Novel gene editing technologies and a greater understanding of cancer biology could unleash the full power of CAR T in both blood and solid tumors. But which therapies will succeed?
Cambridge Healthtech Institute’s Sixth Annual CAR Ts, TCRs and TILs conference focuses on the latest research, protein engineering and clinical strategies driving the development of adoptive cell therapies across a wide range of
indications. Clinical progress with Chimeric Antigen Receptors (CAR), T Cell Receptors (TCR), Tumor Infiltrating Lymphocytes (TIL), and NK cells will be addressed as well as new strategies for commercialization will be reviewed.
Final Agenda
WEDNESDAY, APRIL 10
7:15 am Registration (Commonwealth Hall) and Morning Coffee (Harbor Level)
7:25 - 8:25 PANEL DISCUSSION: Women in Science – Inspired Professional and Personal Stories (Continental breakfast provided) (Waterfront 1&2)
Moderator:
Jennifer S. Chadwick, PhD, Director of Biologic Development, BioAnalytix, Inc.; Co-Chair, Mentors Advisors and Peers Program, Women In Bio, Boston Chapter
Panelists:
Joanna Brewer, PhD, Vice President, Platform Technologies, AdaptImmune
Charlotte A. Russell, MD, DMSc, CMO, Alligator Bioscience
Susan Richards, PhD, Presidential Scientific Fellow, Translational Medicine Early Development, Sanofi R&D
Kristi Sarno, Senior Director, Business Development, Pfenex
8:30 Chairperson’s Opening Remarks
Bob Valamehr, PhD, Chief Development Officer, Fate Therapeutics
8:40 KEYNOTE PRESENTATION: Mechanisms of CAR Treatment Success and Failure Based on Clinical Experience in Lymphoma and Leukemia
Adrian Bot, PhD, Vice President, Translational Sciences, Kite Pharma, a Gilead Company
As CAR T cell therapy is now standard of care in certain B cell malignancies, novel data point to mechanistic aspects related to treatment success or failure, essential to advance next-generation therapies. In this presentation, we cover factors influencing
clinical outcomes: product T cell fitness, integrating the number and polyfunctionality of specialized T cell subsets, tumor burden and immune microenvironment, and biological aspects intrinsic to the cancerous process.
9:10 Resistance to CART19 Therapy: Mechanisms and Novel Therapeutic Strategies
Marco Ruella, MD, Clinical
Instructor, Associate Director, Dr. June’s Laboratory, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania
Chimeric Antigen Receptor T cell (CAR T) have generated impressive clinical results for CD19+ B cell leukemia and lymphoma. However, a significant subset of patients still does not respond or eventually relapses. I will discuss the mechanisms of resistance
to CART19 and present future developments.
9:40 Novel Targets and Technologies for CAR T Cells in Multiple Myeloma and Acute Myeloid Leukemia
Katrin Mestermann, PhD, Post-Doc, Max Eder Research Group‚ CAR T-Cell Engineering, Department of Medicine II, University Hospital Würzburg
Translational research in CAR T cell immunotherapy involves a rapidly increasing portfolio of novel target antigens, CAR designs, and technologies to enhance safety, efficacy and physician control. This talk will review the latest developments from our
program including novel targets in hematology and oncology, and novel technologies for high-throughput screening, ultra-fast manufacturing, and real-time control over CAR T cells after administration in vivo.
10:10 Coffee Break in the Exhibit Hall with Poster Viewing (Commonwealth Hall)
10:15 Women in Science Speed Networking in the Exhibit Hall (Commonwealth Hall)
10:55 Targeting TCR-β Constant Domain for Immunotherapy of T Cell Malignancies
Matthieu Ferrari, PhD, Senior Scientist, Protein Engineering, Autolus
Unlike B cell depletion, pan-T cell aplasia is prohibitively toxic. We report a new targeting strategy based on the mutually exclusive expression of T cell receptor β-chain constant domains 1 and 2 (TRBC1 and TRBC2). Unlike nonselective approaches
targeting the entire T cell population, TRBC-targeted immunotherapy could eradicate a T cell malignancy while preserving sufficient normal T cells to maintain cellular immunity.
11:25 FEATURED PRESENTATION: Allogeneic CAR T: The Next Revolution in Cell Therapy
Barbra Sasu, PhD,
CSO, Allogene
While allogeneic CAR T research is at an earlier stage, encouraging Phase 1 clinical data demonstrates the promise of this therapy for more patients. The talk will highlight the clinical data available to date and the overall research strategy to
develop a pipeline of allogeneic CAR T therapies across a range of hematological and solid tumor indications.
11:55 Gene Edited Off-the-Shelf Immunotherapies
Andre Choulika, PhD., Chairman and CEO, Cellectis
A limitation of the current autologous approach is that CAR T-cells must be manufactured on a "per patient basis". Cellectis has developed a platform for generating chimeric antigen receptor (CAR)-redirected T-cells from third-party healthy donors
using transcription activator-like effector nucleases (TALEN®). Nuclease mediated inactivation of the TCR alpha abrogates the potential for T-cells bearing alloreactive TCR's to mediate Graft versus Host Disease (GvHD). Additional gene inactivation
events can be incorporated, permitting resistance to lymphodepleting or chemotherapeutic agents, resistance to tumor inhibition or suppression of cross T-cell reactions. Such allogeneic “off-the-shelf” CAR T-cell products will permit
a wider application of CAR technology and potentially lead to a new paradigm in cancer treatment.
12:25 The Functional Capacity of Immune Cells Predicts Clinical Outcome Across IO Therapies
Will
Singleterry, PhD, Director, Business Development, IsoPlexis
Using single cell proteomics to measure the functional capacity or ‘fitness’ of immune cells has correlated with and been predictive of clinical outcome in CAR-T, TIL, Cancer Vaccine and Checkpoint Inhibitor therapy. This talk will
review several of these data sets and discuss applications of IsoPlexis’ single cell technology.
12:40 Mammalian Display Antibody Discovery for Integral Membrane Proteins
Ryan Cawood, PhD, Oxford Genetics
Through co-expression of integral membrane targets and scFv molecule libraries in a mammalian cells we show that cells that exhibit self-labelling can be purified and lead molecules identified via NGS analysis. Lead candidates are then suitable for
either CAR-T or antibody reformatting.
12:55
Luncheon Presentation I: Genetically Modified Cell Lines for Immuno-Oncology Cell-Based Assay Development
Stacy Ward, PhD,
Senior Research & Development Scientist, Cell Design Studio, MilliporeSigma12:55
MilliporeSigma’s Cell Design Studio™ cell line engineering service offering is the premier research partner for generating customized cell-based assays and immunotherapy research models. Our team has generated new monoallelic HLA panel
expression cell lines and tumor-associated antigen panels, which express individual tumor antigens at varying levels in biologically-relevant cell lines. In this presentation, we will discuss the breadth of these lines and discuss their utility
in immuno-oncology and therapeutic testing.
1:25 Luncheon Presentation II (Sponsorship Opportunity Available)
1:55 Session Break
2:10 Chairperson
Adrian Bot, PhD, Vice President, Translational Sciences, Kite Pharma, a Gilead Company
2:15 Rejection-Resistant T Cell Platform for an Off-the-Shelf Therapy
Maksim Mamonkin, PhD, Assistant Professor, Center for Cell and Gene Therapy, Baylor College of Medicine
‘Off-the-shelf’ (OTS) T cell products pre-manufactured from healthy donors are readily available and less costly than autologous products, offering similar therapeutic potency. However, immune rejection by host T- and NK-cells may limit
the persistence of OTS cells and compromise their anti-tumor activity. We engineered alloimmune defense receptors (ADRs) that enable OTS T cells to recognize and eliminate alloreactive lymphocytes resulting in complete protection from immune rejection
while retaining full functionality.
2:45 Translation of Pluripotent Cell-Derived T and NK Cells as a Cornerstone Approach for Off-the-Shelf Cancer Immunotherapy
Bob Valamehr, PhD,
Chief Development Officer, Fate Therapeutics
Pluripotent cell technology represents a powerful approach to make cell-based immunotherapies available to a wide range of patients through the generation of a consistent and renewable “off-the-shelf” source of cellular therapeutics. I
will discuss our progress towards developing unique and effective strategies to create a renewable source of genetically engineered “off-the-shelf” T and NK cells with augmented function. Updates on IND filings and FIH progress will
also be given.
3:15 Epitope Identification and Clinical Immune Monitoring in Gene Therapy and Immune Oncology Programs
Emilee Knowlton, PhD,
Immunology, Sales Specialist, Sales, ProImmune, Inc.
Epitope discovery is a crucial element in the development of vaccine candidates and drug therapeutics. In the Immune-oncology space, identifying neoepitopes and tumor-associated antigens provide new targets for cancer diagnostics and enable the tracking
of patient responses to treatment. ProImmune provides industry-leading tools for antigen characterization, epitope mapping and immune monitoring. In this presentation, case studies will be shared that detail how ProImmune’s integrated platform
has identified novel epitopes in the immune-oncology field.
3:45 Refreshment Break in the Exhibit Hall with Poster Viewing (Commonwealth Hall)
4:45 Problem-Solving Breakout Discussions - Click here for details(Commonwealth
Hall)
5:45 Networking Reception in the Exhibit Hall with Poster Viewing (Commonwealth Hall)
7:00 End of Day
THURSDAY, APRIL 11
8:00 am Registration (Commonwealth Hall) and Morning Coffee (Harbor Level)
8:30 Chairperson’s Remarks
Adrian Bot, PhD, Vice President, Translational Sciences, Kite Pharma, a Gilead Company
8:35 Combining Innate and Adaptive Immunity: NK Receptors for CAR T Cell Therapy
Simon Bornschein, PhD, Scientist, Celyad
The success of CAR T therapy against B-cell malignancies generated high expectations for all cancers, but the target remains the challenge. NKG2D binds to 8 different ligands present on a broad range of tumors yet largely absent on healthy tissue
indicating a potential breadth of applicability of the approach. Our approache to exploring the therapeutic power of NKG2D CAR T cells in the autologous (CYAD-01) and allogeneic (CYAD-101) setting will be discussed.
9:05 Gene Editing of Stem Cells for Universal SPEAR T-Cell Therapy
Joanna Brewer, PhD, Vice
President, Platform Sciences, AdaptImmune
Adoptive T cell therapy using autologous material for CAR and TCR therapies show considerable promise. However, an off-the-shelf product will speed up the time to treat patients and provide a consistent and unlimited source of therapeutic cells. Stem
cells are also amenable to genetic modification, allowing them to remain hidden from the immune system for long-term persistence of differentiated T cells expressing enhanced affinity TCRs.
9:35 Organize, Optimize, and Measure Biologics R&D with Modern Software
Alya Bhimji, PhD, Field Applications Scientist, Benchling
Benchling is a biologics-native informatics platform used by over 160,000 scientists to configure biologics workflows and run day-to-day R&D. This presentation will highlight how Benchling has helped leading biopharma companies to organize, optimize,
and measure their biologics R&D.
10:05 Coffee Break in the Exhibit Hall with Poster Viewing (Commonwealth Hall)
11:05 ImmTAC™: Engineering Soluble Bispecific TCRs, with High Specificity and Affinity, to Treat Cancer
Vijaykumar Karuppiah, PhD., Senior Scientist, Immunore
11:15 Immatics' Discovery and Validation Platform for Tumor-Specific T Cell Receptors
Sara Yousef, PhD., Research Scientist, Immatics
11:25 Functional TCR-T Cell Screening Using Single-Cell Droplet Microfluidics
Weian Zhao, PhD., Associate Professor, Department of Pharmaceutical Sciences, University of California, Irvine
11:35 Tumor Infiltrating Lymphocytes Therapy for Solid Tumors
Chantale Bernatchez, PhD, Assistant Professor, Department of Melanoma Medical Oncology - Research, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center
In TIL therapy T cells are grown from solid tumor samples and expanded to large numbers ex vivo to be infused back to the patient. The therapy has been very successful in metastatic melanoma with a 42% clinical response
rate at our institution and others with most of the responses being durable. Despite great results we are at this point investigating why the other half of the patients would not respond. Through molecular and immunological assays we are trying
to define biomarkers that could predict response to therapy. Another focus of our research is to test the efficacy of TIL therapy in other solid tumor types.
12:05 pm Advancements in Tumor Infiltrating Lymphocytes in Treatment of Solid Tumors
Kelly DiTrapani, VP, Medical Affairs, Iovance Biotherapeutics
Iovance is developing TIL, a one-time cell therapy treatment that leverages and enhances the body’s natural defenses against certain solid tumors. TIL is being investigated in several multi-center Phase 2 clinical trials and preliminary results
have demonstrated safety and efficacy in melanoma, head and neck and cervical cancer patients. While available immunotherapies for solid tumors, such as anti-PD-1 antibodies have shown promise, additional agents are needed for patients who may
progress on such therapies or are intolerant.
12:35 End of CAR Ts, TCRs and TILs