Author: Tomita, Yusuke; Sato, Ryo; Ikeda, Tokunori; Sakagami, Takuro
Title: BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: in silico analyses and a hypothesis Cord-id: yip5so4z Document date: 2020_8_20
ID: yip5so4z
Snippet: Abstract The world is facing the rising emergency of SARS-CoV-2. The outbreak of COVID-19 has caused a global public health and economic crisis.Recent epidemiological studies have shown that a possible association of BCG vaccination program with decreased COVID-19-related risks, suggesting that BCG may provide protection against COVID-19. Non-specific protection against viral infections is considered as a main mechanism of BCG and clinical trials to determine whether BCG vaccine can protect heal
Document: Abstract The world is facing the rising emergency of SARS-CoV-2. The outbreak of COVID-19 has caused a global public health and economic crisis.Recent epidemiological studies have shown that a possible association of BCG vaccination program with decreased COVID-19-related risks, suggesting that BCG may provide protection against COVID-19. Non-specific protection against viral infections is considered as a main mechanism of BCG and clinical trials to determine whether BCG vaccine can protect healthcare workers from the COVID-19 are currently underway. We hypothesized that BCG may carry similar T cell epitopes with SARS-CoV2 and evaluated the hypothesis by utilizing publicly available database and computer algorithms predicting human leukocyte antigen (HLA) class Iâ€binding peptides. We foundthatBCG contains similar 9-amino acids sequences with SARS-CoV2. These closely-related peptides had moderate to high binding affinity for multiple common HLA class I molecules, suggesting that cross-reactive T cells against SARS-CoV2 could be generated by BCG vaccination.
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