15P Topical strategy to prevent skin toxicities from bispecific-EGFR inhibitors by blocking drug-receptor interactions in skin

Results: Through the highly efficient isolation and immortalization of tumor-or TLSderived B cells, our approach captures the B cell diversity and all Ig-isotypes from all tissues.As opposed to the labor intensive and costly approach of ex vivo BCR sequencing and subsequent recombinant antibody production and validation, our B cell Tumor Libraries (TuLibs) secrete antibodies into the culture supernatant while retaining indefinite expansion capabilities, allowing for immediate functional screening of antibodies and rapid identification of unique tumor-specific B cell clones.Moreover, our immortalized B cells retain the ability to undergo somatic-hypermutation, allowing for in vitro affinity maturation of immortalized B cell clones against targets of interest.Conclusions: Altogether, Kling Biotherapeutic's proprietary platform allows the comprehensive functional screening and affinity maturation of human and animal B cell repertoires from multiple tissues sources.TuLibs represents a significant advancement in our ability to identify new immuno-functional targets and antibodies for biopharmaceutical development of tumor targeted therapies.

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Publication Details

Journal
ESMO Open
Published
2025-03-01
DOI
https://doi.org/10.1016/j.esmoop.2025.104171
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
0.00
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article

15P Topical strategy to prevent skin toxicities from bispecific-EGFR inhibitors by blocking drug-receptor interactions in skin

Ofra Benny, Sharon Merims, L. Weinstein, L. Aharonov et al.
ESMO Open
HER2/EGFR in Cancer Research
article

15P Topical strategy to prevent skin toxicities from bispecific-EGFR inhibitors by blocking drug-receptor interactions in skin

Ofra Benny, Sharon Merims, L. Weinstein, L. Aharonov, Y. Hazut
article en

Abstract

Results: Through the highly efficient isolation and immortalization of tumor-or TLSderived B cells, our approach captures the B cell diversity and all Ig-isotypes from all tissues.As opposed to the labor intensive and costly approach of ex vivo BCR sequencing and subsequent recombinant antibody production and validation, our B cell Tumor Libraries (TuLibs) secrete antibodies into the culture supernatant while retaining indefinite expansion capabilities, allowing for immediate functional screening of antibodies and rapid identification of unique tumor-specific B cell clones.Moreover, our immortalized B cells retain the ability to undergo somatic-hypermutation, allowing for in vitro affinity maturation of immortalized B cell clones against targets of interest.Conclusions: Altogether, Kling Biotherapeutic's proprietary platform allows the comprehensive functional screening and affinity maturation of human and animal B cell repertoires from multiple tissues sources.TuLibs represents a significant advancement in our ability to identify new immuno-functional targets and antibodies for biopharmaceutical development of tumor targeted therapies.

ESMO OpenVol. 10
Hebrew University of Jerusalem (IL), Nazareth Hospital EMMS (IL), Hadassah Medical Center (IL)
Zero hunger
Openalex Percentile: Top 94%
HER2/EGFR in Cancer Research
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15P Topical strategy to prevent skin toxicities from bispecific-EGFR inhibitors by blocking drug-receptor interactions in skin — Ofra Benny, Sharon Merims, et al. · ESMO Open (2025) | TGRS Research Map | TGRS