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Challenges in the therapy of NeuroHIV As ART alone is insufficient to fully suppress HIV-1 replication, including the transcription and translation of HIV-1 provirus in both T-cell reservoirs and non-CD4 T-cell reservoirs, there is a critical need to develop new brain-penetrating agents that can effectively target both CNS and peripheral immune cells to simultaneously silence HIV-1 and reduce the risk of neuroinflammation

The complementary mechanisms of amylin and GLP-1 pathways have generated significant scientific interest, with researchers exploring whether combined receptor activation produces synergistic improvements in weight and metabolic outcomes