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Scientific Program
4th Annual Summit on Cell and Gene Therapy, will be organized around the theme “To support Cell Therapy Research from bench to clinic”
Cell Therapy 2021 is comprised of 19 tracks and 82 sessions designed to offer comprehensive sessions that address current issues in Cell Therapy 2021.
Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
The capability to make specific modifications to the human gene has been an objective in medical since; gene is the recognition of the basic unit for heredity. Therefore, gene therapy is defined as the capability of genetic improvement through the correction of modified genes or specific modifications that target therapeutic treatment. This therapy became possible through the advances of genetics and bioengineering that enabled manipulating vectors for delivery of extra chromosomal material to target cells. One of the major focuses on this technique is the optimization of delivery vehicles (vectors) that are mostly plasmas, unstructured or viruses. These viruses are more often investigated due to their excellence of infected cells and inserting their genetic material.
Stem Cell Therapies Meeting | Regulatory and Ethical Issues of Therapies Conference | Clinical Trials and Research in Cell and Gene Therapies Meetings
- Track 1-1Substitution of the adenosine deaminize deficiency
- Track 1-2Substitution of α 1-antitrypsin
- Track 1-3Improvement of immune function
- Track 1-4Tumour removal
- Track 1-5Chemo protection
- Track 1-6Enzymatic substitution
- Track 1-7Cytokine release
The U.S. Food and Drug Administration's (FDA's) new Paediatric Rule makes it more likely that children will receive improved treatment, because physicians will have more complete information on how drugs affect children and the suitable doses for each age group (FDA, 1998e). The rule also allows FDA to require industry to test already marketed products in studies with paediatric populations in certain fascinating circumstances, such as when a drug is commonly prescribed for use in children but when the absence of adequate testing and labelling could be significant risks. The aim of this session is to examine many interrelated legal and regulatory issues, as well as the interrelated social and ethical concerns, in the evaluation of the effects of drugs and biologics on paediatric populations.
Cellular Therapies Meetings | Bioengineering Therapeutics Conferences | Immunotherapy Conferences
- Track 2-1Anchoring Studies to "Minimal Risk"
- Track 2-2Current Regulations Guiding Clinical Research
- Track 2-3Placebo-Controlled Trials
- Track 2-4Consent, Assent, and Determination of Risk
Almost every cell and gene therapy the clinical trial is dissimilar in some way. Working with living organisms presents new and dissimilar challenges to the traditional clinical trial model. With over 400 decades CGT professionals globally, ICON has developed tools and best practices to transform CGT trial design and implementation. From site selection to study start up through implementation, ICON supply project management, clinical services, product-specific logistics solutions, data flow, regulatory strategy and central laboratory services.
Advanced Gene Therapeutics Conference | Clinical Trials and Research in Cell and Gene Therapies Meeting | Stem Cell in Drug Development Conference
Therapeutics Engineering assembles understanding of bodily responses to imputable materials and drug delivery devices. These focus on the biomaterial selection and fusion and also in depth study of drug design, manufacturing, and delivery. We will be getting trained in Nano-materials, material properties, transport phenomena, biochemical engineering, and metabolic engineering. Application areas include analyse therapeutics, biomimetic, and drug delivery systems.
- Advancing technologies to detect and differentiate disease states and treatment responses (i.e., biomarkers) rapidly and precisely
- Developing low-cost sensors that detect subtle, early changes in health status, allowing for more rapid, effective interventions
- Synthesizing injectable microstructure biomaterials to reduce functionally debilitating scarring
- Creating methods and devices to deliver drugs across biological barriers, and to precisely target therapies to specific tissues and cells
- Building and miniaturizing fully implantable, bio artificial devices to carry out the natural functions of failed organs
- Building a solution for kidney failure
- Drug delivery for a leading cause of blindness
- Speeding genetic analysis of individual cells for disease biomarkers
- Delivering targeted, personalized cancer therapy to metastatic tumours
- Developing metabolic imaging technologies to detect cancer biomarkers
- Using microstructures to reduce debilitating scars after heart attacks
Regulatory and Ethical Issues of Therapies Conferences | Immunotherapy Conferences | Stem Cell Therapies Meeting
Vaccination consists of appealing the immune system with a contagious agent, or components of a contagious agent, modified in such a manner that there is no harm or disease, but securing that when the host is resisted with that contagious agent, the immune system can appropriately neutralize it before it causes any illness. A hundred years vaccination has been bring out by one of two match: either introducing specific antigens against which the immune system reacts directly; or introducing live attenuated infectious agents that replicate within the host without causing disease synthesize the antigens that subsequently prime the immune system.
- No risk for infection
- Antigen presentation by both MHC class I and class II molecules
- Polarise T-cell response toward type 1 or type 2
- Immune response focused on the antigen of interest
- Ease of development and production
- Stability for storage and shipping
- Cost-effectiveness
- Obviates need for peptide synthesis, expression and purification of recombinant proteins and use of toxic adjuvants
- Long-term persistence of immune gene
Nanotechnology in Stem Cell Conference | Bioengineering Therapeutics Conferences | Immunotherapy Conferences
Epigenetics is rising to eminence in biology as a mechanism by which environmental factors have intermediate-term effects on gene expression without changing the underlying genetic sequence. It can occur through the specific methylation of DNA bases and modification of histones. There are wide-feeding implications for the gene-environment contest and epigenetic mechanisms are causing a revaluation of many traditional concepts such as heritability. The reversible nature of epigenetics also provides conceivable treatment or prevention prospects for diseases previously thought hard-coded into the gene. Therefore, we consider how growing knowledge of epigenetics is altering our understanding of biology and medicine, and its implications for future research.
Regulatory and Ethical Issues of Therapies Conferences | Immunotherapy Conferences | Stem Cell Therapies Meeting
- Track 6-1Covalent modifications
- Track 6-2RNA transcripts
- Track 6-3MicroRNAs
- Track 6-4mRNA
- Track 6-5sRNAs
- Track 6-6Prions
- Track 6-7Structural inheritance
- Track 6-8Nucleosome positioning
- Track 6-9Genomic architecture
Human gene therapy and its function for the treating the human genetic disorders, such as cystic fibrosis, cancer, and other diseases, are considered. Gene therapy is defined as a technique in which a functioning gene is stuck in into a human cell to correct a genetic error or else to introduce a new functioning to the cell. Many methods, including viral vectors and non-viral vectors, have been developed for both ex vivo and in vivo gene transfer into cells. There are several safety and ethical issues related to manipulating the human gene that need to be resolved. Current gene therapy efforts focus on gene insertion into stem cells only. The current human gene project provides the sequences of a vast number of human genes, leading to the identification, characterization, and understanding of genes that are responsible for many human diseases
- Replacing a disease-causing gene with a healthy copy of the gene
- Inactivating a disease-causing gene that is not functioning properly
- Introducing a new or modified gene into the body to help treat a disease
Stem Cell in Cardiovascular Disease Conferences | Genetic Vaccines Meeting | Clinical Trials and Research in Cell and Gene Therapies Conferences
- Track 7-1Plasmid DNA.
- Track 7-2Viral vectors
- Track 7-3Bacterial vectors
- Track 7-4Human gene editing technology
- Track 7-5Patient-derived cellular gene therapy products
At the present scenario Cancer therapies are not basing on surgery, radiation, and chemotherapy. Because all these three methods cause a risk damage to normal tissues or incomplete destruction of the cancer. Nano- therapy means to target chemotherapies and also collectively to cancerous cells and neoplasms, guide in surgical resection of tumour and enhance the therapeutic competence of radiation-based and the other current based treatment methods. All these together can decrease the risk to the patient and an increased probability of survival.
Human Gene Therapy Conference | Nanotechnology in Stem Cell Conference | Molecular Epigenetics Meeting
- Track 8-1Delivering Chemotherapy
- Track 8-2Nano-enabled Immunotherapy
- Track 8-3Delivering or Augmenting Radiotherapy
- Track 8-4Delivering Gene Therapy
There are many types of cancer treatment. Which types of treatment that you can prescribe will depend on the type of cancer that you have and how advanced it is. Some people who were facing with cancer will have only one treatment. But most people have a rear case in combination of treatments, such as surgery with chemotherapy and also with radiation therapy. When you need a treatment for cancer, you have a lot to think and learn about. It is normal to feel affected and confused. But, talking with your doctor and learning about which type of treatment you may have can help you feel better and can control the fear.
Stem Cell in Cardiovascular Disease Conferences | Genetic Vaccines Meeting | Clinical Trials and Research in Cell and Gene Therapies Conference
- Track 9-1Surgery
- Track 9-2Radiation Therapy
- Track 9-3Chemotherapy
- Track 9-4Immunotherapy
- Track 9-5Targeted Therapy
- Track 9-6Hormone Therapy
- Track 9-7Stem Cell Transplant
- Track 9-8Precision Medicine
Immunotherapy is considered as a type of cancer treatment that helps your immune system to fight against cancer. The immune system helps your body to fight with infections and other diseases. It is consists of organs and white blood cells and tissues of the lymph system.Immunotherapy is a type of biological therapy. Organic therapy is a type of treatment that we use from the substances made from living organisms to treat cancer.
Stem Cell Therapies Meetings | Regulatory and Ethical Issues of Therapies Conference | Nanotechnology in Stem Cell Conference
- Track 10-1Immune checkpoint inhibitors
- Track 10-2T-cell transfer therapy
- Track 10-3Monoclonal antibodies
- Track 10-4Immune system modulators
Stem Cell Research & Therapy is the major domain for translating analysis into stem cell therapies. An international peer-reviewed conference, it publishes high-quality open research access articles with a special stress on basic, translational and clinical research into stem cell therapeutics and regenerative therapies, including animal models and clinical trials. The conference also provides reviews, viewpoints, commentaries, reports and strategies. They are some specified stem cells given below.
Stem Cell Therapies Meetings | Cell and Gene Therapy Conferences | Nanotechnology in Stem Cell Conference .
- Track 11-1Adult stem cells
- Track 11-2Embryonic stem cells
- Track 11-3Induced pluripotent stem cells
- Track 11-4Cancer stem cells
- Track 11-5Stem cell differentiation, proliferation and migration
- Track 11-6Cell culture and manufacture
- Track 11-7Stem cell therapy/transplantation
- Track 11-8Ethical, legal and social aspects
Cell therapy (also called cellular transplantation, cell therapy, or cytotherapy) is a therapy in which possible cells are injected, implant or embed into a patient in order to effectuate a medicinal effect, for example, by transplanting T-cells capable of fighting cancer cells via cell-mediated immunity in the course of immunotherapy, or grafting stem cells to regenerate diseased tissues.
Cell therapy commenced in the nineteenth century when scientists experimented by injecting animal material in a try to prevent and treat illness. However, such try didn’t produced any positive benefit, the next research was found in the mid twentieth century that human cells could be used to help prevent the human body rejecting transplanted organs, leading in time to successful bone marrow transplantation has become common practice in treatment for patients that have compromised bone marrow after disease, infection, radiation or chemotherapy.
Cell and Gene Therapy Meeting | Cell Science and Stem Cell Research | Nanotechnology in Stem Cell Conference
- Track 12-1Allogeneic Cell Therapy
- Track 12-2Autologous Cell Therapy
- Track 12-3Xenogeneic Cell Therapy
The number of individuals with chronicle wounds has been increasing worldwide due to a fading population, diabetes, obesity, and cardiovascular disease. In the U.S, almost seven million people have chronic skin ulcers. Many restorative approaches have been used. Whatever, the treatment comes out are not always ideal because of failure to achieve complete wound closure in around 60% of cases, scarring, and high rate of recurrence. However, there is a need of more effective therapies. Stem cells offer promising possibilities. Pre-clinical studies have shown that bone- or adipose tissue-derived mesenchyme stem cells (MSCs) have a competitive advantage over other types of stem cells due to their better defined multi potent differentiating potential, paracrine effects, immune modulatory properties, and safety. Therefore, large controlled clinical trials are needed to examine the capabilities of MSCs in humans and to assess their safety profile. In this review, we highlight emerging treatments in tissue regeneration and repair and provide some perspectives on how to translate current knowledge about stem cells-both multi potent and pluripotent-into the clinical approach for treating patients on heal wounds
Cellular Therapies Meetings | Bioengineering Therapeutics Conferences | Immunotherapy Conference
- Track 13-1Novel Stem Cell Therapy For Knees
- Track 13-2Novel Stem Cell Therapy For Arthritis
- Track 13-3Novel Stem Cell Therapy For Cancer
- Track 13-4Novel Stem Cell Therapy For Hair loss
The skin gradually re-establishes itself for the duration of grown-up life, and the hair follicle experiences a never ending cycle of development and decay. Microorganisms (Stem Cell’s) lives in the epidermis and hair follicle guarantee the support of grown-up skin equilibrium and hair recovery; however they likewise take part in the fix of the epidermis after wounds.
- Stem Cells With In Adult Skin Epithelium
- Signalling And Stem Cell Fate Specification In The Skin
- Bone Morphogenetic Protein Signalling
- Notch Signalling
Stem Cell in Cardiovascular Disease Conferences | Regulatory and Ethical Issues of Therapies Conference | Genetic Vaccines Meeting
Cardiovascular Diseases (CVD) includes congestive heart failure stroke and hypertension, coronary artery disease. Most of these diseases may occur when there is a less oxygen supply to heart cells / Cardiomyocytes which damaged as being supplied by less oxygen as well as less blood which we can treated by stem cell therapy by inducing some bone-marrow derived mononuclear cells, umbilical cord blood cells, Mesenchyme stem cells or Cardiac stem cells in to the damaged portion of heart . These cells interspersed in to heart and secrete certain portions and paracrine factors that repair of the damaged area by cardiac tissue Regeneration.
Nanotechnology in Stem Cell Conference | Bioengineering Therapeutics Conferences | Immunotherapy Conferences
- Track 15-1LQT Syndromes
- Track 15-2Timothy Syndrome
- Track 15-3LEOPARD Syndrome
- Track 15-4Duchene Muscular Dystrophy (DMD)
- Track 15-5Becker Muscular Dystrophy (BMD)
- Track 15-6Hutchinson Gilford Provera (HGPS)
In recent years, stem cell nanotechnology has emerged as a replacement of exciting field. Experimental and Theoretical studies of interaction between nanostructures or nanomaterial’s and stem cells have created nice advances. The importance of nanotechnology, nanostructures, and nanomaterial’s to the elemental developments in stem cells-based therapies for injuries and degenerative diseases has been recognized. In general, the consequences of properties and structure of nanomaterials on the accretion and differentiation of stem cells became a replacement of integrative border in reconstruction medicine and material science
Advanced Gene Therapeutics Conference | Clinical Trials and Research in Cell and Gene Therapies Meeting | Stem Cell in Drug Development Conference
- Track 16-1Nanoparticles: Cell Tracking, And Endocytosis
- Track 16-2Nano vaccines
- Track 16-3Nanomaterial’s And Nano engineering
- Track 16-4Nanotechnology For Genetic Engineering
- Track 16-5Nanotechnology For Creating Stem Cell Niche
- Track 16-6Nanoparticle Toxicity To Stem Cells
Undefined cell treatment has been opened another way in the territory of medication disclosure and improvement. Biopharmaceutical organizations have been working in interpreting fundamental utilizations of undefined cell advances in the medication improvement forms in order to diminish the high weakening rate generally arrange sedate applicants, which has been developing at a quick place in the previous decade.
Approach of unformed microorganism advances has given new expectation to fabricate imaginative cell models. The always developing systems utilized for detachment of human/creature embryonic foundational microorganisms (ESCs), bone marrow-determined mesenchyme developed cells, umbilical line undifferentiated organisms, grown-up tissue-particular neural immature microorganisms and human instigated pluripotent foundational microorganisms (iPSC) have prompted the headway of varied high throughput and combinatorial screening advancements consequently supplementing the a part of undifferentiated organism models in sedate disclosure
Regulatory and Ethical Issues of Therapies Conferences | Molecular Epigenetics Meeting | Bioengineering Therapeutics Conferences
- Track 17-1Cancer Clinical Trails
- Track 17-2Clinical Research And Bioethics
- Track 17-3Drug Screening Tools
- Track 17-4Stem Cell Biology And Regenerative Medicine
- Track 17-5Drug Safety And Regulations
Stem cells are constant cells found in cell living organisms that get separated through a cell division and then gets separate into a particular cell. The two properties of foundational microorganisms which are used to separate them in very body cell are self-restoration and proficiency. Because of their prospective job in different conducts, a foundational microorganism is subjected as inside and outside examination of Extensive Research Science.
Stem Cell in Cardiovascular Disease Conferences | Genetic Vaccines Meeting | Clinical Trials and Research in Cell and Gene Therapies Conferences.
- Track 18-1Biology of Human Embryonic Stem Cells.
- Track 18-2• Genomics and Genetics in Somatic Cell Biology
- Track 18-3Cell signal in Somatic Cell Differentiation.
- Track 18-4In-vitro culturing of Stem Cells.
- Track 18-5Applications of Somatic Stem Cells.
Stem cells are the basic materials of body cells from that all different cells will be specialized and functions are generated. Below the proper condition with in the body or a laboratory, stem cells divide to create a lot of cells called daughter cells.
These daughter cells will either become new stem cells (self-renewal) or else become specialized cells with a more specific function, such as blood cells, brain cells, heart muscle cells or bone cells. No different cell with in the body has the natural ability to generate new type of cell.
- Increase understanding of how diseases occur
- Generate healthy cells to replace diseased cells (regenerative medicine)
- Test new drugs for safety and effectiveness
Cellular Therapies Meetings | Bioengineering Therapeutics Conferences | Immunotherapy Conferences.
- Track 19-1Embryonic stem cells
- Track 19-2Adult cells altered to have properties of embryonic stem cells
- Track 19-3Adult stem cells
- Track 19-4Perinatal stem cells