# IL-7: a potential next-generation adjuvant for immune cell therapies

**Authors:** Richard S. Hotchkiss, John F. DiPersio, Cassian Yee, Russell K. Pachynski, Marcel R. M. Van Den Brink

PMC · DOI: 10.3389/fimmu.2025.1736931 · Frontiers in Immunology · 2026-01-02

## TL;DR

This paper explores how IL-7, a cytokine, can enhance immune cell therapies by improving T-cell function and numbers, potentially leading to better cancer treatments.

## Contribution

The paper highlights IL-7 as a promising next-generation adjuvant for immune cell therapies based on clinical experience and potential future applications.

## Key findings

- IL-7 is well-tolerated and increases CD4 and CD8 T-cell numbers and function.
- IL-7 has been used in various clinical settings, including cancer and lymphopenia, with positive outcomes.
- The authors suggest IL-7 can address major limitations in adoptive cell therapies.

## Abstract

Cell-based immune therapies ranging from CAR-T cells to tumor infiltrating lymphocytes (TILs) and endogenous T-cell products, have produced unprecedented clinical responses in hematologic malignancies and are currently under active investigation for solid tumors. Nevertheless, several key challenges continue to limit the durability and breadth of clinical benefit. IL-7 is a pleiotropic cytokine that increases both the number and function of lymphocytes. Although not yet clinically approved, IL-7 has been used in over 620 adult and pediatric patients for a variety of reasons including, for example, to hasten bone marrow recovery after allogenic stem cell transplantation, to reverse lymphopenia due to HIV and idiopathic etiologies, to treat patients with various malignancies, and to boost vaccine responses. IL-7 is generally well-tolerated and effective in producing a durable increase in the number and function of CD4 and CD8 T cells. Recently, IL-7 has been used clinically in multiple myeloma patients receiving CAR-T cell therapy, in patients with urothelial cancer who are receiving checkpoint inhibitors, in patients undergoing endogenous lymphocyte cell therapy, and in critically-ill lymphopenic patients with COVID-19. The authors, all of whom have used IL-7 clinically, discuss how IL-7 effectively addresses all the major problems currently limiting adoptive cell therapies. Peering into the future, we believe that IL-7 will be a major advance as an adjuvant treatment in many cell therapies and hope that this commentary will expedite IL-7’s testing in multiple clinical settings.

## Linked entities

- **Proteins:** IL7 (interleukin 7)
- **Diseases:** multiple myeloma (MONDO:0009693), lymphopenia (MONDO:0003783), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** multiple myeloma (MESH:D009101), HIV (MESH:D015658), urothelial cancer (MESH:D014523), malignancies (MESH:D009369), hematologic malignancies (MESH:D019337), COVID-19 (MESH:D000086382), lymphopenia (MESH:D008231)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12808468/full.md

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Source: https://tomesphere.com/paper/PMC12808468