Call of projets - 2014

WP1 - Task1.4 -A new anti-CMV strategy to prevent primary infection during HSCT - Partners : F. Haspot and I. Anegon (UMR 1064)

Immunocompromised patients are at high risks of HCMV reactivation, which might be associated with severe end organ diseases and increased mortality in transplant patients. Thus, we used CRISPR/Cas9 to specifically target the UL122/123 HCMV’s essential. The multiplex CRISPR/Cas9 system (three gRNA) was much more efficient than the singleplex (one gRNA) approach targeting the same gene. Target gene expression, concomitant genome replication and virion release were significantly impaired by the multiplex strategy. Our anti-HCMV strategy based on three gRNAs efficiently blocked viral replication. A further anti-HCMV CRISPR/Cas9 system is under development to be able to target latently infected cells. This provides the basis for the development of an anti-HCMV CRISPR/Cas9 therapy.

WP1 - Task1.5 -Functional Contribution of MICA Polymorphic variants to Immune Responses in Organ Transplantation and in Cancer - Partners : B. Charreau (UMR 1064) & N. Gervois (UMR1232)

This project explores the emergent concept that some MICA gene polymorphisms encode for non-conventional MICA proteins which may affect MICA expression, regulation and functions. Our study focus on the genetic variant MICA A5.1 that associates with MICA*008, the most common allele, and on two MICA alleles encoding novel MICA isoforms that we recently identified (Charreau B. et al., EP13305955.0 5/7/2013, patented). Overall these 3 MICA alleles account for around 70% of the general population and of our transplant donors. The principal aim of this project is to determine how some frequent MICA gene polymorphisms encoding for non-conventional and/or truncated MICA proteins will affect MICA expression (membrane-bound and circulating proteins) and regulation on endothelial cells and melanoma cells, NKG2D-dependent NK cell activation and CD8 T-cell costimulation, and to decipher their contribution to the control of tumor progression and MICA alloimmunization in kidney transplantation.

WP2 - Task4.3 Adoptive cell therapy for glioblastoma – characterization of tumor cell targets and analysis of their recognition by human t lymphocytes in vitro - Partners : E. Scotet (Team 1) and C. Pecqueur (Team 9) (UMR1232)

This project had several objectives centered on the study of human glioblastoma (GBM) biology and immunotherapy in novel physiological models in vitro and in vivo (eg., humanized xenografts in NSG mice). Promising results have been obtained with both in vitro and in vivo activities. Transcriptomic and functional studies have identified relevant GBM NKR-related molecules that are targeted by human Vg9Vd2 T cells. The funding of the project byt the Labex IGO has fostered the establishment of new local, national and international collaborations and the submission of additional national and EU network projects. A better characterization of the self-ligands recognized by Vg9Vd2 T cells on GBM cells is currently performed as well as the definition of some biomarkers (that may allow the pre-selection of the patients affected by the GBM sub-type that seem to optimally respond to the Vg9Vd2 ACT, in order to maximize the number of patients that may benefit from the treatment.

Call of projets - 2016

WP1 - Task 1.8. CD8+CD28neg T cells, a threat to transplantation? - Partner 1 : N. Degauque (UMR1064) - Partner 2 : F. Haspot (UMR1064) - Partner 3 : C. Pecqueur (UMR1232)

Kidney transplantation is the treatment of choice for End-Stage Renal dysfunction from patient survival perspective as well as from an economical point-of-view. Preventing the occurrence of acute rejection is not anymore an issue. However, minimal success had been obtained to prevent late chronic rejection and current immunosuppressive drugs are associated with increased infections, viral reactivations and malignancies. It is thus critical to design innovative strategies to control the pathogenic cells involved in chronic rejection. We have shown that kidney transplant recipients with a high frequency of effector memory CD8 T cells re-expressing CD45RA (EMRA) exhibit a 2-fold higher risk of kidney dysfunction. Our preliminary results highlight that pre-existing or neo-formed pathogenic CD8+CD28- T cells are a barrier for long-term graft acceptance that cannot be control by actual IS drugs nor by the newly developed costimulation blockade drugs. The aim of the project is to characterize the development of pathogeneic CD8+CD28- T cells after kidney transplantation and to evaluate in humanized mouse model the ability to control their immune function by metabolic interferences. The project is divided into 3 tasks
Task #1. To investigate the adaptation of the metabolism of CD8 T cell subsets after kidney transplantation
Task #2. To develop humanized mouse models to study CD8+CD28- T cells pathogenicity
Task #3. To test the ability of metabolic interferences to control the immune response of CD8+CD28- T cells in preclinical models.

WP2 - Task 4.4. Engineered CAR-Tregs - licensed to specific control of immune responses in transplantation - Partner 1 : C. Guillonneau (UMR1064) - Partner 2 : X. Saulquin (UMR1232)  

The establishment of tolerance for organ transplants is a major goal in the field of transplantation. Indeed, transplanted patients take immunosuppressive drugs suppressing all the immune system for the rest of their life, and although these drugs have allowed remarkable success, unwanted side effects still lead to high morbidity and mortality, even when avoiding excessive immunosuppression. We previously reported the suppressive properties of rat CD8+CD45RClow T cells and demonstrated their potential for cell therapy in transplantation. We showed that antigen-specific CD8+ Tregs had superior potential compared to polyclonal Tregs. This project aim to confer antigen-specificity using chimeric antigen receptors (CARs) directed to donor antigens and evaluate the potential of such strategy in transplantation.

WP2 - Task 4.5. Boosting anti-tumor response by conferring metabolic autonomy to T cells - Partners : C. Louvet (UMR1064) & B. Vanhove (UMR1064)

Blockade of immune activation checkpoints and gene-engineering of T cells with anti tumor T cell receptors (TCR) or chimeric antigen receptors (CAR) have recently produced impressive results in the clinic for a variety of cancers. However, additional therapeutic weapons will likely be needed to reach tumor clearance, especially in solid tumors. The tumor microenvironment can exert strong suppressive effects on T cells, often considered as counter-regulatory mechanisms triggered by the T cells themselves. Beyond immune checkpoint targeting, we believe that conferring functional advantages to T cells by genetic engineering could be decisive to tip the balance in favor of immunity. Such strategies could be implemented through adoptive cell transfer (ACT) therapies but still remain poorly explored notably because most of the attention is currently focused on TCR/CAR. In this project, we explore the therapeutic potential of engineering critical enzyme-encoding genes with the aim to boost selective metabolic pathways in preclinical models of solid cancers.

WP3 - Task7.4 -Combining adoptive T cell transfer of engineered PD-1 deficient specific T cells with a-radioimmunotherapy for melanoma treatment - Partner 1: Team 3 UMR1232 (N. Labarriere) - Partner 2: Team 1 UMR1232 (E. Scotet) - Partner 3: Team 2 UMR1064 (TH. Nguyen) - Partner 4: Team 13 UMR1232 (J. Gaschet)

The overall objective of this proposal is to assess, through a set of complementary in vitro and in vivo experimental approaches (eg, NSG mice engrafted with PDL-1 expressing human melanoma tumors), the anti-tumor efficacy of an innovative treatment combining ACT, with high avidity PD-1ko melanoma specific T lymphocytes, and α-RIT. This will be achieved through the implementation and the completion of the following milestones:
1/ Silencing of PDCD1 gene in high-avidity human melanoma-specific CD8+ αβ T lymphocytes. This step will be achieved by transfection or transduction of T lymphocytes with PDCD1-specific gRNA and Cas9. The design and validation of these tools will rely on the expertise of the local GenoCell Edit facility (Partner ≠3), specialized in this technology. The selection, amplification and in vitro validation of PD-1 inactivated melanoma-specific CD8+ αβ T cells will be performed by Partner ≠1.

2/ Anti-tumor efficiency of engineered CD8+ αβ T cells in vivo. The efficiency of engineered PD-1neg melanoma specific T cells to control the growth of human PDL-1 expressing melanoma tumors will be measured in NSG mice, and compared to that obtained with wild-type counterpart T cells (Partners ≠2 and ≠1).
3/ Development of radiolabeled anti-PDL-1 mAb. A commercially available anti-human PDL-1 specific mAb will be conjugated and labeled with Astatine-211 (for therapy) or Zirconium-89 (for molecular imaging) (Partner ≠4).

4/ Anti-tumor efficiency of PDL-1-specific α-RIT in vivo. The objective is to document in NSG mice engrafted with human PDL-1 expressing melanoma tumors the efficiency of α-RIT targeting PDL-1 on tumor growth and to characterize the expression of PDL-1 on remaining or resistant melanoma cells (Partners #2 and #4).
5/ Anti-tumor efficiency of combined ACT and α-RIT strategies in vivo. The impact of α-RIT immunotherapy targeting PDL-1 molecules expressed on melanoma cells, prior infusion of PD-1ko specific T cells will be assessed in NSG mice carrying human melanoma tumor grafts (Partners ≠1, ≠2 and ≠4).