Research
Interests:
Our
laboratory is concerned with understanding mechanisms of immune
damage associated with infection with human immune deficiency virus
(HIV). While recent advances in the chemotherapy of HIV infection
have dramatically improved the prognosis for sufferers of this disease,
perhaps half of all patients do not enjoy the full benefit of treatment,
because of drug resistance or difficulty tolerating therapy. Thus,
the need for new therapies is underlined by increasing recognition
of the limitations of currently available anti-HIV treatments. Based
on evidence that host immunity can provide protection from progression
of HIV disease, our approach is to evaluate methods of enhancing
HIV-specific T cell immunity. Our work is patient-oriented, involving
analysis of cellular immune responses in materials derived from
HIV-infected individuals. Our long-term goal is to translate findings
from such investigations into novel approaches to treatment of HIV
disease.
There
are two main projects currently under way in the laboratory:
1.
We are conducting an analysis of the potent immune modulatory drug
thalidomide in patients with chronic HIV disease. Recently, we described
the activity of this compound as a costimulator of T cells, and
subsequently demonstrated the immune stimulatory effect of this
agent when administered to patients with HIV infection. Our data
suggest that this drug may have activity as an immune adjuvant,
and may be used to enhance desirable immune responses directed against
HIV, and to boost responses to vaccines. To test this, we are conducting
a controlled clinical trial in patients with chronic HIV infection.
Endpoints include boosted HIV-specific CD8 and CD4 T cell responses,
and enhanced priming of T cell responses to an experimental immunogen.
Together with in depth immunologic analysis, we are conducting studies
of viral turnover and genetic diversity to see whether treatment-associated
changes in immune function correspond to changes in viral replication.
In parallel with these clinical studies, we are pursuing a laboratory-based
investigation to analyze the cellular and molecular mechanisms of
action of thalidomide and potent analog drugs derived from the parent
molecule.
2.
HIV-infected patients exhibit a wide range of immune system destruction
at the time that treatment with anti-HIV chemotherapy is initiated.
Although some studies have shown that the extent of immune destruction,
as measured by peripheral blood CD4+ T cell counts, predicts to
some extent the degree of immune recovery following effective treatment,
there has been very little analysis of the recovery of HIV-specific
T cell immunity as a function of pre-treatment immune damage. We
are presently devising highly sensitive ex vivo assays of HIV-specific
cellular immune function to enable us to address questions such
as these. In this regard, our central approach is to exploit the
extraordinary efficiency of dendritic cells to stimulate antigen-specific
T cell responses, taking advantage of recent advances that have
facilitated generating these cells from patient blood. The large
and highly diverse HIV-infected population of patients attending
University of Miami-affiliated clinics allows us to design studies
to investigate questions such as these.
Selected
Publications:
Larsson
M, Fonteneau JF, Lirvall M, Haslett P, Lifson JD, Bhardwaj N. Activation
of HIV-1 specific CD4 and CD8 T cells by human dendritic cells:
roles for cross-presentation and non-infectious HIV-1 virus. AIDS.
2002 Jul 5;16(10):1319-29.
Larsson
M, Wilkens DT, Fonteneau JF, Beadle TJ, Merritt MJ, Kost RG, Haslett
PA, Cu-Uvin S, Bhardwaj N, Nixon DF, Shacklett BL. Amplification
of low-frequency antiviral CD8 T cell responses using autologous
dendritic cells.
AIDS. 2002 Jan 25;16(2):171-80.
Hanekom
WA, Hughes J, Haslett PA, Apolles P, Ganiso V, Allin R, Goddard
E, Hussey GD, Kaplan G. The immunomodulatory effects of thalidomide
on human immunodeficiency virus-infected children. J
Infect Dis. 2001 Nov 1;184(9):1192-6. |