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NIAID Fact Sheet
New Treatments for HIV Infection: Prolonging and Improving Life

May 25, 1999

When AIDS was first recognized in 1981, patients with the disease were unlikely to live longer than a year or two. Today, advances in understanding the human immunodeficiency virus (HIV) and how it causes AIDS have helped scientists to develop an effective arsenal of drugs that, when used in combination, can help many people with HIV disease live longer and healthier lives. The addition of a new class of anti-HIV drugs to combination therapies has contributed to the first drop in the U.S. AIDS death rates since the beginning of the epidemic. (See the graph on AIDS death rates.) The story of this achievement highlights the pivotal contributions of both basic research and the Institute's collaborations with academia and industry to develop effective treatments for HIV disease.

Since HIV was identified in 1983, NIAID-supported scientists have led efforts to understand how the virus attacks the immune system and causes disease. This research demonstrated that substantial amounts of HIV are present, primarily in the lymphoid tissue, from the earliest stages of infection; that levels of HIV typically increase as HIV disease progresses; and that HIV remains infectious and actively replicates even while trapped and hidden in immune cells. Such basic research discoveries provide the rationale for using drugs that delay or prevent HIV disease by suppressing HIV replication.


Early Anti-HIV Treatments

For several years, the only drugs available for treating HIV infection were nucleoside analogue reverse transcriptase (RT) inhibitors. These drugs interfere with the action of a specific HIV enzyme (RT) involved in the replication cycle of HIV. The first anti-HIV drug, zidovudine (AZT), was originally developed in 1964 as a possible cancer treatment but was found to be ineffective against tumor cells. However, collaboration between the National Cancer Institute and the pharmaceutical company Burroughs Wellcome led to the discovery in the early 1980s of AZT's ability to suppress HIV replication in the test tube and paved the way for clinical trials of AZT.

Burroughs Wellcome, with input from NIH and the Food and Drug Administration, successfully conducted testing of AZT in HIV-infected individuals. Subsequently, NIAID's AIDS Clinical Trials Group (ACTG) conducted several clinical trials in partnership with industry to test four other nucleoside RT inhibitors: zalcitabine (ddC), didanosine (ddI), stavudine (D4T), and lamivudine (3TC). All five drugs are now licensed in the United States. Additional ACTG studies demonstrated the benefits of AZT therapy for preventing mother-to-infant transmission of HIV and for lowering the risk for developing AIDS in persons with HIV infection.

Unfortunately, HIV rapidly develops resistance to these and other anti-HIV drugs. Researchers have attacked the problem of drug resistance -- which is particularly harmful because of HIV's high rate of replication and mutation -- by using regimens of multiple anti-HIV drugs. NIAID-supported researchers were among the first to show (in 1995) that treatment with combinations of AZT and other nucleoside analogue RT inhibitors was more effective than treatment with AZT alone. In addition, combining 3TC with AZT slowed the virus from developing resistance to AZT and, in some cases, restored AZT sensitivity in patients who carried virus that had become resistant to the drug. As a result of these NIAID-supported studies, combination therapy emerged as the preferred treatment modality for HIV infection.


A New Class of Anti-HIV Drugs

Meanwhile, basic research supported by NIAID and others was providing information about additional mechanisms of HIV replication that offered new targets for anti-HIV drugs. For example, Institute-supported basic research was pivotal to discovering and defining the importance of the HIV protease enzyme, which is used by the virus to produce infectious HIV particles. Other Institute-supported scientists helped determine the precise three-dimensional structure of HIV protease, a crucial step in designing drugs that block the action of the enzyme. NIAID also supported researchers who helped drug-screening efforts by developing simple, rapid tests to measure the inhibition of protease activity. Many of these basic research advances were made by investigators of NIAID's National Cooperative Drug Discovery Groups for Treatment of HIV program, which encourages collaboration among scientists from academia, industry, and government.

These accomplishments set the stage for the Institute's successful collaboration with the pharmaceutical industry in developing the new class of anti-HIV drugs known as protease inhibitors. Building on these findings, NIAID actively promoted the protease enzyme as a potential target for drug development and supported pharmaceutical companies' initial drug discovery efforts throughout the late 1980s and early 1990s. The Institute worked closely with several industrial partners as they designed, produced, and clinically tested protease inhibitors. This collaboration helped speed product development. The first licensed protease inhibitor went to market in December 1995. Additional protease inhibitors were approved in 1996 and 1997.



Anti-HIV Drugs

Anti-HIV Drugs

The diagram above shows (1) the virus entering the cell, (2-3) conversion of viral RNA to DNA using the enzyme reverse transcriptase and incorporation of the viral genome into the DNA of the host cell, (4) viral proteins cleaved by protease for assembly of new viral particles, (5) new virus particles budding from the surface of the host cell. It also shows the steps in the viral life cycle that are interrupted by (A) reverse transcriptase inhibitors and (B) protease inhibitors.


Potent Combination Therapies

Because two-drug combination therapy was proven more effective than monotherapy, the next logical step was to test three-drug combinations that included the new protease inhibitors. Since 1996, several NIAID-supported research groups and collaborating pharmaceutical companies reported that triple-drug combinations with a protease inhibitor reduced the levels of HIV circulating in the blood so dramatically that the virus often was undetectable with standard tests. In papers published in September 1997, investigators supported by the Institute conclusively demonstrated that triple-drug combinations with a protease inhibitor and two other anti-HIV drugs were more effective than one- or two-drug regimens for long-term suppression of HIV.



AIDS Deaths in the United States from January 1986 to June 1998

AIDS Deaths in the United States from January 1986 to June 1998

Estimates Adjusted for Reporting Delays

Data Reported to CDC through December 31, 1998

The increased use of potent combinations of anti-HIV drugs has led to a significant decline in AIDS deaths in the United States in the past 2 years.


New Avenues for Therapies

The success in many patients of the new combination therapies, when used according to Federal guidelines, has been encouraging, at least in the short term. These heartening results, however, are not the end of the story. HIV's ability to mutate and become resistant to currently available drugs is a persistent threat, and many patients do not benefit from or cannot tolerate complex combination regimens. NIAID is supporting research to develop more potent therapies that have fewer toxic effects and are easier to administer. Also crucial are less expensive treatments for the more than 30 million persons worldwide who are infected with HIV.



Spinoffs From NIAID Research on HIV/AIDS

NIAID basic and clinical research on HIV/AIDS has contributed to "spinoff" advances in other areas of research. Information about viruses, infectious microbes, and the immune system gleaned from HIV/AIDS research is providing insights on new ways to fight other diseases.
  • Methods used to design drugs that target different phases of the HIV life cycle are being applied to the development of drugs to treat other viral diseases such as hepatitis C, influenza, and cytomegalovirus (CMV) infections.

  • The successful strategy of using combination drug regimens to fight HIV is being applied to other viral diseases such as hepatitis B and C.

  • The anti-HIV drug lamivudine was recently licensed in the United States for treatment of chronic hepatitis B. The drug has been approved for this purpose in several other countries, including China.

  • Research to develop treatments for opportunistic infections in HIV-infected persons has produced new treatments to prevent and control diseases such as CMV retinitis, Pneumocystis carinii pneumonia, Mycobacterium avium complex, cryptococcal meningitis, and herpes simplex. Many of these therapies are now used by individuals with immune systems weakened by treatments for cancer or transplants.

  • Findings from a collaborative study about the effectiveness of a short-course TB prevention regimen offer hope for reducing the risk for TB in persons infected with HIV. The short-course regimen has the potential for reducing the cost of TB prevention programs, improving compliance with the prophylactic regimen, and possibly treating latent TB infection in HIV-negative individuals.

  • An African study testing antibacterial washes as a means of preventing HIV transmission from mother to infant yielded unexpected results. The inexpensive antiseptic, which was applied to the mother's birth canal during labor and to the newborn immediately after birth, generally did not reduce HIV transmission. However, the washes did reduce the number of deaths related to infections as well as the rate of infections in both mothers and newborns.

  • Sensitive and rapid techniques developed or refined for the diagnosis and monitoring of HIV infection are now being used for other diseases such as hepatitis, TB, Lyme disease, herpes simplex, and encephalitis.

  • Retroviral vectors derived from HIV/AIDS research are being adapted for use in gene transfer therapy for cancer patients. Scientists also are investigating gene-based therapies to help patients with hepatitis and chronic granulomatous disease.


These concerns underscore the need for NIAID's continued effort to find new therapies for HIV infection. Basic researchers at NIAID laboratories have helped explain why HIV can rebound in patients who discontinue combination therapy, and they are working to develop new ways to attack pools of latently infected cells that serve as hiding places for HIV. NIAID scientists also have opened new avenues for therapies with the discovery of coreceptors for HIV's entry into immune cells. (See Chemokines and HIV Coreceptors)

Since 1993, NIAID's Strategic Program for Innovative Research on AIDS Treatment (SPIRAT) has supported basic and clinical research on novel approaches to treatment. Scientists supported by SPIRAT and other NIAID research programs are contributing to the discovery and development of the next generation of anti-HIV treatments. Such strategies may include therapies that combat drug resistance by targeting a broader range of mechanisms in the HIV replication cycle, treatments designed to rebuild the damaged immune system of infected individuals, and gene therapy to protect cells from HIV infection or interfere with HIV function in already infected cells. NIAID also plays a central role in international efforts to develop an HIV vaccine. As the story of the AIDS epidemic continues to unfold, NIAID research will continue to provide the foundation for new breakthroughs in improving the quality and duration of life for people infected with HIV.




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