Antibody fragment prevents hemorrhages associated with new Alzheimer's treatments

by Autonomous University of Barcelona

edited by Lisa Lock, reviewed by Alexander Pol

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In 2025, the European Medicines Agency approved two antibodies for Alzheimer's disease: lecanemab (Leqembi^TM, from Biogen) and donanemab (Kisunla, from Eli Lilly and Co.), both based on immunotherapy (the use of molecules from the immune system to treat diseases). These antibodies, obtained in the laboratory, act against the Aβ peptide, a protein fragment that accumulates in the brains of patients with Alzheimer's disease. Elimination of this protein by the immune system helps slow the characteristic cognitive decline of the disease.

These two antibodies are the first disease-modifying therapies for Alzheimer's. They stop and, in some cases, even partially reverse this devastating condition. However, a frequent and characteristic side effect of these drugs is cerebral bleeding, detectable by magnetic resonance imaging. The brain does not have the molecules and cells that make up the systemic immune system, so the entry of antibodies into the brain is not desirable under healthy conditions, although it is necessary for these treatments to be effective.

The incidence of bleeding in clinical trials ranged from 10% to 27% of treated patients, with a particularly high incidence in individuals carrying a specific apolipoprotein allele: APOEε4. In Europe, these treatments can be administered only to people with one or no copy of the APOEε4 allele, a genetic variant associated with a higher risk of Alzheimer's.

The Protein Design and Immunotherapy group at the UAB, led by Chair Professor Sandra Villegas of the Department of Biochemistry and Molecular Biology, has been working for years on the hypothesis that full-length antibodies could be unsafe for the treatment of neurodegenerative diseases because they recruit systemic immune system cells into the brain. This undesirable recruitment can disrupt the blood-brain barrier and cause bleeding.

"That is why we designed the monocatenary antibody fragment (scFv-h3D6) targeting the Aβ peptide, which does not have the region responsible for recruiting these immune cells, and we have broadly demonstrated its efficacy at the molecular, cellular and cognitive scale in mice," says Professor Sandra Villegas.

Now, in collaboration with Dr. Silvia Lope-Piedrafita, a UAB researcher and expert in magnetic resonance, and Dr. Mar Hernández-Guillamon, a researcher at the Vall d'Hebron Research Institute and expert in the APP23 mouse model, the group has used magnetic resonance imaging to visualize the bleeding caused by the full-length antibody bapineuzumab, from which the developed fragment derives, and compare it with the effects of administering only the antibody fragment.

The results, published in Biomolecules, notably show that bleeding does not occur when the antibody fragment is administered, while therapeutic effects are maintained.

Villegas says, "The work shows that antibody fragments can offer a safer alternative than intact antibodies, which paves the way for new research into an effective and safe drug for Alzheimer's disease."

More information

Silvia Lope-Piedrafita et al, ScFv-h3D6 Prevents Bapineuzumab-Induced Hemorrhagic Events in the APP23 Mouse Model of Alzheimer's Disease, Biomolecules (2025). DOI: 10.3390/biom15111602

Key medical concepts

Alzheimer's DiseaseApolipoprotein E4

Clinical categories

NeurologyClinical pharmacology Provided by Autonomous University of Barcelona Who's behind this story?

Lisa Lock

BA art history, MA material culture. Former museum editor, paramedic, and transplant coordinator. Editing for Science X since 2021. Full profile →

Alexander Pol

PhD nano-engineering from Delft University. Published researcher and journal reviewer. Brings scientific insight to content standards. Full profile →

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