Table 1. Selected recent immunotherapy for HIV-1 infection.
Immunotherapy | Treatment | Responses | Reference |
---|---|---|---|
Promoting immune responses | |||
Cytokines | IL-2 during ART treatment interruptions | No evidence of improved HIV-1-specific immunity | [35] |
IL-7 dose escalation trial in ART-treated patients | Increases in CD4+ T-cell numbers | [37] | |
IL-21 administered to SIV-infected Rhesus macaques | Increases in natural killer-cell and CD8+ T-cell function and Th17 cells and a reduction in bacterial translocation and immune activation | [38,39] | |
Drugs | Immunomodulatory drugs | Enhanced T-cell responses to dendritic cells electroporated with GAG or NEF mRNA | [46] |
Correcting immune activation and dysfunction | |||
Drugs | Aspirin | Reductions in CD38, HLA-DR, and sCD14 | [40] |
COX-2 inhibitor celecoxib | Celecoxib reduced the expression CD38 and inflammatory markers | [41] | |
Antibodies | Anti-PD-1 | Blocking PD-1 results in increased cytokine expression in HIV-1 patients | [27] |
Anti-CLTA4 treatment of SIV-infected macaques | Decreased TGF-β, IDO, and viral RNA in SIV-infected macaques | [30] | |
Anti-CCR5 Maraviroc | Reduction in CD38 HLA-DR-expressing CD4+ T cells and normalized CD8+ T-cell skewing | [32] | |
Probiotics | Symbiotic plus dietary fiber | No alteration in bacterial translocation | [48] |
Prebiotic and probiotic | Reductions in bacterial DNA, CD4+ T-cell counts, and IL-6 | [49] |
ART, antiretroviral therapy; COX-2, cyclooxygenase type 2; IDO, indoleamine 2,3-dioxygenase; IL, interleukin; SIV, simian immunodeficiency virus; TGF-β, transforming growth factor-beta.