In recent years, there have been significant advances in anti-HIV treatment, especially the use of multiple antiretroviral drugs. These drugs attack different parts of HIV's life cycle simultaneously, increasing their effectiveness against the virus. This treatment, called highly active antiretroviral therapy (HAART), allows many infected people to control their disease and lead relatively normal lives even in the absence of a cure.
HAART not only reduces the total amount of HIV in infected people's bodies, but also maintains their immune system function and effectively prevents opportunistic infections.
According to the recommendations of the World Health Organization (WHO), all people with HIV should receive antiretroviral therapy (ART). This strategy not only prolongs the lives of patients, but also reduces the spread of the virus in society. However, these treatment regimens are complex and require strict medication compliance, and patient participation is particularly important in selecting treatment options. As research deepens, it becomes increasingly important to explore HIV-related stigma, barriers to treatment intervention, and solutions to overcome these barriers.
Currently, anti-HIV drugs mainly include six categories, each of which works at different stages of the HIV life cycle. The general combination consists of two nucleoside reverse transcriptase inhibitors (NRTIs) as a base, followed by a non-nucleoside reverse transcriptase inhibitor (NNRTI), a protease inhibitor (PI) or an integrase inhibitor (INSTI).
Entry inhibitors work by preventing HIV from entering host cells. This type of drug includes Maraviroc and Enfuvirtide.
Nucleotide reverse transcriptase inhibitorsNRTI drugs achieve their effects by inhibiting the reverse transcription process of HIV. Typical drugs include Zidovudine and Lamivudine.
This class of drugs inhibits the activity of reverse transcriptase by binding to an allosteric site on the enzyme. The first and second generation NNRTIs include Nevirapine and Rilpivirine.
This class of drugs specifically targets the integrase enzyme, preventing HIV DNA from integrating into the genetic material of host cells. Raltegravir is the first FDA-approved integrase inhibitor.
Protease inhibitorsProtease inhibitors reduce the release of infectious viruses by interfering with viral maturation. Common drugs include Darunavir and Atazanavir, which are highly recommended for first-line treatment.
The importance of combination therapy lies in the rapid mutation nature of HIV. By combining multiple drugs, the chance of the virus developing drug-resistant mutations can be reduced. Standard HAART therapy usually uses three drugs, and this "triple cocktail" has been shown to effectively control the virus.
"A single antiretroviral drug cannot suppress HIV for a long time and must be used in combination to achieve long-term effectiveness."
Although antiretroviral therapy has significantly improved the quality of life of HIV patients, researchers are still exploring how to further reduce the disease burden on patients. Recent studies have shown that increasing interleukin-2 (IL-2) has a certain effect on improving the immune cells of HIV patients, but it has not shown a significant improvement in mortality and infection rates.
Over time, approaches to antiretroviral treatment have evolved. Many experts agree that antiretroviral therapy should be started at any CD4 count to reduce the risk of disease progression.
According to WHO guidelines, an appropriate antiretroviral treatment regimen is "safe, simple and effective."
Multiple drug treatments for HIV have significantly improved the quality of life of patients and effectively controlled the spread of the virus. With the advancement of medicine, will there be a cure for HIV in the future, or will maintaining a chronic disease status become the new normal?