PMID- 32863070 OWN - NLM STAT- MEDLINE DCOM- 20200928 LR - 20201218 IS - 1873-2518 (Electronic) IS - 0264-410X (Print) IS - 0264-410X (Linking) VI - 38 IP - 41 DP - 2020 Sep 22 TI - BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis. PG - 6352-6356 LID - S0264-410X(20)31086-0 [pii] LID - 10.1016/j.vaccine.2020.08.045 [doi] AB - 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-CoV-2 and evaluated the hypothesis by utilizing publicly available database and computer algorithms predicting human leukocyte antigen (HLA) class I-binding peptides. We foundthatBCG contains similar 9-amino acid sequences with SARS-CoV-2. 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-CoV-2 could be generated by BCG vaccination. CI - Copyright (c) 2020 The Authors. Published by Elsevier Ltd.. All rights reserved. FAU - Tomita, Yusuke AU - Tomita Y AD - Department of Respiratory Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan. Electronic address: y-tomita@kumadai.jp. FAU - Sato, Ryo AU - Sato R AD - Laboratory of Stem Cell and Neuro-Vascular Biology, Genetics and Developmental Biology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, United States. FAU - Ikeda, Tokunori AU - Ikeda T AD - Laboratory of Clinical Pharmacology and Therapeutics, Faculty of Pharmaceutical Sciences, Sojo University, Japan; Department of Medical Information Sciences and Administration Planning, Kumamoto University Hospital, Japan. FAU - Sakagami, Takuro AU - Sakagami T AD - Department of Respiratory Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20200820 PL - Netherlands TA - Vaccine JT - Vaccine JID - 8406899 RN - 0 (BCG Vaccine) RN - 0 (Epitopes, T-Lymphocyte) RN - 0 (Histocompatibility Antigens Class I) RN - 0 (Viral Vaccines) SB - IM MH - Amino Acid Sequence/genetics MH - BCG Vaccine/*immunology MH - Betacoronavirus/genetics/*immunology MH - CD8-Positive T-Lymphocytes/*immunology MH - COVID-19 MH - Coronavirus Infections/*prevention & control MH - Cross Reactions/immunology MH - Epitopes, T-Lymphocyte/genetics/*immunology MH - Histocompatibility Antigens Class I/immunology MH - Humans MH - Mycobacterium bovis/genetics/immunology MH - Pandemics/*prevention & control MH - Pneumonia, Viral/*prevention & control MH - SARS-CoV-2 MH - Viral Vaccines/immunology PMC - PMC7440160 OTO - NOTNLM OT - Bacillus Calmette-Guerin (BCG) OT - COVID-19 OT - Human leukocyte antigen (HLA) OT - Pandemic OT - Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) COIS- Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. EDAT- 2020/08/31 06:00 MHDA- 2020/09/29 06:00 PMCR- 2020/08/20 CRDT- 2020/09/01 06:00 PHST- 2020/06/04 00:00 [received] PHST- 2020/07/13 00:00 [revised] PHST- 2020/08/18 00:00 [accepted] PHST- 2020/08/31 06:00 [pubmed] PHST- 2020/09/29 06:00 [medline] PHST- 2020/09/01 06:00 [entrez] PHST- 2020/08/20 00:00 [pmc-release] AID - S0264-410X(20)31086-0 [pii] AID - 10.1016/j.vaccine.2020.08.045 [doi] PST - ppublish SO - Vaccine. 2020 Sep 22;38(41):6352-6356. doi: 10.1016/j.vaccine.2020.08.045. Epub 2020 Aug 20.