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Study
puts Indian population at higher risk of fast progression
of HIV infections
Jayashree
Padmini - New Delhi
A Study undertaken by researchers at the All India Institute
of Medical Sciences (AIIMS) indicates a possible genetic
predisposition and fast progression of HIV in infected
Indian population. Reviewing the data on the distribution
patterns of molecular subtypes of HLA (human leukocyte
antigen) class I and class II extended haplotypes in
India with reference to global distributions, the AIIMS
researchers come to the conclusion that Indian HIV positive
population is at higher risk of faster disease progression.
The project, study of Genetic Diversity of Indian population
sponsored by the Department of Biotechnology, was conducted
by Dr N K Mehra, prof and head, and Dr Gurvinder Kaur
of the Department Transplant Immunology & Immunologicals
at AIIMS.
The study being undertaken over a period of 2001-2004,
in 2000 odd sample population from Delhi has also come
across several novel genes associated with HLA in Chromosome
6. "The data available from this study indicates
that Indian HIV positive population is genetically programmed
for disease progression at a faster rate compared to
our western counterparts," explained Dr N K Mehra.
In view of the findings of the HLA study, the team has
submitted a proposal to the Indian Council of Medical
Research to undertake a multi-centric study on a bigger
population group across the country.
Dr N K Mehra said, "The long term goals of the
study will be to identify genetic markers to predict
predisposition to HIV and disease progression."
Similar studies are going on in the western world also
on the role of HLA antigen and susceptibility of HIV
infection. "We would require about Rs 2 to 3 crore
to take up a large study on at least two-three defined
ethnic groups in the country on HIV viral load &
CD4 T-cell count. We need to follow up for around five
years to establish the prevalence as well as to identify
genetic markers," informed Dr Mehra.
The report says that since there is selective predominance
of different HLA alleles and haplotypes in different
populations, a dedicated screening effort is required
at the global level to develop MHC-based (MHC - major
histocompatibility complex) vaccines against infectious
diseases. This will lead to the development of multivalent,
poly-epitope, subtype-specific HIV vaccines that are
specific to the target geographical location. At present
the range and diversity of the genetic and ethnic background
of HIV-1 infected individuals are hardly known.
As the HIV-1 is a highly variable virus, the viral epitopes
that trigger a protective response might differ depending
on the HLA type of the individual, the genetic subtype
of the infectious virus, and the predominant virus that
causes the epidemic in a certain geographical region.
Hence the need to study seropositive/negative populations.
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