KAIST researchers reprogram tumor immune cells to target cancer

Scientists at KAIST in South Korea have developed a novel therapy that transforms a tumor's own immune cells into potent cancer fighters directly inside the body. By injecting lipid nanoparticles into tumors, the treatment reprograms macrophages to produce cancer-recognizing proteins, overcoming barriers in solid tumor treatment. Early animal studies show promising reductions in tumor growth.

Tumors often harbor immune cells called macrophages, which are equipped to attack cancer but are typically suppressed by the tumor's environment. A team at KAIST, led by Professor Ji-Ho Park from the Department of Bio and Brain Engineering, has devised a strategy to reactivate these cells on-site. Announced on December 30, the breakthrough involves injecting a specially designed drug that macrophages absorb readily.

The drug consists of lipid nanoparticles delivering mRNA encoding chimeric antigen receptor (CAR) proteins—devices that enable cells to recognize and target cancer—along with an immune-boosting compound. Once absorbed, the macrophages produce these CAR proteins themselves, evolving into what the researchers call "CAR-macrophages." These enhanced cells not only engulf cancer cells directly but also rally nearby immune responses, amplifying the overall anticancer effect.

Solid tumors, such as those in gastric, lung, and liver cancers, pose unique challenges due to their dense structure, which hinders immune cell infiltration and function. Existing CAR-macrophage therapies require extracting cells from patients, modifying them in labs, and reinfusing them—a process that is costly and logistically complex. The KAIST approach bypasses these steps by leveraging macrophages already present in the tumor microenvironment.

In experiments with animal models of melanoma, a severe form of skin cancer, the therapy significantly curbed tumor growth. Notably, the immune activation extended beyond the treated site, hinting at potential systemic benefits. Professor Ji-Ho Park emphasized the innovation: "This study presents a new concept of immune cell therapy that generates anticancer immune cells directly inside the patient's body." He added that it addresses key limitations of prior methods, including delivery efficiency and the suppressive tumor setting.

The research, with Jun-Hee Han as first author, appeared in the journal ACS Nano in 2025. Supported by Korea's National Research Foundation, it underscores advances in in situ immunotherapy.

Makala yanayohusiana

Illustration of triple-drug therapy inducing necroptosis in leukemia cells, triggering immune response in preclinical study.
Picha iliyoundwa na AI

Triple-drug therapy drives necroptosis and boosts immune attack on leukemia in preclinical study

Imeripotiwa na AI Picha iliyoundwa na AI Imethibitishwa ukweli

Researchers at the Institut Pasteur and Inserm have developed a triple-drug strategy that induces necroptosis in malignant B cells, triggering a strong anti-tumor immune response in preclinical models of leukemia. By reprogramming how cancer cells die, the approach enabled complete leukemia elimination in animals and may offer a new avenue for treating B cell-related blood cancers, according to findings published in Science Advances.

Researchers at KAIST have developed an injection that transforms immune cells within tumors into active cancer-killing agents, bypassing the need for complex lab procedures. The method uses lipid nanoparticles to deliver instructions directly to macrophages, enabling them to recognize and attack cancer cells while boosting broader immune responses. In animal tests, the approach significantly slowed tumor growth in melanoma models.

Imeripotiwa na AI Imethibitishwa ukweli

Scientists at the Icahn School of Medicine at Mount Sinai report an experimental CAR T-cell strategy that targets tumor-associated macrophages—the immune cells many tumors use as a protective shield—rather than attacking cancer cells directly. In preclinical mouse models of metastatic ovarian and lung cancer, the approach reshaped the tumor microenvironment and extended survival, with some animals showing complete tumor clearance, according to a study published online January 22 in Cancer Cell.

Researchers at Northwestern University have developed a more effective therapeutic vaccine for HPV-related cancers by rearranging components in a DNA-based nanoparticle. This structural adjustment significantly enhances the immune system's ability to target and destroy tumors. The findings, published in Science Advances, highlight the importance of molecular arrangement in vaccine design.

Imeripotiwa na AI Imethibitishwa ukweli

Cold Spring Harbor Laboratory researchers report that engineered anti-uPAR CAR T cells cleared senescence-linked cells in mice, improving intestinal regeneration, reducing inflammation and strengthening gut barrier function. The approach also aided recovery from radiation-related intestinal injury and showed regenerative signals in experiments using human intestinal and colorectal cells, raising the possibility of future clinical trials.

Trinity College Dublin researchers report that electrically stimulating human macrophages shifted them toward an anti‑inflammatory, tissue‑repairing state in laboratory tests, pointing to potential therapies for injuries and inflammatory disease. The peer‑reviewed findings appear in Cell Reports Physical Science.

Imeripotiwa na AI Imethibitishwa ukweli

A research team led by Jinyong Wang at the Chinese Academy of Sciences says it has developed a three-step laboratory process that can generate large numbers of induced natural killer (iNK) cells — including CD19 CAR-engineered versions — starting from CD34+ stem and progenitor cells from umbilical cord blood. In a Nature Biomedical Engineering study published in October 2025, the researchers reported output on the order of tens of millions of NK cells from a single starting CD34+ cell in their system and showed anti-tumour activity in mouse models of blood cancers, while also reporting sharply reduced viral-vector use for CAR delivery compared with approaches that modify mature NK cells.

Jumatatu, 16. Mwezi wa tatu 2026, 16:23:31

Engineered antibody shrinks tumors body-wide in early cancer trial

Jumapili, 1. Mwezi wa tatu 2026, 09:17:42

Oregon State researchers report iron-based nanomaterial that eliminates breast-cancer tumors in mice

Ijumaa, 13. Mwezi wa pili 2026, 11:07:36

CAR T-cell therapy may slow ALS progression

Jumatano, 11. Mwezi wa pili 2026, 05:11:35

FDA fast-tracks first inhalable gene therapy for lung cancer

Jumanne, 20. Mwezi wa kwanza 2026, 03:55:31

UBC researchers show how to reliably generate helper T cells from stem cells by tuning Notch signaling

Alhamisi, 15. Mwezi wa kwanza 2026, 14:16:51

Northwestern antibody targets pancreatic cancer's immune evasion

Jumanne, 23. Mwezi wa kumi na mbili 2025, 01:57:35

MIT and Stanford create tool to expose cancer to immune system

Jumatatu, 15. Mwezi wa kumi na mbili 2025, 15:24:19

Scientists alter mast cells to fight cancer tumors

Jumatatu, 24. Mwezi wa kumi na moja 2025, 21:29:12

Scientists map proteins that let carcinomas change identity

Jumamosi, 22. Mwezi wa kumi na moja 2025, 16:34:36

Nasal nanodrops wipe out glioblastoma tumors in mice

 

 

 

Tovuti hii inatumia vidakuzi

Tunatumia vidakuzi kwa uchambuzi ili kuboresha tovuti yetu. Soma sera ya faragha yetu kwa maelezo zaidi.
Kataa