Literature DB >> 26572785

The meningeal lymphatic system: a route for HIV brain migration?

Susanna L Lamers1, Rebecca Rose2, Lishomwa C Ndhlovu3, David J Nolan4, Marco Salemi4, Ekaterina Maidji5, Cheryl A Stoddart5, Michael S McGrath5.   

Abstract

Two innovative studies recently identified functional lymphatic structures in the meninges that may influence the development of HIV-associated neurological disorders (HAND). Until now, blood vessels were assumed to be the sole transport system by which HIV-infected monocytes entered the brain by bypassing a potentially hostile blood-brain barrier through inflammatory-mediated semi-permeability. A cascade of specific chemokine signals promote monocyte migration from blood vessels to surrounding brain tissues via a well-supported endothelium, where the cells differentiate into tissue macrophages capable of productive HIV infection. Lymphatic vessels on the other hand are more loosely organized than blood vessels. They absorb interstitial fluid from bodily tissues where HIV may persist and exchange a variety of immune cells (CD4(+) T cells, monocytes, macrophages, and dendritic cells) with surrounding tissues through discontinuous endothelial junctions. We propose that the newly discovered meningeal lymphatics are key to HIV migration among viral reservoirs and brain tissue during periods of undetectable plasma viral loads due to suppressive combinational antiretroviral therapy, thus redefining the migration process in terms of a blood-lymphatic transport system.

Entities:  

Keywords:  HIV brain infection; Lymphatic system; Macrophage-targeted therapy; Meninges; Neurological disease

Mesh:

Substances:

Year:  2015        PMID: 26572785      PMCID: PMC4868798          DOI: 10.1007/s13365-015-0399-y

Source DB:  PubMed          Journal:  J Neurovirol        ISSN: 1355-0284            Impact factor:   2.643


  53 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-23       Impact factor: 11.205

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Authors:  Dionna W Williams; Eliseo A Eugenin; Tina M Calderon; Joan W Berman
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3.  FDC:TFH Interactions within Cervical Lymph Nodes of SIV-Infected Rhesus Macaques.

Authors:  Rajnish S Dave; Ravi K Sharma; Roshell R Muir; Elias Haddad; Sanjeev Gumber; Francois Villinger; Artinder P Nehra; Zafar K Khan; Brian Wigdahl; Aftab A Ansari; Siddappa N Byrareddy; Pooja Jain
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4.  Tissue-resident macrophages can contain replication-competent virus in antiretroviral-naive, SIV-infected Asian macaques.

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Journal:  JCI Insight       Date:  2017-02-23

5.  HIV Maintains an Evolving and Dispersed Population in Multiple Tissues during Suppressive Combined Antiretroviral Therapy in Individuals with Cancer.

Authors:  Rebecca Rose; Susanna L Lamers; David J Nolan; Ekaterina Maidji; N R Faria; Oliver G Pybus; James J Dollar; Samuel A Maruniak; Andrew C McAvoy; Marco Salemi; Cheryl A Stoddart; Elyse J Singer; Michael S McGrath
Journal:  J Virol       Date:  2016-09-29       Impact factor: 5.103

6.  HIV DNA Is Frequently Present within Pathologic Tissues Evaluated at Autopsy from Combined Antiretroviral Therapy-Treated Patients with Undetectable Viral Loads.

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10.  Development of a Novel In Vitro Primary Human Monocyte-Derived Macrophage Model To Study Reactivation of HIV-1 Transcription.

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