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Poster Display & Cocktail

17P - KBA1413: An antibody derived from a cured AML patient, recognizes a unique glycoepitope shared by AML, MDS and several solid cancer cells

Date

03 Mar 2025

Session

Poster Display & Cocktail

Presenters

Martijn Kedde

Citation

Annals of Oncology (2025) 10 (suppl_2): 1-7. 10.1016/esmoop/esmoop104162

Authors

M. Kedde1, V. Clerico Mosina2, B. Pieters2, B. Monica1, K. Maijoor1, E. Frankin1, R. Schotte3, A. Bakker1, R. Roovers1, M. Koslowski4, S. Gullà5

Author affiliations

  • 1 Preclinical, Kling Biotherapeutics, 1105 BA - Amsterdam/NL
  • 2 Protein Sciences, Kling Biotherapeutics, 1105 BA - Amsterdam/NL
  • 3 Translational Research Dept., Kling Biotherapeutics, 1105 BA - Amsterdam/NL
  • 4 Ceo, Kling Biotherapeutics, 1105 BA - Amsterdam/NL
  • 5 Cso, Kling Biotherapeutics, 1105 BA - Amsterdam/NL

Resources

This content is available to ESMO members and event participants.

Abstract 17P

Background

The use of human B cells for antigen- and antibody discovery is on the rise due to the emergence of new techniques to tap into the human antigen-experienced B cell repertoire. To identify new targets for immunotherapy, we screened the B-cell repertoire of a patient with high-risk acute myeloid leukemia (AML) who mounted a potent graft versus leukemia immune response following allogeneic stem cell transplantation.

Methods

KBA1413 is a fully human antibody identified using Kling’s proprietary B cell screening platform, Kling-Select. KBA1413 derives from the B cells of an AML patient who remains in long term remission following allogeneic hematopoietic stem cell transplantation.

Results

The antibody recognizes a unique, previously undescribed, sialylated epitope present on CD43 (CD43s). This epitope is expressed on across all AML subtypes and on myelodysplastic syndrome (MDS), as illustrated by KBA1413 reactivity to with freshly isolated blasts of over 60 randomly selected AML and MDS patients. In addition, KBA1413 also recognizes several solid tumor indications, including melanoma and breast cancer. KBA1413 triggers NK-mediated antibody dependent cell-mediated cytotoxicity (ADCC) against AML cells both in vitro and in vivo in human immune system mice xenografted with AML cells, suggesting that KBA1413 played a role in the graft versus leukemia response of the original donor patient.

Conclusions

To increase its therapeutic potential KBA1413 was made into a bispecific T-cell engaging antibody (bTCE) that induced potent cytotoxicity in vitro and in vivo on cell lines and primary AML. Bifunctional targeting of AML with KBA1413 and a CD33 binder induced potent ADCC activitycytotoxicity in vitro, outperforming single agent activity. To increase the affinity of KBA1413, we further optimized binding of KBA1413 with employed the Kling-Evolve platform, this allows for the in vitro maturation of B cell clones against targets of interest. We are further exploring the therapeutic potential of KBA1413 with affinity matured variants produced with Kling-Evolve.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Kling Biotherapeutics.

Funding

Has not received any funding.

Disclosure

M. Kedde: Financial Interests, Institutional, Stocks/Shares: Kling Biotherapeutics; Financial Interests, Institutional, Project Lead: Kling Biotherapeutics. V. Clerico Mosina: Financial Interests, Institutional, Stocks/Shares: Kling Biotherapeutics. B. Pieters, B. Monica, K. Maijoor, E. Frankin, R. Schotte, A. Bakker: Financial Interests, Institutional, Stocks/Shares: Kling Biotherapeutics. R. Roovers, M. Koslowski, S. Gullà: Financial Interests, Institutional, Stocks/Shares: Kling Biotherapeutics; Financial Interests, Institutional, Leadership Role: Kling Biotherapeutics.

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