SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Dallas Tiffany)
 

Search: WFRF:(Dallas Tiffany) > (2024) > Reducing neonatal F...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Reducing neonatal Fc receptor binding enhances clearance and brain-to-blood ratio of TfR-delivered bispecific amyloid-β antibody

Schlein, Eva (author)
Uppsala universitet,Institutionen för folkhälso- och vårdvetenskap
Andersson, Ken G. (author)
BioArctic AB, Biotechnol, Stockholm, Sweden.
Dallas, Tiffany (author)
Uppsala universitet,Molekylär geriatrik
show more...
Syvänen, Stina (author)
Uppsala universitet,Molekylär geriatrik
Sehlin, Dag, 1976- (author)
Uppsala universitet,Molekylär geriatrik
show less...
 (creator_code:org_t)
Taylor & Francis, 2024
2024
English.
In: mAbs. - : Taylor & Francis. - 1942-0862 .- 1942-0870. ; 16:1
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Recent development of amyloid-β (Aβ)-targeted immunotherapies for Alzheimer’s disease (AD) have highlighted the need for accurate diagnostic methods. Antibody-based positron emission tomography (PET) ligands are well suited for this purpose as they can be directed toward the same target as the therapeutic antibody. Bispecific, brain-penetrating antibodies can achieve sufficient brain concentrations, but their slow blood clearance remains a challenge, since it prolongs the time required to achieve a target-specific PET signal. Here, two antibodies were designed based on the Aβ antibody bapineuzumab (Bapi) – one monospecific IgG (Bapi) and one bispecific antibody with an antigen binding fragment (Fab) of the transferrin receptor (TfR) antibody 8D3 fused to one of the heavy chains (Bapi-Fab8D3) for active, TfR-mediated transport into the brain. A variant of each antibody was designed to harbor a mutation to the neonatal Fc receptor (FcRn) binding domain, to increase clearance. Blood and brain pharmacokinetics of radiolabeled antibodies were studied in wildtype (WT) and AD mice (AppNL-G-F). The FcRn mutation substantially reduced blood half-life of both Bapi and Bapi-Fab8D3. Bapi-Fab8D3 showed high brain uptake and the brain-to-blood ratio of its FcRn mutated form was significantly higher in AppNL-G-F mice than in WT mice 12 h after injection and increased further up to 168 h. Ex vivo autoradiography showed specific antibody retention in areas with abundant Aβ pathology. Taken together, these results suggest that reducing FcRn binding of a full-sized bispecific antibody increases the systemic elimination and could thereby drastically reduce the time from injection to in vivo imaging.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Alzheimer's disease (AD)
amyloid-beta (a beta)
bispecific antibody
blood-brain barrier (BBB)
neonatal Fc receptor (FcRn)
receptor mediated transcytosis (RMT)

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

  • mAbs (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Find more in SwePub

By the author/editor
Schlein, Eva
Andersson, Ken G ...
Dallas, Tiffany
Syvänen, Stina
Sehlin, Dag, 197 ...
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Neurosciences
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
and Biochemistry and ...
Articles in the publication
mAbs
By the university
Uppsala University

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view