• International Congress on Gene Therapy and Cell Therapy
  • Persian

Gene and cell therapy, a definitive solution to treating disease

The science of gene therapy and cell therapy is known today as one of the definitive ways to treat diseases in the world.

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Application of Gene therapy and cell therapy

Treatment of genetic diseases

Gene therapy can be used as a treatment for genetic diseases. In this method, defective or missing genes are introduced into the cells of the patient's body to restore the correct functioning of cells and tissues to normal. Diseases such as hemophilia, cystic fibrosis, genetic heart diseases and neurological diseases are among the diseases that can be treated or controlled with these methods.

Cancer treatment

Gene therapy has become a key player in cancer treatment, particularly as a targeted and precise method. This involves transferring specific genes into cancer cells to inhibit their growth, boosting the body's immune system to recognize and destroy cancer cells, or modifying blood stem cells to treat cancers such as leukemia and lymphoma.

Treatment of neurological diseases

The use of gene and cell therapy in neurological diseases such as Parkinson's, Alzheimer's, amyotrophic lateral sclerosis (ALS), and muscular atrophy can significantly improve the quality of life of patients. Stem cells can be used as a potential treatment for the regeneration and repair of damaged neural tissues.

Treatment of autoimmune and inflammatory diseases

Gene therapy and cell therapy can be effective in treating autoimmune diseases such as lupus, rheumatoid arthritis, and multiple sclerosis (MS). Stem cells can help repair tissues and regulate the function of the immune system, while gene therapy seeks to correct abnormal inflammatory responses in the body.

Treatment of organ failures

Gene therapy and cell therapy are used to treat organ failures such as kidney failure, liver failure, and heart failure. Using stem cells or gene modification, it is possible to regenerate and repair damaged tissues and improve the normal function of organs.

Treatment of blood and immune disorders

Gene therapy can be used to treat blood diseases such as thalassemia and sickle cell anemia, and immune disorders such as primary immunodeficiency and immunodeficiency. Gene editing or the use of blood stem cells makes it possible to treat and improve the condition of these patients.

About the Gene therapy and cell therapy Congress

The 1st International Congress on Gene Therapy and Cell Therapy is a pioneering scientific event aimed at addressing the latest breakthroughs, challenges, and future directions in the rapidly evolving fields of gene- and cell-based therapeutics. This congress brings together leading scientists, clinicians, biotechnologists, healthcare professionals, and regulatory experts from across the globe to explore innovative strategies that are transforming the landscape of modern medicine.

Held with the goal of fostering international collaboration and promoting interdisciplinary dialogue, the congress provides a unique platform for sharing scientific knowledge, clinical experiences, and translational research outcomes. Through keynote lectures, scientific panels, poster sessions, and industry exhibitions, the event will cover a wide range of topics, including gene editing technologies, stem cell applications, immunotherapies, clinical trial design, bioethics, and regulatory frameworks.

Outlook for the International Gene therapy and cell therapy Congress

The vision of the 1st International Congress on Gene Therapy and Cell Therapy is to establish a dynamic, interdisciplinary, and globally connected platform that accelerates the development, translation, and clinical implementation of advanced gene- and cell-based therapies.

This congress aspires to become a premier international forum where scientists, clinicians, industry leaders, and policy-makers come together to share cutting-edge research, innovative technologies, and strategic insights aimed at improving human health through personalized and regenerative medicine.

  • Interdisciplinary and multidimensional research
  • Creating global standards and strategies
  • Advances in the treatment of diseases

Congress Participation Guide

We are with you at the Permanent Secretariat of the International Gene therapy and cell therapy Congress.

1. Where do I start to attend the Gene therapy and cell therapy Congress?

From the Create User Account section, create your own user account for free and register for the Congress after entering the site's user area.

2. How to submit an article?

After creating a user account and logging into your user area, you can send your abstracts to the congress refereeing section from the article submission section. Articles can be submitted in English.

3. What is the procedure for participating in the congress on the day of the event?

The online studio platform is separate for the workshops and congress sections. For the workshops section, you must use the Windows version of Online Studio, and to view the congress, you must use the mobile version of Online Studio, which will be notified through the user area.

The importance of membership in the country's Gene therapy and cell therapy family

Knowledge of new gene and cell therapy methods

One of the most important achievements of the International Gene and Cell Therapy Congress is familiarization with various methods related to clinical treatment.

Increasing awareness of gene and cell therapy

One of the main goals of the Gene and Cell Therapy Congress is to inform about the latest scientific achievements in gene and cell therapy in Iran and the world.

Understanding the scientific community of gene and cell therapy

Connecting different scientific communities around gene and cell therapy and forming scientific, professional, and business connections with each other.

Gene and cell therapy: the definitive solution to treating cancer and diseases