JNJ-78306358, a first-in-class bispecific T cell engaging antibody targeting CD3 and HLA-G

JNJ-78306358 是一种首创的双特异性 T 细胞接合抗体,靶向 CD3 和 HLA-G。

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作者:Nataša Obermajer,Adam Zwolak,Kelly van de Ven,Shana Versmissen,Krista Menard,Katharine Rogers,Ted Petley,Dan Weinstock,Jason Aligo,Jaymala Patel,Ken Tian,Lorraine Angelillo,Fang Yi,Stephen Jarantow,Keith Schutsky,Yoshitomo Hamuro,Diana Alvarez Arias,Kristel Buyens,Tsun-Wen Sheena Yao,Vince Torti,Aleksandra Brajic,Brian Geist,Marjolein van Heerden,Gerald Chu,Bie Verbist,Maté Ongenaert,Julien Häsler,Kathryn Packman,Jacintha Shenton,Laurie Lenox,Jacalyn Clawson,Regina J Brown,Josh Lauring,James G Greger,Dirk Brehmer,Sanjaya Singh,Matthew V Lorenzi,Sylvie Laquerre

Abstract

T cell-redirecting bispecific antibodies (bsAbs) to treat advanced stage solid tumors are gaining interest after recent clinical successes. The immune checkpoint human leukocyte antigen G (HLA-G) is expressed in several tumor types while in normal tissues expression is limited. Here, we describe JNJ-78306358, a T cell-redirecting bispecific antibody (bsAb) to treat advanced stage solid tumors. JNJ-78306358 binds with high affinity to the α3 subunit of HLA-G on cancer cells and with purposely engineered weaker affinity to CD3ε on T cells. JNJ-78306358 induced potent T cell-mediated cytotoxicity of HLA-G-expressing solid tumors in vitro and in vivo. JNJ-78306358 also blocked the interaction of HLA-G with its receptors in vitro, indicating that immune checkpoint blocking may contribute to its anti-tumor activity. These results suggest that T cell-redirection against HLA-G could be a potent and effective treatment for a wide range of solid tumor indications.

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