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Analysis of Simian Immunodeficiency Virus-specific CD8+ T-cells in Rhesus Macaques by Peptide-MHC-I Tetramer Staining
Published on: December 23, 2016
Parallel loss of myeloid and plasmacytoid dendritic cells from blood and lymphoid tissue in simian AIDS
Kevin N Brown1, Anita Trichel, Simon M Barratt-Boyes
1Department of Infectious Diseases and Microbiology, Graduate School of Public Health, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Abstract:
The loss of myeloid (mDC) and plasmacytoid dendritic cells (pDC) from the blood of HIV-infected individuals is associated with progressive disease. It has been proposed that DC loss is due to increased recruitment to lymph nodes, although this has not been directly tested. Similarly as in HIV-infected humans, we found that lineage-negative (Lin(-)) HLA-DR(+)CD11c(+)CD123(-) mDC and Lin(-)HLA-DR(+)CD11c(-)CD123(+) pDC were lost from the blood of SIV-infected rhesus macaques with AIDS. In the peripheral lymph nodes of SIV-naive monkeys the majority of mDC were mature cells derived from skin that expressed high levels of HLA-DR, CD83, costimulatory molecules, and the Langerhans cell marker CD1a, whereas pDC expressed low levels of HLA-DR and CD40 and lacked costimulatory molecules, similar to pDC in blood. Surprisingly, both DC subsets were depleted from peripheral and mesenteric lymph nodes and spleens in monkeys with AIDS, although the activation status of the remaining DC subsets was similar to that of DC in health. In peripheral and mesenteric lymph nodes from animals with AIDS there was an accumulation of Lin(-)HLA-DR(moderate)CD11c(-)CD123(-) cells that resembled monocytoid cells but failed to acquire a DC phenotype upon culture, suggesting they were not DC precursors. mDC and pDC from the lymphoid tissues of monkeys with AIDS were prone to spontaneous death in culture, indicating that apoptosis may be a mechanism for their loss in disease. These findings demonstrate that DC are lost from rather than recruited to lymphoid tissue in advanced SIV infection, suggesting that systemic DC depletion plays a direct role in the pathophysiology of AIDS.
Insights
Dendritic cells (DCs), including myeloid (mDC) and plasmacytoid (pDC) types, are depleted from blood and lymphoid tissues in advanced SIV infection. This loss, driven by apoptosis, contributes to AIDS pathogenesis rather than increased recruitment to lymph nodes.
Area of Science:
- Immunology
- Virology
- Pathophysiology
Background:
- Loss of myeloid (mDC) and plasmacytoid dendritic cells (pDC) in HIV-infected individuals correlates with disease progression.
- Previous hypotheses suggested DC loss was due to increased recruitment to lymph nodes, but this remained untested.
Purpose of the Study:
- To investigate the distribution and status of myeloid and plasmacytoid dendritic cells in SIV-infected rhesus macaques.
- To determine if DC loss in AIDS is due to recruitment to lymph nodes or other mechanisms.
Main Methods:
- Flow cytometry analysis of blood, peripheral lymph nodes, and mesenteric lymph nodes in SIV-naive and SIV-infected rhesus macaques.
- Assessment of DC phenotype, activation status, and apoptosis in lymphoid tissues.
- In vitro culture of dendritic cells from lymphoid tissues to evaluate survival.
Main Results:
- SIV-infected macaques exhibited loss of mDC and pDC from blood, similar to HIV-infected humans.
- Contrary to expectations, both mDC and pDC subsets were depleted from peripheral and mesenteric lymph nodes and spleens in SIV-infected macaques with AIDS.
- Accumulation of monocytoid-like cells, not DC precursors, was observed in lymph nodes of AIDS macaques.
- Dendritic cells from lymphoid tissues of AIDS macaques showed increased susceptibility to spontaneous apoptosis in culture.
Conclusions:
- Dendritic cell loss in advanced SIV infection involves depletion from lymphoid tissues, not increased recruitment.
- Increased apoptosis of dendritic cells in lymphoid tissues is a key mechanism for their depletion during AIDS.
- Systemic dendritic cell depletion plays a direct role in the pathophysiology of AIDS.

