HIV Infections Clinical Trial
Official title:
Can Anthelminthic Treatment Delay the Progression of HIV? Randomised Open-label Trial Testing Presumptive Anthelminthic Treatment on Progression of HIV in ART-naïve HIV-positive Patients in a Rural African Setting With Presumed High Prevalence of Helminth Infections.
This study focuses on one of the major health issues of Sub-Saharan Africa: multi-parasitism
and co-infections. In particular this study aims to elucidate the interaction of helminths
with HIV.
There is good reason to suspect a detrimental effect of helminth infection on the course of
HIV infection. We hypothesize, that treatment of helminths in HIV- and helminth co-infected
individuals leads to a reduction of HIV viral load. With a lower HIV RNA level one would
expect a slower decline of CD4 cells and hence also a slower progression of the disease.
Ideally this would lead to a prolongation of the chronic phase of HIV infection and to a
delay in the time when anti-retroviral treatment needs to be started.
* Background: On the basis of immunological considerations and in vitro trials on
co-infections there is strong reason to suspect a detrimental effect of helminth infection
on the course of HIV. The immunological answer very efficiently evoked by helminth infection
is aimed at hijacking and suppressing the immune system in order to suit the requirements of
the specific helminth. This permits helminths to cause chronic infection, often persisting
over years and allowing some infecting worms to grow to several centimetres of length within
their host. However, this immune modulation also affects non-related antigens (for example
HIV) which would actually require a different line of immunological action.
Some clinical trials have been able to confirm this detrimental effect of helminths on HIV
infection, while other trials failed to do so. A recent Cochrane review on clinical trials
with HIV and helminth co-infection found an overall slight reduction of HIV viral load if
helminth infection was treated. However there was no measurable effect on CD4 count or
clinical staging of HIV. This might be explained by the fact that these trials were very
heterogeneous in their set-up and were run for too short a time (max 6 months) to allow
sufficient answers to these questions.
According to mathematical models, even a relatively modest reduction of HIV RNA by 0.5 log
could delay the need to start combined antiretroviral therapy by about 3.5 years and
potentially prolong the symptom-free phase of HIV-infection by nearly 1 year. On a
population scale this could lead to substantial savings with regard to drug and clinical
costs and on an individual level to an invaluable gain in drug-free and ideally also
symptom-free life years.
- Objective: To assess the impact of presumptive anthelminthic treatment on HIV
progression in patients infected with HIV in a rural setting with presumed high
prevalence of helminth infection.
- Methods: Randomised open-label trial of presumptive triple anthelminthic treatment in
HIV positive patients not yet requiring anti-retroviral treatment.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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