TY - JOUR
T1 - Solving the mystery of the FMC63-CD19 affinity
AU - Seigner, Jacqueline
AU - Zajc, Charlotte U.
AU - Dötsch, Sarah
AU - Eigner, Caroline
AU - Laurent, Elisabeth
AU - Busch, Dirk H.
AU - Lehner, Manfred
AU - Traxlmayr, Michael W.
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - The majority of approved CAR T cell products are based on the FMC63-scFv directed against CD19. Surprisingly, although antigen binding affinity is a major determinant for CAR function, the affinity of the benchmark FMC63-scFv has not been unambiguously determined. That is, a wide range of affinities have been reported in literature, differing by more than 100-fold. Using a range of techniques, we demonstrate that suboptimal experimental designs can cause artefacts that lead to over- or underestimation of the affinity. To minimize these artefacts, we performed SPR with strictly monomeric and correctly folded soluble CD19, yielding an FMC63-scFv affinity of 2–6 nM. Together, apart from analyzing the FMC63-scFv affinity under optimized conditions, we also provide potential explanations for the wide range of published affinities. We expect that this study will be highly valuable for interpretations of CAR affinity-function relationships, as well as for the design of future CAR T cell generations.
AB - The majority of approved CAR T cell products are based on the FMC63-scFv directed against CD19. Surprisingly, although antigen binding affinity is a major determinant for CAR function, the affinity of the benchmark FMC63-scFv has not been unambiguously determined. That is, a wide range of affinities have been reported in literature, differing by more than 100-fold. Using a range of techniques, we demonstrate that suboptimal experimental designs can cause artefacts that lead to over- or underestimation of the affinity. To minimize these artefacts, we performed SPR with strictly monomeric and correctly folded soluble CD19, yielding an FMC63-scFv affinity of 2–6 nM. Together, apart from analyzing the FMC63-scFv affinity under optimized conditions, we also provide potential explanations for the wide range of published affinities. We expect that this study will be highly valuable for interpretations of CAR affinity-function relationships, as well as for the design of future CAR T cell generations.
UR - http://www.scopus.com/inward/record.url?scp=85180723354&partnerID=8YFLogxK
U2 - 10.1038/s41598-023-48528-0
DO - 10.1038/s41598-023-48528-0
M3 - Article
AN - SCOPUS:85180723354
VL - 13
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 23024
ER -