty necrosis compared to grade I. Some inflammatory cytokines expressed by intrahepatic inflammatory cells in chronic HCV patients promote inflammation and injury (pro‐inflammatory) such as TNF‐α. Other cytokines aid in resolving inflammation and injury (anti‐inflammatory) such as IL‐28. The balance between these cytokines will determine the degree of inflammatory state. None of the investigated cytokines proved its clear cut role in affecting response to therapy, however, their levels varied between responders and non‐responders for further investigations to clarify.</p> </abstract> … (more)
- Is Part Of:
- Apmis. Volume 123:Issue 1(2015:Jan.)
- Journal:
- Apmis
- Issue:
- Volume 123:Issue 1(2015:Jan.)
- Issue Display:
- Volume 123, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 123
- Issue:
- 1
- Issue Sort Value:
- 2015-0123-0001-0000
- Page Start:
- 18
- Page End:
- 27
- Publication Date:
- 2014-08-06
- Subjects:
- Pathology -- Periodicals
Microbiology -- Periodicals
Immunology -- Periodicals
572 - Journal URLs:
- http://www.blackwell-synergy.com/loi/apm ↗
https://onlinelibrary.wiley.com/journal/16000463 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apm.12301 ↗
- Languages:
- English
- ISSNs:
- 0903-4641
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1568.740000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3902.xml