The findings of this review confirm that the importance of vitamin D metabolites or analogues which can provide a helpful platform to target some kinds of cancer, particularly when used in combination with existing therapies. Moreover, the correlation between vitamin D deficiencies with cardiovascular diseases and rheumatoid arthritis (RA) progression might suggest a pivotal role of vitamin D in either initiation or progression of these diseases.
Background:
Mycobacterium tuberculosis (Mtb) is considered as one of the most efficacious
human pathogens. The global mortality rate of TB stands at approximately 2 million, while about 8 to
10 million active new cases are documented yearly. It is, therefore, a priority to develop vaccines that
will prevent active TB. The vaccines currently used for the management of TB can only proffer a certain
level of protection against meningitis, TB, and other forms of disseminated TB in children; however,
their effectiveness against pulmonary TB varies and cannot provide life-long protective immunity.
Based on these reasons, more efforts are channeled towards the development of new TB vaccines. During
the development of TB vaccines, a major challenge has always been the lack of diversity in both the
antigens contained in TB vaccines and the immune responses of the TB sufferers. Current efforts are
channeled on widening both the range of antigens selection and the range of immune response elicited
by the vaccines. The past two decades witnessed a significant progress in the development of TB vaccines;
some of the discovered TB vaccines have recently even completed the third phase (phase III) of a
clinical trial.
Objective:
The objectives of this article are to discuss the recent progress in the development of new
vaccines against TB; to provide an insight on the mechanism of vaccine-mediated specific immune
response stimulation, and to debate on the interaction between vaccines and global interventions to end
TB.
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