Chemokine networks and altered leukocyte traffic in acute simian immunodeficiency virus infection. Candice Cynclare Clay

ISBN: 9780549670162

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NOOKstudy eTextbook

186 pages


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Chemokine networks and altered leukocyte traffic in acute simian immunodeficiency virus infection.  by  Candice Cynclare Clay

Chemokine networks and altered leukocyte traffic in acute simian immunodeficiency virus infection. by Candice Cynclare Clay
| NOOKstudy eTextbook | PDF, EPUB, FB2, DjVu, AUDIO, mp3, RTF | 186 pages | ISBN: 9780549670162 | 4.49 Mb

Human immunodeficiency virus (HIV) debilitates the host immune system by targeting critical immune cells, namely CD4 T lymphocytes and monocytes or macrophages. The migration of HIV-infected leukocytes into tissues directly impacts disease pathogenesis by mediating viral dissemination, establishing viral reservoirs and providing new target cells for infection in various sites. The main goal of this dissertation is to examine leukocyte trafficking parameters and chemokine networks in the acute phase of simian immunodeficiency virus (SIV) infection in the nonhuman primate model for acquired immunodeficiency syndrome (AIDS).-The project presented in Chapter 1 focuses on the establishment of an in vivo leukocyte trafficking model and on defining homeostatic T lymphocyte migration patterns by tracking fluorescein dye-labeled leukocytes.

In a second project (Chapter 2), T cell trafficking parameters are examined in acute SIV infection to determine if chemokine networks and T cell migration are altered. Increased T lymphocyte homing towards the small intestine is observed in SIV-infected compared to uninfected animals, which correlates with an induction of proinflammatory chemokines in this tissue. The small intestine represents a major site of CD4 T cell depletion in acute SIV infection and the observed gut-specific T cell trafficking likely provides additional target cells for viral infection and contributes to both peripheral blood and mucosal CD4 T cell decline.

The third project (Chapter 3) focuses on monocyte migration into the central nervous system in acute SIV infection and monocytes role as Trojan Horse for virus import into the brain. Migration of dye-labeled monocytes across the blood-brain barrier is unambiguously demonstrated and neuroinflammation characterized.

In chapter 4, I extend upon the monocyte brain-trafficking studies and develop an in vitro SIV infection model to further evaluate the impact of SIV infection on monocyte migratory parameters and their neuroinvasive potential. These studies demonstrate dysregulation of chemokines and leukocyte migratory circuits in acute SIV infection expected to contribute to CD4 T lymphocyte decline and viral dissemination via monocytes into the brain. Such studies are expected to lead to novel drug targeting and treatment options that inhibit acute and chronic (neuro-) inflammation by targeting specific cells subsets and their migratory signals.



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