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Innovative Genetically Engineered Immune Cells Offer Hope for Organ Transplant Rejection Prevention

Innovative Genetically Engineered Immune Cells Offer Hope for Organ Transplant Rejection Prevention

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Researchers develop a targeted immunotherapy using genetically engineered immune cells to prevent organ rejection, offering hope for more precise and effective transplant treatments.

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A recent breakthrough by researchers at the Medical University of South Carolina introduces a novel approach to reducing organ transplant rejection through genetically modified immune cells. The team has engineered a new type of immune cell capable of specifically targeting and neutralizing B-cells that produce harmful anti-HLA antibodies responsible for rejecting transplanted organs. This cutting-edge strategy involves the use of chimeric anti-HLA antibody receptors (CHARs), which are added to regulatory T-cells (Tregs). These receptors detect and bind to problematic B-cells, prompting Tregs to suppress their activity, thereby preventing immune attacks on the transplanted tissue.

This targeted immunosuppression approach is a significant advancement over the traditional use of broad-spectrum immunosuppressant drugs, which can weaken the entire immune system and lead to adverse side effects. By honing in on specific immune components, this method aims to preserve overall immune function while preventing rejection.

The study, led by Dr. Leonardo Ferreira, involved testing these engineered cells with samples from dialysis patients prone to kidney transplant rejection. Results demonstrated a marked reduction in anti-HLA antibody levels, suggesting the potential effectiveness of this tailored immune modulation. This development is particularly promising for pre-sensitized patients—those with prior exposure to specific HLA variants like HLA-A2—who typically face greater challenges in finding compatible organs.

Additionally, the research highlights the importance of maintaining immune balance: while immune responses are vital for fighting infections, they must be precisely regulated to avoid unnecessary tissue damage or rejection. The CHAR-based strategy exemplifies how innovative biotech can enhance immune regulation, making organ transplants safer and more accessible for patients with limited options.

Overall, this research opens new avenues for organ transplant treatment, aiming to improve long-term outcomes and reduce reliance on generalized immunosuppressants, potentially transforming transplant medicine in the future.

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