Javascript must be enabled to continue!
Abstract 2228: PD1/CTLA4 humanized mice - A great model for pre-clinical toxicology and efficacy evaluation of macromolecular drugs
View through CrossRef
Abstract
Immune checkpoint antibodies have conferred huge cancer immunotherapeutic effect (CITE). Besides, severe immunotherapy related adverse events (irAE) occurred in combination therapy such as anti-PD1 combines with anti-CTLA4 antibodies greatly limit the development of cancer therapy. Animal models which can recapitulate both clinical irAE and CITE will be benefit for developing safer immune-checkpoint-targeting reagents. However, no animal models were found can be used for preclinical safety evaluation of drugs up to now. Given this fact, PD1/CTLA4 double-humanized mice models were established in both BALB/c (BALB/c-hPD1/hCTLA4) and C57BL/6 (B6-hPD1/hCTLA4) background, which by replacing the mouse extracellular domain of CTLA4 and PD1 with human segments while retaining mouse intact intracellular part, respectively. Our data showed that strong CITE against anti-hCTLA4 treatment observed in models from both BALB/c and B6 background. Apparent inhibition of tumor growth also emerged on subcutaneously engrafted CT26 tumor in BALB/c-hPD1/hCTLA4 mice by anti-PD1/CTLA4 bispecific antibody treatment. Meanwhile, severe irAEs which have been observed in clinical patients, such as joint swelling, skin inflammation, heart damage and infiltration of inflammatory cells in different tissues and organs could be reproduced in BALB/c-hPD1/hCTLA4 mice. Consistent with previous reports, we could not observe similar irAEs under drugs treatment at the same dose in C57BL/6-hPD1/hCTLA4 mice. Our data indicated that adult BALB/c-hPD1/hCTLA4 mice, but not C57BL/6-hPD1/hCTLA4 mice, were more sensitive to irAEs. Taken together, adult PD1/CTLA4 humanized mice in BALB/c background can not only be used to screen humanized antibodies, but also have tremendous values for preclinical safety evaluation.
Citation Format: Cunxiang Ju, Mingkun Zhang, Rui Mao, Ma Xiuying, Jin Tang, Shuai Li, Jingjing Wang, Hongyan Sun, Jing Zhao, Xiang Gao. PD1/CTLA4 humanized mice - A great model for pre-clinical toxicology and efficacy evaluation of macromolecular drugs [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 2228.
American Association for Cancer Research (AACR)
Title: Abstract 2228: PD1/CTLA4 humanized mice - A great model for pre-clinical toxicology and efficacy evaluation of macromolecular drugs
Description:
Abstract
Immune checkpoint antibodies have conferred huge cancer immunotherapeutic effect (CITE).
Besides, severe immunotherapy related adverse events (irAE) occurred in combination therapy such as anti-PD1 combines with anti-CTLA4 antibodies greatly limit the development of cancer therapy.
Animal models which can recapitulate both clinical irAE and CITE will be benefit for developing safer immune-checkpoint-targeting reagents.
However, no animal models were found can be used for preclinical safety evaluation of drugs up to now.
Given this fact, PD1/CTLA4 double-humanized mice models were established in both BALB/c (BALB/c-hPD1/hCTLA4) and C57BL/6 (B6-hPD1/hCTLA4) background, which by replacing the mouse extracellular domain of CTLA4 and PD1 with human segments while retaining mouse intact intracellular part, respectively.
Our data showed that strong CITE against anti-hCTLA4 treatment observed in models from both BALB/c and B6 background.
Apparent inhibition of tumor growth also emerged on subcutaneously engrafted CT26 tumor in BALB/c-hPD1/hCTLA4 mice by anti-PD1/CTLA4 bispecific antibody treatment.
Meanwhile, severe irAEs which have been observed in clinical patients, such as joint swelling, skin inflammation, heart damage and infiltration of inflammatory cells in different tissues and organs could be reproduced in BALB/c-hPD1/hCTLA4 mice.
Consistent with previous reports, we could not observe similar irAEs under drugs treatment at the same dose in C57BL/6-hPD1/hCTLA4 mice.
Our data indicated that adult BALB/c-hPD1/hCTLA4 mice, but not C57BL/6-hPD1/hCTLA4 mice, were more sensitive to irAEs.
Taken together, adult PD1/CTLA4 humanized mice in BALB/c background can not only be used to screen humanized antibodies, but also have tremendous values for preclinical safety evaluation.
Citation Format: Cunxiang Ju, Mingkun Zhang, Rui Mao, Ma Xiuying, Jin Tang, Shuai Li, Jingjing Wang, Hongyan Sun, Jing Zhao, Xiang Gao.
PD1/CTLA4 humanized mice - A great model for pre-clinical toxicology and efficacy evaluation of macromolecular drugs [abstract].
In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24.
Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 2228.
Related Results
Abstract 5120: NPRL2 gene therapy induces effective antitumor immunity in KRAS/STK11 mutant anti-PD1 resistant metastatic human NSCLC in a humanized mouse model
Abstract 5120: NPRL2 gene therapy induces effective antitumor immunity in KRAS/STK11 mutant anti-PD1 resistant metastatic human NSCLC in a humanized mouse model
Abstract
NPRL2/TUSC4 is a potent tumor suppressor gene whose expression is reduced in many cancers including NSCLC. Restoration of NPRL2 expression in cancer cells i...
Abstract 1497: Identification of discrepancy between CTLA4 expression and CTLA4 activation in gastric cancer
Abstract 1497: Identification of discrepancy between CTLA4 expression and CTLA4 activation in gastric cancer
Abstract
Objective: Recently, immune checkpoints blockers showed higher anti-tumor activity for advanced gastric cancer (GC). The purpose of the study is to find ...
Abstract IA18: Interrogating anti-PD1 immunotherapy resistance mechanisms
Abstract IA18: Interrogating anti-PD1 immunotherapy resistance mechanisms
Abstract
Background: The response rate of 15-20% with anti-PD1 targeting in head and neck squamous cell carcinoma (HNSCC) highlights the need for strategies to overc...
Abstract PO-040: Integration of anti-TIGIT and anti-Lag3 with NBTXR3-mediated immunoradiation therapy improves abscopal effect and induces long-term memory against cancer
Abstract PO-040: Integration of anti-TIGIT and anti-Lag3 with NBTXR3-mediated immunoradiation therapy improves abscopal effect and induces long-term memory against cancer
Abstract
Introduction: TIGIT and Lag3 are inhibitory receptors expressed on cytotoxic CD8+ T cells and NK cells and directly inhibit the activation and proliferation...
Abstract 4125: Rencofilstat exerts a dominant role in synergistic anti-PD1-combination effects in a fatty liver model of hepatocellular carcinoma
Abstract 4125: Rencofilstat exerts a dominant role in synergistic anti-PD1-combination effects in a fatty liver model of hepatocellular carcinoma
Abstract
Rencofilstat is a clinical-phase drug candidate that inhibits multiple cyclophilin isomerases and affects many cellular processes. The objectives of this st...
Evolutionary fingerprint in rodent PD1 confers weakened activity and enhanced tumor immunity compared to human PD1
Evolutionary fingerprint in rodent PD1 confers weakened activity and enhanced tumor immunity compared to human PD1
SUMMARYMechanistic understanding of the immune checkpoint receptor PD1 is largely based on mouse models, but human and mouse PD1 orthologs exhibit only 59.6% identity in amino acid...
Abstract 1650: Humanized mouse models for preclinical evaluation of novel immune cell therapies, checkpoint inhibitors, and immune cell engagers
Abstract 1650: Humanized mouse models for preclinical evaluation of novel immune cell therapies, checkpoint inhibitors, and immune cell engagers
Abstract
Background The preclinical evaluation of novel immune therapies demands humanized mouse models with functional human immune cells. In previous studies we ha...
TIGIT acts as an immune checkpoint upon inhibition of PD1 signaling in autoimmune diabetes
TIGIT acts as an immune checkpoint upon inhibition of PD1 signaling in autoimmune diabetes
IntroductionChronic activation of self-reactive T cells with beta cell antigens results in the upregulation of immune checkpoint molecules that keep self-reactive T cells under con...

