Enhancing the immune response against acute myeloid leukemia using specialized antibodies
Official title: Promoting immunity against acute myeloid leukemia through Fc effector-optimized antibody inhibitory of MICA/B shedding
Funded at Icahn School of Medicine at Mount Sinai · NIH-10992151 · Data updated 2026-11-12
This study is looking at a new way to help your immune system fight acute myeloid leukemia (AML) by using special antibodies that keep important signals on leukemia cells from disappearing, making it easier for your body's immune cells to find and destroy the cancer.
Quick facts
| Grant type | R37 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Icahn School of Medicine at Mount Sinai NIH-funded |
| Lab location | 1 site (New York, United States) |
| Project start | February 6, 2023 |
| Project end | November 30, 2027 |
| Funding year | 2025 |
| Award (this year) | $520,895 |
| NIH project number | 5R37CA269982-03 |
| Project ID | NIH-10992151 on NIH RePORTER |
Who could benefit from this research
✓Could help
Ideal candidates for this research are patients diagnosed with acute myeloid leukemia who are seeking innovative treatment options.
✕Less likely to help
Patients with other types of leukemia or those who do not have acute myeloid leukemia may not benefit from this research.
What this research studies
This research focuses on improving the immune system's ability to fight acute myeloid leukemia (AML) by using specially designed antibodies that prevent the shedding of important surface proteins on leukemia cells. These proteins, known as MICA and MICB, act as signals to alert immune cells, such as natural killer (NK) cells and macrophages, to attack the cancer cells. The study aims to develop a new version of an antibody that enhances the recognition and destruction of AML cells by these immune cells, potentially leading to better treatment outcomes for patients. By blocking the mechanisms that allow leukemia cells to evade the immune response, this research seeks to create a more effective therapeutic approach for AML.
Why it matters
Potential benefit: If successful, this research could lead to more effective treatments for patients with acute myeloid leukemia, improving their chances of recovery.
How similar studies have gone: Previous research has shown promising results with similar antibody-based approaches in enhancing immune responses against cancer, indicating potential for success in this novel application.
Where this research is happening
-
Icahn School of Medicine at Mount Sinai
New York, United States Active
Researchers
- Principal investigator: Ferrari de Andrade, Lucas — Icahn School of Medicine at Mount Sinai
- Study coordinator: Ferrari de Andrade, Lucas
Related research
Other NIH-funded projects on the same topics.
-
Targeting the SCP4 pathway in acute myeloid leukemia (AML)
Aims to uncover how the SCP4 signaling pathway drives AML and how it could be blocked to help patients.
-
Interferon-γ plus donor immune cells to fight AML/MDS after partial donor transplant
This project tests a therapy that adds a signaling protein, IFN-γ, with donor immune cells to help treat relapsed AML/MDS after a haploidentical stem cell transplant.
-
Targeting the protein housekeeping system in adult leukemia
Researchers are testing a new approach to treat acute myeloid leukemia by disrupting how AML cells manage their proteins, with the goal of helping patients live longer and healthier lives.
-
Understanding how epigenetic helper proteins drive AML and how to target them
A scientist team is studying how accessory proteins in gene-regulating complexes affect acute myeloid leukemia and whether they can be targeted for safer, more precise therapies.
-
Targeting FLVCR1-enabled choline use in a aggressive AML subtype
A new approach aims to block how a specific leukemia subtype (CG-AML) takes up choline to feed its growth, potentially slowing or stopping the disease.
-
Advancing CD70-targeted CAR-NK Therapy for AML
A patient-focused look at a new cell therapy that uses engineered NK cells to target AML by hitting CD70, aiming to reduce relapse with potentially fewer blood cell problems.
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.