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)

<p>Autophagy is a homeostatic process in the eukaryotic cells which contributes towards degradation</p><p>of unwanted cellular constituents, killing of the invading intracellular microbes and generation of cell</p><p>mediated immunity (CMI). The professional antigen pre...

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Main Author: Om Parkash (Author)
Format: Book
Published: Journal of Vaccines and Immunology - Peertechz Publications, 2018-03-21.
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042 |a dc 
100 1 0 |a Om Parkash  |e author 
245 0 0 |a 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) 
260 |b Journal of Vaccines and Immunology - Peertechz Publications,   |c 2018-03-21. 
520 |a <p>Autophagy is a homeostatic process in the eukaryotic cells which contributes towards degradation</p><p>of unwanted cellular constituents, killing of the invading intracellular microbes and generation of cell</p><p>mediated immunity (CMI). The professional antigen presenting cells (APCs) like: macrophages and</p><p>dendritic cells, present microbial antigens (derived from engulfed and killed microbe) in combination</p><p>with MHC-II to generate IFN-γ producing CD4+ Th1 cells. Over the years, inducing IFN-γ+ CD4+ Th1</p><p>mediated CMI has remained, predominantly, as the target for developing anti TB vaccine. In individuals,</p><p>where Mycobacterium tuberculosis (MTB) bacilli invading the APCs evade induction of autophagy, anti</p><p>TB vaccine may not be effective due to lack of presentation of MTB derived antigens to generate and</p><p>re-stimulate vaccine generated memory CD4+ Th1 cells. On the other hand, induction of autophagy in</p><p>the APCs kills the invading MTB bacilli and may suffi ciently present microbial antigens to generate and</p><p>re-stimulate vaccine generated IFN-γ producing CD4+ Th1 memory cells. The re-stimulated memory cells</p><p>then differentiate to effector CD4+ Th1 cells to release IFN-γ which further takes part in activation of</p><p>antimicrobial activity in APCs thereby leading to protection of the vaccinees and sustaining the vaccine</p><p>generated CMI. Keeping all these points in view, a hypothesis has been described here, wherein it has been</p><p>suggested that measuring autophagy activation status in combination with prevalence of IFN-γ producing</p><p>memory/effector CD4+ Th1 cells against vaccine antigens may prove to be promising biomarkers for</p><p>assessing protective effi cacy of anti TB vaccine(s).</p> 
540 |a Copyright © Om Parkash et al. 
546 |a en 
655 7 |a Mini Review  |2 local 
856 4 1 |u https://doi.org/10.17352/jvi.000022  |z Connect to this object online.