Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Transcriptomic profiles conducive to immune-mediated tumor rejection in human breast cancer skin metastases treated with Imiquimod


Imiquimod is a topical toll-like-receptor-7 agonist currently used for treating basal cell carcinoma. Recently, imiquimod has demonstrated tumor regression in melanoma and breast cancer skin metastases. However, the molecular perturbations induced by imiquimod in breast cancer metastases have not been previously characterized. Here, we describe transcriptomic profiles associated with responsiveness to imiquimod in breast cancer skin metastases. Baseline and post-treatment tumor samples from patients treated with imiquimod in a clinical trial were profiled using Nanostring technology. Through an integrative analytic pipeline, we showed that tumors from patients who achieved a durable clinical response displayed a permissive microenvironment, substantiated by the upregulation of transcripts encoding for molecules involved in leukocyte adhesion and migration, cytotoxic functions, and antigen presentation. In responding patients, Imiquimod triggered a strong T-helper-1 (Th-1)/cytotoxic immune response, characterized by the coordinated upregulation of Th-1 chemokines, migration of Th-1 and cytotoxic T cells into the tumor, and activation of immune-effector functions, ultimately mediating tumor destruction. In conclusion, we have shown that topical imiquimod can induce a robust immune response in breast cancer metastases, and this response is more likely to occur in tumors with a pre-activated microenvironment. In this setting, imiquimod could be utilized in combination with other targeted immunotherapies to increase therapeutic efficacy.


Breast cancer is the second cause of death in women and the second most common cancer to metastasize to the skin after melanoma1. Treatment of breast cancer skin metastases remains a challenge. Initial management usually consists of resection and radiotherapy but skin metastases often recur and can lead to chest wall ulceration, bleeding, and pain.

Imiquimod is a Toll-like Receptor (TLR)-7 agonist that can activate the innate immune system and shape the ensuing adaptive immune response. Imiquimod induces the production of several pro-inflammatory cytokines such as IFN-α, TNF-α, IL-1, IL-6, and IL-8 and leads to the recruitment and activation of dendritic cells2,3,4. In basal and squamous cell carcinoma, imiquimod induces infiltration of the tumor with effector T cells, increases production of IFN-γ, granzyme, perforin, and apoptosis5,6. Genome-wide transcriptomic analysis of basal cell carcinoma before and after treatment has defined key molecular events induced by imiquimod7. Such transcripts are involved in the activation of specific chemokine-chemokine receptor ligand pathways conducive to a T-helper 1 (Th-1) immune response and the induction of immune-effector genes. These pathways are also activated during other forms of immunity-mediated tissue-specific destruction, such allograft rejection8, graft-versus-host disease and flares of autoimmunity, and were termed as the Immunologic Constant of Rejection (ICR)9,10,11. The ICR signature was further refined and is now represented by twenty transcripts in four functional categories: CXCR3/CCR5 chemokines (including CXCL9, CXCL10, CCL5), Th1 signaling (including IFNG, IL12B, TBX21, CD8A, STAT1, IRF1, CD8B), effector (including GNLY, PRF1, GZMA, GZMB, GZMH) and immune regulatory functions (including CD274, CTLA4, FOXP3, IDO1, PDCD1)12,13,14. High expression of the ICR has been found to be associated with favorable prognosis in multiple tumor types and responsiveness to immunotherapeutic approaches such as IL-2, adoptive therapy and checkpoint inhibition10,15,16,17.

In melanoma, several case reports have shown regression of cutaneous metastases with imiquimod either alone18,19 or in combination with other therapies20,21,22. This tumor regression was associated with an increase in T cell infiltrate and upregulation of ICR genes such as CCL5, CXCL9, CXCL10 important for homing of cytotoxic T cells as well as markers of dendritic cell (CD80, CD86) and T cell activation (CD69)23.

Activation of the adaptive immune response has been shown to be associated with better prognosis in breast cancer. An increase in the number of tumor infiltrating lymphocytes is associated with greater likelihood of complete pathological response after chemotherapy across breast cancer subtypes, and reduced risk of relapse and death particularly in triple negative breast cancers24,25,26,27,28,29,30,31. Interestingly, most of the prognostic and predictive transcriptomic classifiers described so far in breast cancer include ICR genes. Type I immunity is believed to be especially important for immunotherapy, with CD8+ T cells inducing cytotoxicity and CD4+ T helper cells inducing cytokine secretion and promotion of antigen presentation of tumor32. In a recent trial, topical imiquimod in combination with intravenous nab-paclitaxel resulted in an antitumor response of 72% in the treatment of mostly hormone receptor negative breast cancer cutaneous metastases33 suggesting that activation of the immune system may play an important role in the treatment of breast cancer skin metastases. Imiquimod may play an even more important role in hormone receptor positive breast cancer, since it is the subtype with the least amount of CD8+ infiltrating T cells34.

We have previously shown that topical imiquimod, as a single agent, can induce an antitumor response in 20% of skin metastases of mainly hormone receptor positive breast cancers and can promote an immunogenic tumor microenvironment35. An increase in CD4+ and CD8+ infiltrating T cells after treatment was seen in one of the responders but not in the other, and cytokine measurement in tumor supernatant was variable, suggesting the need for a more sensitive assay to characterize the effects of imiquimod on the tumor microenvironment in breast cancer skin metastases. Furthermore, in two additional patients who achieved long-term benefit, an antitumor antigen response was induced by imiquimod (in-situ vaccination effect) and subsequently expanded by endocrine therapy leading to durable complete remissions.36

Here, by using an integrative analysis we describe transcriptomic profiles associated with responsiveness to imiquimod treatment. This is the first study to characterize the transcriptomic changes induced by imiquimod in breast cancer skin metastases.



Ten patients were enrolled and treated with imiquimod for eight weeks as previously described35. The clinical trial was approved by the New York University Institutional Review Board. All research was performed in accordance with the New York University Institutional Review Board guidelines and regulations, a written informed consent was obtained from all patients. Same-site tumor biopsies were obtained at baseline and after 8 weeks of imiquimod treatment. Paraffin embedded tumor tissue was available from 8/10 patients for this study, as samples from two patients had insufficient quantity for further analysis. Two of the patients had stable disease during the initial study and were found to have a systemic complete clinical response after subsequent treatment with fulvestrant after study completion (including the treated skin metastases). On follow up, these two patients also had disease remission for two years. We initially sought to characterize the tumor microenvironment of these two patients due to their unusual complete response on hormone therapy and long duration of disease remission and labeled these patients as complete responders (CR). An additional patient had a local partial tumor response (greater than 50% tumor shrinkage) after eight weeks of imiquimod treatment and was labeled as a partial responder (PR). Patients with CR and PR were considered as having derived clinical benefit (CB). Five of the eight patients did not have a clinical response and were defined as non-responders (NR).

Gene Expression

Paraffin blocks were carefully evaluated for tumor content and cut into seven sections of 10 um thickness for RNA extraction. Samples were deparaffinized with xylene and extracted using the RNeasy FFPE kit (Qiagen #73504), according to manufacturer’s instructions. Extracted FFPE RNA quality and quantity were analyzed on an agilent Bioanalyzer 2100 using a nano chip. Smear analysis was performed to determine the percent of RNA greater than 300nt for optimized hybridization according to Nanostring’s protocol. Adjusted inputs for each RNA sample were calculated to input 100 ng of RNA greater than 300nt. RNA was hybridized using the Nanostring nCounter® Human v1.1 PanCancer Immune Profiling Panel (770 transcripts) according to the manufacturer’s protocol. Hybridizations were processed on the nCounter Prep Station, and prepped cartridges were scanned on the Nanostring Digital Analyzer using 280 field of view counts.


The evaluation of tumor-infiltrating lymphocytes (TIL) density was performed by Immunohistochemistry (IHC) on paraffin embedded tumor tissues as previously described35 and correlated with clinical response. Tumor sections (thickness 4 μm) were deparaffinized and rinsed in distilled water. Heat induced epitope retrieval was carried out in 10 mmol/L citrate buffer. CD3, CD4, CD8 (Ventana Medical Systems), and Forkhead Box Protein P3 antibody (FoxP3, Ebiosciences) antibodies were used. Detection was carried out on a NEXes instrument (Ventana Medical Systems) using the manufacturer’s reagent buffer and detection kits. After washing in distilled water, slides were counterstained with hematoxylin, dehydrated, and mounted with permanent media. Appropriate positive and negative controls were included with the study sections. IHC-positive cells were counted manually in 5 representative high-power fields (HPF, 400), to derive the average number per HPF, by a pathologist blinded to the response.

Statistical Analysis

Data were normalized using the housekeeping genes present in the panel and by applying negative control subtraction (nSover 2.6 package). Quantile normalization using preprocessCore v1.38 and Log2 transformation was applied to the expression matrix. PCA plots were generated using scatterplot3d v0.3. Consensus clustering based on the ICR genes was performed using consensusclusterPlus v1.40 (maxK = 7, 5000 repetitions, Ward D2 as interlinking). Based on such clustering, samples were classified as ICR High, ICR Medium, and ICR Low, with ICR High and ICR Low samples as the highest and lowest expression of the ICR z-score, respectively.

Singe sample gene set enrichment (ssGSEA)37,38 using GSVA package v1.24.2 was applied to calculate enrichment scores for leukocyte populations using cell-specific transcripts included in the Nanostring panel (Supplementary Table S1) as well as the enrichment score for the ICR genes. The fold changes of these scores were expressed as the ratio of Anti Loge of the mean enrichment scores and were plotted with their confidence interval using forestplot v1.7.2. Differentially expressed genes (DEGs) or differences in the enrichment scores were calculated by paired or unpaired t-test for the post- vs pre-treatment and CR vs NR analysis respectively using 2-tailed p value of 0.05 as significance cut off. Fold change was expressed by the Anti-Log2 of the Log2 fold change, which is the difference between the mean of the Log2 values of the two categories in comparison. Enrichment analysis of the DEGs was performed using Nanostring annotations (immune response categories, Supplementary Table S2) specific for this panel. In all comparisons of response status, only the CR and NR samples were included as these samples represent tumors with two opposite biologic behaviors. PR data were however displayed in the heatmaps and boxplots in comparison with CR and NR samples. Post- vs pre-treatment comparisons were performed by including all samples. Boxplots for single gene expression and ICR score were plotted using ggplot2 v 2.2.1. Dotted heatmaps were used to represent the ssGSEA enrichment z-scores and the percentage of genes with an absolute fold change of more than 1.5 for each immune cell signature. These plots were generated using the ComplexHeatmap v1.14 package. Immunohistochemistry data were compared by Wilcoxon signed-rank test.


Patient characteristics

Paired tissues from eight patients with breast cancer skin metastases enrolled on a clinical trial of imiquimod therapy were included in this study. Patient demographics are summarized in Table 1. The majority of the women were post-menopausal (62.5%), all had invasive ductal carcinoma, and the majority of tumors were high grade (87.5%) and hormone receptor positive (87.5%), 50% were HER2 positive. Patients were designated as CR (n = 2), PR (n = 1), and NR (n = 5) as described above.

Table 1 Patient characteristics.

Transcriptome changes induced by imiquimod treatment and baseline predictive markers

Principal component analysis (PCA) based on all the transcripts is shown in Fig. 1A. Using a PC1 arbitrary cut-off of −10 3/3 tumors from patients responding to the treatment but only 1/5 tumors from non-responding patients were found to cluster. The number of overlapping genes among the comparisons used for the detection of the DEGs (e.g., post vs pre-treatment, pre-treatment CR vs NR, and post-treatment CR vs NR) are shown in Fig. 1B. Comparing all patients post- versus pre-treatment, 53 DEGs were identified (Table 2, Fig. 1B,C). Several genes related to innate immunity were upregulated in the post-treatment group. These included genes related to lymphocyte activation (SH2D1A, SLAMF1), lymphocyte adhesion (SELL), cytolysis (PRF1), NK cell activation (KLRC1), T cell (CD3G, CD347) and cytotoxic T cell (CD8A) function, and antigen presentation (HLA-C). Although some genes were downregulated, overall, pathway enrichment analysis revealed a positive modulation of the immune response underlined by the activation of cytotoxic mechanisms (Fig. 1D and Supplementary Table S3). Downregulated genes included several MAPK-related genes (MAP2K4, MAPK1, MAPK11 and MAP3K5), which are also involved in oncogenic signaling, and genes related to IL-17/Th-17 and IL-13 signaling (Table 2 and Supplementary Table S3).

Figure 1

Transcriptomic changes according to treatment and response status. (A) Principle component analysis (PCA) based on all transcripts. (B) Venn diagrams of DEGs, (separated by down and upregulated, p < 0.05) red circles: paired t-test, post- vs pre-treatment samples; blue circles: unpaired t-test, pre-treatment complete responder (CR) vs pre-treatment non responder (NR), excluding the partial responder (PR) sample from the statistical test; green circles: unpaired t-test, post-treatment complete responder (CR) vs post-treatment non responder (NR), excluding the partial responder sample from the statistical test. (C) Heatmaps based on the DEGs in B; samples are ordered according to treatment and ICR score in the left panel, and using hierarchical clustering in the middle and right panel; the PR sample was clustered according to the DEG as in B; genes are ordered according to hierarchical clustering in all panels; Hormone receptor (HR) status, HER2 receptor (HER2) status and ICR classification are shown. For the ICR classification, samples were clustered using consensus clustering based on 20 ICR genes in 3 groups with low (ICR low), intermediate (ICR medium), and high (ICR high) expression of the ICR genes (see methods). (D) Top enriched Nanostring pathways (Immune Response Categories).

Table 2 DEG post vs pre-treatment.

In baseline samples, prior to treatment with imiquimod, 45 genes were differentially expressed in CR vs NR samples (Table 3, Fig. 1B). Interestingly, the PR clustered between CR and NR (Fig. 1C). Upregulated genes included leukocyte adhesion and migration molecules (ITGAX, ITGAM, ITGB2, and FUY7), chemokine receptor (CX3CR1), T-cell cytotoxic markers (CD8A, and GZMK), and genes associated with antigen presentation (HLA-DMA, HLA-DBP1, and HLA-DPA1). Enrichment analysis corroborated the existence of a permissive microenvironment in lesions from patients with clinical benefit from imiquimod, substantiated by the activation of the antigen processing pathway, which was accompanied by the downregulation of some cytokines such as IFN lambda 1 (IFNL1) IL34, and IL23, which is involved in Th-17 signaling (Fig. 1D).

Table 3 DEG CR vs NR (pre-treatment).

After imiquimod treatment, CR versus NR differed in 57 DEGs (Table 4, Fig. 1B). In this analysis, the PR clustered together with the CR. CR patients had higher levels of several immune genes (Fig. 1C), including chemokines and chemokine receptors (CXCL13, CXCL9, CCL5, CCR5, CXCR3, CCR7, CXCR4), markers of lymphocyte activation (LAG3, TXK), NK cells (KLRC2, KLRD1, NCR1), neutrophils (LCN2), and markers of effector function (GNLY, GZMB, GZMK, GZMA), and innate immunity (TNFRSF1B, IL7R). S100A7, which is involved in the regulation of cell cycle progression and proliferation, was also over-expressed. The top enriched pathways in the CR group included NK and T-cell functions, chemokines and (immune) regulation (Fig. 1D).

Table 4 DEG CR vs NR (post-treatment).

Applying multiple hypothesis correction of a 0.25 false discovery rate (q values provided in Tables 2, 3 and 4), yielded 5 genes in the pre-treatment comparison (MPPED1, ITGAM, HLA-DPB1, HLA-DPA1, and GZMK, all upregulated in the CR vs NR samples) and 18 genes in the post-treatment comparison (ICAM2, GZMA, CD48, ITK, STAT4, HLA-A, KLRK1, RUNX3, CXCR4, KLRC2, LCN2, IL7R, CCL5, CXCL9, and CCR5, upregulated in CR vs NR samples and CD1A, USP9Y, and IRAK1, upregulated in NR vs CR samples). The majority of the transcripts upregulated in CR samples relate to chemoattraction, antigen presentation (pre-treatment comparison), and cytotoxic mechanisms (post-treatment comparison). No genes passed the 0.25 false discovery rate in the pre vs post-treatment comparison likely due to the dilution of the signal caused by the hypo-responsive samples.

Responders to imiquimod treatment had higher levels of T cells and cytotoxic cells

Single sample gene set enrichment analysis (ssGSEA) was used to estimate the variation in leukocyte subpopulations in each sample. Post- vs pre-treatment comparison revealed that overall, imiquimod consistently enhanced T cell (p = 0.011) and cytotoxic T cell (p = 0.017) infiltration (Fig. 2A). Before treatment, CR patients had a lower level of T central-memory (Tcm) cells (p = 0.038) and a higher level of macrophages (p = 0.0057), T cell (p = 0.039) and NKCD56 bright cells (p = 0.012) as compared to NR patients. The relative depletion of Tcm cells could be the result of a proportional enrichment of activated T-cell after treatment. Thus, CR patients displayed a baseline pre-activated immune microenvironment (Fig. 2B).

Figure 2

Variation in leukocyte subpopulations according to treatment and response status as estimated by transcriptomic analysis. (A–C) Forest plots based on fold changes of leukocyte subpopulation enrichment score. The enrichment score for each leukocyte subpopulation is calculated by single sample gene set enrichment analysis (ssGSEA). Fold changes (FC) are calculated as the ratio of Anti Loge of the enrichment scores. FC > 1 consists of increased enrichment score in post- vs pre-treatment sample in (A), increased enrichment score in pre-treatment CR vs pre-treatment NR samples in (B), and increased enrichment score in post-treatment complete responder vs post-treatment non responder samples (C). p-values are from paired (A) and unpaired (B,C) t-test. The PR was not included in the analysis. Red dots highlight the significant findings (p < 0.05, two-tailed).

In CR patients, there was a strong activation of the cytotoxic response (p = 0.012) accompanied by upregulation of the ICR genes (Fig. 2C) (p = 0.023) and by a switch from immature dendritic cells (iDC) (p = 0.0228) to activated dendritic cells (aDCs) (p = 0.096) in post-treatment compared to baseline biopsy. At the individual sample level, the magnitude of the cytotoxic response was maximal in responding patients, with similar levels among the two CR and the PR (Fig. 3A,B).

Figure 3

Single sample enrichment scores and consistent changes induced by imiquimod. (A) Dotted heatmaps representing the single sample gene set enrichment analysis (ssGSEA) of immune signatures with at least 3 genes present in the nanostring data, with labels for response (NR, PR, CR), treatment (post and pre), hormone receptor (HR) status, HER2 receptor (HER2) status and ICR classification, samples are ordered according treatment and ICR score. (B) Matching dotted heatmap representing the percentage of genes in the signature up or downregulated more the 1.5 fold between post and pre-treatment, with inversely regulated genes canceling each other out, cut-off at 15%.

A nonsignificant trend for higher CD3, CD8, CD4, and FOXP3 positive cells, as evaluated by immunohistochemistry, was observed in CR vs NR pre-treatment samples and was also present after treatment. However, among the responding patients, IHC evaluation detected increase of TILs (consistent across all the markers) only in the PR patient (Supplementary Figure 1), who had a local response at the time of the biopsy. This observation suggests that molecular profiling might be more sensitive than IHC in detecting changes in the functional orientations of the tumor microenvironment preceding the clinical response.

Responders to imiquimod treatment displayed consistent upregulation of the ICR score

We analyzed the immunologic constant of rejection (ICR) score (ie., the mean log2 expression of the ICR genes, Fig. 4A,B) across samples, and compared its expression in CR versus NR, pre- and post-treatment. The ICR score was significantly higher in the post-treatment CR vs NR samples (p = 0.021) while it did not differ among the two categories at baseline (Fig. 4C). Interestingly, the PR sample clustered with the CR samples. The ICR genes with significantly higher levels in CR vs NR samples after treatment are shown in Fig. 4D. Most of the ICR genes had similar and consistent trends (Supplementary Figure 2). An exception was represented by FOXP3, which displayed a non significant lower level in post-treatment CR vs NR samples.

Figure 4

ICR gene expression according to treatment and response status. (A) Schematic representation of ICR genes divided by functional categories. (B) Heatmap based on ICR gene expression, with labels for response (NR, PR and CR), treatment (post and pre), hormone receptor (HR) status, HER2 receptor (HER2) status and ICR classification. (C) Boxplot of the ICR score expressed as the mean log2 expression of the ICR genes according to treatment and response status. (D) Boxplots of representative ICR genes: CD8A (Th1 signaling), CXCL9 and CCL5 (CXCR3 and CCR5 signaling), GZMA, GZMB and GNLY (effector functions); p values displayed here were calculated using unpaired t-test including only CR and NR. PR data was displayed in the boxplots for comparison with the other two categories.


This is the first study to characterize the transcriptional changes induced by imiquimod in breast cancer skin metastases. The CR samples showed a pre-activated immune microenvironment at baseline, substantiated by the enrichment of genes related to antigen processing and a proportional enrichment of T cells, NKCD56 bright cells and macrophages. Macrophages have often been shown to be a negative prognostic factor, although M1 macrophages, which sustain anti-tumor immune response, have been associated with favorable prognosis39,40. However, coordinated activation of the cytotoxic response was observed only after treatment, suggesting that despite a permissive microenvironment observed at baseline, tumor destruction in responding lesions requires a strong switch from chronic to acute inflammation, which is captured by the ICR genes.

Only a limited proportion of DEG overlaps between pre-treatment CR vs NR, post-treatment CR vs NR, and post-vs pre-treatment lesions. The lack of overlap among DEG post- vs pre-treatment with the ones detected in the post-treatment CR vs NR comparison might be the result of the dilution of the signal in the post-vs pre-treatment comparison due to the inclusion of the NR samples. The differences observed in pre- and post-treatment CR vs NR samples might be the consequence of a differential functional activation of the immune response at these time points. Baseline CR samples are dominated by a sub-inflamed microenvironment typified by the upregulation of antigen-processing related genes, while post-treatment differences are characterized by the coordinated activation of cytotoxic mechanisms conducive to immune-mediated rejection. Nevertheless, 40% (3/7) of the upregulated genes overlapping between at least two comparisons reflect the activation of a cytotoxic response (CD8A, GZMK, KLRK1) while the remaining ones are related to immune modulation. This observation suggests that the full activation of a pre-existing, yet incomplete, cytotoxic response is critical to induce immune-mediated tumor rejection in this setting.

Clinical response to imiquimod treatment was associated with a higher ICR score validating the ICR hypothesis in metastatic breast cancer. The ICR consists of Th-1 signaling genes, CXCR3 and CCR5 chemokines, effector function genes, and immune regulatory genes. High expression levels of these genes have been correlated with better prognosis in melanoma, ovarian, colorectal, hepatocellular, lung, as well as breast cancer10,12,14, and in lesions more likely to respond to immunotherapy10,15,16,17. Recently, Ayers et al. identified and validated an immune gene signature correlating with clinical benefit to PD1 blockade41. This 18-gene signature includes IFN-γ–inducible genes (STAT1, HLA-E), transcripts related to antigen presentation (HLA-DQA1, HLA-DRB1, PSMB10, CMKLR1), chemokines and chemokine ligands (CCL5, CXCL9, CXCR6), cytotoxic activity (CD8A, NKG7), and regulatory functions (TIGIT, LAG3, CD274 (PDLI), CD276, and PDCD1LG2(PDL2)) and as such highly overlaps with the ICR genes42.

LAG-3 was identified as one of the DEGs upregulated with a 6.6 fold change in the CR group post-treatment. LAG-3 is a receptor expressed by activated T lymphocytes and is considered a marker of T cell exhaustion leading to reduced effector function and expression of inhibitory receptors43. Blockade of LAG-3 is hypothesized to synergize with other immune checkpoint inhibitors such as anti-PD-144. Phase II data of imiquimod with nab-paclitaxel also showed that patients with a poor clinical response had higher circulating levels of PD-1+ T cells suggesting that combination therapy with anti-PD-1 and/or anti-LAG-3 may increase treatment responses33. Previous clinical trial data, of mostly estrogen receptor positive metastatic breast cancer, suggest that when combined with chemotherapy, a LAG-3 inhibitor in metastatic breast cancer can increase the number of activated monocytes, dendritic cells, NK cells and CD8 T cells with promising response rates45. Our data suggests that LAG-3 may play an important role in breast cancer skin metastases as well and LAG-3 inhibition and PD-1 inhibition should be considered in combination with imiquimod as possible treatment modalities.

Interestingly, the PR sample had the same immune gene expression signature post-treatment (clustering together with the 2 CR samples) as the complete responders (Fig. 1C). Our subsequent long-term analyses of tumor antigen-specific immune responses point to the important role of imiquimod treatment inducing the adaptive response, which then got augmented during endocrine therapy in both patients as they continued to derive clinical benefit and entered a long-lasting CR36. This likely explains the unexpected and durable complete response from fulvestrant since a previous large phase 3 study of fulvestrant monotherapy demonstrated that a complete response is very rare46. This further suggests that the genes upregulated by imiquimod are associated with long term immunogenic effects which can improve the efficacy of subsequent therapies. Whereas upregulation of ICR genes has been previously correlated with better response to chemotherapy and trastuzumab29,47, our data suggests that activation of these pathways may also improve response to subsequent hormonal therapy.

Limitations of our study are the small number of patients and the short duration of treatment. The delayed CR in two patients who displayed immune activation within the metastases after eight weeks of treatment with imiquimod suggests the possibility that a longer treatment might increase response rates. Genes differentially expressed detected by univariate analysis are subject to false discovery. The possibility to incur into a Type I error (i.e., the rejection of a true null hypothesis) is partially attenuated by the use of the integrative pipeline presented here. By combining deconvolution and enrichment analyses, more permissive cut-off p values can be used to detect biological relevant phenomena. Nevertheless, this dataset should be considered as a discovery set, and further validation using orthogonal platforms as deep phenotyping and proteomic approaches are warranted.

The strength of this study is the use of gene array analysis in paired samples derived from a prospective clinical trial with long-term follow-up of patients. This sensitive technique for characterizing immune changes induced by imiquimod treatment was able to detect at 8 weeks intratumoral changes associated with not only immediate but also future clinical benefit, which could not be derived from histologic analysis35.

Metastatic breast cancer, especially with cutaneous metastases, remains very difficult to treat. Long-term clinical response to therapy in metastatic cancer is rare. Promoting immunogenicity in the tumor microenvironment may enhance efficacy of other therapies such as chemotherapy, endocrine therapy, targeted therapies or even newer immunotherapeutics. Imiquimod has been shown to be a potent activator of the innate immune system, which then supports adaptive immune response in cancer, and we demonstrate that this is the case in metastatic breast cancer as well. Encouragingly, although hormone receptor positive breast cancer appears to be the least immunogenic type of breast cancer34, we have shown that imiquimod can induce a robust anti-tumor immune response leading to clinical response in the three patients with hormone receptor positive disease described here. This is in line with a recent report of successful immunotherapy in a patient with metastatic hormone receptor positive breast cancer48. Future trials are needed to investigate the use of imiquimod in combination with other therapies.

Data Availability

The normalized Nanostring data used in the current study is available as Supplementary File 1.


  1. 1.

    Tan, A. R. Cutaneous manifestations of breast cancer. Semin. Oncol. 43, 331–334 (2016).

    Article  Google Scholar 

  2. 2.

    Takeda, K. & Akira, S. TLR signaling pathways. Seminars in Immunology 16, 3–9 (2004).

    CAS  Article  Google Scholar 

  3. 3.

    Weeks, C. E. & Gibson, S. J. Induction of interferon and other cytokines by imiquimod and its hydroxylated metabolite R-842 in human blood cells in vitro. J. Interferon Res. 14, 81–85 (1994).

    CAS  Article  Google Scholar 

  4. 4.

    Urosevic, M. et al. Disease-independent skin recruitment and activation of plasmacytoid predendritic cells following imiquimod treatment. J. Natl. Cancer Inst. 97, 1143–1153 (2005).

    CAS  Article  Google Scholar 

  5. 5.

    Schön, M. et al. Tumor-selective induction of apoptosis and the small-molecule immune response modifier imiquimod. J. Natl. Cancer Inst. 95, 1138–1149 (2003).

    Article  Google Scholar 

  6. 6.

    Huang, S. J. et al. Imiquimod enhances IFN-gamma production and effector function of T cells infiltrating human squamous cell carcinomas of the skin. J. Invest. Dermatol. 129, 2676–2685 (2009).

    CAS  Article  Google Scholar 

  7. 7.

    Panelli, M. C. et al. Sequential gene profiling of basal cell carcinomas treated with imiquimod in a placebo-controlled study defines the requirements for tissue rejection. Genome Biol. 8, R8 (2007).

    Article  Google Scholar 

  8. 8.

    Spivey, T. L. et al. Gene expression profiling in acute allograft rejection: challenging the immunologic constant of rejection hypothesis. J Transl Med 9, 174 (2011).

    CAS  Article  Google Scholar 

  9. 9.

    Wang, E., Worschech, A. & Marincola, F. M. The immunologic constant of rejection. Trends Immunol. 29, 256–262 (2008).

    Article  Google Scholar 

  10. 10.

    Galon, J., Angell, H. K., Bedognetti, D. & Marincola, F. M. The continuum of cancer immunosurveillance: prognostic, predictive, and mechanistic signatures. Immunity 39, 11–26 (2013).

    CAS  Article  Google Scholar 

  11. 11.

    Wang, E., Bedognetti, D. & Marincola, F. M. Prediction of response to anticancer immunotherapy using gene signatures. J. Clin. Oncol. 31, 2369–2371 (2013).

    CAS  Article  Google Scholar 

  12. 12.

    Bedognetti, D., Hendrickx, W., Marincola, F. M. & Miller, L. D. Prognostic and predictive immune gene signatures in breast cancer. Curr Opin Oncol 27, 433–444 (2015).

    CAS  Article  Google Scholar 

  13. 13.

    Bedognetti, D., Hendrickx, W., Ceccarelli, M., Miller, L. D. & Seliger, B. Disentangling the relationship between tumor genetic programs and immune responsiveness. Curr. Opin. Immunol. 39, 150–158 (2016).

    CAS  Article  Google Scholar 

  14. 14.

    Hendrickx, W. et al. Identification of genetic determinants of breast cancer immune phenotypes by integrative genome-scale analysis. Oncoimmunology 6, e1253654 (2017).

    Article  Google Scholar 

  15. 15.

    Herbst, R. S. et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients. Nature 515, 563–567 (2014).

    CAS  Article  ADS  Google Scholar 

  16. 16.

    Bedognetti, D. et al. CXCR3/ CCR5 pathways in metastatic melanoma patients treated with adoptive therapy and interleukin-2. Br. J. Cancer 109, 2412–2423 (2013).

    CAS  Article  Google Scholar 

  17. 17.

    Bedognetti, D., Wang, E. & Marincola, F. M. Meta-analysis and metagenes: CXCL-13-driven signature as a robust marker of intratumoral immune response and predictor of breast cancer chemotherapeutic outcome. Oncoimmunology 3, e28727 (2014).

    Article  Google Scholar 

  18. 18.

    Bong, A. B. et al. Imiquimod, a topical immune response modifier, in the treatment of cutaneous metastases of malignant melanoma. Dermatology (Basel) 205, 135–138 (2002).

    CAS  Article  Google Scholar 

  19. 19.

    Rivas-Tolosa, N. et al. Local cryosurgery and imiquimod: A successful combination for the treatment of locoregional cutaneous metastasis of melanoma: A case series. J. Dermatol. 43, 553–556 (2016).

    CAS  Article  Google Scholar 

  20. 20.

    Joseph, R. W. et al. Treatment of in-transit and metastatic melanoma in two patients treated with ipilimumab and topical imiquimod. Melanoma Res. 26, 409–412 (2016).

    Article  ADS  Google Scholar 

  21. 21.

    Leventhal, J. S., Odell, I. D., Imaeda, S., Maverakis, E. & King, B. A. Treatment of melanoma in-transit metastases with combination intralesional interleukin-2, topical imiquimod, and tretinoin 0.1% cream. JAAD Case Rep 2, 114–116 (2016).

    Article  Google Scholar 

  22. 22.

    Shi, V. Y. et al. 100% Complete response rate in patients with cutaneous metastatic melanoma treated with intralesional interleukin (IL)-2, imiquimod, and topical retinoid combination therapy: results of a case series. J. Am. Acad. Dermatol. 73, 645–654 (2015).

    CAS  Article  Google Scholar 

  23. 23.

    Mauldin, I. S. et al. Topical treatment of melanoma metastases with imiquimod, plus administration of a cancer vaccine, promotes immune signatures in the metastases. Cancer Immunol. Immunother. 65, 1201–1212 (2016).

    CAS  Article  Google Scholar 

  24. 24.

    Salgado, R. et al. The evaluation of tumor-infiltrating lymphocytes (TILs) in breast cancer: recommendations by an International TILs Working Group 2014. Annals of oncology: official journal of the European Society for Medical Oncology 26, 259–271 (2015).

    CAS  Article  Google Scholar 

  25. 25.

    Loi, S. et al. Tumor infiltrating lymphocytes are prognostic in triple negative breast cancer and predictive for trastuzumab benefit in early breast cancer: results from the FinHER trial. Ann. Oncol. 25, 1544–1550 (2014).

    CAS  Article  Google Scholar 

  26. 26.

    Ali, H. R. et al. Association between CD8+ T-cell infiltration and breast cancer survival in 12,439 patients. Ann. Oncol. 25, 1536–1543 (2014).

    CAS  Article  Google Scholar 

  27. 27.

    Mahmoud, S. M. A. et al. Tumor-infiltrating CD8+ lymphocytes predict clinical outcome in breast cancer. J. Clin. Oncol. 29, 1949–1955 (2011).

    Article  Google Scholar 

  28. 28.

    Adams, S. et al. Prognostic value of tumor-infiltrating lymphocytes in triple-negative breast cancers from two phase III randomized adjuvant breast cancer trials: ECOG 2197 and ECOG 1199. J. Clin. Oncol. 32, 2959–2966 (2014).

    Article  Google Scholar 

  29. 29.

    Denkert, C. et al. Tumor-associated lymphocytes as an independent predictor of response to neoadjuvant chemotherapy in breast cancer. J. Clin. Oncol. 28, 105–113 (2010).

    CAS  Article  Google Scholar 

  30. 30.

    Giraldo, N. A. et al. The immune contexture of primary and metastatic human tumours. Curr. Opin. Immunol. 27, 8–15 (2014).

    CAS  Article  Google Scholar 

  31. 31.

    Loi, S. et al. Prognostic and predictive value of tumor-infiltrating lymphocytes in a phase III randomized adjuvant breast cancer trial in node-positive breast cancer comparing the addition of docetaxel to doxorubicin with doxorubicin-based chemotherapy: BIG 02–98. J. Clin. Oncol. 31, 860–867 (2013).

    CAS  Article  Google Scholar 

  32. 32.

    Zitvogel, L., Galluzzi, L., Kepp, O., Smyth, M. J. & Kroemer, G. Type I interferons in anticancer immunity. Nat. Rev. Immunol. 15, 405–414 (2015).

    CAS  Article  Google Scholar 

  33. 33.

    Salazar, L. G. et al. Topical Imiquimod Plus Nab-paclitaxel for Breast Cancer Cutaneous Metastases: A Phase 2 Clinical Trial. JAMA. Oncology 3, 969–973 (2017).

    Google Scholar 

  34. 34.

    Stanton, S. E., Adams, S. & Disis, M. L. Variation in the Incidence and Magnitude of Tumor-Infiltrating Lymphocytes in Breast Cancer Subtypes. JAMA Oncology 2, 1354–1360 (2016).

    Article  Google Scholar 

  35. 35.

    Adams, S. et al. Topical TLR7 agonist imiquimod can induce immune-mediated rejection of skin metastases in patients with breast cancer. Clin. Cancer Res. 18, 6748–6757 (2012).

    CAS  Article  Google Scholar 

  36. 36.

    Janosky, M. et al. MAGE-specific T cells detected directly ex-vivo correlate with complete remission in metastatic breast cancer patients after sequential immune-endocrine therapy. J Immunother Cancer 2, 32 (2014).

    Article  Google Scholar 

  37. 37.

    Bindea, G. et al. Spatiotemporal dynamics of intratumoral immune cells reveal the immune landscape in human cancer. Immunity 39, 782–795 (2013).

    CAS  Article  Google Scholar 

  38. 38.

    Hänzelmann, S., Castelo, R. & Guinney, J. GSVA: gene set variation analysis for microarray and RNA-seq data. BMC Bioinformatics 14, 7 (2013).

    Article  Google Scholar 

  39. 39.

    Mantovani, A., Romero, P., Palucka, A. K. & Marincola, F. M. Tumour immunity: effector response to tumour and role of the microenvironment. Lancet 371, 771–783 (2008).

    CAS  Article  Google Scholar 

  40. 40.

    Wathen, W. F. Petri dish to operatory: bridging the gap. J. Dent. Res. 69, 502–502 (1990).

    CAS  Article  Google Scholar 

  41. 41.

    Ayers, M. et al. IFN-γ-related mRNA profile predicts clinical response to PD-1 blockade. J. Clin. Invest. 127, 2930–2940 (2017).

    Article  Google Scholar 

  42. 42.

    Turan, T. et al. Immune oncology, immune responsiveness and the theory of everything. J Immunother Cancer 6, 8 (2018).

    Article  Google Scholar 

  43. 43.

    Kok, M. LAG-3: another brake to release in breast cancer? Ann. Oncol., (2017).

    CAS  Article  Google Scholar 

  44. 44.

    Burugu, S., Gao, D., Leung, S., Chia, S. K. & Nielsen, T. O. LAG-3+ tumor infiltrating lymphocytes in breast cancer: clinical correlates and association with PD-1/PD-L1 + tumors. Ann. Oncol., (2017).

    CAS  Article  Google Scholar 

  45. 45.

    Brignone, C. et al. First-line chemoimmunotherapy in metastatic breast carcinoma: combination of paclitaxel and IMP321 (LAG-3Ig) enhances immune responses and antitumor activity. J Transl Med 8, 71 (2010).

    Article  Google Scholar 

  46. 46.

    Di Leo, A. et al. Results of the CONFIRM phase III trial comparing fulvestrant 250 mg with fulvestrant 500 mg in postmenopausal women with estrogen receptor-positive advanced breast cancer. J. Clin. Oncol. 28, 4594–4600 (2010).

    Article  Google Scholar 

  47. 47.

    Perez, E. A. et al. Genomic analysis reveals that immune function genes are strongly linked to clinical outcome in the North Central Cancer Treatment Group n9831 Adjuvant Trastuzumab Trial. J. Clin. Oncol. 33, 701–708 (2015).

    CAS  Article  Google Scholar 

  48. 48.

    Zacharakis, N. et al. Immune recognition of somatic mutations leading to complete durable regression in metastatic breast cancer. Nat. Med. 24, 724–730 (2018).

    CAS  Article  Google Scholar 

Download references


The work was supported in part by the AMA Foundation Seed Grant (to MR and SA) and in part by the Breast Cancer Research and Education Fund (New York State Department of Health, # #DOH01-C31850GG-3450000, to ME and SA). Opinions expressed here are solely those of the authors and do not necessarily reflect those of the Health Research Science Board, the New York State Department of Health, or the State of New York. This work (DB and WH work: gene expression integrative analysis) was supported in part by Qatar National Reserach Fund (NPRP10-0126-170262 “Identification of molecular determinants of breast cancer immune responsiveness by integrative genome-scale analysis”, awarded to DB).

Author information




M.R. and S.A. contributed to the conception of the study and provided financial support. M.R., W.H., M.E., F.M.M., D.B., and S.A. contributed to the study design, analysis and interpretation of data, and to manuscript writing. A.H., L.C., C.L., K.R., S.D., and F.D. contributed to the development of methodology and acquisition of data (histology and gene arrays).

Corresponding authors

Correspondence to Davide Bedognetti or Sylvia Adams.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Rozenblit, M., Hendrickx, W., Heguy, A. et al. Transcriptomic profiles conducive to immune-mediated tumor rejection in human breast cancer skin metastases treated with Imiquimod. Sci Rep 9, 8572 (2019).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links