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Dengue Virus Serotype-2 Impairs Proliferation of Healthy Donors' T Lymphocytes
被引:5
|作者:
Fuentes-Miranda, C. J.
[1
]
Sanchez-Garcia, F. J.
[1
]
Coker, A. R.
[2
]
Rojas-Espinosa, O.
[1
]
Salinas-Tobon, R.
[1
]
Moreno-Altamirano, M. M. B.
[1
]
机构:
[1] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Dept Inmunol, Mexico City 11340, DF, Mexico
[2] UCL, Ctr Amyloidosis & Acute Phase Prot, Div Med, London, England
关键词:
T lymphocytes;
Dengue virus;
Cell proliferation;
NF-AT;
NF-kappa B;
Intracellular Ca2+;
CYTOKINE PRODUCTION;
HEMORRHAGIC-FEVER;
INTERFERON-GAMMA;
CELL RESPONSES;
INFECTION;
INTERLEUKIN-2;
MACROPHAGES;
ACTIVATION;
TARGETS;
REPLICATION;
D O I:
10.1159/000357180
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Objectives: T lymphocytes are not infected by dengue virus (DENV), nevertheless it is possible that exposure to DENV may affect their function. T lymphocytes from DENV-infected individuals are impaired in their proliferative capacity, although this effect has been attributed to altered function of antigen-presenting cells rather than to an intrinsic defect on T lymphocytes. Here we analyzed whether T lymphocytes from healthy donors became impaired in their proliferative capacity following in vitro exposure to DENV serotype-2 (DENV-2), as well as the possible mechanisms for this. Methods: Isolated CD4+ and CD8+ T lymphocytes from healthy donors were in vitro exposed to DENV-2, before polyclonal activation, cell proliferation, IL-2 synthesis. IL-2R alpha expression, nuclear translocation of NF-AT and NF-kappa B, and intracellular calcium flux were assessed. Results: In vitro exposure of both CD4+ and CD8+ T lymphocytes from healthy donors to DENV-2 impairs cell proliferation, IL-2 synthesis, and IL-2Ra (CD25) cell membrane expression. Signalling wise, exposure to DENV-2 impairs the nuclear translocation of NF-AT, downstream of intracellular calcium mobilization, as well as that of NF-kappa B. Conclusion: In the course of a dengue infection, direct exposure of T lymphocytes to DENV could affect cell-mediated immune responses. (C) 2014 S. Karger AG, Basel
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页码:83 / 92
页数:10
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