Differential partial activation phenotype and production of tumour necrosis factor-α by conventional dendritic cells in response to lipopolysaccharide in HIV+ viraemic subjects and HIV+ controllers
Version of Record online: 7 NOV 2014
© 2014 British Society for Immunology
Clinical & Experimental Immunology
Volume 178, Issue 3, pages 489–503, December 2014
How to Cite
Camacho-Sandoval, R., Del Río Estrada, P. M., Rivero-Arrieta, A., Reyes-Terán, G. and Bonifaz, L. C. (2014), Differential partial activation phenotype and production of tumour necrosis factor-α by conventional dendritic cells in response to lipopolysaccharide in HIV+ viraemic subjects and HIV+ controllers. Clinical & Experimental Immunology, 178: 489–503. doi: 10.1111/cei.12430
- Issue online: 7 NOV 2014
- Version of Record online: 7 NOV 2014
- Accepted manuscript online: 5 AUG 2014 04:51AM EST
- Manuscript Accepted: 29 JUL 2014
- Mexican Government (Comisiónde Equidad y Género de la H. Cámara de Diputados)
- Fundación México Vivo
- Consejo Nacional de Ciencia y Tecnología (CONACyT). Grant Numbers: 134511, 232303
Fig. S1. Gating strategy to identify dendritic cell (DC) subsets.
Fig. S2. CD86 and CD47 expression are correlated positively.
Fig. S3. Frequency of IL-12 + conventional dendritic cells (cDC) in lipopolysaccharide (LPS)-treated peripheral blood mononuclear cells (PBMCs) is similar between viraemic subjects and controls.
Fig. S4. Toll-like receptor (TLR)-4 and TLR-8 expression in conventional dendritic cells (cDC).
Fig. S5. Interleukin (IL)-1β cytokine production by peripheral blood mononuclear cells (PBMCs) after lipopolysaccharide (LPS) stimulation differs between controls and viraemic subjects.
Fig. S6. Gating strategy to identify B cells, natural killer (NK) cells, CD4+ T cells and monocytes.
Fig. S7. Differential frequency of interleukin (IL)-1β in conventional dendritic cells (cDC) after lipopolysaccharide (LPS)-treated peripheral blood mononuclear cells (PBMCs) between viraemic subjects and controllers.
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