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Tumor-conditional anti-CTLA4 uncouples antitumor efficacy from immunotherapy-related toxicity
Chien-Chun Steven Pai, … , Gillian Kingsbury, Lawrence Fong
Chien-Chun Steven Pai, … , Gillian Kingsbury, Lawrence Fong
Published December 10, 2018
Citation Information: J Clin Invest. 2019;129(1):349-363. https://doi.org/10.1172/JCI123391.
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Research Article Immunology Oncology

Tumor-conditional anti-CTLA4 uncouples antitumor efficacy from immunotherapy-related toxicity

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Abstract

While immune checkpoint blockade leads to potent antitumor efficacy, it also leads to immune-related adverse events in cancer patients. These toxicities stem from systemic immune activation resulting in inflammation of multiple organs, including the gastrointestinal tract, lung, and endocrine organs. We developed a dual variable domain immunoglobulin of anti-CTLA4 antibody (anti-CTLA4 DVD, where CTLA4 is defined as cytotoxic T lymphocyte–associated antigen-4) possessing an outer tumor-specific antigen-binding site engineered to shield the inner anti-CTLA4–binding domain. Upon reaching the tumor, the outer domain was cleaved by membrane type-serine protease 1 (MT-SP1) present in the tumor microenvironment, leading to enhanced localization of CTLA4 blockade. Anti-CTLA4 DVD markedly reduced multiorgan immune toxicity by preserving tissue-resident Tregs in Rag 1–/– mice that received naive donor CD4+ T cells from WT C57BL/6j mice. Moreover, anti-CTLA4 DVD induced potent antitumor effects by decreasing tumor-infiltrating Tregs and increasing the infiltration of antigen-specific CD8+ T lymphocytes in TRAMP-C2–bearing C57BL/6j mice. Treg depletion was mediated through the antibody-dependent cellular cytotoxicity (ADCC) mechanism, as anti-CTLA4 without the FcγR-binding portion (anti-CTLA4 DANA) spared Tregs, preventing treatment-induced toxicities. In summary, our results demonstrate an approach to anti-CTLA4 blockade that depletes tumor-infiltrating, but not tissue-resident, Tregs, preserving antitumor effects while minimizing toxicity. Thus, our tumor-conditional anti-CTLA4 DVD provides an avenue for uncoupling antitumor efficacy from immunotherapy-induced toxicities.

Authors

Chien-Chun Steven Pai, Donald M. Simons, Xiaoqing Lu, Michael Evans, Junnian Wei, Yung-hua Wang, Mingyi Chen, John Huang, Chanhyuk Park, Anthony Chang, Jiaxi Wang, Susan Westmoreland, Christine Beam, Dave Banach, Diana Bowley, Feng Dong, Jane Seagal, Wendy Ritacco, Paul L. Richardson, Soumya Mitra, Grace Lynch, Pete Bousquet, John Mankovich, Gillian Kingsbury, Lawrence Fong

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Figure 7

Immune landscape within tumors after different CTLA4 blockades.

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Immune landscape within tumors after different CTLA4 blockades.
C57BL/6j...
C57BL/6j male mice were implanted with TRAMP-C2 tumors at day 0, and tumors were allowed to grow for 40 days. Mice were randomized into different treatment groups and received different treatments at days 40, 43, 46, and 49. Tissues were harvested at day 52 and analyzed by flow cytometry. (A) Tumors were harvested from each treatment group and analyzed for different immune subsets by flow cytometry. (B) Total numbers of CD4+ T cells per tumor weight. CD4+ T cells were pregated on live CD45+CD3+CD8– T cells. (C) Percentage of ICOS expression among CD4+Foxp3– T cells. (D) Percentage of CD4+Foxp3+ among CD3+ cells. (E) Total number of infiltrating CD8+ T cells per tumor weight. (F) Total numbers of CD8+CD25+ T cells per tumor weight. (G) Percentage of Ki-67 among CD3+CD8+ T cells. (H) Percentage of Spas-1–reactive CD8+ T cells among CD3+ cells. Two independent experiments were conducted. Data were shown as 5 mice per group from 1 representative experiment. Bars represent mean ± SEM. *P < 0.05; **P < 0.01; ***P < 0.001, 1-way ANOVA with post hoc Tukey’s test.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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