Editorial: Modulation of Human Immune Parameters by Anticancer Therapies

Abstract

Editorial on the Research Topic Modulation of Human Immune Parameters by Anticancer Therapies Immunoncology is among the most important hallmarks of immunotherapy revolution of cancer medicine. Here, we compiled reviews and original research articles reflecting current developments in immunoncology. Novel therapies modulate the complex interaction between tumor and immune system (Figure 1). Multiparametric flow cytometry (FCM) is a key analytical tool contributing over 1,000 research articles/year to the field. As a quantitative single-cell technology, FCM reliably and reproducibly identifies rare populations, detects subtle changes in modulatory signals, and assesses time-sensitive antigenic expression patterns. State-of-the-art equipment, fast sophisticated software, and flexibly labeled monoclonal antibodies allow rapid analyses with high sensitivity and specificity, even in routine applications. Lambert et al. explain how new analytes are added to the portfolio of diagnostic and research laboratories. Sample preparation, antibody titration, and appropriate controls are central in cytometric analysis and must be controlled with the necessary rigor and reproducibility (1). Figure 1 Tumor-immune-interactions and investigation by flow cytometry. Although tumor cell analysis is a key application of cytometry (2, 3), this research topic is dedicated to the modulation of immune parameters, and we only included work focusing on tumor-immune-cell interaction and its disease-course impact. Dendritic cells (DCs) are crucial in tumor protection (4). Lu et al. dissect the interaction of DCs with non-small cell lung cancer (NSCLC) cells, which can induce an immunosuppressive microenvironment and evade immune surveillance. Analysis of costimulatory molecules and pro-/anti-inflammatory cytokines reveals new subpopulations of CD1c+ DCs in coculture with NSCLC. Particularly, the expression of signal molecules and pro-inflammatory cytokines are suppressed, whereas the secretion of anti-inflammatory cytokines by DCs is upregulated, suggesting that NSCLC can induce tolerogenic DCs, blocking DC-mediated anti-tumor immunity. Chemokines and their corresponding receptors play a pivotal role in orchestrating trafficking of immune cells to fulfill their next tasks. CXCL10 has been associated with T cell recruitment into tumors. Meng et al. link an increased CXCL10 expression and T cell infiltration with autophagy inhibition in gastric cancer (GC). Since autophagy was associated with GC cell survival and therapy resistance, autophagy inhibition is considered a potential GC treatment strategy, which might also favorably effect T cell recruitment into the tumor. Inflammation is central in tumorigenesis underlining close interactions between immune system and tumor. Besides adaptive immunity, innate immunity is crucial in tumor defense (5). Stein et al. address the role of the inflammatory cytokine TNF-α in colorectal cancer (CRC). CRC has commonly good prognosis, if detected early. With distant metastasis, 5-year survival rate drops below 10% with little therapeutic progress. The metastasis-associated oncogene in CRC 1 (MACC1) is involved in CRC metastasis, induces cell proliferation and motility, supports cell survival, and redirects metabolism. Also, in several other solid cancers, MACC1 is a potential target for late forms of metastasis. The authors demonstrate that TNF-α triggers upregulation of MACC1 mRNA and protein via induction of c-Jun expression, resulting in promoted CRC-cell migration. MACC1 induction was successfully inhibited by MACC1 and c-Jun knockdown as well as anti–TNF-α and anti-TNFR1 blocking antibodies, providing potential therapeutic targets for treating inflammation-associated CRC. Tumor-immune-cell interactions are decisive in the disease course but not yet fully understood and addressed by Plesca et al. In various cancers, high densities of CD45RO+ T-helper1 cells and CD8+ T cells are associated with improved outcome, M2 macrophages rather with worsened prognosis (5). This can also be applied to the expected response to anti-programmed cell-death-protein 1 (PD-1). Anti–PD-1 therapy affects an increased density of tumor-infiltrating T cells in responders, and increased frequency of melanoma-infiltrating TCF7+CD8+ T cells. However, tumor-infiltrating PD-1+CD38hi CD8+ T-cells are associated with anti–PD-1 resistance that favors implementation of immunoprofiling before checkpoint inhibition therapy. Based on the manifold relationships between immune system and tumor, the numerous parallels between immunopathology and tumor therapy are not surprising. Khoy et al. present Natalizumab in multiple sclerosis (MS) as a typical example for immune therapies and precursor of today’s antibody therapies for tumors. MS is a chronic demyelinating disease of the CNS with an autoimmune component. Among the recently available disease-modifying therapies, Natalizumab, a monoclonal antibody against VLA-4 integrin, effectively inhibits cell migration to tissues including the CNS, thereby inhibiting disease progression. Since also immune function is impaired, immunomonitoring during therapy is important to detect adverse effects. Klöß et al. report on challenging examples that bridge between treatment of cancer and immune-mediated diseases, major hurdles are suitable experimental models reflecting the complex tumor-immune-interactions during treatment for identifying new therapies. In addition to patient-derived tumor xenotransplants (PDX) (humanized) mouse models, ex vivo approaches to cancer modeling like microfluidic human organs-on-chips are shown. Better understanding of treatment mechanisms and side effects permitted the development of novel targeted cell-, drug-, and biological-based therapies. Progress of...