Identifier |
wh_ch58_p3325_1 |
Title |
Walsh & Hoyt: Life Cycle |
Creator |
Lynn K. Gordon, MD |
Affiliation |
UCLA |
Subject |
Infectious Diseases; Retroviruses; Retrovirus Diseases; Lentiviruses; Life Cycle |
Description |
The lentivirus life cycle commences with attachment of virus, initially through gp120, to the host cell via the surface receptor CD4 and coreceptors such as CXCR4, CKR5, CKR2b, or CKR3. Productive infection does not require dividing host cells, but rather occurs in terminally differentiated cells, increasing the number of potential host cells for lentiviral infections and increasing the potential gene delivery value for lentiviral vectors in gene therapy. Although direct infection of cells may ultimately lead to cell death or depletion, functional impairment may result from secondary dysfunction of other cell types leading to systemic signs or symptoms, thought to be relevant in HIV-associated encephalopathy or diarrhea. Primary host target cells include T lymphocytes, monocytes/macrophages, dendritic cells, and microglial cells. |
Date |
2005 |
Language |
eng |
Format |
application/pdf |
Type |
Text |
Source |
Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition |
Relation is Part of |
Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology |
Collection |
Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu |
Publisher |
Wolters Kluwer Health, Philadelphia |
Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
Rights Management |
Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
ARK |
ark:/87278/s6991gfd |
Setname |
ehsl_novel_whts |
ID |
185664 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6991gfd |