Chu Xiaojie, Li Wei, Hines Margaret G, Lyakhov Ilya, Mellors John W, Dimitrov Dimiter S
Center for Antibody Therapeutics, Division of Infectious Diseases, Department of Medicine, University of Pittsburgh Medical School, Pittsburgh, PA, United States.
Comp IL, LLC, Carnegie, PA, United States.
Front Oncol. 2023 Oct 9;13:1194972. doi: 10.3389/fonc.2023.1194972. eCollection 2023.
The high expression of uPAR has been linked to tumor progression, invasion, and metastasis in several types of cancer. Such overexpression of uPAR makes it a potential target for immunotherapies across common cancers such as breast, colorectal, lung, ovarian cancer, and melanoma. In our study, two high-affinity and specific human V domain antibody candidates, designed as clones 3 and 115, were isolated from a phage-displayed human V antibody library. Domain-based bispecific T- cell engagers (DbTE) based on these two antibodies exhibited potent killing of uPAR-positive cancer cells. Thus, these two anti-uPAR domain antibodies are promising candidates for treating uPAR positive cancers.
uPAR的高表达与多种癌症的肿瘤进展、侵袭和转移有关。uPAR的这种过表达使其成为乳腺癌、结直肠癌、肺癌、卵巢癌和黑色素瘤等常见癌症免疫治疗的潜在靶点。在我们的研究中,从噬菌体展示的人V抗体库中分离出两个高亲和力和特异性的人V结构域抗体候选物,设计为克隆3和115。基于这两种抗体的基于结构域的双特异性T细胞衔接器(DbTE)对uPAR阳性癌细胞表现出有效的杀伤作用。因此,这两种抗uPAR结构域抗体是治疗uPAR阳性癌症的有前景的候选药物。