Tuberculosis:
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Tuberculosis
is a chronic bacterial infection, which causes more death world-wide than
any other infectious disease. The bacteria
Mycobacterium tuberculosis
is spread through the air and usually affects the lungs, though some other
organs are sometimes involved. Most who are infected with M. tuberculosis
do not develop active tuberculosis. However, in weak immune systems, the
chances are raised
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With
appropriate antibiotic therapy, most cases of tuberculosis can be cured,
but drug-resistant strains are becoming more prevalent. Drug resistance
occurs when the patient fails to take all of their medicine, thus the remaining
strain grows resistant to the antibiotic. This may also occur if the patient
is treated with too few drugs or small doses
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During
the nineteenth century, tuberculosis claimed more lives in the United States
than any other disease. Improvements in housing, sanitation, and medicine
reduced dramatically those numbers. By the 1980's the number of cases was
little over twenty-two thousand. After 1985, however, the tides changed.
The HIV/AIDS epidemic was one factor. This with weakened immune systems
are vulnerable to reactivation of latent infection. Another cause is the
increase of immigrants from countries where tuberculosis is more common.
Increased poverty and drug use spread the disease. There has been poor
compliance to treatment regimes, especially amongst disadvantaged groups,
encouraging mutations and multi-drug resistant strains. The number of residents
in long-term care facilities has increased. With age, the immune system
declines, and latent infections become active
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Tuberculosis
is caused by repeated exposure to airborne droplets contaminated with the
rod-shaped bacterium, M. tuberculosis. Sometimes, rarely, the bacteria
is M. africanum or M. bovis. M. tuberculosis, like other mycobacterium,
has an unusual cell wall, a waxy coating high in lipid count. Little is
known about the membranes structure or function. This cell wall seems to
allow the bacterium to survive in macrophage, cells of the immune system
which ordinarily degrade invaders with enzymes. The coat also blocks many
common drugs. Mycobacterium are called "acid fast", because their fatty
cell walls prevent decolorization by acid solutions after staining for
diagnostic procedures. M. tuberculosis is difficult to study in a lab environment.
It multiplies slowly-- only once every twenty-four hours-- and they form
clump, making working with and counting them difficult. It is airborne,
and so can only be studied under very secure conditions
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Only
those with active tuberculosis can spread it, but the droplet nuclei remain
airborne for long periods of time. They are small enough to bypass the
defenses of the upper respiratory system, such as hairs and excretions
of the mucosae. Infection begins when the bacterium reach the alveoli,
where they multiply within macrophages. Those who have been undergoing
treatment for at least two weeks are not usually infectious
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The
macrophages ingest the bacterium. Some are killed immediately, other multiply.
Rarely, most time is HIV-sufferers and children, the infection spreads
to other body sites, sometime resulting in life-threatening bacterial meningitis.
During the two to eight weeks after infection, macrophages show pieces
of the bacilli on the cells surface to other leukocytes, called T-cells.
The T-cells release an elaborate set of chemical signals. The response
it called cell-mediated hypersensitivity. This hypersensitivity will show
the characteristic red welt in response to the tuberculin skin test (PDD
test). Some T-cell signals produce inflammatory reactions. Others activate
cells to kill bacterium and wall off infected macrophages in hard, grey
capsules called tubercles. The immune system and the infection maintain
a stand-off, sometimes for years. In the tubercles, tuberculosis bacilli
may persist within the macrophages, but multiplication and spread is confined.
Most undergo a complete healing of the initial infection. The tubercles
calcify and become useless. A skin test and perhaps a chest x-ray my provide
the only evidence of the struggle
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Only
about ten percent f people infected with the disease develop active tuberculosis.
The risk is highest in the first year after the initial infection. Active
tuberculosis results from the spread of bacterium from the alveoli through
the bloodstream or lymphatic system to other parts of the lungs or lymph
nodes. In about fifteen percent of cases, the bacterium cam travel to the
skin, kidneys, bones, and reproductive or urinary systems. At the new sites,
the body fights as before and kill the bacilli, but tissue is also killed.
The dead cells and tissues form granulomas with the consistency of soft
cheese, where the bacterium survive, though they do not flourish. Early
signs of active tuberculosis may include weight lose, fever, sweats, and
loss of appetite. As more tissue is destroyed and granulomas expand, cavities
develop in the lungs, sometimes breaking the bronchi, allowing a large
number of bacteria to escape when the sufferer coughs. As the disease progresses,
the granulomas may liquify, perhaps the result of enzymes from the immune
cells. The liquid is a rich growth medium for the bacteria, who multiply
and spread quickly, creating further lesion and chest pain, coughing, and
bloody sputum when a blood vessel is broken. Shortness of breath does not
come until the lungs are extensively damaged
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The
skin test, or Montoux test, can identify most of those infected with tuberculosis.
A substance known as purified protein derivative in injected hypodermically
into the antibrachial and observed for 48 to 72 hours. A red welt is positive
for infection, previous or current, active or not. If the test is positive,
x-rays may show the lesions and cavities of active tuberculosis. Samples
of sputum are also taken for cultures
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Recently,
researchers have developed a test utilizing nucleic acids to diagnose tuberculosis.
Luminescent chemicals from fireflies are also being experimented with to
find out what drugs may be used to kill the bacterium
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The
death rate among untreated tuberculosis sufferers is about fifty percent,
but with treatment, that number can be taken down to ten. The drugs isoniazid
and rifampin are given in tandem for or at least six months, and pyrazinamide
for the first two. This is refereed to as short-course chemotherapy. Sometimes
ethambutol is also given. A second line of drugs is often needed, with
serious side effects, the treatment itself lasting from 18 months to two
years
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In
parts of the world where tuberculosis is common, a weakened strain of it
is given as a vaccine, which helps prevent spread, but does not stop the
initial infection. It makes the skin test pointless, however, and is not
used in the United States
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