Correction to: J ImmunoTher Cancer (2019) 7:288
https://doi.org/10.1186/s40425-019-0778-7
Following publication of the original article [1], the authors have reported that Fig. 2 and Additional file 1: Figure S1, S2 partially show red scripts.
In Fig. 2:
A: Red font “MHC-I (MFI x 103)” should change to black font;
C: Red font “0.07” and “M-MDSC” should change to black font.
In Additional file 1: Figure S1, S2:
S1: Red font “Spleen” and “Tumor” should change to black font;
S2: Red font “C”, “D”, “E”, “F”, “G”, “H” should change to black font.
The correct version of the figures can be found below.
The corrections have been implemented in the original article as well.
We apologize for the inconvenience.
Reference
Metzger, et al. J ImmunoTher Cancer. 2019;7:288. https://doi.org/10.1186/s40425-019-0778-7.
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Additional information
The original version of this article was revised: the authors have reported that Figure 2 and S2 partially show red scripts.
Supplementary information
Additional file 1: Figure S1.
. Gating strategy for the identification of MDSC populations. Figure S2. Poly(I:C)c reduces macrophage frequency and activates macrophages, cDC, B and NK cells. Figure S3. Poly(I:C)c triggers transcriptional reprogramming of MDSC. Figure S4. Significantly regulated genes in PMN- and M-MDSC upon poly(I:C)c therapy.
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Metzger, P., Kirchleitner, S.V., Kluge, M. et al. Correction to: Immunostimulatory RNA leads to functional reprogramming of myeloid-derived suppressor cells in pancreatic cancer. j. immunotherapy cancer 7, 349 (2019). https://doi.org/10.1186/s40425-019-0830-7
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DOI: https://doi.org/10.1186/s40425-019-0830-7