TY - JOUR
T1 - Proceedings of the 2017 ISEV symposium on “HIV, NeuroHIV, drug abuse, & EVs”
AU - Hu, Guoku
AU - Yelamanchili, Sowmya
AU - Kashanchi, Fatah
AU - Haughey, Norman
AU - Bond, Vincent C.
AU - Witwer, Kenneth W.
AU - Pulliam, Lynn
AU - Buch, Shilpa
N1 - Funding Information:
The work in Buch lab was supported by the National Institutes of Health Grants DA040397, MH112848 (to S.B.), DA042704, and DA033150 (to G.H.). The project described was also supported by the NIH, National Institute of Mental Health, 2P30MH062261. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Funding Information:
We thank the International Society for Extracellular Vesicle (ISEV) for their continued support in enabling us to host the symposium in Toronto, Canada in May 2017. Work in the Kashanchi Lab acknowledges the following persons: Catherine DeMarino, Stacey Boyd, Michelle Pleet, and Angela Schwab. Work in the Pulliam Lab acknowledges Bing Sun, Pranjali Dalvi, and Norina Tang. Work in the Haughey Lab acknowledges the following persons: Alex M. Dickens, Luis B. Tovar-y?Romo, Seung-Wan Yoo, Amanda L. Trout, Mihyun Bae, Marlene Kanmogne, Bezawit Megra, Dionna W. Williams, Kennith W. Witwer, Mar Gacias, Nino Tabatadze, Robert Cole, Patrizia Casaccia, Joan W. Berman, and Daniel C. Anthony. Work in the Bond Lab acknowledges the following persons: Jane Chu, Michelle Lang, William Roth, Alexander Quarshie, Eduardo Lani Volpe Da Silveira, Kenneth A. Rogers, Martin N. Shelton, Mafuz Khan, Chunxia Zhao, Richard Barnard, Praveen K. Amancha, Wendy Armstrong, Cameron Tran, and Emory University Center for AIDS Research. Work in the Witwer lab acknowledges Dillon C. Muth and Zhaohao Liao, as well as collaborators Matias Ostrowski and Clotilde Th?ry. Work in the Buch Lab acknowledges Ke Liao, Fang Niu, Lu Yang, Shannon Callen, and Howard S. Fox. International Society for Extracellular Vesicles ISEV 2017 Annual Meeting Toronto, Canada 17?21 May 2017 Conference Summary Report: Program for HIV Satellite Symposium ?HIV, NeuroAIDS, drug abuse & EVs? May 17, 2017 The authors declare that they have no conflict of interest.
Funding Information:
The work in Kashanchi lab was supported by the Department of Energy Grant DE-SC0001599, the National Institutes of Health Grants AI078859, AI074410, and AI043894 (to F. K.) and Grant NS086453 (to G. C. S.), and in part by NIAID, NCI, and the National Institute on Drug Abuse.
Funding Information:
This work in the Bond Lab was supported by the UNCF/Merck Graduate Research Dissertation Fellowship, the American Medical Association Foundation, CRECD Grant 8R25MD007589–10, and NIH NIGMS MBRS Grant R25 GM058268; NIMHD 8G12MD007602 and 8U54MD007588 from NIMHD, Georgia Research Alliance grant GRA.VAC08.W, and Emory CFAR grant P30 A1050409.
Funding Information:
This work in the Pulliam lab was supported by the National Institutes of Health grant MH112483 (to L.P.) The work in Haughey lab was supported by the National Institutes of Health grants: P30MH075673, R01MH110245, and R01DA040390 (to NH).
Publisher Copyright:
© 2017, Journal of NeuroVirology, Inc.
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Despite the success of combination antiretroviral therapy (cART), there is increased prevalence of HIV-associated neurocognitive disorders (HAND) in HIV-1-infected individuals on cART, which poses a major health care challenge. Adding further complexity to this long-term antiretroviral use is the comorbidity with drugs of abuse such as morphine, cocaine, and methamphetamine, which can in turn, exacerbate neurologic and cognitive deficits associated with HAND. Furthermore, HIV proteins, such as the transactivator of transcription (Tat) and the envelope protein (gp120), as well as antiretrovirals themselves can also contribute to the progression of neurodegeneration underlying HAND. In the field of NeuroHIV and drug addiction, EVs hold the potential to serve as biomarkers of cognitive dysfunction, targets of therapy, and as vehicles for therapeutic delivery of agents that can ameliorate disease pathogenesis. Based on the success of a previous Satellite Symposium in 2015 at the ISEV meeting in Washington, experts again expanded on their latest research findings in the field, shedding light on the emerging trends in the field of Extracellular Vesicle (EV) biology in NeuroHIV and drug abuse. The satellite symposium sought to align experts in the fields of NeuroHIV and drug abuse to share their latest insights on the role of EVs in regulating neuroinflammation, neurodegeneration, peripheral immune response, and HIV latency in HIV-infected individuals with or without the comorbidity of drug abuse.
AB - Despite the success of combination antiretroviral therapy (cART), there is increased prevalence of HIV-associated neurocognitive disorders (HAND) in HIV-1-infected individuals on cART, which poses a major health care challenge. Adding further complexity to this long-term antiretroviral use is the comorbidity with drugs of abuse such as morphine, cocaine, and methamphetamine, which can in turn, exacerbate neurologic and cognitive deficits associated with HAND. Furthermore, HIV proteins, such as the transactivator of transcription (Tat) and the envelope protein (gp120), as well as antiretrovirals themselves can also contribute to the progression of neurodegeneration underlying HAND. In the field of NeuroHIV and drug addiction, EVs hold the potential to serve as biomarkers of cognitive dysfunction, targets of therapy, and as vehicles for therapeutic delivery of agents that can ameliorate disease pathogenesis. Based on the success of a previous Satellite Symposium in 2015 at the ISEV meeting in Washington, experts again expanded on their latest research findings in the field, shedding light on the emerging trends in the field of Extracellular Vesicle (EV) biology in NeuroHIV and drug abuse. The satellite symposium sought to align experts in the fields of NeuroHIV and drug abuse to share their latest insights on the role of EVs in regulating neuroinflammation, neurodegeneration, peripheral immune response, and HIV latency in HIV-infected individuals with or without the comorbidity of drug abuse.
KW - Drug abuse
KW - Extracellular vesicles (EVs)
KW - HIV-associated neurocognitive disorders (HAND)
KW - Human immunodeficiency virus (HIV)
KW - NeuroHIV
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U2 - 10.1007/s13365-017-0599-8
DO - 10.1007/s13365-017-0599-8
M3 - Article
C2 - 29147885
AN - SCOPUS:85034227478
SN - 1355-0284
VL - 23
SP - 935
EP - 940
JO - Journal of neurovirology
JF - Journal of neurovirology
IS - 6
ER -