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									<identifier>oai:www.peertechzpublications.org:10.17352/jvi.000022</identifier>
									<datestamp>2018-03-21</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Measuring autophagy level along with vaccine reactive IFN-+CD4+ Th1 cells may be a promising approach to understand effi cacy of anti TB vaccine(s)
										</dc:title><dc:creator>Om Parkash</dc:creator><dc:description>&lt;p&gt;Autophagy is a homeostatic process in the eukaryotic cells which contributes towards degradation&lt;/p&gt;&lt;p&gt;of unwanted cellular constituents, killing of the invading intracellular microbes and generation of cell&lt;/p&gt;&lt;p&gt;mediated immunity (CMI). The professional antigen presenting cells (APCs) like: macrophages and&lt;/p&gt;&lt;p&gt;dendritic cells, present microbial antigens (derived from engulfed and killed microbe) in combination&lt;/p&gt;&lt;p&gt;with MHC-II to generate IFN-γ producing CD4+ Th1 cells. Over the years, inducing IFN-γ+ CD4+ Th1&lt;/p&gt;&lt;p&gt;mediated CMI has remained, predominantly, as the target for developing anti TB vaccine. In individuals,&lt;/p&gt;&lt;p&gt;where Mycobacterium tuberculosis (MTB) bacilli invading the APCs evade induction of autophagy, anti&lt;/p&gt;&lt;p&gt;TB vaccine may not be effective due to lack of presentation of MTB derived antigens to generate and&lt;/p&gt;&lt;p&gt;re-stimulate vaccine generated memory CD4+ Th1 cells. On the other hand, induction of autophagy in&lt;/p&gt;&lt;p&gt;the APCs kills the invading MTB bacilli and may suffi ciently present microbial antigens to generate and&lt;/p&gt;&lt;p&gt;re-stimulate vaccine generated IFN-γ producing CD4+ Th1 memory cells. The re-stimulated memory cells&lt;/p&gt;&lt;p&gt;then differentiate to effector CD4+ Th1 cells to release IFN-γ which further takes part in activation of&lt;/p&gt;&lt;p&gt;antimicrobial activity in APCs thereby leading to protection of the vaccinees and sustaining the vaccine&lt;/p&gt;&lt;p&gt;generated CMI. Keeping all these points in view, a hypothesis has been described here, wherein it has been&lt;/p&gt;&lt;p&gt;suggested that measuring autophagy activation status in combination with prevalence of IFN-γ producing&lt;/p&gt;&lt;p&gt;memory/effector CD4+ Th1 cells against vaccine antigens may prove to be promising biomarkers for&lt;/p&gt;&lt;p&gt;assessing protective effi cacy of anti TB vaccine(s).&lt;/p&gt;</dc:description>
										<dc:publisher>Journal of Vaccines and Immunology - Peertechz Publications</dc:publisher>
										<dc:date>2018-03-21</dc:date>
										<dc:type>Mini Review</dc:type>
										<dc:identifier>https://doi.org/10.17352/jvi.000022</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Om Parkash et al.</dc:rights>
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