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Alfa-TILTM Platform

Tumor-Infiltrating Lymphocyte (TIL) therapy represents a transformative advancement in cancer immunotherapy, leveraging a patient's own immune system to target solid tumors. As interest in personalized cellular therapy surges, TIL has emerged as a clinically promising, tumor-specific approach with growing relevance in preclinical innovation and therapeutic discovery. Alfa Cytology offers cutting-edge preclinical TIL development services through our proprietary Alfa-TIL™ platform. Engineered for efficiency, our solution enables high-quality TIL preparation from minimal tumor input with significantly reduced turnaround times. Backed by a team of experienced scientists and streamlined laboratory workflows, Alfa-TIL™ empowers research partners to accelerate TIL-based therapeutic discovery with precision and confidence.

Overview of Alfa-TILTM

Tumor-Infiltrating Lymphocyte (TIL) therapy is a promising form of adoptive cell therapy (ACT) that utilizes a patient's own immune system to target cancer. By isolating lymphocytes from tumor tissues—cells already sensitized to tumor-specific antigens—and expanding them ex vivo, this therapy reinfuses these potent immune cells back into the patient. Unlike engineered therapies such as CAR-T, TILs are polyclonal and inherently tumor-reactive, allowing for broad recognition of patient-specific tumor neoantigens.

Fig. 1 General scheme of the preparation of TILs. (Zhao, Y., et al., 2022) Fig. 1 General scheme of the preparation of TILs. (Zhao, Y., et al., 2022)

Building upon these advancements, Alfa-TIL™ provides a cutting-edge platform for the development of preclinical TIL therapies. It offers a robust, modular, and highly customizable service pipeline, designed with flexibility and speed in mind. Alfa-TIL™ platform empowers researchers to efficiently explore, optimize, and refine TIL therapies for a broad range of cancers. By integrating advanced technologies, it simplifies the entire TIL development process—from the isolation of tumor-reactive lymphocytes to functional modifications and in-depth profiling. This versatility enables researchers to accelerate therapeutic discoveries, optimize experimental designs, and transition seamlessly from preclinical research to clinical trial readiness. Alfa-TIL™ not only supports fundamental research but also ensures translational value, providing the necessary tools to drive the development of next-generation immunotherapies.

Mechanisms of Alfa-TILTM

The development of TIL therapy has been significantly influenced by advances in the understanding of tumor immunology. Tumors are not static, and their ability to evade the immune system is one of the main challenges in cancer therapy. TIL therapy takes advantage of the fact that certain immune cells infiltrate tumor tissues naturally, recognizing the tumor as foreign. This observation led to the hypothesis that expanding these naturally occurring immune cells outside the body and reinfusing them could harness their inherent tumor-specific recognition capability. Over the decades, advances in cytokine support (e.g., IL-2), lymphodepletion protocols, and manufacturing processes have significantly improved the efficacy and feasibility of TIL-based interventions.

Natural Tumor Reactivity

TILs are naturally primed against tumor antigens, providing an intrinsic capacity for tumor elimination without the need for genetic modification.

Polyclonality

The polyclonal nature of TILs allows them to recognize and target a diverse range of tumor-associated antigens, addressing potential tumor variability.

Tumor Microenvironment Adaptation

TILs are capable of adapting to the suppressive tumor microenvironment, overcoming obstacles such as immune checkpoints and inhibitory cytokines.

Advantages of Alfa-TILTM

Company Name TIL Platforms Features
Competitor 1 Platform 1 Clinical-stage, autologous manufacturing, single-center GMP pipeline; lengthy culture.
Competitor 2 Platform 2 Engineered TIL with membrane-bound IL-15 for enhanced persistence; preclinical/early-stage candidate.
Competitor 3 Platform 3 Enriches most tumor-reactive T cells before expansion; combination with viral immunotherapies.
Competitor 4 Platform 4 Streamlined manufacturing, academic-origin platform adapted for cost-effective development.
Alfa Cytology-Alfa-TILTM Alfa-TILTM Low-input tissue, rapid isolation/expansion, customizable genetic engineering, in vitro/in vivo validation, multi-omics profiling.

Workflow of TIL Therapy Development

Low-Input & Rapid TIL Isolation and Expansion

Alfa-TIL™ provides reliable and time-efficient TIL isolation and expansion services using small amounts of tumor tissue. Our protocol is optimized to generate high-quality, viable TIL populations within a short processing timeline—making it ideal for preclinical studies where sample availability is limited or time is a critical factor.

TIL Genetic Engineering for Functional Enhancement

Alfa-TIL™ enables targeted gene modifications to enhance TIL function, durability, or resistance to immunosuppressive signals. Researchers can access services for the introduction of custom constructs or genome edits to evaluate next-generation TIL designs in a controlled preclinical setting.

Multi-Omics TIL Profiling

Alfa-TIL™ supports transcriptomic and immune phenotyping analysis of TILs to reveal functional signatures, clonality, and exhaustion states. Services include bulk RNA sequencing, TCR repertoire analysis, and high-dimensional flow cytometry to guide product optimization and target discovery.

Preclinical TIL Functional Validation

Alfa-TIL™ offers in vitro and in vivo assays to evaluate TIL antitumor activity, including cytotoxicity, cytokine release, and efficacy in animal models. These services support early functional characterization and candidate selection.

TIL Therapy for Diverse Cancer Types

TIL-based immunotherapy has shown promise across a broad spectrum of solid tumors, particularly those characterized by high mutational burden, immune infiltration, or viral antigens. Alfa-TIL™ platform supports preclinical TIL development across diverse tumor types. Our low-input isolation, genetic engineering, and functional validation services enable rapid assessment of tumor-specific TIL performance across multiple disease contexts.

Breast Cancer

Cervical Cancer

Melanoma

Why Choose Us?

  • Proprietary Alfa-TIL™ workflow optimized for low-input tumor samples
  • Expertise in TIL genetic enhancement, functional validation, and multi-omics profiling
  • Fully preclinical-focused—ideal for early discovery and proof-of-concept studies

Partner with Alfa-TIL™ and leverage our agile, expert-driven TIL development solutions tailored for preclinical R&D. Whether you're working on TIL discovery, engineering, or functional evaluation, our team is here to help you move forward—faster, and with confidence. Contact us today to explore collaboration opportunities and request a custom proposal.

Reference

  1. Zhao, Y., et al. Genetically engineered oncolytic bacteria as drug delivery systems for targeted cancer theranostics. Acta biomaterialia. 2022, 14(17): 4160.

For research use only.