A newly discovered PD-L1 B-cell epitope peptide vaccine (PDL1-Vaxx) exhibits potent immune responses and effective anti-tumor immunity in multiple syngeneic mice models and (synergizes) in combination with a dual HER-2 B-cell vaccine (B-Vaxx)

表位 肽疫苗 癌症研究 免疫疗法 抗体 抗体依赖性细胞介导的细胞毒性 免疫检查点 免疫系统 单克隆抗体 医学 T细胞 免疫学 癌症疫苗 癌症 病毒学 内科学
作者
Linlin Guo,Jay Overholser,Heather Darby,Nicholas J. Ede,Pravin T. P. Kaumaya
出处
期刊:OncoImmunology [Landes Bioscience]
卷期号:11 (1) 被引量:12
标识
DOI:10.1080/2162402x.2022.2127691
摘要

Blockade of checkpoint receptors with monoclonal antibodies against CTLA-4, PD-1 and PD-L1 has shown great clinical success in several cancer subtypes, yielding unprecedented responses albeit a significant number of patients develop resistance and remain refractory. Both PD-1/PD-L1 and HER-2 signaling pathway inhibitors have limited efficacy and exhibits significant toxicities that limit their use. Ongoing clinical studies support the need for rationale combination of immuno-oncology agents to make a significant impact in the lives of cancer patients. We introduce the development of a novel chimeric PD-L1 B-cell peptide epitope vaccine (amino acid 130–147) linked to a “promiscuous” T cell measles virus fusion (MVF) peptide (MVF-PD-L1(130); PDL1-Vaxx) or linked to tetanus toxoid (TT3) TT3-PD-L1 (130) via a linker (GPSL). These vaccine constructs are highly immunogenic and antigenic in several syngeneic animal models. The PD-L1 vaccines elicited high titers of polyclonal antibodies that inhibit tumor growth in multiple syngeneic cancer models, eliciting antibodies of different subtypes IgG1, IgG2a, IgG2b and IgG3, induced PD-1/PD-L1 blockade, decreased proliferation, induced apoptosis and caused ADCC of tumor cells. The PDL1-Vaxx induces similar inhibition of tumor growth versus the standard anti-mouse PD-L1 antibody in both syngeneic BALB/c and C57BL/6J mouse models. The combination of PDL1-Vaxx with HER-2 vaccine B-Vaxx demonstrated synergistic tumor inhibition in D2F2/E2 carcinoma cell line. The anti-PDL1-Vaxx block PD-1/PD-L1 interaction and significantly prolonged anti-tumor responses in multiple syngeneic tumor models. The combination of HER-2 vaccine (B-Vaxx) with either PDL1-Vaxx or PD1-Vaxx demonstrated synergistic tumor inhibition. PDL1-Vaxx is a promising novel safe checkpoint inhibitor vaccine.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研狗应助粗暴的迎彤采纳,获得40
刚刚
彭于晏应助mikebai采纳,获得10
1秒前
1秒前
Qingchun完成签到,获得积分10
1秒前
二三三完成签到,获得积分10
1秒前
1秒前
2秒前
678发布了新的文献求助10
2秒前
2秒前
跳跃靖发布了新的文献求助10
2秒前
2秒前
粉色发布了新的文献求助10
3秒前
3秒前
科研通AI6.2应助lin采纳,获得10
3秒前
我是树完成签到,获得积分10
3秒前
木木SCI完成签到 ,获得积分10
3秒前
3秒前
彳亍君发布了新的文献求助10
4秒前
4秒前
李玉梅发布了新的文献求助10
5秒前
tutou完成签到,获得积分10
6秒前
zhhhh发布了新的文献求助10
6秒前
科研通AI6.1应助凯蒂jiang采纳,获得30
6秒前
6秒前
必胜发布了新的文献求助20
6秒前
跳跃的千柳完成签到,获得积分10
7秒前
Haburu完成签到,获得积分10
7秒前
斯文败类应助怡然的迎波采纳,获得10
7秒前
科研小白完成签到,获得积分10
7秒前
7秒前
Rosechanel完成签到,获得积分20
7秒前
Ava应助背后期待采纳,获得10
7秒前
8秒前
DN完成签到,获得积分10
8秒前
lky1017发布了新的文献求助10
8秒前
云馨完成签到,获得积分10
9秒前
lin完成签到,获得积分10
9秒前
pluto应助XuBo采纳,获得10
9秒前
FashionBoy应助翟文艳采纳,获得30
9秒前
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Organometallic Chemistry of the Transition Metals 800
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6437367
求助须知:如何正确求助?哪些是违规求助? 8251874
关于积分的说明 17556725
捐赠科研通 5495671
什么是DOI,文献DOI怎么找? 2898496
邀请新用户注册赠送积分活动 1875293
关于科研通互助平台的介绍 1716275