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F.Seghrouchni1,2*,
M.Amicosante3, L.Baassi1,2, K.Sadki1,
V.Colizzi4,
A.Benjouad2, R.El Aouad1
1Department of Immunology-Virology, National Institute of
Hygiene, Rabat, (MOROCCO)
2Laboratory and UFR of Biochemistry and Immunology,
Department of Biology,
University Mohamed V-Agdel, Rabat, (MOROCCO)
3Department of Internal Medicine, University of Rome “Tor
Vergata”, Rome, (ITALY)
4Department of Biology, University of Rome “Tor Vergata”,
Rome, (ITALY) |
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Tuberculosis (TB) remains a
global health problem and effective control of TB is dependent on the
availability of efficient vaccines and diagnostic tests. However, the
above require the identification of highly specific antigens of
Mycobacterium tuberculosis (M.tb), that are safe enough to be
used in vivo and structurally stable for broad technical application.
However, the purified or recombinant antigens of M.tb are
immunologically quite complex. The potential use of these reagents is
also limited by the technical problems related to their production. HLA-promiscuous
T-cell multi-epitopic peptides (HLA-p.T-c.m-EP) are designed on the
basis of the prediction of sequences that bind to MHC molecules and
their interaction with T-cell receptors in stimulating the immune
system. The gain in time, cost and facile investigation provided by
selection of such HLA-p.T-c.m-EP using bioinformatics, makes possible
the analysis of the immunological aspect of a high number of M.tb
gene products with the aim of better understanding their involvement in
immune host defense against M.tb. This approach could also
provide a rational basis for the development of a subunit vaccine for
TB. Furthermore, the ability of these epitopic peptides to induce
differential responses specifically to distinct stages of the disease
might offer a relevant perspective for better diagnosis of TB. This
review describes the structural and functional characteristics of
HLA-p.T-c.m-EP and emphasizes their use as novel agents for development
of diagnostics and vaccines. |