International Conference on Advanced Cell and Gene Therapy

Join Us at the 3rd International Conference on Advanced Cell and Gene Therapy

Dates: September 19- 20 / 2025

Location: Barcelona, Spain

Dear Doctors, Healthcare Professionals, Researchers, and Students

Researchers Fusion are excited to extend a warm invitation to you for the 3rd International Conference on Advanced Cell and Gene Therapy, taking place as an interactive on September 19-20, 2024. This congress promises to be a dynamic platform for sharing cutting-edge research, exploring innovative therapies, and discussing the latest trends in combating Advanced Cell and Gene Therapy.

Advanced Cell and Gene Therapy refers to cutting-edge medical treatments that involve modifying or manipulating cells or genes to treat or cure diseases, particularly those that have no effective conventional treatments. These therapies are at the forefront of regenerative medicine and have the potential to address a wide range of genetic, chronic, and degenerative conditions.

Here’s a breakdown of what each entails:

1. Cell Therapy
Cell therapy involves the transplantation or infusion of living cells to repair or replace damaged tissues or organs. The goal is often to restore normal function, regenerate tissue, or modulate the immune system. Some of the main types of cell therapy include:

Stem Cell Therapy: Uses stem cells (cells capable of developing into many different types of cells) to regenerate damaged tissue or organs. These cells can be obtained from embryos, adult tissues, or reprogrammed cells (induced pluripotent stem cells, or iPSCs).
Tissue Engineering: Combines cells with biomaterials to create new tissues or organs for implantation.
Immunotherapy (e.g., CAR-T): This is a form of cell therapy where the patient’s immune cells are modified outside the body and then reinfused to target and destroy cancer cells.
2. Gene Therapy
Gene therapy involves modifying a person’s genes to treat or prevent disease. It can be used to:

Replace a mutated gene with a healthy one.
Inactivate a faulty gene.
Introduce a new or modified gene to help treat a disease.
Gene therapy is particularly useful for genetic disorders like cystic fibrosis, muscular dystrophy, and certain types of inherited blindness. The delivery of genetic material into a patient's cells is typically carried out through viral vectors (modified viruses that can safely transport the gene into cells) or non-viral methods (such as nanoparticles).

Why to Attend?
Expert Speakers: Hear from leading experts in the field who will share their insights and discoveries.
Networking Opportunities: Connect with peers, colleagues, and mentors from around the globe.
Educational Sessions: Gain knowledge from comprehensive sessions covering various aspects of infectious diseases.
Research Presentations: Showcase your research findings and contribute to the advancement of knowledge.
Virtual Exhibition: Explore the latest advancements in diagnostics, treatments, and technologies.

Who Should Attend?
Doctors and Healthcare Practitioners
Researchers and Scientists
Students and Academicians
Public Health Officials