HIV Infections Clinical Trial
Official title:
Pilot Study of an ACh-E Inhibitor Upon Immune Activation Markers in HIV-1 Infected Patients Receiving Highly Active Antiretroviral Therapy (HAART) Showing an Incomplete Immune Response.
The purpose of this study is to determine whether the addition of Pyridostigmine to Highly Active Antiretroviral Therapy (HAART) increases the number of CD4+ T-cells in discordant patients in which viral load diminishes, but T-cell levels remain low after the initiation of treatment.
In HIV-1 infected patients, HAART suppresses viral replication, reflected by a reduced viral
load, and a recovery in the frequency of CD4+ T-cells. The latter is associated with a
reduced risk for developing opportunistic infectious diseases, and death. T-cell recovery,
however, is highly variable within individuals, suggesting that virological eradication is
but one factor of it.
A phenomenon known as Immune Discordance has been well known. It reflects a subpopulation -as
high as 30% of patients- in whom there is an adequate suppression of viral replication, but
CD4+ cell levels rise modestly (below safety levels). In this setting, patients remain
susceptible to develop opportunistic infections, have disease progression, and die. Various
mechanisms have been proposed, but one common factor is enhanced CD4+-cell activation,
leading to cell dysfunction and apoptosis.
It is known that an inflammatory response is able to activate the anti-inflammatory
cholinergic pathway, in which acetylcholine (ACh) is released and in turn activates nicotinic
receptors in macrophages. The result is a diminished synthesis of inflammatory cytokines such
as TNF-α, and IL-1. We have recently shown in an ex-vivo, proof-of-concept study carried in
HIV-infected subjects in early phases of the infection (not requiring specific treatment)
that Pyridostigmine diminishes CD4+-cell activation and an increase in the subpopulation of
regulatory T-cells (T-reg).
Pyridostigmine, an ACh-esterase inhibitor, has been shown to be safe in other populations,
including healthy Gulf War military personnel, and patients with Myasthenia Gravis. Its
hypothetical effect is by reducing the degrading rate of the naturally occurring ACh
(released by the vagus nerve) by the enzyme ACh-esterase. This in turn enhances its coupling
to nicotinic receptors in macrophages that, according to our previous study (unpublished
data), improves the T-cell milieu, diminishes T-cell activation (a well known trigger for
apoptosis), and enhances T-reg proliferation.
The purpose of this study is to determine whether the addition of Pyridostigmine to Highly
Active Antiretroviral Therapy (HAART) increases the number of CD4+ T-cells in discordant
patients in which viral load diminishes, but T-cell levels remain low after the initiation of
treatment.
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