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AIDS--acquired immune deficiency
syndrome--was first reported in the United States in 1981 and
has since become a major worldwide epidemic. AIDS is caused
by the human immunodeficiency virus (HIV). By killing or
impairing cells of the immune system, HIV progressively
destroys the body's ability to fight infections and certain
cancers. Individuals diagnosed with AIDS are susceptible to
life-threatening diseases called opportunistic infections,
which are caused by microbes that usually do not cause
illness in healthy people.
More than 500,000 cases of AIDS have been
reported in the United States since 1981, and as many as
900,000 Americans may be infected with HIV. The epidemic is
growing most rapidly among minority populations and is a
leading killer of African-American males. According to the
U.S. Centers for Disease Control and Prevention (CDC), the
prevalence of AIDS is six times higher in African-Americans
and three times higher among Hispanics than among
whites.
Transmission
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HIV is spread most commonly by sexual
contact with an infected partner. The virus can enter the
body through the lining of the vagina, vulva, penis, rectum
or mouth during sex.
HIV also is spread through contact with
infected blood. Prior to the screening of blood for evidence
of HIV infection and before the introduction in 1985 of
heat-treating techniques to destroy HIV in blood products,
HIV was transmitted through transfusions of contaminated
blood or blood components. Today, the risk of acquiring HIV
from such transfusions is extremely small.
HIV frequently is spread among injection
drug users by the sharing of needles or syringes contaminated
with minute quantities of blood of someone infected with the
virus. However, transmission from patient to health-care
worker or vice-versa via accidental sticks with contaminated
needles or other medical instruments is
rare.
Women can transmit HIV to their fetuses
during pregnancy or birth. Approximately one-quarter to
one-third of all untreated pregnant women infected with HIV
will pass the infection to their babies. HIV also can be
spread to babies through the breast milk of mothers infected
with the virus. If the drug AZT is taken during pregnancy,
the chance of transmitting HIV to the baby is reduced
significantly.
Although researchers have detected HIV in
the saliva of infected individuals, no evidence exists that
the virus is spread by contact with saliva. Laboratory
studies reveal that saliva has natural compounds that inhibit
the infectiousness of HIV. Studies of people infected with
HIV have found no evidence that the virus is spread to others
through saliva such as by kissing. However, the risk of
infection from so-called "deep" kissing, involving the
exchange of large amounts of saliva, is unknown. Scientists
also have found no evidence that HIV is spread through sweat,
tears, urine or feces.
Studies of families of HIV-infected people
have shown clearly that HIV is not spread through casual
contact such as the sharing of food utensils, towels and
bedding, swimming pools, telephones or toilet seats. HIV is
not spread by biting insects such as mosquitoes or
bedbugs.
HIV can infect anyone who practices risky
behaviors such as:
Having another sexually transmitted
disease such as syphilis, herpes, chlamydia or gonorrhea
appears to make someone more susceptible to acquiring HIV
infection during sex with an infected
partner.
Early Symptoms
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Many people do not develop any symptoms
when they first become infected with HIV. Some people,
however, have a flu-like illness within a month or two after
exposure to the virus. They may have fever, headache, malaise
and enlarged lymph nodes (organs of the immune system easily
felt in the neck and groin). These symptoms usually disappear
within a week to a month and are often mistaken for those of
another viral infection.
More persistent or severe symptoms may not
surface for a decade or more after HIV first enters the body
in adults, and within two years in children born with HIV
infection. This period of "asymptomatic" infection is highly
variable. Some people may begin to have symptoms in as soon
as a few months, whereas others may be symptom-free for more
than 10 years. During the asymptomatic period, however, HIV
is actively infecting and killing cells of the immune system.
HIV's effect is seen most obviously in a decline in the blood
levels of CD4+ T cells (also called T4 cells)--the immune
system's key infection fighters. The virus initially disables
or destroys these cells without causing
symptoms.
As the immune system deteriorates, a
variety of complications begins to surface. One of the first
such symptoms experienced by many people infected with HIV is
lymph nodes that remain enlarged for more than three months.
Other symptoms often experienced months to years before the
onset of AIDS include a lack of energy, weight loss, frequent
fevers and sweats, persistent or frequent yeast infections
(oral or vaginal), persistent skin rashes or flaky skin,
pelvic inflammatory disease that does not respond to
treatment or short-term memory loss. Some people develop
frequent and severe herpes infections that cause mouth,
genital or anal sores, or a painful nerve disease known as
shingles. Children may have delayed development or failure to
thrive.
AIDS
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The term AIDS applies to the most advanced
stages of HIV infection. Official criteria for the definition
of AIDS are developed by the U.S. Centers for Disease Control
and Prevention (CDC) in Atlanta, Ga., which is responsible
for tracking the spread of AIDS in the United
States.
In 1993, CDC revised its definition of
AIDS to include all HIV-infected people who have fewer than
200 CD4+ T cells. (Healthy adults usually have CD4+ T-cell
counts of 1,000 or more.) In addition, the definition
includes 26 clinical conditions that affect people with
advanced HIV disease. Most AIDS-defining conditions are
opportunistic infections, which rarely cause harm in healthy
individuals. In people with AIDS, however, these infections
are often severe and sometimes fatal because the immune
system is so ravaged by HIV that the body cannot fight off
certain bacteria, viruses and other
microbes.
Opportunistic infections common in people
with AIDS cause such symptoms as coughing, shortness of
breath, seizures, dementia, severe and persistent diarrhea,
fever, vision loss, severe headaches, wasting, extreme
fatigue, nausea, vomiting, lack of coordination, coma,
abdominal cramps, or difficult or painful
swallowing.
Although children with AIDS are
susceptible to the same opportunistic infections as adults
with the disease, they also experience severe forms of the
bacterial infections to which children are especially prone,
such as conjunctivitis (pink eye), ear infections and
tonsillitis.
People with AIDS are particularly prone to
developing various cancers such as Kaposi's sarcoma or
cancers of the immune system known as lymphomas. These
cancers are usually more aggressive and difficult to treat in
people with AIDS. Hallmarks of Kaposi's sarcoma in
light-skinned people are round brown, reddish or purple spots
that develop in the skin or in the mouth. In dark-skinned
people, the spots are more pigmented.
During the course of HIV infection, most
people experience a gradual decline in the number of CD4+ T
cells, although some individuals may have abrupt and dramatic
drops in their CD4+ T-cell counts. A person with CD4+ T cells
above 200 may experience some of the early symptoms of HIV
disease. Others may have no symptoms even though their CD4+
T-cell count is below 200.
Many people are so debilitated by the
symptoms of AIDS that they are unable to hold steady
employment or do household chores. Other people with AIDS may
experience phases of intense life-threatening illness
followed by phases of normal functioning.
A small number of people initially
infected with HIV 10 or more years ago have not developed
symptoms of AIDS. Scientists are trying to determine what
factors may account for their lack of progression to AIDS,
such as particular characteristics of their immune systems or
whether they were infected with a less aggressive strain of
the virus or if their genetic make-up may protect them from
the effects of HIV.
Diagnosis
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Because early HIV infection often causes
no symptoms, it is primarily detected by testing a person's
blood for the presence of antibodies (disease-fighting
proteins) to HIV. HIV antibodies generally do not reach
detectable levels until one to three months following
infection and may take as long as six months to be generated
in quantities large enough to show up in standard blood
tests.
People exposed to HIV should be tested for
HIV infection as soon as they are likely to develop
antibodies to the virus. Such early testing will enable them
to receive appropriate treatment at a time when they are most
able to combat HIV and prevent the emergence of certain
opportunistic infections (see
Treatment below). Early testing also alerts
HIV-infected people to avoid high-risk behaviors that could
spread HIV to others.
HIV testing is done in most doctors'
offices or health clinics and should be accompanied by
counseling. Individuals can be tested anonymously at many
sites if they have particular concerns about
confidentiality.
Two different types of antibody tests,
ELISA and Western Blot, are used to diagnose HIV infection.
If a person is highly likely to be infected with HIV and yet
both tests are negative, a doctor may test for the presence
of HIV itself in the blood. The person also may be told to
repeat antibody testing at a later date, when antibodies to
HIV are more likely to have developed.
Babies born to mothers infected with HIV
may or may not be infected with the virus, but all carry
their mothers' antibodies to HIV for several months. If these
babies lack symptoms, a definitive diagnosis of HIV infection
using standard antibody tests cannot be made until after 15
months of age. By then, babies are unlikely to still carry
their mothers' antibodies and will have produced their own,
if they are infected. New technologies to detect HIV itself
are being used to more accurately determine HIV infection in
infants between ages 3 months and 15 months. A number of
blood tests are being evaluated to determine if they can
diagnose HIV infection in babies younger than 3
months.
Treatment
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When AIDS first surfaced in the United
States, no drugs were available to combat the underlying
immune deficiency and few treatments existed for the
opportunistic diseases that resulted. Over the past 10 years,
however, therapies have been developed to fight both HIV
infection and its associated infections and
cancers.
The Food and Drug Administration has
approved a number of drugs for the treatment of HIV
infection. The first group of drugs used to treat HIV
infection, called reverse transcriptase (RT) inhibitors,
interrupt an early stage of virus replication. Included in
this class of drugs are AZT (also known as zidovudine), ddC
(zalcitabine), ddI (dideoxyinosine), d4T (stavudine), and 3TC
(lamivudine). These drugs may slow the spread of HIV in the
body and delay the onset of opportunistic infections.
Importantly, they do not prevent transmission of HIV to other
individuals.
Non-nucleoside reverse transcriptase
inhibitors (NNRTIs) such as delvaridine (Rescriptor) and
nevirapine (Viramune) are also available for use in
combination with other antiretroviral
drugs.
More recently, a second class of drugs has
been approved for treating HIV infection. These drugs, called
protease inhibitors, interrupt virus replication at a later
step in its life cycle. They include ritonavir (Norvir),
saquinivir (Invirase), indinavir (Crixivan), and nelfinavir
(Viracept). Because HIV can become resistant to both classes
of drugs, combination treatment using both is necessary to
effectively suppress the virus.
Currently available antiretroviral drugs
do not cure people of HIV infection or AIDS, however, and
they all have side effects that can be severe. AZT may cause
a depletion of red or white blood cells, especially when
taken in the later stages of the disease. If the loss of
blood cells is severe, treatment with AZT must be stopped.
DdI can cause an inflammation of the pancreas and painful
nerve damage.
The most common side effects associated
with protease inhibitors include nausea, diarrhea and other
gastrointestinal symptoms. In addition, protease inhibitors
can interact with other drugs resulting in serious side
effects.
A number of drugs are available to help
treat opportunistic infections to which people with HIV are
especially prone. These drugs include foscarnet and
ganciclovir, used to treat cytomegalovirus eye infections,
fluconazole to treat yeast and other fungal infections, and
TMP/SMX or pentamidine to treat
Pneumocystis carinii pneumonia
(PCP).
In addition to antiretroviral therapy,
adults with HIV whose CD4+ T-cell counts drop below 200 are
given treatment to prevent the occurrence of PCP, which is
one of the most common and deadly opportunistic infections
associated with HIV. Children are given PCP preventive
therapy when their CD4+ T-cell counts drop to levels
considered below normal for their age group. Regardless of
their CD4+ T-cell counts, HIV-infected children and adults
who have survived an episode of PCP are given drugs for the
rest of their lives to prevent a recurrence of the
pneumonia.
HIV-infected individuals who develop
Kaposi's sarcoma or other cancers are treated with radiation,
chemotherapy or injections of alpha interferon, a genetically
engineered naturally occurring protein.
Prevention
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Since no vaccine for HIV is available, the
only way to prevent infection by the virus is to avoid
behaviors that put a person at risk of infection, such as
sharing needles and having unprotected sex.
Because many people infected with HIV have
no symptoms, there is no way of knowing with certainty
whether a sexual partner is infected unless he or she has
been repeatedly tested for the virus or has not engaged in
any risky behavior. The Public Health Service recommends that
people either abstain from sex or protect themselves by using
latex condoms whenever having oral, anal or vaginal sex with
someone they aren't certain is free of HIV or other sexually
transmitted diseases. Only condoms made of latex should be
used, and water-based lubricants should be used with latex
condoms.
Although some laboratory evidence shows
that spermicides can kill HIV organisms, scientists are still
evaluating the usefulness of spermicides in preventing HIV
infection.
The risk of HIV transmission from a
pregnant woman to her fetus is significantly reduced if she
takes AZT during pregnancy, labor and delivery, and her baby
takes it for the first six weeks of life.
Research
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NIAID-supported investigators are
conducting an abundance of research on HIV infection,
including the development and testing of HIV vaccines and new
therapies for the disease and some of its associated
conditions. More than a dozen HIV vaccines are being tested
in people, and many drugs for HIV infection or
AIDS-associated opportunistic infections are either in
development or being tested. Researchers also are
investigating exactly how HIV damages the immune system. This
research is suggesting new and more effective targets for
drugs and vaccines. NIAID-supported investigators also
continue to document how the disease progresses in different
people.
For information about studies of new HIV
therapies, call the AIDS Clinical Trials Information Service:
1-800-TRIALS-A
1-800-243-7012 (TDD/Deaf Access)
For federally approved treatment
guidelines on HIV/AIDS, call the HIV/AIDS Treatment
Information Service:
1-800-HIV-0440
1-800-243-7012 (TDD/Deaf Access)
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