HIV Gene Therapy
HIV gene therapy is designed to remove or control HIV infection by addressing the virus's genetic material. Approaches include modifying immune cells' genes to withstand infection, adding antiviral genes, and utilizing CRISPR to remove viral DNA from infected cells. These novel techniques aim to give long-term control or even a cure for HIV, changing virus management.
Related Conference of HIV Gene Therapy
March 09-10, 2026
21th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
Singapore City, Singapore
June 18-19, 2026
16th International Conference on Human Genetics and Genetic Diseases
Singapore City, Singapore
June 18-19, 2026
19th International Conference on Genomics & Pharmacogenomics
Singapore City, Singapore
HIV Gene Therapy Conference Speakers
Recommended Sessions
- Advanced Gene Therapeutics
- Cancer Therapies
- CAR T-cell Therapy
- Cell Culture and Bioprocessing
- Cell Science and Stem Cell Research
- Cellular Therapies
- Clinical Trials and Research in Cell and Gene Therapies
- Diabetes Gene Therapy
- Genetic Vaccines
- HIV Gene Therapy
- Human Gene Therapy
- Molecular Epigenetics
- Nano-Therapy
- Nanotechnology in Stem Cell
- Novel Stem Cell Therapy
- Skin Cell Therapy
- Stem Cell Engineering
- Stem Cell in Cardiovascular Disease
- Stem Cell in Drug Development
- Stem Cell Therapies
- Viral Gene Therapy
Related Journals
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- Biomaterials and Nanotechnology in Regenerative Medicine - Stemgen 2026 (Japan)
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- Ethical, Legal, and Social Implications in Stem Cell Research - Stemgen 2026 (Japan)
- Future Trends: Organoids, Bioengineering, and Next-Generation Therapies - Stemgen 2026 (Japan)
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