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AIDS AND INJECTION
DRUG USERS
Central to the "risk-AIDS" hypothesis is the notion that chronic injection
drug use causes AIDS (Duesberg, 1992), a view that is contradicted
by numerous studies.
Although some evidence suggests injection drug use can cause certain
immunologic abnormalities, such as reduction in natural killer (NK)
cell activity (reviewed in Kreek, 1990), the specific immune deficit
that leads to AIDS--a progressive reduction of CD4+ T cells resulting
in persistent CD4+ T lymphocytopenia--is rare in HIV-seronegative
injection drug users in the absence of other immunosuppressive conditions
(Des Jarlais et al., 1993; Weiss et al., 1992).
In a survey of 229 HIV-seronegative injection drug users in New
York City, mean CD4+ T cell counts of the group were consistently
over 1000/mm3 (Des Jarlais et al., 1993). Only two individuals had
two CD4+ T cell measurements of fewer than 300/mm3, one of whom
died with cardiac disease and non-Hodgkin's lymphoma listed as the
cause of death. In a study of 180 HIV-seronegative injection drug
users in New Jersey, the participants' average CD4+ T cell count
was 1169/mm3 (Weiss et al., 1992). Two of these individuals, both
with generalized lymphocytopenia, had CD4+ T cell counts less than
300/mm3.
In the MACS, median CD4+ T cell counts of 63 HIV-seronegative injection
drug users rose from 1061/mm3 to 1124/mm3 in a 15 to 21 month follow-up
period (Margolick et al., 1992). In a cross-sectional study, 11
HIV-seronegative, long-term heroin addicts had mean CD4+ T cell
counts of 1500/mm3, while 11 healthy controls had CD4+ T cell counts
of 820 cells/mm3 (Novick et al., 1989).
Recent data also refute the notion that a certain lifetime dosage
of injection drugs is sufficient to cause AIDS in HIV-seronegative
individuals. In a Dutch study, investigators compared 86 HIV-seronegative
individuals who had been injecting drugs for a mean of 7.6 years
with 70 HIV-seropositive people who had injected drugs for a mean
of 9.1 years. Upon enrollment in 1989, CD4+ T cell counts were 914/mm3
in the HIV-seronegative group, and 395/mm3 in the seropositive group.
By 1994, there were 25 deaths attributable to AIDS-defining conditions
in the seropositive group; among HIV-seronegative individuals, eight
deaths occurred, none due to AIDS-defining diseases (Cohen, 1994a).
Excess mortality among HIV-infected injection drug users as compared
to HIV-seronegative users has also been observed by other investigators.
In a prospective Italian study of 2,431 injection drug users enrolled
in drug treatment programs from 1985 to 1991, HIV-seropositive individuals
were 4.5 times more likely to die than HIV-seronegative subjects
(Zaccarelli et al., 1994). No deaths due to AIDS-defining conditions
were seen among 1,661 HIV-seronegative individuals, 41 of whom died
of other conditions, predominantly overdose, liver disease and accidents.
Among 770 individuals who were HIV-seropositive at study entry or
who seroconverted during the study period, 89 died of AIDS-related
conditions and 52 of other conditions.
In HIV-seropositive individuals, a number of investigators have
found no statistical association between injection drug use and
decline of CD4+ T cell counts (Galli et al., 1989, 1991; Schoenbaum
et al., 1989; Margolick et al., 1992, 1994; Montella et al., 1992;
Alcabes et al., 1993b, 1994; Galai et al., 1995), nor a difference
in disease progression between active versus former users of injection
drugs (Weber et al., 1990; Galli et al., 1991; Montella et al.,
1992; Italian Seroconversion Study, 1992).
Taken together, these studies suggest that any negative effects
of injection drugs on CD4+ T cell levels are limited and may explain
why many investigators have found that HIV-seropositive injection
drug users have rates of disease progression that are similar to
other HIV-infected individuals (Rezza et al., 1990; Montella et
al., 1992; Galli et al., 1989; Selwyn et al., 1992; Munoz et al.,
1992; Italian Seroconversion Study, 1992; MAP Workshop, 1993; Pezzotti
et al., 1992; Margolick et al., 1992, 1994; Alcabes, 1993b, 1994;
Galai et al., 1995).
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