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HAART
AND ITS CONTROVERSIES
A.
Meliço Silvestre
Direcção do Departamento de Doenças
Infecciosas, Hospitais da Universidade de Coimbra, Portugal
Since
the beginning of HAART clinical practice, we are now, seven
years after, trying to analyse the results and discuss the
controversial of this important improvement, trying to maximize
results for the welfare of our patients and dealing with
viral load/CD4+ count paradigm.
Meanwhile, we all know, clinicians and researchers, the
multitude of unanswered questions. When so many questions
are placed, we deliberately stress the experience and modest
contribution of our clinical and basic research team.
The virus is evolving. In Portugal we are facing non-B subtypes
and recombinant strains, not knowing until now the effectiveness
of our drugs over them. Could this lead to the begging of
new epidemics?
The viral proteins, stressed by antiretrovirals, are mutating
and resisting to medica-
tion
but is this so linear?
The apparent efficacy of HAART can not destroy viral sanctuaries,
being calculated that we probably need more than 60 years
to eradicate the infection. This led us to Blood Brain Barrier
and what is behind AIDS dementia and PML
What about patient genetic factors? What is the clinical
importance of MDR1 gene expression on antiretrovirals cell
penetration?
Another problem that we face is the antiretrovirals adherence.
New easily taken regimens are entering the market, but arent
we forgetting social/psychological patients support?
And when we achieve to constrain the virus and we have an
immune reconstitution syndrome?
And what about metabolic disorders?
We clinicians and researchers face an enormous task ...
always underlining that our main thought is the HIV patient.
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