Monocyte Traffic, Dorsal Root Ganglion Histopathology, and Loss of Intraepidermal Nerve Fiber Density in SIV Peripheral Neuropathy

Jessica R. Lakritz, Ayman Bodair, Neal Shah, Ryan O'Donnell, Michael J. Polydefkis, Andrew D. Miller, Tricia H. Burdo

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


HIV-associated sensory neuropathy remains the most common neurological complication of HIV infection and is characterized by dorsal root ganglion (DRG) inflammation and intraepidermal nerve fiber density (IENFD) loss. Chronic peripheral immune cell activation and accumulation may cause damage to the DRG, but has not been fully investigated yet. By using an SIV-infected, CD8-lymphocyte-depleted rhesus macaque model, we defined immune cells surrounding DRG neurons and their role in DRG pathology, measured cell traffic from the bone marrow to the DRGs using 5-bromo-2-deoxyuridine (BrdU) pulse, and serially measured IENFD. We found an increase in CD68+ and CD163+ macrophages in DRGs of SIV-infected animals. MAC387+ recently recruited monocytes/macrophages were increased, along with BrdU+ cells, in the DRGs of SIV-infected macaques. We demonstrated that 78.1% of all BrdU+ cells in DRGs were also MAC387+. The number of BrdU+ monocytes correlated with severe DRG histopathology, which included neuronophagia, neuronal loss, and Nageotte nodules. These data demonstrate that newly recruited MAC387+BrdU+ macrophages may play a significant role in DRG pathogenesis. IENFD decreased early (day 21), consistent with the development of sensory neuropathy in SIV-infected macaques. Decreased IENFD was associated with elevated BrdU+ cells in the DRG. These data suggest that increased recruitment of macrophages to DRG is associated with severe DRG histopathology and IENFD loss.

Original languageEnglish (US)
Article number2026
Pages (from-to)1912-1923
Number of pages12
JournalAmerican Journal of Pathology
Issue number7
StatePublished - Jul 1 2015

ASJC Scopus subject areas

  • Pathology and Forensic Medicine


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