Hepatitis C virus ( HCV ) infection is a major public wellness load throughout the universe ( Alter and Seeff, 2000 ; Lauer and Walker, 2001 ) . It is considered to be the most common blood borne infection in the U.
S. with an estimated 4 million HCV septic persons in the U.S.
( Recommendations for prevention,1998 ) , and 180 million people are estimated to be affected by HCV globally ( Davis et al. , 2003 ; Rosen, 2011 ) .Hepatitis C virus ( HCV ) infection causes important liver disease and badness of the disease ranges widely from symptomless chronic infection to liver cirrhosis and even hepatocellular carcinoma ( HCC ) ( Lauer and Walker, 2001 ; Asselah et al. , 2009 ) .
However both familial and environmental factors have a major impact on the natural history of HCV infection ( Asselah et al. , 2009 ) .Acute hepatitis C is defined as the diagnostic infection and histories for the first six months after infection with HCV. Merely 15 % of the persons are affected by acute HCV infection and no anti-HCV antibody is detected at the first visual aspect of symptoms, in about one tierce of the septic people ( Maheshwari et al.
, 2008 ) . Viral infection elicits an initial immune response that is responsible for riddance of the virus in 15 % to 45 % of patients during acute hepatitis C ( AHC ) ( Santantonio et al. , 2008 ) .
Chronic hepatitis C can be described as an symptomless infection with HCV that remains for more than six months. It is involved in infiltration of inflammatory cells ( Leroy et al. , 2003 ) . In comparing to the other viral infections, the typical property of HCV infection is that the bulk of the individuals get chronic infection ( up to 80 % ) after viral exposure ( Lauer and Walker, 2001 ; McHutchison, 2004 ) . Upon HCV infection, many patients advancement to chronic hepatitis C as their early innate immune response and subsequently adaptative immune response have failed in uncluttering the virus. Furthermore, in many septic individuals with chronic HCV, the uneffective inflammatory response consequences in the fibrogenesis and the development of cirrhosis ( Heydtmann and Adams, 2009 ) .
Hepatitis C virus ( HCV ) is a member of Hepacivirus genus of the Flaviviridiae household ( Pedersen et al. , 2007 ; Asselah et al. , 2009 ) , represented by six genotypes and a big figure of subtypes ( Simmonds et al. , 2005 ; Pederson et al.
, 2007 ) . It is a non-cytopathic and hepatotropic RNA virus ( Heydtmann and Adams, 2009 ) , that replicates in the liver ( Lauer and Walker, 2001 ) . HCV comprises of the polyprotein that is processed into structural proteins ( nucleus and envelope proteins 1 and 2 ) , nonstructural proteins ( NS2 to NS5 ) , and a protein of unknown map ( p7 ) ( Lauer and Walker, 2001 ; Dustin and Rice, 2007 ) .The HCV virion is made up of 9.6 kilobits individual stranded positive RNA genome with extremely invariant 5? and 3? untranslated parts ( Rehermann and Nascimbeni, 2005 ; Wieland and Chisari, 2005 ) . It is contained in a mirid bug and is enveloped by a lipid bilayer, within which two different glycoproteins are anchored ( Asselah et al.
, 2009 ) .When the host cell is infected with virus, the viral genome is uncoated and maps as a templet for the interlingual rendition of individual polyprotein that is processed by host and viral peptidases. The synthesis of negative-strand RNA is initiated by the non-structural viral proteins and so negative-strand RNA acts as a reproduction templet for the extension of new positive-strand viral genomes ( Rehermann and Nascimbeni, 2005 ; Wieland and Chisari, 2005 ) . Viral reproduction is extremely fast ; more than 10 trillion viral atoms are estimated to be produced per twenty-four hours, even in the chronic stage of infection ( Neumann et al. , 1998 ) .Viral reproduction is carried out through an RNA-dependent RNA polymerase that lacks proof-reading capableness, contributes to the coevals of sequence diverseness but related quasispecies within an septic person, showing a major challenge with regard to host immune response and chronic infection ( Bowen and Walker, 2005 ; Rehermann and Nascimbeni, 2005 ; Dustin and Rice, 2007 ) .
Hepatocytes are the major mark of HCV, but the other marks of virus may include monocytes, lymph cells and endothelial cells ( Lai et al. , 2006 ; Pham et al. , 2008 ) . HCV is considered to be the common cause of chronic hepatitis and is one of the most important etiological agents of postransfusional hepatitis ( Balanescu et al. , 2012 ) .
Studies on HCV infection had been carried out in septic patients ( Lechner et al. , 2000 ; Takaki et al. , 2000 ) and Pan troglodytess ( Thimme et al.
, 2002 ; Shoukry et al. , 2004 ) .
Cytokines ; molecular weight of less than 30 kDa ; are defined as regulative proteins or glycoproteins ; secreted by white blood cells and assorted other cells in the organic structure in response to assorted stimulations. More than 200 cytokines have been identified ( Goldsby, 2003 ) .
Cytokines play an indispensable function in modulating the host responses to infection, immune responses, redness and injury ( Dinarello, 2000 ) .Structural surveies have indicated that cytokines are classified into four groups: the hematopoietin household, the interferon household, the chemokine household and the tumour mortification factor household ( Goldsby, 2003 ) .Cytokines can be categorized as proinflammatory and anti-inflammatory cytokines. Proinflammatory cytokines are involved in doing the disease worse by advancing redness whereas anti-inflammatory cytokines map to cut down redness and advance mending procedure ( Dinarello, 2000 ) .
Harmonizing to some research workers ; cytokines are responsible for both immunoregulation and immune damage ( Woitas et al. , 1999 ; Cianci et al. , 2005 ; Wright et al. , 2005 ) .
CYTOKINES AND HEPATITIS C VIRUS:
Hepatitis C virus ( HCV ) is considered to be the chief cause of hepatocellular hurt that is related with the complicated immunologic systems ( Zekri et al. , 2005 ) . In order to modulate immune responses, cytokines have major influence in commanding the implicit in pathogenesis and the ensuing consequence of HCV infection ( Amini and Poustchi, 2012 ) .
Host immune defence against HCV infection is regulated by both humoral and cell-mediated immune responses but it is indicated that cell-mediated immune response to the cytokine system is involved in the immunopathogenesis of chronic hepatitis C ( Jacobson et al. , 2001 ) .Cytokines consist of a complicated web of molecules that are responsible for modulating the inflammatory response and the homeostasis of organ maps. Furthermore, cytokines participate in many physiological and pathological actions happening in the liver ; which include ordinance of liver growing, regeneration and other inflammatory procedures such as viral liver disease, liver fibrosis and cirrhosis ( Zekri et al. , 2005 ) . During chronic HCV infection, cytokines play a cardinal function in the ordinance of hepatic redness and fibrogenesis ( Zhang et al.
, 2012 ) .It is indicated that cytokines themselves are manipulated by polymorphisms in their cistrons. However most of the familial discrepancies that confer a important hazard for chronic HCV infection have been localized in cistrons responsible for cytokine synthesis and the ultimate immune response ( Amini and Poustchi, 2012 ) .
ROLE OF INTERFERONS IN HCV INFECTION:
Interferons belong to the multigene household of inducible cytokines ( Blatt et al. , 1996 ; Diaz et al. , 1996 ; Young, 1996 ; Roberts et al. , 1998 ; Stark et al.
, 1998 ) . Interferon was foremost discovered as an antiviral agent by Isaacs and Lindenmann more than 50 old ages ago ( Isaacs and Lindenmann, 1957 ) . More than 10 mammalian IFN species and several races have been reported ( Pestka, 2007 ) and all IFNs possess antiviral activity ( Pestka et al. , 1987 ; Samuel, 1988 ; Stark et al. , 1998 ) .
IFNs are categorized into three chief groups: type I, type II and type III IFNs ( Heim, 2012 ) . The type I IFNs comprises all IFN?s, IFN? , IFN? , IFN? , IFN? and IFN? ( Pestka, 2007 ) . Type II IFNs include merely one category i.e. , IFN? ( Heim, 2012 ) , and type III IFNs have been identified as IFN?1, IFN?2 and IFN?3 and these are besides known as IL29, IL28A and IL28B severally ( Kotenko et al. , 2003 ; Sheppard et al. , 2003 ) .
Upon viral infection, cells produce IFN?s, IFN? and IFN?s ( Heim, 2012 ) .Two major tracts have been reported that are involved in the sensing of the viral genomes and in the initiation of type I and type II interferons: the toll-like receptor ( TLR ) dependant tract ( Iwasaki and Medzhitov, 2004 ; Akira et al. , 2006 ) and the cytosolic tract affecting the binding of viral genome to the RNA helicases retinoic acid inducible gene-I ( RIG-I ) and melanoma distinction antigen 5 ( MDA5 ) ( Yoneyama, 2004 ; Yoneyama and Fujita, 2007 ) .Interferons are non merely involved in the initial host response to HCV, but besides play important function in an immune response to chronic stage of hepatitis C which lasts for many old ages and later consequences in the cirrhosis and hepatocellular carcinoma ( Heim, 2012 ) .
The invariably activated endogenous IFN system has been observed in the liver of many septic patients with chronic hepatitis C and the look of 100s of IFN stimulated cistrons ( ISGs ) in hepatocytes have been indicated ( MacQuillan et al.,2003 ; Asselah et al.,2003 ; Chen et al. , 2005 ; Asselah et al. , 2008 ; Sarasin et al. , 2008 ) .
Role of type I interferons including IFN-? , -? and -? against viral infection are related with innate immune responses ( Dinging et al. , 2012 ) . The merchandises of interferon-stimulated cistrons ( ISGs ) include the cellular factors that mediate this defence mechanism. However small information is available about antiviral potency, mark specificity and the mechanism of action of most ISG merchandises ( Schoggins et al.
, 2011 ) . Direct signaling tracts by viral infection are involved in the IFN cistron written text and IFN activates the innate cellular antiviral response which serves to suppress the viral reproduction ( Yang et al. , 2011 ) .Suppression in production of HCV virion by impacting the viral RNA and protein synthesis, encouragement of immune lysis of HCV septic cells, repressive actions on hepatic fibrosis and negative consequence on HCV induced carcinogenesis ; are some of the outstanding maps of type-II interferon i.e.
IFN- ? ( Cecere et al. , 2004 ) . In add-on to these, self-generated viral riddance is besides related with IFN-? production in HCV infection ( Major et al. , 2002 ; Thimme et al. , 2002 ) .
Type-III interferon ( IFN- ? , including IL-29, IL-28A and IL-28B ) ; a new subfamily of interferon ; are associated with the suppression of viral reproduction in vitro and in vivo ( Dinging et al. , 2012 ) . However cistrons encoding these type-III interferon members are found to be clustered on human chromosome 19q13. Structurally, they are related to IL-10 superfamily of cytokines but their maps are similar to type-I interferons as they are besides activated by viral infections and possess anti-viral activity in vitro ( Kotenko et al. , 2003 ; Sheppard et al. , 2003 ) .Recent surveies have shown that there is an association of familial discrepancies near the IL28B cistron and ISG look in the liver ( Honda et al.
, 2010 ; Urban et al. , 2010 ; Dill et al. , 2011 ) but the mechanism of initiation of ISGs linked with IL28B genotype is still vague ( Heim,2012 ) . Furthermore, viral extinguishing procedures that are responsible for HCV to prevail, in malice of such powerful activation of hepatic IFN system, are non good understood. It is indicated that activated endogenous IFN system is non merely involved in HCV clearance, but besides suppresses the response to IFN- based therapies ( Chen et al. , 2005 ; Asselah et al. , 2008 ; Sarasin et al.
, 2008 ) .
ROLE OF CHEMOKINES IN HCV INFECTION:
Chemokines are a ace household of cytokines ; molecular weight of 8-10 kDa. These are chemotactic cytokines that induce leukocyte migration and are involved in orchestrating the immune response to viruses, including hepatitis C virus ( Murdoch and Finn, 2000 ; Rossi and Zlotnik, 2000 ; Heydtmann and Adams, 2009 ) .
In order to advance the cell migration, chemokines bind to specific G-protein coupled receptors, expressed on different mark cells that finally enhance the immune responses during ague and chronic redness ( Murdoch and Finn, 2000 ; Rossi and Zlotnik, 2000 ) . Although chemokines are indispensable for riddance of virus, but these are besides responsible for redness and tissue harm due to inappropriate continuity of their look in chronic hepatitis C infection ( Heydtmann and Adams, 2009 ) .On the footing of different figure of aminic acids between the N-terminal cystein residues, chemokines are classified into four households: the CC, the CXC, the CX3C, and the XC households ( Kang and Shin, 2011 ) .
Chemokines in acute HCV infection:
The function of chemokines in acute HCV infection is non good defined and in order to analyze ordinance of chemokines in acute HCV infection HCV-infected Pan troglodytes theoretical accounts had been used ( Landford et al. , 2004 ; Major et al. , 2004 ; Shin et al. , 2011 ) .
In response to HCV RNA, pattern acknowledgment receptors induce the production of type I interferon ( IFN ) in early stage of HCV infection RNA ( Havey et al. , 2003 ; Helbig et al. , 2004 ; Shin et al. , 2006 ; Decalf et al. , 2007 ; Takahashi et al. , 2010 ; Shin et al. , 2011 ) that is followed by production of Th1-associated chemokines after two to eight hebdomads of HCV infection ( Shin et al. , 2006 ; Shin et al.
, 2011 ) . In acute stage of HCV infection, CXCR3-associated chemokines ( CXCL9, CXCL10, and CXCL11 ) and CCR5-associated chemokines ( CCL3, CCL4, and CCL5 ) are considered to be indispensable for efficient antiviral T cell response ( Kang and Shin, 2011 ) .
Chemokines in chronic HCV infection:
The function of chemokines in chronic HCV infection is wholly different from their functions in acute stage of HCV infection. During acute HCV infection, chemokines take portion in enlisting of antiviral T cells that leads to viral clearance whereas in chronic HCV infection chemokines are responsible for redness.The increased degree of chemokines in the peripheral blood and the liver during chronic HCV infection, consequences in the development of redness ( Qin et al. , 1998 ; Loetscher et al. , 1998 ; Shields et al. , 1999 ; Kunkel et al.
, 2002 ; Boisvert et al. , 2003 ; Leroy et al. , 2003 ; Heydtmann et al.
, 2006 ) .Due to relentless HCV virus, there is invariably augmented production of chemokines to the liver and consequences in chronic liver hurt without viral clearance. It is observed that many of the liver-infiltrating HCV-specific T cells isolated from chronic HCV-infected patients may affect in the continuity of chronic redness that directs to uninterrupted hepatic hurt, despite being exhausted. There are many chemokines associated with liver redness in chronic HCV infection. It is indicated that during chronic HCV infection, the virus replicates persistently within the hepatocytes therefore protracting the production of chemokines and as a effect leads to uninterrupted hepatic hurt without viral riddance by enlisting of inflammatory cells to the liver ( Kang and Shin, 2011 ) .
ROLE OF Th1 AND Th2 CYTOKINES IN HCV INFECTION:
Immunoregulatory cytokines and T lymph cells are of critical importance in the host defence against HCV infection ( Zekri et al. , 2005 ) .
On the footing of differences in cytokine secernment, activated CD4+ T cells can be classified into two subsets: Th1 and Th2 subsets ( Gioia et al. , 2005 ; Lanzilli et al. , 2005 ) .
Th1 and Th2 cytokines are of import in viral infections and perturbations in the ordinance of these cytokines result in viral continuity and outgrowth of chronic disease. Recent surveies have shown that Th1 cytokines are prevailing in chronic hepatitis C and are associated with liver immunopathology ( Gigi et al. , 2008 ) .The unsuccessful event of self-generated clearance of virus and chronic continuity of virus is associated with an unequal Th1 unsusceptibility every bit good as weak HCV-infected T cell response at an inflammatory site. In order to bring on the Th1 unsusceptibility, production of interleukin-12 ( IL-12 ) is required, taking to the riddance of pathogens and viruses ( Cecere et al.
, 2004 ) .T-helper type 1 ( Th1 ) cytokines ( IL-2, IFN-? ) are needed for host anti-viral responses, while T-helper type 2 ( Th2 ) cytokines ( IL-4, IL-10 ) can stamp down the development of these effecters. Cacciarelli et Al.
observed increased degrees of IL-2, IL-4, IL-10, and IFN-? in patients infected with chronic HCV. It was reported that after handling HCV-infected patients with interferon therapy, degrees of IL-4 and IL-10 had decreased and resulted in lessened activity of HCV RNA ( Cacciarelli et al. , 1996 ) .Another survey has indicated that patients infected with chronic HCV infection exhibited augmented degrees of Th1 cytokines, including IL-2, IL-2R, and IFN-? ; whereas degrees of Th2 cytokines IL-4 and IL-6 were lower in the patients as compared to command topics ( Cribier et al. , 1998 ) .Experimental surveies have indicated that antigen-specific Th1 unsusceptibility and proinflammatory cytokines are involved in liver hurt related to HCV and viral clearance ( Schvoerer et al.
, 2003 ; Wright et al. , 2005 ; Katia et al. , 2006 ) , nevertheless small is known about pathogenesis of chronic HCV infection ( Wang et al. , 2012 ) .
ROLE OF PRO-INFLAMMATORY CYTOKINES IN HCV INFECTION:
In chronic hepatitis C, an elevated serum degree of proinflammatory cytokines has been observed ( Tilg et al. , 1992 ; Larrea et al. , 1996 ) . TNF-? and IL-1 ( ? and ? ) are considered to be important proinflammatory cytokines that are expressed by kupffer cells and T-cells in the liver ( Beutler and Cerami 1989 ; Winwood and Arthur 1993 ; Hoffmann et al.
, 1994 ) . Apart from the kupffer cells, freshly recruited macrophages from go arounding monocytes may besides move as a beginning of cytokines ( Tsukamoto, 1999 ) .It has been demonstrated that proinflammatory cytokines besides produce in endothelial cells of liver sinusoids, activated hepatic stellate cells ( HSCs ) , and bilious epithelial cells ( Hoffmann et al.
, 1994 ; Tsukamoto, 1999 ) .The map of cytokines derived from hepatocytes, is non yet clearly defined. Although surveies carried out on intrahepatic inflammatory cytokine cistrons in human chronic HCV infection have pointed out that an augmented hepatic look of the Th1 cytokines ( IL-2 and IFN- ? ) is related with HCV liver hurt ( Napoli et al.
, 1996 ; Bertoletti et al. , 1997 ; McGuinness et al. , 2000 ) . As compared to healthy individuals, the untreated chronic HCV-infected patients had shown an elevated degree of TNF-? messenger RNA in the liver and mononucleate cells ( Larrea et al. , 1996 ; McGuinness et al.
, 2000 ) .Proinflammatory cytokines may include IL-6 and IL-18, where IL-6 serves in immune responses ( Li et al. , 2004 ) and degrees of IL-18 are associated with metabolic and viral hepatic diseases ( Vacchiet et al.
, 2005 ) .As the pathogenesis of chronic HCV infection is concerned, an increased degree of proinflammatory cytokines had been observed in serum of patients ( Tilg et al. , 1992 ; Larrea et al. , 1996 ) and upregulation of intrahepatic Th1-like cytokines had besides indicated ( Napoli et al.
, 1996 ) . It was reported that HCV becomes immune to suppression by cytokines and due to this ground ; cytokines play a outstanding function in liver harm instead than commanding viral reproduction ( Shapiro et al. , 1998 ; Koziel, 1999 ) .
ROLE OF OTHER INTERLEUKINS IN HCV INFECTION:
Interleukins ( IL ) belong to one of the households of cytokines and these are secreted by some leucocytes and may move upon other leucocytes ( Goldsby, 2003 ) . Some of the interleukins associated with HCV infection are discussed here.Interleukin-17 ( IL-17 ) cytokine household has late been identified ; involved in host immune responses against intracellular pathogens and chronic inflammatory conditions. Although small information is available about the map of IL-17 bring forthing cells in HCV infection but it is indicated that T cells bring forthing IL-17/IL-22 are found in liver and circulating degrees of IL-17 are non associated with liver fibrosis ( Foster et al.
, 2012 ) . However, Chang et Al. had reported positive correlativity between IL-17 and badness of liver redness. In chronic HCV infected patients, serum IL-17 degrees are found to be higher ( Balanescu et al. , 2012 ) .Interleukin-33 ( IL-33 ) is a freshly described cytokine ; belongs to the household of IL-1. Epithelial tissues and vascular endothelial cells may bring forth IL-33 ( Schmitz et al. , 2005 ) .
However, less information is available on part of IL-33 to the pathogenesis of HCV infection.Wuang et Al. reported that IL-33 is considered to be a infective agent taking to chronic hepatitis C related liver hurt and is associated with the development of Th2 response ( Wuang et al.
, 2012 ) .The biological function of IL-33 is associated with the initiation of Th2 cell distinction and activation of mast cells, ensuing in Th2 cytokine production and Th2 response. Furthermore, the effects of IL-33 besides include pneumonic and mucosal Th2 redness ( Schmitz et al. , 2005 ) .
ROLE OF TGF-? CYTOKINE IN HCV INFECTION:
Transforming growing factor beta ( TGF-? ) is described as a major profibrogenic cytokine and HCV-specific CD8+T cells are involved in production of TGF-? .
It has a protective function in HCV-infected liver along with other T-cell derived factors, involved in bettering HCV liver disease patterned advance ( Li et al. , 2012 ) .TGF household of proteins has of import functions in ordinance of cellular procedures including growing, distinction, extracellular matrix formation and immune-suppression ( Blobe et al. , 2000 ; Hayashi and Sakai, 2012 ) . TGF-? and proinflammatory cytokines are known to be indispensable go-betweens of progressive fibrosis and carcinogenesis ( Zhang et al.
, 2012 ) .In chronic infection, HCV-specific immune effecter responses may take to liver harm and hepatic stellate cells ( HSC ) are considered as chief effecters of liver fibrosis ( Li et al. , 2012 ) .
During acute stage, adaptative effecter T cells play a important function in commanding HCV infection ( Missale et al. , 1996 ) , whereas in chronic infection, continuity of inefficient effecter T cell responses is responsible for tissue harm and inflammatory reactions, directing to fibrosis and eventually cirrhosis ( Li et al. , 2012 ) . It is reported that TGF-? produced locally by regulatory/immunosuppressive T cells ( Tregs ) inhibits instead than enhances hepatic fibrogenesis. Tregs are related with HCV pathogenesis ; nevertheless Treg functions in HCV disease patterned advance are non good understood ( Li et al.
, 2012 ) .TGF-? is a cytokine with several functions, including capableness of directing T cell line of descent committedness towards either proinflammatory Th17 T cells or anti-inflammatory Treg, depending on presence of extra factors, such as IL-6 ( Wahl, 2007 ) .TGF-? mediated suppressive activity against HCV-specific effecter map had antecedently been detected in peripheral blood of patients infected with chronic hepatitis C and a new population of non-classical human Tregs responsive to HCV that produced the Treg-associated cytokine TGF-? , had identified ( Alatrakchi et al. , 2007 ) .
Harmonizing to some surveies, Tregs are considered to be related with HCV continuity in chronic HCV infection ( Billerbeck et al. , 2007 ; Li et al. , 2008 ; Alatrakchi and Koziel, 2009 ) . Although TGF-? may play an indispensable function in anti-inflammation by locally protecting against environing tissue harm ( Li et al. , 2012 ) .It is concluded that in response to infection with HCV, cytokines are either involved in modulating the immune response in order to extinguish the virus or in liver harm by impairing the immune system. Cytokines are considered to be both positively and negatively correlated with HCV infection.