To study the safety and effectiveness of CAR-T Cell therapy on HIV patients whose plasma HIV has been successfully suppressed after cART, which is expected to enhance the res-constitution of HIV-specific immune function to assist the eradication of HIV reservoir.
Despite the advent of combined antiretroviral therapy (cART), the persistence of viral reservoirs remains a major barrier to curing human immunodeficiency virus type 1 (HIV-1) infection. Recently, the shock and kill strategy, by which HIV-1 reservoirs could be eradicated following reactivation of latent HIV-1 by latency-reversing agents (LRAs), has been extensively practiced. It is important to reestablish virus-specific and reliable immune surveillance to eradicate the reactivated virus-harboring cells.the VC-CAR-T cells effectively induced the cytolysis of LRA-reactivated HIV-1-infected CD4 T lymphocytes isolated from infected individuals receiving successful cART. Our previous study demonstrated that the special features of genetically engineered CAR-T cells make them a particularly suitable candidate for therapeutic application in efforts to reach a functional HIV cure. In this clinical trial, we intend to study the safety and effectiveness of CAR-T Cell Therapy on HIV patients whose plasma HIV has been successfully suppressed after cART, by observing the adverse events, HIV-1 reservoir and the immune index.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
HIV-1 specific chimeric antigen receptor cells
Guangzhou 8th People's Hospital
Guangzhou, Guangdong, China
RECRUITINGIncidence of treatment-associated adverse events of CAR-T cell therapy
To observe the adverse events of VC-CAR-T cell therapy on HIV-infected patients during the clinical trial
Time frame: 6 Months
HIV-1 reservoir
To assay the HIV loads in the peripheral blood Mono-nuclear cells and plasma
Time frame: 6 Months
HIV viral load rebound time
To assay the HIV viral load rebound period after discontinuing cART
Time frame: 6 months
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