The Study to help AIDS Research Effort (SHARE) studies the natural
history of infection with human immuno deficiency virus, type 1 (HIV-
1). SHARE, along with similar sites in Chicago, Pittsburgh, and Los
Angeles, forms the Multicenter AIDS Cohort Study (MACS). MACS
participants, including 1447 enrolled in SHARE, have been followed
semiannually since 1984 and have provided questionnaire data,
physical exam data, laboratory data ( including HIV-1 serostatus and
T - cell subset measurements), and a large repository of plasma,
serum, cryopreserved peripheral blood mononuclear cells and other
specimens. Evaluating and following the prevalent and incident cases
of HIV-1 infection in the MACS including 584 in SHARE, has provided
key insights into risk factor s for infection with HIV-1, progression
of HIV-1 infection once it is established, host defense against HIV-
1, genetic factors affecting HIV-1 pathogenesis, and use and efficacy
of different forms of therapy for HIV-1 infection and for
opportunistic pathogens. SHARE and the MACS have made key
contributions to defining the importance of the measurement of t-
helper (CD4+) lymphocytes, plasma viral load, and immune activation
as pathogenic and prognostic factors in HIV-1 infection. SHARE has
also played a leading role in the MACS neuropsychological studies.
The current project request the continuation of the follow up of the
SHARE cohort from 1999 to 2003. Expected survival and enrollment of
the HIV-1 infected cohort members through this time period is 89%
Specific Aims of the renewal include defining the long-term efficacy
and safety of newer highly active antiretroviral treatments (HAART)
and new clinical outcomes associated with HAART - induced increases
in survival (e.g, neurological and oncological diseases with long
incubation periods); defining prognostic markers for people taking
HAART; and following cohort members for full characterization of
outcomes. These aims can be addressed only with continued follow up
of this extremely well-characterized cohort. Other studies that
depend on such follow up, but will be carried out with collaborators
rather than being directly addressed in this application, include
virological and immunological mechanisms of HIV-1 pathogenesis, and
laboratory correlates of disease progression or non-progression. The
MACS should continue to play a leading role in studies designed to
lead to better treatments and preventive vaccines for HIV-1
infection.
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We apologize for the inconvenience.
- The DCCPS Team.