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Saturday, November 22, 2008
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A
BRIEF HISTORY
OF THE EMERGENCE
OF AIDS
In 1981, clinical investigators in
New York and California observed among young, previously healthy, homosexual men
an unusual clustering of cases of rare diseases, notably Kaposi's sarcoma (KS)
and opportunistic infections such as Pneumocystis carinii pneumonia (PCP), as
well as cases of unexplained, persistent lymphadenopathy (CDC, 1981a,b, 1982a;
Masur et al., 1981; Gottlieb et al., 1981; Friedman-Kien, 1981). It soon became
evident that these men had a common immunologic deficit, an impairment in cell-mediated
immunity resulting from a significant loss of "T-helper" cells, which bear the
CD4 marker (Gottlieb et al., 1981; Masur et al., 1981; Siegal et al., 1981; Ammann
et al., 1983a).
The widespread occurrence of KS and
PCP in young people with no underlying disease or history of immunosuppressive
therapy was unprecedented. Searches of the medical literature, autopsy records
and tumor registries revealed that these diseases previously had occurred at
very low levels in the United States (CDC, 1981b; CDC, 1982f).
KS, a very rare skin neoplasm, had
affected mostly older men of Mediterranean origin or cancer or transplant patients
undergoing immunosuppressive therapy (Gange and Jones, 1978; Safai and Good,
1981). Before the AIDS epidemic, the annual incidence of Kaposi's sarcoma in
the United States was 0.02 to 0.06 per 100,000 population (Rothman, 1962a; Oettle,
1962). In addition, a more aggressive form of KS that generally occurred in
younger individuals was seen in certain parts of Africa (Rothman, 1962b; Safai,
1984a). By 1984, never-married men in San Francisco were found to be 2,000 times
more likely to develop KS than during the years 1973 to 1979 (Williams et al.,
1994). As of Dec. 31, 1994, 36,693 patients with AIDS in the United States with
a definitive diagnosis of KS had been reported to the CDC (CDC, 1995b).
PCP, a lung infection caused by a
pathogen to which most individuals are exposed with no undue consequences, was
extremely rare prior to 1981 in individuals other than those receiving immunosuppressive
therapy or among the chronically malnourished, such as certain Eastern European
children following World War II (Walzer, 1990). A 1967 survey, for example,
found only 107 U.S. cases of PCP reported in the medical literature up to that
point, virtually all among individuals with underlying immunosuppressive conditions
or who had undergone immunosuppressive therapy (Le Clair, 1969). In that year,
CDC became the sole supplier in the United States of pentamidine isethionate,
then the only recommended PCP therapy, and began collecting data on each PCP
case diagnosed and treated in this country. After reviewing requests for pentamidine
in the period 1967 to 1970, researchers found only one case of confirmed PCP
without a known underlying condition (Walzer et al., 1974). In the period immediately
prior to the recognition of AIDS, January 1976 to June 1980, CDC received only
one request for pentamidine isethionate to treat an adult in the United States
who had PCP and no underlying disease (CDC, 1982f). In 1981 alone, 42 requests
for pentamidine were received to treat patients with PCP and no known underlying
disorders (CDC, 1982f). By Dec. 31, 1994, 127,626 individuals with AIDS in the
United States with definitive diagnoses of PCP had been reported to the CDC
(CDC, 1995b).
Another rare opportunistic disease,
disseminated infection with the Mycobacterium avium complex (MAC), also was
seen frequently in the first AIDS patients (Zakowski et al., 1982; Greene et
al., 1982). Prior to 1981, only 32 individuals with disseminated MAC disease
had been described in the medical literature (Masur, 1982a). By Dec. 31, 1994,
the CDC had received reports of 28,954 U.S. AIDS patients with definitive diagnoses
of disseminated MAC (CDC, 1995b).
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