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Alternative Activation of Human Plasmacytoid DCs In Vitro and in Melanoma Lesions: Involvement of LAG-3  Chiara Camisaschi, Annamaria De Filippo, Valeria.

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Presentation on theme: "Alternative Activation of Human Plasmacytoid DCs In Vitro and in Melanoma Lesions: Involvement of LAG-3  Chiara Camisaschi, Annamaria De Filippo, Valeria."— Presentation transcript:

1 Alternative Activation of Human Plasmacytoid DCs In Vitro and in Melanoma Lesions: Involvement of LAG-3  Chiara Camisaschi, Annamaria De Filippo, Valeria Beretta, Barbara Vergani, Antonello Villa, Elisabetta Vergani, Mario Santinami, Antonello Domenico Cabras, Flavio Arienti, Frédéric Triebel, Monica Rodolfo, Licia Rivoltini, Chiara Castelli  Journal of Investigative Dermatology  Volume 134, Issue 7, Pages (July 2014) DOI: /jid Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 The lymphocyte activation gene 3 (LAG-3) defines a discrete subpopulation of human plasmacytoid dendritic cells (pDCs). The pDCs, identified in healthy donor (HD) peripheral blood mononuclear cells (PBMCs) by multiparametric FACS analysis as BDCA-2+ CD123high according to the gating strategy reported in (a), or isolated as untouched cells by immunomagnetic bead sorting and checked for purity by assessing blood dendritic cell antigen 2 (BDCA-2) expression (b), were analyzed for the expression of LAG-3. FSC, forward scatter; SSC, side scatter. (c) The frequency of LAG-3+ pDCs evaluated in pDCs gated in PBMCs (n=17) or in purified pDCs (n=9) is reported. Purified pDCs cultured with IL-3 or IL-3 plus CpG for 24 hours at 37 °C were analyzed for the expression of the maturation/activation markers CD80, CD83, and LAG-3. (d) The mean percentages with error bars of cells expressing these markers (n=5). Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

3 Figure 2 The lymphocyte activation gene 3-positive (LAG-3+) plasmacytoid dendritic cells (pDCs) are enriched in melanoma-associated pDCs (MA-pDCs) and display a partially activated phenotype. pDCs were identified by multiparametric FACS analysis as described for Figurein the peripheral blood mononuclear cells (PBMCs) of healthy donors (PBMC DON), stage III and IV melanoma patient (PBMC PT), and melanoma-invaded lymph nodes (LN) and cutaneous metastasis (CUT) (MA-pDC). The gated pDCs were then analyzed for the expression of (a) LAG-3, and (b) CD80, CD83, CD86, and tumor necrosis factor–related apoptosis-inducing ligand (TRAIL). pDCs from (c) healthy donor PBMCs (PBMC DON pDC), (d) melanoma patient PBMCs (PBMC PT pDC), and (e) melanoma-associated pDCs (MA-pDCs) were further gated as LAG-3+ or LAG-3- and analyzed for the expression of the indicated markers. The P-value was calculated using paired t-tests. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

4 Figure 3 Chemotaxis of lymphocyte activation gene 3-positive (LAG-3+) plasmacytoid dendritic cells (pDCs). (a) pDCs purified from healthy donor (HD) peripheral blood mononuclear cells (PBMCs) were added to the upper chambers of a 96-transwell plate in complete medium. The lower chambers contained complete medium (Med), complete medium plus CCL5 (CCL5), or medium conditioned by the melanoma cell lines plus IL-3 (supernatant (SN) Me204 and SN LM65). CCL5, chemokine (C-C motif) ligand 5. The number of pDCs that migrated into the lower chambers is reported in histogram (mean±SEM, n=4). (b) pDCs were tested for migration to the different media described for a in independent chemotaxis experiments. Migrated and nonmigrated pDCs were then assessed for their LAG-3 expression by FACS analysis. The percentage of LAG-3+ pDCs is reported in the histogram (mean±SEM, n=4). Only significant P-values are reported. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

5 Figure 4 Lymphocyte activation gene 3 (LAG-3) triggering induces plasmacytoid dendritic cell (pDC) activation. Healthy donor (HD) pDCs were cultured in complete medium (Med) alone or added with the stimulating agents indicated in each histogram (a–c and g–i; Mel, HLA-DR+ melanoma cell line LM65). (d, j) The ratio between the quantity of IL-6 produced by pDCs stimulated as indicated in the y axis (n=5); (e, k) the ratios between IFNα and IL-6 produced by pDCs stimulated as indicated (n=5). (f) The percentages of regulatory T cells (Tregs; Foxp3+IL-10+ in gated CD3) induced in CD4+CD25- T cells cultured with the indicated stimuli (n=2). (l) The ex vivo percentages of IL-6+ and IFNα+ pDCs in melanoma-invaded lymph node (LNs; black dots) and in cutaneous metastasis (red dots). The P-value was calculated using paired t-tests. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

6 Figure 5 Lymphocyte activation gene 3-positive (LAG-3+) plasmacytoid dendritic cells (pDCs) localized at tumor site are positive for IL-6. Consecutive sections of melanoma-invaded lymph nodes (LNs) were stained with anti-BDCA-2 antibody (Ab) to identify pDCs (a, left column) and anti-IL-6 Ab (a, right column); arrows indicate the presence of BDCA-2+ and IL-6+ cells, respectively. Scale bar=200 μm. (b, d, e) Confocal analysis of the blood dendritic cell antigen 2 (BDCA-2; green), LAG-3 (blue), and IL-6 (red) molecules shows the presence of triple-positive cells. (c) By immunohistochemistry (IHC), a pDC positive for the expression of BDCA-2 is evidenced in the proximity of the tumor area (scale bar=50 μm). Consecutive sections were also stained with anti-MART-1 (red) and anti-HLA-DR (green) Abs. LAG-3+BDCA-2+ pDCs, in direct contact with MART-1+ melanoma cells, and MART-1+HLA-DR+ cells are reported in (f) and (g), respectively. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

7 Figure 6 Monocytes (Mos) are induced to produce CCL2 (chemokine (C-C motif) ligand 2) by the supernatants (SNs) of plasmacytoid dendritic cells (pDCs) activated by melanoma cells. Monocytes purified from healthy donor (HD) peripheral blood mononuclear cells (PBMCs) were incubated for 48 hours at 37 °C in pDC-conditioned medium consisting of the SNs of overnight cocultures of purified immature pDCs plus IL-3 or purified pDCs and HLA-DR+ melanoma cells plus IL-3 in the presence or absence of a blocking anti-IL-6 mAb. Mel, HLA-DR+ melanoma cell line LM65. As a control, the monocytes were incubated with a medium conditioned overnight with IL-3 and melanoma cells. CCL2 expression was evaluated in monocytes by intracellular staining and FACS analysis. The percentage of monocytes competent for CCL2 release is indicated in each dot plot. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

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