Possible Cross-Reactivity between SARS-CoV-2 Proteins, CRM197 and Proteins in Pneumococcal Vaccines May Protect Against Symptomatic SARS-CoV-2 Disease and Death
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Root-Bernstein, R. (2020). Age and Location in Severity of COVID-19 Pathology: Do Lactoferrin and Pneumococcal Vaccination Explain Low Infant Mortality and Regional Differences?. BioEssays.
Pawlowski, C., Puranik, A., Bandi, H., Venkatakrishnan, A.J., Agarwal, V., Kennedy, R., O’Horo, J.C., Gores, G.J., Williams, A.W., and Halamka, J. (2020). Exploratory analysis of immunization records highlights decreased SARS-CoV-2 rates in individuals with recent non-COVID-19 vaccinations. medRxiv.
Watanabe, Y., Allen, J.D., Wrapp, D., McLellan, J.S., and Crispin, M. (2020). Site-specific glycan analysis of the SARS-CoV-2 spike. Science, eabb9983.
Shajahan, A., Supekar, N.T., Gleinich, A., and Azadi, P. (2020). Deducing the N- and O-glycosylation profile of the spike protein of novel coronavirus SARS-CoV-2. Glycobiology.
WHO (2009). Recommendations to Assure the Quality, Safety and Efficacy of Pneumococcal Conjugate Vaccines, World Health Organization.
Lee, 2020, Quality Improvement of Capsular Polysaccharide in Streptococcus pneumoniae by Purification Process Optimization, Front. Bioeng. Biotechnol., 8, 39, 10.3389/fbioe.2020.00039
Morais, V., Dee, V., and Suárez, N. (2018). Purification of Capsular Polysaccharides of Streptococcus pneumoniae: Traditional and New Methods. Front. Bioeng. Biotechnol., 6.
Yu, 1999, Pneumococcal Capsular Polysaccharide Preparations May Contain Non-C-Polysaccharide Contaminants That Are Immunogenic, Clin. Diagn. Lab. Immunol., 6, 519, 10.1128/CDLI.6.4.519-524.1999
Yu, 2003, Immunogenic Protein Contaminants in Pneumococcal Vaccines, J. Infect. Dis., 187, 1019, 10.1086/368200
Briles, 1999, The pspC Gene of Streptococcus pneumoniae Encodes a Polymorphic Protein, PspC, Which Elicits Cross-Reactive Antibodies to PspA and Provides Immunity to Pneumococcal Bacteremia, Infect. Immun., 67, 6533, 10.1128/IAI.67.12.6533-6542.1999
Ogunniyi, 2001, Protection against Streptococcus pneumoniae Elicited by Immunization with Pneumolysin and CbpA, Infect. Immun., 69, 5997, 10.1128/IAI.69.10.5997-6003.2001
Resemann, 2016, Cross Reactive Material 197 glycoconjugate vaccines contain privileged conjugation sites, Sci. Rep., 6, 20488, 10.1038/srep20488
Rudensky, 1991, Sequence analysis of peptides bound to MHC class II molecules, Nature, 353, 622, 10.1038/353622a0
Hemmer, 2000, Minimal peptide length requirements for CD4+ T cell clones—Implications for molecular mimicry and T cell survival, Int. Immunol., 12, 375, 10.1093/intimm/12.3.375
Miles, 2013, Peptide length determines the outcome of TCR/peptide-MHCI engagement, Blood, 121, 1112, 10.1182/blood-2012-06-437202
Cunningham, 1989, Human and murine antibodies cross-reactive with streptococcal M protein and myosin recognize the sequence GLN-LYS-SER-LYS-GLN in M protein, J. Immunol., 143, 2677, 10.4049/jimmunol.143.8.2677
Kanduc, 2009, Quantifying the possible cross-reactivity risk of an HPV16 vaccine, J. Exp. Ther. Oncol., 8, 65
2009, Autoreactive T-cell receptor (Vbeta/D/Jbeta) sequences in diabetes are homologous to insulin, glucagon, the insulin receptor, and the glucagon receptor, J. Mol. Recognit., 22, 177, 10.1002/jmr.930
2014, Rethinking Molecular Mimicry in Rheumatic Heart Disease and Autoimmune Myocarditis: Laminin, Collagen IV, CAR, and B1AR as Initial Targets of Disease, Front. Pediatr., 2, 85
2012, T Cell Receptor Variable Regions in Diabetes Bind to Each Other, to Insulin, Glucagon or Insulin Receptor, and to Their Antibodies, Open Autoimmun. J., 4, 10, 10.2174/1876894601204010010
2015, How to Make a Non-Antigenic Protein (Auto) Antigenic: Molecular Complementarity Alters Antigen Processing and Activates Adaptive-Innate Immunity Synergy, Anti-Cancer Agents Med. Chem., 15, 1242, 10.2174/1871520615666150716105057
Takiishi, 2017, Intestinal barrier and gut microbiota: Shaping our immune responses throughout life, Tissue Barriers, 5, e1373208, 10.1080/21688370.2017.1373208
Damian, 1965, Molecular Mimicry in Biological Adaptation, Science, 147, 824, 10.1126/science.147.3660.824.c
Moise, 2014, Immune camouflage: Relevance to vaccines and human immunology, Hum. Vaccines Immunother., 10, 3570, 10.4161/hv.36134
Moise, 2016, T cell epitope redundancy: Cross-conservation of the TCR face between pathogens and self and its implications for vaccines and autoimmunity, Expert Rev. Vaccines, 15, 607, 10.1586/14760584.2016.1123098
2016, Autoimmunity and the microbiome: T-cell receptor mimicry of “self” and microbial antigens mediates self tolerance in holobionts, BioEssays, 38, 1068, 10.1002/bies.201600083
Root-Bernstein, R. (2017). Human Immunodeficiency Virus Proteins Mimic Human T Cell Receptors Inducing Cross-Reactive Antibodies. Int. J. Mol. Sci., 18.
FDA (2020, June 28). Package Insert. PNEUMOVAX 23 1983, Available online: https://www.fda.gov/media/80547/download.
CDC (2020, June 28). About Diphtheria, Tetanus, and Pertussis Vaccines, Available online: https://www.cdc.gov/vaccines/vpd/dtap-tdap-td/hcp/about-vaccine.html.
Grifoni, 2020, Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals, Cell, 181, 1489, 10.1016/j.cell.2020.05.015
Mateus, J., Grifoni, A., Tarke, A., Sidney, J., Ramirez, S.I., Dan, J.M., Burger, Z.C., Rawlings, S.A., Smith, D., and Phillips, E.J. (2020). Selective and cross-reactive SARS-CoV-2 T cell epitopes in unexposed humans. Science, eabd3871.
Sette, 2020, Pre-existing immunity to SARS-CoV-2: The knowns and unknowns, Nat. Rev. Immunol., 20, 1
Merckx, 2020, Transmission of SARS-CoV-2 by Children, Dtsch. Arztebl. Int., 117, 553
Zhang, 2020, Secondary Transmission of Coronavirus Disease from Presymptomatic Persons, China, Emerg. Infect. Dis., 26, 1924, 10.3201/eid2608.201142
Kam, 2020, A Well Infant with Coronavirus Disease 2019 with High Viral Load, Clin. Infect. Dis., 71, 847, 10.1093/cid/ciaa201
Qian, 2020, COVID-19 Transmission Within a Family Cluster by Presymptomatic Carriers in China, Clin. Infect. Dis., 71, 861, 10.1093/cid/ciaa316
Ye, 2020, Delivery of infection from asymptomatic carriers of COVID-19 in a familial cluster, Int. J. Infect. Dis., 94, 133, 10.1016/j.ijid.2020.03.042
Puolakkainen, 2000, Picornavirus proteins share antigenic determinants with heat shock proteins 60/65, J. Med. Virol., 62, 383, 10.1002/1096-9071(200011)62:3<383::AID-JMV11>3.0.CO;2-#
Misko, 1999, Crossreactive recognition of viral, self, and bacterial peptide ligands by human class I-restricted cytotoxic T lymphocyte clonotypes: Implications for molecular mimicry in autoimmune disease, Proc. Natl. Acad. Sci. USA, 96, 2279, 10.1073/pnas.96.5.2279
Trama, 2014, HIV-1 Envelope gp41 Antibodies Can Originate from Terminal Ileum B Cells that Share Cross-Reactivity with Commensal Bacteria, Cell Host Microbe, 16, 215, 10.1016/j.chom.2014.07.003
Williams, 2015, Diversion of HIV-1 vaccine-induced immunity by gp41-microbiota cross-reactive antibodies, Science, 349, aab1253, 10.1126/science.aab1253
Ross, 1990, Elimination of Mycoplasmal Plate Agglutination Cross-Reactions in Sera from Chickens Inoculated with Infectious Bursal Disease Viruses, Avian Dis., 34, 663, 10.2307/1591261
Bordenave, 1973, L’idiotypie comparée des anticorps de lapins différents contresalmonella abortus-equi et contre le virus de la mosaique du tabac. observation d’une réactivité croisée entre certains idiotypes d’anticorps contre ces deux matériels antigéniques, Eur. J. Immunol., 3, 726, 10.1002/eji.1830031114
2005, Vaccination markers: Designing unique antigens to be added to vaccines to differentiate between natural infection and vaccination, Vaccine, 23, 2057, 10.1016/j.vaccine.2005.01.008
Ashford, J.W., Franklin, R., Young, A., Neumann, B., Fernandez, R., Joannides, A., Reyahi, A., and Modis, Y. (2020). Faculty Opinions recommendation of Homologous protein domains in SARS-CoV-2 and measles, mumps and rubella viruses: Preliminary evidence that MMR vaccine might provide protection against COVID-19. Fac. Opin. Post Publ. Peer Rev. Biomed. Lit.
Ashford, J.W., Gold, J.E., Tilley, L.P., and Baumgartl, W. (2020). Faculty Opinions recommendation of MMR Vaccine Appears to Confer Strong Protection from COVID-19: Few Deaths from SARS-CoV-2 in Highly Vaccinated Populations. Fac. Opin. Post Publ. Peer Rev. Biomed. Lit.
Chumakov, K., and Gallo, R. (2020, April 21). Could an Old Vaccine be a Godsend for New Coronavirus? Using the Oral Polio Vaccine Could Prevent or Reduce the Spread of COVID-19 to Immunized Individuals. USA Today. 21 April 2020. Available online: https://www.usatoday.com/story/opinion/2020/04/21/oral-polio-vaccine-has-potential-treat-coronavirus-column/5162859002/.
Netea, 2020, Trained Immunity: A Tool for Reducing Susceptibility to and the Severity of SARS-CoV-2 Infection, Cell, 181, 969, 10.1016/j.cell.2020.04.042
Gualerzi, 2020, Stop playing with data: There is no sound evidence that Bacille Calmette-Guérin may avoid SARS-CoV-2 infection (for now), Acta Bio Med. Atenei Parm., 91, 207
Hamiel, 2020, SARS-CoV-2 Rates in BCG-Vaccinated and Unvaccinated Young Adults, JAMA, 323, 2340, 10.1001/jama.2020.8189
Pereira, 2020, The need for fast-track, high-quality and low-cost studies about the role of the BCG vaccine in the fight against COVID-19, Respir. Res., 21, 1, 10.1186/s12931-020-01439-4
Bosmans, 1987, Purification, partial characterization, and identification of a skin-reactive protein antigen of Mycobacterium bovis BCG, Infect. Immun., 55, 245, 10.1128/iai.55.1.245-252.1987
Harboe, 1992, Protein Antigens of Mycobacteria Studied by Quantitative Immunologic Techniques, Clin. Infect. Dis., 14, 313, 10.1093/clinids/14.1.313
Romain, 1993, Identification of a Mycobacterium bovis BCG 45/47-kilodalton antigen complex, an immunodominant target for antibody response after immunization with living bacteria, Infect. Immun., 61, 742, 10.1128/iai.61.2.742-750.1993
Aguilo, 2017, Reactogenicity to major tuberculosis antigens absent in BCG is linked to improved protection against Mycobacterium tuberculosis, Nat. Commun., 8, 16085, 10.1038/ncomms16085
Mustafa, 2006, Immunogenicity of Mycobacterium tuberculosis Antigens in Mycobacterium bovis BCG-Vaccinated and M. bovis-Infected Cattle, Infect. Immun., 74, 4566, 10.1128/IAI.01660-05
Morens, 2008, Predominant Role of Bacterial Pneumonia as a Cause of Death in Pandemic Influenza: Implications for Pandemic Influenza Preparedness, J. Infect. Dis., 198, 962, 10.1086/591708
Stefani, 2013, Prevention of Cervical Cancer in Women: Human Papillomavirus DNA Testing in Atypical Pap Smears, J. Virol. Antivir. Res., 2, 1, 10.4172/2324-8955.1000104
Cucchiari, D., Pericàs, J.M., Riera, J., Gumucio, R., Coloma, E., Nicolás, D., and Hospital Clínic 4H Team (2020). Pneumococcal superinfection in COVID-19 patients: A series of 5 cases. Med. Clín.
Clancy, C.J., and Nguyen, M.H. (2020). COVID-19, superinfections and antimicrobial development: What can we expect?. Clin. Infect. Dis.
Rawson, T.M., Moore, L.S.P., Zhu, N., Ranganathan, N., Skolimowska, K., Gilchrist, M., Satta, G., Cooke, G., and Holmes, A. (2020). Bacterial and Fungal Coinfection in Individuals With Coronavirus: A Rapid Review To Support COVID-19 Antimicrobial Prescribing. Clin. Infect. Dis., 530.
Xia, 2020, Clinical and CT features in pediatric patients with COVID-19 infection: Different points from adults, Pediatr. Pulmonol., 55, 1169, 10.1002/ppul.24718
Wang, 2020, Coronavirus disease 2019 in elderly patients: Characteristics and prognostic factors based on 4-week follow-up, J. Infect., 80, 639, 10.1016/j.jinf.2020.03.019
Zhang, J.-J., Dong, X., Cao, Y.-Y., Yuan, Y.-D., Yang, Y.-B., Yan, Y.-Q., Akdis, C.A., and Gao, Y. (2020). Clinical characteristics of 140 patients infected with SARS-CoV-2 in Wuhan, China. Allergy.
Liu, 2019, Viral and Bacterial Etiology of Acute Febrile Respiratory Syndrome among Patients in Qinghai, China, Biomed. Environ. Sci., 32, 438
Guan, 2020, Clinical Characteristics of Coronavirus Disease 2019 in China, N. Engl. J. Med., 382, 1708, 10.1056/NEJMoa2002032
Zhou, 2020, Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: A retrospective cohort study, Lancet, 395, 1054, 10.1016/S0140-6736(20)30566-3
Zhu, 2020, Co-infection with respiratory pathogens among COVID-2019 cases, Virus Res., 285, 198005, 10.1016/j.virusres.2020.198005
Lavoignet, 2019, White blood cell count and eosinopenia as valuable tools for the diagnosis of bacterial infections in the ED, Eur. J. Clin. Microbiol. Infect. Dis., 38, 1523, 10.1007/s10096-019-03583-2
Debray, 2019, Eosinopenia as a marker of diagnosis and prognostic to distinguish bacterial from aseptic meningitis in pediatrics, Eur. J. Clin. Microbiol. Infect. Dis., 38, 1821, 10.1007/s10096-019-03614-y
Poelen, 2019, Prediction and Validation of Immunogenic Domains of Pneumococcal Proteins Recognized by Human CD4+ T Cells, Infect. Immun., 87, e00098-19, 10.1128/IAI.00098-19
Briles, 2000, The potential to use PspA and other pneumococcal proteins to elicit protection against pneumococcal infection, Vaccine, 18, 1707, 10.1016/S0264-410X(99)00511-3
Ferreira, 2009, Characterization of Protective Mucosal and Systemic Immune Responses Elicited by Pneumococcal Surface Protein PspA and PspC Nasal Vaccines against a Respiratory Pneumococcal Challenge in Mice, Clin. Vaccine Immunol., 16, 636, 10.1128/CVI.00395-08
Schachern, 2014, Pneumococcal PspA and PspC proteins: Potential vaccine candidates for experimental otitis media, Int. J. Pediatr. Otorhinolaryngol., 78, 1517, 10.1016/j.ijporl.2014.06.024
Lagousi, T., Basdeki, P., Routsias, J.G., and Spoulou, V. (2019). Novel Protein-Based Pneumococcal Vaccines: Assessing the Use of Distinct Protein Fragments Instead of Full-Length Proteins as Vaccine Antigens. Vaccines, 7.
Masomian, M., Ahmad, Z., Gew, L.T., and Poh, C.L. (2020). Development of Next Generation Streptococcus pneumoniae Vaccines Conferring Broad Protection. Vaccines, 8.
Fedson, 2011, Pneumococcal polysaccharide vaccination for adults: New perspectives for Europe, Expert Rev. Vaccines, 10, 1143, 10.1586/erv.11.99
Mahamat, 2013, Additive preventive effect of influenza and pneumococcal vaccines in the elderly, Hum. Vaccines Immunother., 9, 128, 10.4161/hv.22550
Choi, Y.H., and Miller, E. (2020). Potential impact of Covid-19 response measures on invasive pneumococcal disease in England and Wales. MedRxiv.
National Institute for Communicable Diseases (South Africa) (2020, July 10). Pneumococcal Conjugate Vaccine Use in the Light of the COVID-19 Pandemic. Available online: https://www.nicd.ac.za/diseases-a-z-index/covid-19/advice-for-the-public/pneumococcal-conjugate-vaccine-use-in-the-light-of-the-covid-19-pandemic/.
Statens Serum Institut (2020, April 07). Selected Risk Groups are Offered free Pneumococcal Vaccination. Available online: https://www.sst.dk/da/Nyheder/2020/Udvalgte-risikogrupper-faar-tilbud-om-gratis-vaccination-mod-pneumokokker.
(2020, August 19). New Zealand. Policy on Pneumococcal Vaccination and COVID. Available online: https://www.nzdoctor.co.nz/article/news/pneumococcal-vax-potential-option-improve-outcomes-compromised-patients-face-covid-19.
