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Microbiology · Retroviruses (HIV)

Treatment and Prevention of HIV Infection

Human immunodeficiency virus (HIV)

Modern treatment of HIV infection is based on lifelong antiretroviral therapy (ART), the main goal of which is to suppress viral replication as much as possible. Although a complete cure is not yet possible, a properly selected drug regimen allows the disease to be converted into a chronic condition and significantly prolongs the patient's life.

Main goalReduction of viral RNA levels below the limit of detection
Basis of therapyCombined use of multiple drug classes
VaccinationAn effective vaccine has not yet been developed
ComplicationsControl of opportunistic infections is required
4 min readFor medical studentsUpdated Sep 25, 2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Antiretroviral therapy strategy

For effective viral suppression, exclusively combination therapy is used, also known as cART (combination antiretroviral therapy). Using multiple drugs simultaneously is a critical condition for success.

Practice has shown that monotherapy (treatment with a single drug) is largely ineffective. The HIV virus has a high capacity for mutation, and when only a single drug is used, the pathogen quickly develops resistance to it. The combined approach makes it possible to target the virus from multiple angles, preventing the development of resistance. The main clinical guideline and criterion for treatment success is reducing the concentration of viral RNA in the blood to levels that are undetectable by standard test systems.

Classification of HIV drugs

All drugs used to suppress viral replication are divided into five main classes depending on their mechanism of action. It is important for a student to know representatives of each group:

  1. Nucleoside reverse transcriptase inhibitors. A classic example of a drug from this group is zidovudine.
  2. Non-nucleoside reverse transcriptase inhibitors. A typical representative is nevirapine.
  3. Protease inhibitors. A characteristic example for this group is indinavir.
  4. Integrase inhibitors. An example is the drug raltegravir.
  5. Fusion (entry) inhibitors. This group is additionally subdivided into two subgroups depending on the specific target:
  6. CCR5 coreceptor blockers (example — maraviroc).
  7. gp41 protein blockers (example — enfuvirtide).
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Concomitant treatment and prevention

In addition to suppressing the virus itself, a crucial part of patient management is the treatment of conditions arising against the background of immunodeficiency. A key direction here is the treatment and targeted prevention of opportunistic infections, which pose the main threat to the patient's life.

Regarding the prevention of HIV transmission itself, it is generally divided into two directions:

  • Specific prophylaxis. To date, it is unavailable. All attempts to create an effective vaccine have failed so far, but scientific research in this direction is actively ongoing.
  • Non-specific prophylaxis. This is the main tool for containing the epidemic. It includes large-scale social and anti-epidemic measures, including promotion of safe sex and public education.

Briefly: answers to topical questions

Which drugs belong to nucleoside reverse transcriptase inhibitors?

Nucleoside and nucleotide reverse transcriptase inhibitors include drugs that are false analogs of natural nucleosides. This group includes:

  • Zidovudine (azidothymidine) — a thymidine analog.
  • Stavudine — a thymidine analog.
  • Phosphazide — a nucleotide analog of thymidine.
  • Lamivudine — a cytidine analog.
  • Emtricitabine — a cytidine analog.
  • Zalcitabine — a cytidine analog.
  • Didanosine — an adenine analog.
  • Tenofovir — a nucleotide analog of adenine.
  • Abacavir — a guanine analog.

Fixed combinations of NRTIs are also used, for example, zidovudine + lamivudine or abacavir + lamivudine.

Which drugs belong to HIV protease inhibitors?

HIV protease inhibitors include peptidomimetic substances that cause inactivation of the viral aspartyl protease. This group includes the following drugs:

  • Indinavir — a protease inhibitor.
  • Saquinavir — the first drug from the protease inhibitor group.
  • Atazanavir — a protease inhibitor.
  • Darunavir — a protease inhibitor.
  • Lopinavir — a protease inhibitor.
  • Ritonavir — a protease inhibitor.
  • Fosamprenavir — a protease inhibitor.

In clinical practice, drug combinations are frequently used, for example, lopinavir + ritonavir, darunavir + ritonavir, atazanavir + ritonavir.

Which opportunistic infections are characteristic of the AIDS stage?

The AIDS stage is characterized by the development of severe opportunistic infections of protozoal, fungal, bacterial, and viral origin. The main ones include:

  • Protozoal and parasitic — cerebral toxoplasmosis, cryptosporidiosis, strongyloidiasis (Strongyloides stercoralis), leishmaniasis.
  • Fungal — Pneumocystis pneumonia (Pneumocystis jirovecii), candidiasis (Candida species), cryptococcosis (Cryptococcus neoformans), aspergillosis, histoplasmosis.
  • Bacterial — tuberculosis (the main cause of death), bacterial pneumonia (most often Streptococcus pneumoniae), bacillary angiomatosis, syphilis.
  • Viral — cytomegalovirus infection (CMVI).

Which drugs belong to non-nucleoside reverse transcriptase inhibitors?

Non-nucleoside reverse transcriptase inhibitors include drugs that suppress viral replication by acting on the reverse transcriptase enzyme. This group includes:

  • Nevirapine — a non-nucleoside reverse transcriptase inhibitor.
  • Efavirenz — a non-nucleoside reverse transcriptase inhibitor.
  • Etravirine — a non-nucleoside reverse transcriptase inhibitor.
  • Rilpivirine — a non-nucleoside reverse transcriptase inhibitor.

Some of these drugs, such as rilpivirine, may be used as part of fixed-dose combination antiviral agents.

Which drugs belong to HIV integrase inhibitors?

HIV integrase inhibitors include drugs that prevent the integration of viral DNA into the host cell's genetic material. This group includes:

  • Raltegravir (Isentress) blocks the catalytic center of the integrase enzyme.
  • Dolutegravir has the highest degree of CNS penetration.
  • Elvitegravir is used as part of fixed-dose combination drugs.
  • Bictegravir is also used as part of fixed-dose combinations.

Which antiretroviral therapy regimens are considered first-line?

First-line antiretroviral therapy regimens include starting combinations consisting of three antiretroviral drugs:

  • Backbone — two nucleoside or nucleotide reverse transcriptase inhibitors (2 NRTIs).
  • Third drug — one agent from another group of choice.

Possible starting therapy formulas:

  • 2 NRTIs + 1 protease inhibitor (PI);
  • 2 NRTIs + 1 non-nucleoside reverse transcriptase inhibitor (NNRTI);
  • 2 NRTIs + 1 integrase strand transfer inhibitor (INSTI).

Monotherapy, dual therapy, or three NRTIs are not recommended.

Class and exam questions

Why is monotherapy not used for HIV infection?

Monotherapy is ineffective due to the high frequency of viral mutations. Using only a single drug rapidly leads to the development of HIV resistance to treatment.

Can HIV infection be completely cured with modern therapy?

No, current therapy does not provide a complete cure. However, it effectively reduces viral load and significantly prolongs the patient's life.

Is there a vaccine for HIV?

No, specific prophylaxis in the form of an effective vaccine has not been developed to date, and all previous attempts to create one have failed.

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What else to study on this topic

  • Mechanism of action of reverse transcriptase inhibitors
  • Differences between nucleoside and non-nucleoside inhibitors
  • The role of CCR5 coreceptors and the gp41 protein in the viral cycle
  • Main types of opportunistic infections in HIV

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