Normal functional capacity in circulating myeloid and plasmacytoid dendritic cells in patients with chronic hepatitis C

被引:104
作者
Longman, RS
Talal, AH
Jacobson, IM
Rice, CM
Albert, ML
机构
[1] Inst Pasteur, F-75724 Paris, France
[2] Rockefeller Univ, New York, NY 10021 USA
[3] Cornell Rockefeller Sloan Kettering Tri Inst MD P, New York, NY USA
[4] New York Presbyterian Hosp, New York, NY USA
[5] INSERM, AV0201, Paris, France
关键词
D O I
10.1086/431523
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Initial reports analyzing dendritic cell (DC) function in patients with hepatitis C virus (HCV) infection have been controversial. Here, we enumerate and characterize the function of circulating myeloid and plasmacytoid DCs. The results show lower percentages of myeloid DCs (0.62 vs. 0.83;) and plasmacytoid DCs (0.11 Pp. 05 vs. 0.34;) in patients with chronic HCV infection than in healthy, non-HCV-infected individuals. Pp. 004 Despite the lower numbers of circulating myeloid DCs present, no phenotypic or functional defects were identified. The lower percentage of plasmacytoid DCs resulted in decreased absolute interferon (IFN)-alpha production; however, when analyzed on a per-cell basis, plasmacytoid DCs from HCV-infected patients generated levels of IFN-alpha equivalent to those generated by DCs from healthy, non-HCV-infected individuals. Contrary to data from previous models (which attributed HCV pathogenesis to defects in the DC compartment), our data reveal functional DC subsets in patients with chronic HCV infection. These results are encouraging for DC-based HCV immunotherapy trials.
引用
收藏
页码:497 / 503
页数:7
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