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10.1016/j.cell.2021.01.007 http://scihub22266oqcxt.onion/10.1016/j.cell.2021.01.007 33497610!7803150!33497610     free     free     free       Cell 2021 ; 184 (4): 861-880 Nephropedia Template TP {{tp|p=33497610|t=2021. Adaptive immunity to SARS-CoV-2 and COVID-19 |pdf=|usr=}}{{33497610}} gab.com Text Adaptive immunity to SARS-CoV-2 and COVID-19 JO: Cell http://www.kidney.de/pget.php?&tw=1&pmid=33497610 #FOAvip The adaptive immune system is important for control of most viral infections. The three fundamental components of the adaptive immune system are B cells (the source of antibodies), CD4(+) T cells, and CD8(+) T cells. The armamentarium of B cells, CD4(+) T cells, and CD8(+) T cells has differing roles in different viral infections and in vaccines, and thus it is critical to directly study adaptive immunity to SARS-CoV-2 to understand COVID-19. Knowledge is now available on relationships between antigen-specific immune responses and SARS-CoV-2 infection. Although more studies are needed, a picture has begun to emerge that reveals that CD4(+) T cells, CD8(+) T cells, and neutralizing antibodies all contribute to control of SARS-CoV-2 in both non-hospitalized and hospitalized cases of COVID-19. The specific functions and kinetics of these adaptive immune responses are discussed, as well as their interplay with innate immunity and implications for COVID-19 vaccines and immune memory against re-infection. Twit Text FOAVip Adaptive immunity to SARS-CoV-2 and COVID-19 ????Cell http://www.kidney.de/pget.php?&tw=1&pmid=33497610 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33497610 #FOAvip English Wikipedia <ref>{{Cite pmid|33497610}}</ref> Adaptive immunity to SARS-CoV-2 and COVID-19 #MMPMID33497610 Sette A; Crotty S Cell 2021[Feb]; 184 (4): 861-880 PMID33497610show ga The adaptive immune system is important for control of most viral infections. The three fundamental components of the adaptive immune system are B cells (the source of antibodies), CD4(+) T cells, and CD8(+) T cells. The armamentarium of B cells, CD4(+) T cells, and CD8(+) T cells has differing roles in different viral infections and in vaccines, and thus it is critical to directly study adaptive immunity to SARS-CoV-2 to understand COVID-19. Knowledge is now available on relationships between antigen-specific immune responses and SARS-CoV-2 infection. Although more studies are needed, a picture has begun to emerge that reveals that CD4(+) T cells, CD8(+) T cells, and neutralizing antibodies all contribute to control of SARS-CoV-2 in both non-hospitalized and hospitalized cases of COVID-19. The specific functions and kinetics of these adaptive immune responses are discussed, as well as their interplay with innate immunity and implications for COVID-19 vaccines and immune memory against re-infection. |*Adaptive Immunity[MESH] |Age Factors[MESH] |B-Lymphocytes/immunology[MESH] |COVID-19 Vaccines/immunology[MESH] |COVID-19/complications/epidemiology/*immunology/pathology/virology[MESH] |Clinical Trials as Topic[MESH] |Humans[MESH] |Immunologic Memory[MESH] |Post-Acute COVID-19 Syndrome[MESH] |Race Factors[MESH] |SARS-CoV-2/classification/*physiology[MESH] |Sex Factors[MESH] |T-Lymphocyte Subsets/immunology[MESH]Adaptive immunity to SARS-CoV-2 and COVID-19 (epmc).pdf DeepDyve Pubget Overpricing