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Sökning: onr:"swepub:oai:DiVA.org:mau-66835" > RUBY® - a tetravale...

RUBY® - a tetravalent (2+2) bispecific antibody format with excellent functionality and IgG-like stability, pharmacology and developability properties

Nyesiga, Barnabas (författare)
Malmö universitet,Institutionen för biomedicinsk vetenskap (BMV),Alligator Biosci AB, Med Village, Lund, Sweden
Levin, Mattias (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
Saell, Anna (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
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Rosén, Anna (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
Jansson, Kim (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
Fritzell, Sara (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
Hagerbrand, Karin (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
Weilguny, Dietmar (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
von Schantz, Laura (författare)
Alligator Biosci AB, Med Village, Lund, Sweden
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 (creator_code:org_t)
Taylor & Francis, 2024
2024
Engelska.
Ingår i: mAbs. - : Taylor & Francis. - 1942-0862 .- 1942-0870. ; 16:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Despite the large number of existing bispecific antibody (bsAb) formats, the generation of novel bsAbs is still associated with development and bioprocessing challenges. Here, we present RUBY, a novel bispecific antibody format that allows rapid generation of bsAbs that fulfill key development criteria. The RUBYTM format has a 2 + 2 geometry, where two Fab fragments are linked via their light chains to the C-termini of an IgG, and carries mutations for optimal chain pairing. The unique design enables generation of bsAbs with mAb-like attributes. Our data demonstrate that RUBY bsAbs are compatible with small-scale production systems for screening purposes and can be produced at high yields (>3 g/L) from stable cell lines. The bsAbs produced are shown to, in general, contain low amounts of aggregates and display favorable solubility and stress endurance profiles. Further, compatibility with various IgG isotypes is shown and tailored Fc gamma receptor binding confirmed. Also, retained interaction with FcRn is demonstrated to translate into a pharmacokinetic profile in mice and non-human primates that is comparable to mAb controls. Functionality of conditional active RUBY bsAbs is confirmed in vitro. Anti-tumor effects in vivo have previously been demonstrated, and shown to be superior to a comparable mAb, and here it is further shown that RUBY bsAbs penetrate and localize to tumor tissue in vivo. In all, the RUBY format has attractive mAb-like attributes and offers the possibility to mitigate many of the development challenges linked to other bsAb formats, facilitating both high functionality and developability.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Nyckelord

Antibody format
bispecific antibodies
IgG
immuno-oncology
RUBY (R)
tetravalent

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