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TZ-Ab102
SdAb Discovery to Cancer Treatment
TZ_Ab102 has been developed for precise cancer treatment by targeting
peptide–MHC complexes. In this effort, single-domain antibody (sdAb) emerged as a
promising binder with the required specificity and stability.
Building on this insight, an sdAb was engineered to recognize the WT1-derived
peptide–HLA complex with high affinity, and its potential was demonstrated in a
CAR-T format.
These results highlight the promise of sdAbs as a new class of therapeutics for
pMHC-targeted cancer immunotherapy.

Mode of Action & In vitro Efficacy
Crystal Structure
Cytotoxcity Test (CAR-T)

sdAb
WT1 derived peptide
MHC I
(HLA-A*02:01/β2M)

RMF peptide
p53(R175H) peptide
IL-2 (pg/ml)
1000
500
0
-12
-11
-10
-4
-5
-6
-7
-8
-9
Cell: T2
Log([peptide], M)

RMF peptide
p53(R175H) peptide
IL-2 (pg/ml)
1000
500
0
Cell: 721.221 (HLA-A*02:01+/TAP-)
Log([peptide], M)
-12
-11
-10
-4
-5
-6
-7
-8
-9
Progress
Design
Lead
IND Enabling
Remarks
Asset
Hit
Preclinical Study
TZ-Ab102
Awarded a national
research grant
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