Production of profibrotic cytokines by invariant NKT cells characterizes cirrhosis progression in chronic viral hepatitis

被引:120
作者
de Lalla, C
Galli, G
Aldrighetti, L
Romeo, R
Mariani, M
Monno, A
Nuti, S
Colombo, M
Callea, F
Porcelli, SA
Panina-Bordignon, P
Abrignani, S
Casorati, G
Dellabona, P
机构
[1] Chiron Vaccines, IRIS Res Ctr, I-53100 Siena, Italy
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[3] Bambin Gesu Pediat Hosp, Dept Pathol, Rome, Italy
[4] Bioxell Spa, Milan, Italy
[5] Univ Milan, Ist Ricovero & Cura Carattere Sci, Maggiore Hosp, Dept Internal Med, Milan, Italy
[6] H San Raffaele Sci Inst, Div Gen Surg 1, Milan, Italy
[7] H San Raffaele Sci Inst, DIBIT, Canc Immunotherapy & Gene Therapy Program, Milan, Italy
[8] H San Raffaele Sci Inst, Expt Immunol Unit, Milan, Italy
关键词
D O I
10.4049/jimmunol.173.2.1417
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Invariant (inv)NKT cells are a subset of autoreactive lymphocytes that recognize endogenous lipid ligands presented by CD1d, and are suspected to regulate the host response to cell stress and tissue. damage via the prompt production of cytokines. We investigated invNKT cell response during the progression of chronic viral hepatitis caused by hepatitis B or C virus infection, a major human disease characterized by a diffused hepatic necroinflammation with scarring fibrotic reaction, which can progress toward cirrhosis and cancer. Ex vivo frequency and cytokine production were determined in circulating and intrahepatic invNKT cells from controls (healthy subjects or patients with nonviral benign or malignant focal liver damage and minimal inflammatory response) or chronic viral hepatitis patients without cirrhosis, with cirrhosis, or with cirrhosis and hepatocellular carcinoma. invNKT cells increase in chronically infected livers and undergo a substantial modification in their effector functions, consisting in the production of the type 2 profibrotic IL-4 and IL-13 cytokines, which characterizes the progress ion of hepatic fibrosis to cirrhosis. CD1d, nearly undetectable in noncirrhotic and control livers, is strongly expressed by APCs in cirrhotic ones. Furthermore, in vitro CD1d-dependent activation of invNKT cells from healthy donors elicits IL-4 and IL-13. Together, these findings show that invNKT cells respond to the progressive liver damage caused by chronic hepatitis virus infection, and suggest that these cells, possibly triggered by the recognition of CD1d associated with viral- or stress-induced lipid ligands, contribute to the pathogenesis of cirrhosis by expressing a set of cytokines involved in the progression of fibrosis.
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页码:1417 / 1425
页数:9
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