MIP-1α and MIP-1β are members of the CC subgroup of the ehemokine family. Although these two peptides are structurally and functionally related to one another, as well as to other CC ehemokine family members, each exhibits distinct features which allows it to independently regulate specifi
MIP-1α and MIP-1β induction by dengue virus
✍ Scribed by Tammy A. Spain-Santana; Stephanie Marglin; Francis A. Ennis; Alan L. Rothman
- Book ID
- 102378611
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 134 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0146-6615
- DOI
- 10.1002/jmv.2037
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✦ Synopsis
Abstract
Dengue virus (DV) infection can result in either a mild febrile illness known as dengue fever (DF) or a life‐threatening disease called dengue hemorrhagic fever (DHF). DHF is more prevalent in patients undergoing secondary DV infection. This observation has led to the hypothesis that DHF may be the result of immune reactions to the secondary DV infection; an event termed immunopathology. Two cellular factors, MIP‐1α and MIP‐1β, have been found to be induced by infection with DV. MIP‐1 induction by DV infection was observed in a myelomonocytic cell line, as well as in peripheral blood mononuclear cells isolated from a dengue naive donor. MIP‐1 induction was not due to factors secreted by infected cells. In fact, replication‐competent virus was required to induce MIP‐1. Evidence is also provided that MIP‐1 genes are expressed in patients with dengue disease. It is hypothesized that these chemokines may have roles in the immunopathology of dengue infections and may contribute to fever and bone marrow suppression observed in patients with DV infections. J. Med. Virol. 65:324–330, 2001. © 2001 Wiley‐Liss, Inc.
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