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Murid Herpesvirus-4 Exploits Dendritic Cells to Infect B Cells
被引:52
作者:
Gaspar, Miguel
[1
]
May, Janet S.
[1
]
Sukla, Soumi
[1
]
Frederico, Bruno
[1
]
Gill, Michael B.
[1
]
Smith, Christopher M.
[1
]
Belz, Gabrielle T.
[2
]
Stevenson, Philip G.
[1
]
机构:
[1] Univ Cambridge, Dept Pathol, Div Virol, Cambridge CB2 1QP, England
[2] Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Australia
基金:
英国医学研究理事会;
英国惠康基金;
澳大利亚国家健康与医学研究理事会;
关键词:
EPSTEIN-BARR-VIRUS;
CD8(+) T-CELLS;
GAMMA-HERPESVIRUS;
IN-VIVO;
GAMMAHERPESVIRUS;
68;
LYMPH-NODES;
HUMAN CYTOMEGALOVIRUS;
ANTIGEN PRESENTATION;
SUBCAPSULAR SINUS;
HOST COLONIZATION;
D O I:
10.1371/journal.ppat.1002346
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Dendritic cells (DCs) play a central role in initiating immune responses. Some persistent viruses infect DCs and can disrupt their functions in vitro. However, these viruses remain strongly immunogenic in vivo. Thus what role DC infection plays in the pathogenesis of persistent infections is unclear. Here we show that a persistent, B cell-tropic gamma-herpesvirus, Murid Herpesvirus-4 (MuHV-4), infects DCs early after host entry, before it establishes a substantial infection of B cells. DC-specific virus marking by cre-lox recombination revealed that a significant fraction of the virus latent in B cells had passed through a DC, and a virus attenuated for replication in DCs was impaired in B cell colonization. In vitro MuHV-4 dramatically altered the DC cytoskeleton, suggesting that it manipulates DC migration and shape in order to spread. MuHV-4 therefore uses DCs to colonize B cells.
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页数:15
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