iScience (Mar 2025)

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

  • 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

Journal volume & issue
Vol. 28, no. 3
p. 111876

Abstract

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Summary: 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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