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10.1016/j.addr.2021.01.007

http://scihub22266oqcxt.onion/10.1016/j.addr.2021.01.007
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33465451!7832442!33465451
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suck abstract from ncbi


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pmid33465451      Adv+Drug+Deliv+Rev 2021 ; 171 (ä): 29-47
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  • In silico T cell epitope identification for SARS-CoV-2: Progress and perspectives #MMPMID33465451
  • Sohail MS; Ahmed SF; Quadeer AA; McKay MR
  • Adv Drug Deliv Rev 2021[Apr]; 171 (ä): 29-47 PMID33465451show ga
  • Growing evidence suggests that T cells may play a critical role in combating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Hence, COVID-19 vaccines that can elicit a robust T cell response may be particularly important. The design, development and experimental evaluation of such vaccines is aided by an understanding of the landscape of T cell epitopes of SARS-CoV-2, which is largely unknown. Due to the challenges of identifying epitopes experimentally, many studies have proposed the use of in silico methods. Here, we present a review of the in silico methods that have been used for the prediction of SARS-CoV-2 T cell epitopes. These methods employ a diverse set of technical approaches, often rooted in machine learning. A performance comparison is provided based on the ability to identify a specific set of immunogenic epitopes that have been determined experimentally to be targeted by T cells in convalescent COVID-19 patients, shedding light on the relative performance merits of the different approaches adopted by the in silico studies. The review also puts forward perspectives for future research directions.
  • |*Computer Simulation/trends[MESH]
  • |Animals[MESH]
  • |COVID-19 Vaccines/administration & dosage/immunology/*metabolism[MESH]
  • |COVID-19/immunology/*metabolism/prevention & control[MESH]
  • |Epitopes, T-Lymphocyte/immunology/*metabolism[MESH]
  • |Humans[MESH]


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