CHAPTER 103 • THE ATHLETE WITH HIV 603
concentrations in tears, sputum, saliva, and urine but
it is not considered to be highly infectious in these
forms unless they are blood tinged. No HIV has been
found in sweat (LeBlanc, 1993).
- Primary routes of transmission include intimate
sexual contact; parenteral exposure to blood, blood
products, or blood containing body fluids; and
materno-fetal transmission. - HIV is not transmissible through casual contact,
swimming pools, mosquitoes, saliva, sweat, tears,
urine, feces, and inanimate objects (i.e., wrestling
mats, toilet seats, and sinks) (Dorman, 2000).
DIAGNOSIS
SCREENING TESTS
- HIV antibodies are low or absent in the first few
weeks of infection. They may not be produced until
6 weeks after infection and in some instances may not
be detectable until up to 6 months after infection. This
is referred to as the “window period.” Therefore, anti-
body testing following possible exposure is recom-
mended at 6 weeks, 3 months, 6 months, and 1 year. - The most commonly used screening test is the
enzyme-linked immunosorbant assay(ELISA). This
test can identify HIV antibodies in the blood with a
sensitivity of up to 99.5% (ELISA tests have also been
developed to identify HIV antibodies in saliva or
urine). The specificity of the ELISA test, however, is
lower and may lead to false positive results.
Therefore, a positive ELISA must be confirmed with
further testing. - In standard laboratories, if the ELISA test is positive
it is automatically repeated. Two positive ELISA tests
are routinely then confirmed by the Western Blot test,
which identifies antibodies to proteins of a specific
molecular weight. It is only after these confirmatory
tests are positive that an HIV antibody test should be
reported as being a positive test.
FOLLOW-UP TESTING
- The viral load test is performed via polymerase chain
reaction (PCR) or branched DNA (bDNA) testing and
can detect the HIV virus in the blood. Some viral load
tests are sensitive enough to detect as few as five or
less copies of HIV in the blood. - Although it can be used for diagnostic purposes in
some instances, the viral load test is commonly used
in the known HIV positive patient to help assess prog-
nosis and help manage therapy. It is usually suggested
that a baseline measurement be obtained and then the
test be rechecked within 2–8 weeks of initiating or
changing treatment. It can then be followed every 3–4
months.
•Viral genotype and phenotypic resistance assays can
also help guide specific antiretroviral therapy.
•T-cell tests can identify the CD4 count and the
CD4:CD8 ratio in the blood. This information can be
used to assist with managing treatment and initiating
prophylaxis therapy for opportunistic infections.
ATHLETE SPECIFIC CONCERNS
EFFECTS OF HIV ON THE ATHLETE
EXERCISE AND THEIMMUNERESPONSE
INHEALTHYATHLETES
- According to the theory of psychoneuroimmunology,
any stress may be capable of altering immune func-
tion. Exercise is one such stress. - Immunologic changes with exercise include white
blood cell (WBC) increases with brisk exercise,
which may even occur with heavy exertion of only
30 s. Polymorphonuclear neutrophils(PMNs), mono-
cytes, lymphocytes, and natural killer cells also
increase. This increase is caused by increased cardiac
output; displacement of WBCs from reserve pools in
the lung, liver, and spleen; and an increase in epi-
nephrine, which evokes granulocytosis and lympho-
cytosis. The function of natural killer cells may also
increase as a result of the release of cytokines during
exercise. This response falls off if a person becomes
accustomed to an exercise bout, suggesting that the
response is the result of stress and not the inherent
effects of exercise itself. - The lymphocytosis of exercise is brief and after exer-
cise the lymphocyte count will fall within 5 min. A
further delayed fall to below baseline occurs over the
next hour due to the effects of cortisol, which after
exercise is no longer opposed by epinephrine. Counts
return to baseline within 24 h. - Conversely, a leukocytosis and delayed rise in PMNs
is mediated by cortisol, which releases PMNs from
bone marrow. This returns to baseline in about 24 h.
Strenuous exercise may also evoke an acute phase
reactant response and activate complement, and
release tumor necrosis factor, interferons, interleukins,
and other cytokines (Eichner and Calabrese, 1994). - Chronic exercise can have a negative effect on immune
function if there are prolonged periods of intense train-
ing. Natural killer(NK) cell count and leukocyte func-
tion has been shown to decline in swimmers and
runners during periods of intense training. Overtraining