The safety and efficacy of bispecific T-cell engagers (TCEs) in patients with glioma
Published in Cancer and General & Internal Medicine
Among the most aggressive and resistant tumors of the central nervous system, glioblastoma (GBM) has a poor prognosis and few available treatments. Because of the tumor’s infiltrative nature, immunosuppressive environment, and resistance mechanisms, traditional treatments such as radiotherapy, chemotherapy, and surgery offer only modest survival benefits. Bispecific T-cell engagers (TCEs) have shown promising preclinical and early clinical results, and immunotherapy has become a feasible strategy.
TCEs efficiently promote antigen evasion and strong tumor lysis by directing cytotoxic T lymphocytes (CTLs) to tumor-associated antigens (TAA) such as the EGFRvIII ligands IL-13Rα2, Fn14, and NKG2D ligands (NKG2DLs). Although phase I clinical studies with AMG 596 have shown acceptable safety profiles and early indications of efficacy, preclinical mice have demonstrated prolonged longevity.
However, challenges still exist, including the short half-life of TCEs molecules, limited T-cell infiltration, antigen heterogeneity, and the risk of neurotoxicity or cytokine release syndrome (CRS). Promising developments include novel approaches such as multivalent targeting, DNA-encoded or cell-delivered TCEs, and combinations with immune checkpoint inhibitors (ICIs) or CAR-T cells. With an emphasis on its integration into multimodal treatment approaches, this review highlights the safety, effectiveness, and potential uses of TCEs immunotherapy for gliomas.
See here for the article: https://link.springer.com/article/10.1007/s10238-026-02057-yIF: 3.5 Q2
-Kamyar Bagheri
Follow the Topic
Ask the Editor – Inflammation, Metastasis, Cancer Microenvironment and Tumour Immunology
Got a question for the editor about inflammation, metastasis, or tumour immunology? Ask it here!
Continue reading announcementRelated Collections
With Collections, you can get published faster and increase your visibility.
Clinical Practice
Publishing Model: Open Access
Deadline: Ongoing
Next-Generation Immune Profiling and Integrative Biomarkers for Precision Medicine in Inflammatory Diseases
Inflammatory diseases comprise a diverse group of immune-mediated conditions characterized by complex immune dysregulation, tissue-specific microenvironmental changes, and heterogeneous therapeutic responses. Despite significant progress in immunomodulatory treatments, clinical management remains limited by the lack of reliable and clinically actionable biomarkers to support early diagnosis, patient stratification, treatment selection, and disease monitoring.
Recent advances in immune profiling technologies have greatly improved our understanding of inflammatory disease heterogeneity. Multi-omics approaches, including transcriptomics, single-cell sequencing, spatial biology, and microbiome-associated analyses, are increasingly being used to identify molecular signatures associated with disease progression and therapeutic response. At the same time, artificial intelligence and advanced computational methods are providing new opportunities to integrate complex biological data and improve biomarker discovery.
Certain inflammatory conditions, such as inflammatory bowel diseases (IBD), including ulcerative colitis and Crohn’s disease, have provided important insights into immune heterogeneity and translational biomarker development. However, similar strategies are increasingly being applied across a broader spectrum of inflammatory disorders, highlighting the importance of cross-disease analytical frameworks and shared molecular mechanisms.
Despite these advances, translating high-dimensional molecular findings into clinically useful tools remains a major challenge. Greater emphasis is needed on reproducibility, external validation, and clinically interpretable models that can facilitate the integration of biomarker research into real-world medical practice.
This collection aims to highlight recent advances in immune profiling technologies and integrative biomarker research that support precision medicine across inflammatory diseases. We particularly encourage studies that combine computational analysis with clinical relevance, including biomarker validation, predictive modeling, and translational multi-omics research.
Sub-topics may include but are not limited to:
- Immune profiling and biomarker discovery in inflammatory diseases
- Next-generation immune profiling using bulk, single-cell, spatial, and repertoire sequencing
- Multi-omics integration for disease stratification and endotype identification
- Clinically relevant biomarkers for diagnosis, prognosis, and treatment response
- Artificial intelligence and predictive modeling in inflammatory disease research
- Translational studies linking immune mechanisms with clinical outcomes
Publishing Model: Open Access
Deadline: Dec 31, 2026
Please sign in or register for FREE
If you are a registered user on Research Communities by Springer Nature, please sign in