The document discusses NRF-2, a negative regulator of oxidative stress and inflammation. It travels to the nucleus and binds antioxidant elements, decreasing inflammatory cytokine levels. The study aimed to determine if inhibiting oxidative stress could control HIV replication and improve cell survival. Methods used included PCR, ELISA, Western blotting, and flow cytometry. The conclusions were that these molecular biology techniques helped understand NRF-2's importance, and that NRF-2 activation promotes macrophage survival after HIV infection, aiding patient diagnosis.