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Journal of Clinical Medicine Research

Letter to the Editor

Volume 11, Number 8, August 2019, pages 609-613

Profiling of Target Molecules for Immunotherapy in Mesenchymal Tumors

The use of anti-human signal molecules monoclonal antibodies (mAbs) for malignant tumors therapy has achieved considerable success in recent years. Antibody drug conjugates are powerful new clinical treatment options for lymphomas and solid tumors, and immunomodulatory antibodies have also recently achieved remarkable clinical success. The development of therapeutic antibodies requires a deep understanding of malignant tumor serology, protein-engineering techniques, mechanisms of action and resistance, and the interplay between the immune system and tumorigenesis. This review outlines the fundamental strategies, which are required to establish antibody therapies for patients with mesenchymal tumors through iterative approaches to target and antibody selection, extending from preclinical studies to human trials.

A type of drug blocks certain proteins made by some types of immune system cells, such as T cells and some malignant tumor cells. These proteins help keep immune responses in check, and can keep T cells from killing malignant tumor cells. When these proteins are blocked, the “brakes” on the immune system are released and T cells are able to kill malignant tumor cells better. Examples of checkpoint proteins found on T cells or malignant tumor cells include programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4)/B7-homolog-1(B7-1)/B7-homolog-2(B7-2) (Fig. 1). A significant inverse correlation between PD-L1 expression and intraepithelial CD8-positive T-lymphocyte count suggested that PD-L1 on tumor cells may suppress anti-tumor CD8-positive T cells, also called as cytotoxic T cells [1]. Some immune checkpoint inhibitors (ICIs) are used to treat malignant tumors. The probability of response to ICIs is closely related to the nature of tumor’s immune microenvironment. For instance, non-small cell lung carcinoma has emerged as the prototypical tumor types that are responsive to ICIs, and also has PD-L1 immunohistochemical (IHC) companion diagnostic biomarker, which is used to determine whether pembrolizumab or nivolumab, which are anti-human PD-1 monoclonal immunoglobulin (Ig) G4 antibodies, monotherapy will be given [2, 3]. In contrast, the immune microenvironment of mesenchymal tumors is still poorly understood, and biomarkers predictive of immunotherapy response are greatly needed to establish anti-mesenchymal tumors therapy by ICIs.

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Figure 1. Cancer therapy by inhibition of negative immune regulation by programmed death 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4). The figure shows a primary melanoma and tumor-associated antigens (TAAs) that are taken up by an antigen presenting cell (APC: a Langerhans cell; left). APCs then migrate via afferent lymphatics to the sentinel skin-draining lymph node, where they present TAA to naive T cells. These naive T cells continuously screen the lymphoid organs, extravasating through high endothelial venule (HEV) until their corresponding peptide is presented to them in the context of the major histocompatibility complex (MHC). When a TAA is presented in the T-cell-dependent area of a lymph node to its specific naive T cell (center), the latter requires signal 1 (antigen presentation to the T-cell receptor) and 2 (costimulation) for full activation. It will then proliferate and acquire “antigen memory” and a distinct and different set of adhesion molecules that will allow it to navigate outside of the blood vessels and the lymphoid organs, to the peripheral tissues and organs, like the melanoma metastases where it will be able to be reactivated upon re-presentation of the same TAA. However, in the lymph node, T-cell activation is interrupted when signal 3, mediated through interaction between CTLA-4 and CD80/86, takes over CD28 and CD80/86 interaction. This occurs 24 - 48 h after the initiation of T-cell priming. When the memory T cell is recruited to the melanoma metastasis (right) and activated upon TAA re-presentation, the effector activation is decreased when PD-1 is engaged with its ligand PD-L1 that can be expressed on the tumor cell constitutively or in the context of inflammation. The figure adapted from the C. Robert and C. Verjat figure collection, Institute Gustave Roussy (Villejuif-Paris Sud, Paris, France) is modified.

Diagnoses for mesenchymal tumors are rare and published case series typically lump heterogeneous mesenchymal tumors together. Due to this and because of the use of various different PD-L1 antibodies in different studies, the reported incidence of PD-L1 positivity in mesenchymal tumors has varied greatly in the literature, ranging from 0% to 60% [4-13]. In mesenchymal tumors, high expression of PD-L1 mRNA is associated with shorter metastasis-free survival [14]. In two meta-analyses, the expression of PD-L1 was found to be a poor prognosticator in mesenchymal tumors [15].

ICIs have yielded mixed results in sarcoma. Ipilimumab, which binds to a substance called CTLA-4, had no activity in six patients with synovial sarcoma [16]. Ben-Ami reported that none of 12 patients with uterine leiomyosarcoma responded to nivolumab, which is anti-human PD-1 fully human immunoglobulin (Ig) G4 mAb [17]. Two of four patients with alveolar soft part sarcoma were reported to have partial response to anti-PD-L1 therapy [18]. A microsatellite instability (MSI), low tumor mutation burden (TMB) chondrosarcoma with 1% PD-L1 positivity, was reported to respond to nivolumab [19]. Finally, the SARC028 clinical trial reported that 18% of patients with mesenchymal tumors had an objective response to pembrolizumab. Twenty percent of patients with liposarcoma, 10% with synovial sarcoma and 5% with bone sarcoma had a response. No response was seen in patients with leiomyosarcoma or Ewing sarcoma. Importantly, four of 10 patients with undifferentiated mesenchymal tumors had a response and two of these four patients had at least 1% neoplastic cell PD-L1 positivity. Tumors from all six pembrolizumab unresponsive patients with mesenchymal tumors were PD-L1 negative [9]. High RNA expression of B7-homolog 3 (B7-H3), transforming growth factor beta-1 (TGFB1) and T-cell immunoglobulin and mucin domains-containing protein 3 (TIM3), which are putative immunotherapy targets, has been described in sarcoma, specifically in dedifferentiated liposarcoma, undifferentiated pleomorphic sarcoma and myxofibrosarcoma [20].

Most of the immune-therapeutic focus in mesenchymal tumor types has centered on the PD-1 axis [4, 5, 10-15]. The expression of a few alternate immune-therapeutic targets, such as B7-H3, TGFB1 and TIM3, has been previously described in some mesenchymal tumor types [20, 21]. Pathological studies with anti-PD-1 and/or anti-PD-L1 antibodies have yielded inconsistent findings in mesenchymal tumors partially, because of the inclusion of heterogeneous sarcoma entities in many of the relevant studies [4-12]. Using various criteria and antibodies, most studies show that 40-82% of some mesenchymal tumor types have expression of PD-L1 [4, 11, 12]. The population of mesenchymal tumors had reportedly PD-L1 positivity in 38% of cases, substantially more than the non-mesenchymal tumor population which was PD-L1 positive in 19% of cases. The expression of PD-L1 mRNA in mesenchymal tumors was not significantly different from non-mesenchymal tumor cases and was significantly under expressed in non-mesenchymal tumors. However, PD-L2 emerged as significantly overexpressed in mesenchymal tumors. PD-L2 expresses in both neoplastic and non-neoplastic cells in multiple neoplasms and its expression correlates with pembrolizumab response in head and neck squamous cell carcinoma independent of PD-L1 expression [22]. Along with the high positivity PD-L1 in mesenchymal tumors, the overexpression of PD-L2 in mesenchymal tumors suggests that the communication of PD-1/PD-L1/PD-L2 axis may be a key role of protective mechanism against host immune response in mesenchymal tumors. In turn, this raises the possibility that agents targeting PD-L1 may not be as therapeutically efficacious as agents targeting the PD-1 in mesenchymal tumors, and provides a possible reason for the high response rate of mesenchymal tumors to pembrolizumab [9]. As additional putative immunotherapy targets, B7-H3 and TGFB1 were remarkable in that they were both overexpressed in mesenchymal tumors and non-mesenchymal tumors. B7-H3 is immunohistochemically present in most osteosarcomas, and is associated with a poor prognosis and with poor infiltration by CD8-positive T cells [23]. Our knowledge of its functional significance in other sarcomas is limited, but its known immune-suppressive function and relatively high expression in both mesenchymal tumors and non-mesenchymal tumors suggests that it may be an important immune-suppressor in mesenchymal tumors. Overexpression of TGFB1 as the immune-suppressive cytokine has been described in mesenchymal tumors [20, 21]. Importantly, TGFB1 physiologically induces epithelial to mesenchymal transition (EMT) [24]. The elevated expression of multiple EMT-related factors also induces the process of protection from host immune-system, and these factors are exploitable as immunotherapy targets. Colony-stimulating factor 1 receptor (CSF1R) is well known to associate with macrophages and there is preclinical evidence that its blockade increases CD8-positive T-cell motility and tumor infiltration [25]. The significantly differential expression of TIM3 is observed in mesenchymal tumors or non-mesenchymal tumors. This is in conflict with the previously described overexpression of TIM3 in the Cancer Genome Atlas (TCGA) sarcoma cohort [20]. The reasons for this discrepancy are unclear, although the differences in the specific subtypes of mesenchymal tumors included in ours and TCGA cohort may be an explanation. Notably, other potential immunotherapy targets such as CTLA4 and PD-1 were either under expressed or had no expression difference in mesenchymal tumors and non-mesenchymal tumors. Functional analysis in a responding patient demonstrated rapid in vivo expansion of neo-antigen-specific T-cell clones that were reactive to mutant neo-peptides found in the tumor. These data support the hypothesis that the large proportion of mutant neo-antigens in mismatch repair-deficient (dMMR) makes them sensitive to immune checkpoint blockade, regardless of the malignant tumor tissues of origin. The surging interest in cancer immunotherapy, particularly checkpoint blockade, has further led to a focus on dMMR-positive tumors, which are notable for their substantial CD8-positive T-cell infiltrate [26]. Recent report demonstrated that uterine sarcomas were mismatch repair-deficient [9, 26-28]. Uterine sarcoma, 1.4% of stage I to stage III malignant tumors and 0.6% of stage IV malignant tumors were classified in dMMR-positive tumors [8] (Fig. 2). From these research findings, in uterine sarcoma, numbers of infiltrating CD8-positive T cells are considered to be small. Therefore, as previously reported, the anti-tumor effect of therapy by ICIs on uterine sarcoma is considered to be low.

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Figure 2. Mismatch repair deficiency across tumors. Proportion of tumors deficient in mismatch repair (dMMR) in each malignant tumor subtype, expressed as a percentage. Mismatch repair deficient tumors were identified in tumor subtypes tested, more often in early stage (defined as stage < IV) disease. The figure adapted from reference [8].

The causal relationship between metastatic status and presence of CD8 is currently unclear, although there is preclinical evidence indicating that depletion of cytotoxic CD8-positive T cells plays an important role in the proliferation of metastatic neoplastic cells [27]. The recent research findings suggest that inflammatory status can be used to categorize sarcomas and, possibly, their clinical behavior. Further clinical studies will elucidate whether this type of profiling is also predictive of immunotherapy response. The sample size is small and we were only able to include a smattering of various sarcomas in the mesenchymal tumor category. Further studies will need large numbers of each specific sarcoma histology. Finally, histopathological studies and functional or clinical studies are needed to confirm our findings.

In conclusion, if mesenchymal tumors in particular have a very high rate of positive expression of PD-L1 mRNA and high expression of PD-L2 mRNA, which suggests a mechanism of immune-suppression, therefore uterine sarcoma in mesenchymal tumors types has possibly a high response rate to ICIs. The expression profiling of proteins demonstrated the expression of PD-L1, and positive dMMR in uterine sarcoma [9, 26-29]. Unfortunately in uterine sarcoma, late of dMMR reportedly is low, and does not have high response to ICIs [8, 29]. The clinical evidences of lymphocytes infiltration and negative signal-ligands such like PD-L1 in mesenchymal tumors suggest that the tumor microenvironment plays an important role of anti-tumor by ICIs.

Acknowledgments

We sincerely thank Professor Luc Van Kaer (Vanderbilt University Medical Center) for donation of LMP2-deficiency mouse.

Financial Disclosure

This study was supported in part by grants from the Japan Ministry of Education, Culture, Science and Technology (grants #15K10709 and #24592510), The Foundation of Osaka Cancer Research, The Ichiro Kanehara Foundation for the Promotion of Medical Science and Medical Care, The Foundation for the Promotion of Cancer Research, The Kanzawa Medical Research Foundation, The Shinshu Medical Foundation and The Takeda Foundation for Medical Science.

Conflict of Interest

All authors report no conflict of interest.

Informed Consent

Not applicable.

Author Contributions

TH: execution of research and experimental design. TI: execution of research and experimental design. KS: execution of research. ST: research cooperation. YK: execution of research and research cooperation. DZ: joint experiment and execution of research, HA: joint experiment and execution of research. NY: Joint experiment, execution of research and research supervision. KI: research supervision.

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Journal of Clinical Medicine Research is published by Elmer Press Inc.