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Updated: Jun 6, 2026

Draining Lymph Node Metastasis Model for Assessing the Dynamics of Antigen-Specific CD8+ T Cells During Tumorigenesis
Published on: January 26, 2024
Intratumoral TLR4 agonist therapy elicits antigen-specific T cell clonal expansion in metastatic leiomyosarcoma: a
Jessica S Zhang1, Juliana C K Ng1, Pedro Hermida de Viveiros1
1Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Abstract:
Metastatic soft tissue sarcomas (STSs) are a heterogeneous group of rare mesenchymal tumors whose treatment options are limited. Our group has been interested in utilizing the synthetic toll-like receptor 4 (TLR4) agonist, glycopyranosyl lipid A in stable-emulsion formulation (GLA-SE), in patients with advanced STSs. Here, we report a case series of three patients with metastatic leiomyosarcoma who had superficial lesions amenable to intratumoral (IT) injection. We explored the safety, tolerability, and immunologic effects of IT GLA-SE given at 20 μg weekly for 12 weeks, both alone and in combination with radiotherapy. In this small case series, treatment was well tolerated, with no serious adverse events observed. Clinically, although no patient had significant tumor shrinkage, two had notable stability in their target lesions despite systemic disease progression. Immunologically, IT GLA-SE induced a clonal expansion of T cells intratumorally in one patient and in peripheral blood in another, suggesting an antitumor effect both at the site of injection and systemically. Moreover, GLA-SE elicited clonal expansion of systemic T cells targeting a well-known immunogenic cancer antigen, NY-ESO-1. The augmented expression of T cells targeting NY-ESO-1 in the systemic circulation of our patient following IT-GLA-SE warrants further investigation, given the promising role of NY-ESO-1 in current and future T-cell based immunotherapies. Together, these findings demonstrate the potential of IT GLA-SE to elicit antigen-specific T cell clonal expansion as a component of immunotherapeutic strategies to combat metastatic STSs. Expanded studies are needed to explore the clinical and immunologic effects of IT GLA-SE, particularly in combination with other immunotherapies.
Insights
Intratumoral injection of synthetic toll-like receptor 4 (TLR4) agonist, glycopyranosyl lipid A in stable-emulsion formulation (GLA-SE), showed promising T cell expansion in metastatic soft tissue sarcomas (STSs). Further studies are needed to explore its potential in immunotherapy.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- Metastatic soft tissue sarcomas (STSs) are rare, heterogeneous mesenchymal tumors with limited treatment options.
- The synthetic toll-like receptor 4 (TLR4) agonist, glycopyranosyl lipid A in stable-emulsion formulation (GLA-SE), is being investigated for advanced STSs.
Purpose of the Study:
- To explore the safety, tolerability, and immunologic effects of intratumoral (IT) GLA-SE in patients with metastatic leiomyosarcoma.
- To assess the potential of IT GLA-SE as an immunotherapeutic strategy for STSs.
Main Methods:
- A case series of three patients with metastatic leiomyosarcoma receiving IT GLA-SE (20 μg weekly for 12 weeks) alone or with radiotherapy.
- Evaluation of safety, tolerability, clinical response, and immunologic effects, including T cell clonal expansion.
Main Results:
- Treatment was well tolerated with no serious adverse events.
- Two patients showed notable stability in target lesions despite systemic disease progression.
- IT GLA-SE induced T cell clonal expansion intratumorally and systemically, including expansion of T cells targeting the NY-ESO-1 antigen.
Conclusions:
- Intratumoral GLA-SE demonstrates potential to induce antigen-specific T cell responses in metastatic STSs.
- Further investigation of IT GLA-SE, especially in combination with other immunotherapies, is warranted for advanced STSs.

