In-silico identification of subunit vaccine candidates against lung cancer-associated oncogenic viruses. (March 2021)

• Record Type: Journal Article
• Authors: Lathwal, Anjali; Kumar, Rajesh; Raghava, Gajendra P.S.
• Is Part Of: Computers in biology and medicine. Volume 130(2021)
• Publication Date: 2021-03
• Subjects: Oncogenic viruses -- Lung cancer -- Antigenic epitopes -- Promiscuous epitopes -- Immune-stimulatory potential -- Prediction pipeline -- Subunit vaccine -- Proteome -- Immunoinformatics -- Reverse vaccinology; Medicine -- Data processing -- Periodicals; Biology -- Data processing -- Periodicals; 610.285
• DOI: 10.1016/j.compbiomed.2021.104215
• Languages: English
• ISSNs: 0010-4825

Abstract

Abstract: Globally, ~20% of cancer malignancies are associated with virus infections. Lung cancer is the most prevalent cancer and has a 10% 5-year survival rate when diagnosed at stage IV. Cancer vaccines and oncolytic immunotherapy are promising treatment strategies for better clinical outcomes in advanced-stage cancer patients. Here, we used a reverse vaccinology approach to devise subunit vaccine candidates against lung cancer-causing oncogenic viruses. Protein components (945) from nine oncogenic virus species were systematically analyzed to identify epitope-based subunit vaccine candidates. Best vaccine candidates were identified based on their predicted ability to stimulate humoral and cell-mediated immunity and avoid self-tolerance. Using a rigorous integrative approach, we identified 125 best antigenic epitopes with predicted B-cell, T-cell, and/or MHC-binding capability and vaccine adjuvant potential. Thirty-two of these antigenic epitopes were predicted to have IL-4/IFN-gamma inducing potential and IL-10 non-inducing potential and were predicted to bind 15 MHC-type I and 49 MHC-type II alleles. All 32 epitopes were non-allergenic and 31 were non-toxic. The identified epitopes showed good conservancy and likely bind a broad class of human HLA alleles, indicating promiscuous potential. The majority of best antigenic epitopes were derived from Human papillomavirus and Epstein-Barr virus proteins. Of the 32 epitopes, 25 promiscuous epitopes were related to E1 and E6 envelope genes and were present in multiple viral strains/species, potentially providing heterologous immunity. Further validating our results, 38 antigenic epitopes were also present in the largest experimentally-validated epitope resource, Immune Epitope Database and Analysis Resource. We further narrowed the selection to 29 antigenic epitopes with the highest immunogenic/immune-boosting potential. These epitopes possess tremendous therapeutic potential as vaccines against lung cancer-causing viruses and should be validated in future experiments. All findings are available at https://webs.iiitd.edu.in/raghava/vlcvirus/ . Highlights: Identification of best antigenic epitopes against lung cancer-causing viruses. The identified epitopes may stimulate innate and adaptive immune system. The identified epitopes can work as vaccine adjuvants. The promiscuous epitopes may also provide heterologous immunity across strains/species. Validation of predicted epitopes was done using IEDB dataset.