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Knowledge From London and Berlin: Finding Threads to a Functional HIV Cure
Jingyi Ding1, Yanxi Liu2, Yu Lai3
1Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Frontiers in Immunology
|June 14, 2021
Summary
Functional HIV cure remains elusive despite combination antiretroviral therapy (cART). Gene therapies targeting CCR5 and CXCR4, alongside stem cell treatments, offer promising avenues for a functional cure in HIV patients.
Area of Science:
- Infectious Diseases
- Immunology
- Gene Therapy
Background:
- Combination antiretroviral therapy (cART) extends life for HIV patients but does not eliminate viral reservoirs.
- Two functional HIV cures (Berlin and London Patients) involved CCR5-delta32 mutated stem cell transplants for hematological malignancies.
Purpose of the Study:
- To review advancements in gene therapy and other strategies for achieving a functional cure for HIV.
- To explore the potential of coreceptor-based hematopoietic stem cell gene therapy for HIV treatment.
Main Methods:
- Review of existing literature on HIV cure strategies.
- Discussion of gene-modified autologous hematopoietic stem cells (targeting CCR5 and CXCR4).
- Analysis of combination antiretroviral therapy (cART), conditioning regimens, and shock and kill approaches.
Main Results:
- Hematopoietic stem cell transplantation with CCR5-delta32 mutation has shown success in achieving functional HIV cure.
- Gene therapy targeting coreceptors like CCR5 and CXCR4 demonstrates significant promise for HIV treatment.
- Integration of various strategies like cART, gene therapy, and shock and kill may lead to a functional cure.
Conclusions:
- Coreceptor-based hematopoietic stem cell gene therapy is a rapidly advancing field with potential for HIV functional cure.
- Developing a cure for HIV infection is a high priority, with gene therapy offering novel therapeutic avenues.
- Combined strategies including gene therapy, optimized conditioning, and viral eradication methods are crucial for a widespread functional HIV cure.

