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Saturday, September 06, 2008
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IMMUNOLOGIC
PROFILE
OF PEOPLE
WITH AIDS
It is well established that a number
of viral, rickettsial, fungal, protozoal and bacterial infections can cause transient
T cell decreases (Chandra, 1983). Immune deficiencies due to tumors, autoimmune
diseases, rare congenital disorders, chemotherapy and other factors have been
shown to render certain individuals susceptible to opportunistic infections (Ammann,
1991). As mentioned above, chronic malnutrition following World War II resulted
in PCP in Eastern European children (Walzer, 1990). Transplant recipients treated
with immunosuppressive drugs such as cyclosporin and glucocorticoids often suffer
recurrent diseases due to pathogens such as varicella zoster virus and cytomegalovirus
that also cause disease in HIV-infected individuals (Chandra, 1983; Ammann, 1991).
However, the specific immunologic
profile that typifies AIDS--a progressive reduction of CD4+ T cells resulting
in persistent CD4+ T lymphocytopenia and profound deficits in cellular immunity--is
extraordinarily rare in the absence of HIV infection or other known causes of
immunosuppression. This was recently demonstrated in several surveys that sought
to determine the frequency of idiopathic CD4+ T-cell lymphocytopenia (ICL),
which is characterized by CD4+ T cell counts lower than 300 cells per cubic
millimeter (mm3) of blood in the absence of HIV antibodies or conditions or
therapies associated with depressed levels of CD4+ T cells (reviewed in Fauci,
1993b; Laurence, 1993).
In a CDC survey, only 47 (.02 percent)
of 230,179 individuals diagnosed with AIDS were both HIV-seronegative and had
persistently low CD4+ T cell counts (<300/MM3) IN THE ABSENCE OF CONDITIONS
OR THERAPIES ASSOCIATED WITH IMMUNOSUPPRESSION (SMITH ET AL., 1993).
In the MACS, 22,643 CD4+ T cell determinations
in 2,713 HIV-seronegative homosexual men revealed only one individual with a
CD4+ T cell count persistently lower than 300 cells/mm3, and this individual
was receiving immunosuppressive therapy (Vermund et al., 1993a). A similar review
of another cohort of homosexual and bisexual men found no case of persistently
lowered CD4+ T cell counts among 756 HIV-seronegative men who had no other cause
of immunosuppression (Smith et al., 1993). Analogous results were reported from
the San Francisco Men's Health Study, a population-based cohort recruited in
1984. Among 206 HIV-seronegative heterosexual and 526 HIV-seronegative homosexual
or bisexual men, only one had consistently low CD4+ T cell counts (Sheppard
et al., 1993). This individual also had low CD8+ T cell counts, suggesting that
he had general lymphopenia rather than a selective loss of CD4+ T cells. No
AIDS-defining clinical condition was observed among these HIV-seronegative men.
Studies of blood donors, recipients
of blood and blood products, and household and sexual contacts of transfusion
recipients also suggest that persistently low CD4+ T cell counts are extremely
rare in the absence of HIV infection (Aledort et al., 1993; Busch et al., 1994).
Longitudinal studies of injection-drug users have demonstrated that unexplained
CD4+ T lymphocytopenia is almost never seen among HIV-seronegative individuals
in this population, despite a high risk of exposure to hepatitis B, cytomegalovirus
and other blood-borne pathogens (Des Jarlais et al., 1993; Weiss et al., 1992).
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