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Hepatitis C virus persistence in human hematopoietic cells injected into SCID mice
Author(s) -
Bronowicki JeanPierre,
Loriot MarieAnne,
Thiers Valérie,
Grig Yves,
Zignego Anna Linda,
Bréchot Christian
Publication year - 1998
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.510280127
Subject(s) - peripheral blood mononuclear cell , hepatitis c virus , virology , haematopoiesis , biology , immunology , virus , persistence (discontinuity) , hepatitis c , medicine , stem cell , in vitro , biochemistry , genetics , geotechnical engineering , engineering
The issue of infection of peripheral blood mononuclear cells (PBMC) by the hepatitis C virus (HCV) has potentially important implications, but is still debated. We have used the severe combined immunodeficiency (SCID) mouse model to test for the persistence of HCV in PBMC. Hematopoietic cells isolated from 14 subjects infected by HCV were inoculated intraperitoneally into SCID mice. Serum and blood cell samples from these mice were obtained with a mean follow‐up of 8 weeks. As controls, human fibroblasts and sheep PBMC, preincubated with a human HCV‐positive serum, were inoculated concomitantly into mice and analyzed. HCV‐RNA positive strands were detected in 7 of 26 serum samples and 8 of 26 cell fractions from SCID mice inoculated with HCV‐positive PBMC, after 8 weeks of follow‐up. In contrast, no HCV RNA was detectable in the 10 control mice. HCV‐RNA negative strands were detected in only 2 of 10 tested samples from 2 mice, and both positive mice had been inoculated with PBMC from HCV‐positive subjects with malignant hematopoietic syndrome. Our study offers strong evidence for the persistence of HCV infection in mononuclear cells. Our results are also consistent with a low rate of HCV multiplication. This SCID mouse model might therefore be useful in analyzing the mechanisms of HCV persistence in mononuclear cells.