Human T-cell leukemia virus type 1 p8 protein increases cellular conduits and virus transmission
Author(s) -
Nancy Van Prooyen,
Heather Gold,
Vibeke Andresen,
Owen Schwartz,
Kathryn S. Jones,
Frank W. Ruscetti,
Stephen Lockett,
Prabhakar R. Gudla,
David Venzon,
Genoveffa Franchini
Publication year - 2010
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1009635107
Subject(s) - virus , tropical spastic paraparesis , biology , virology , human t lymphotropic virus 1 , leukemia , t cell , immune system , microbiology and biotechnology , t cell leukemia , immunology , myelopathy , spinal cord , neuroscience
The human T-cell leukemia virus type 1 (HTLV-1) is the cause of adult T-cell leukemia/lymphoma as well as tropical spastic paraparesis/HTLV-1-associated myelopathy. HTLV-1 is transmitted to T cells through the virological synapse and by extracellular viral assemblies. Here, we uncovered an additional mechanism of virus transmission that is regulated by the HTLV-1-encoded p8 protein. We found that the p8 protein, known to anergize T cells, is also able to increase T-cell contact through lymphocyte function-associated antigen-1 clustering. In addition, p8 augments the number and length of cellular conduits among T cells and is transferred to neighboring T cells through these conduits. p8, by establishing a T-cell network, enhances the envelope-dependent transmission of HTLV-1. Thus, the ability of p8 to simultaneously anergize and cluster T cells, together with its induction of cellular conduits, secures virus propagation while avoiding the host's immune surveillance. This work identifies p8 as a viral target for the development of therapeutic strategies that may limit the expansion of infected cells in HTLV-1 carriers and decrease HTLV-1-associated morbidity.
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