All Stories

  1. A structure-function analysis shows SARS-CoV-2 BA.2.86 balances antibody escape and ACE2 affinity
  2. Mapping the interaction sites of human and avian influenza A viruses and complement factor H
  3. Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection
  4. The SARS-CoV-2 neutralizing antibody response to SD1 and its evasion by BA.2.86
  5. B cell maturation restored ancestral germlines to control Omicron BA.2.86
  6. The antiviral potential of the antiandrogen enzalutamide and the viral‐androgen signaling interplay in seasonal coronaviruses
  7. A pan-influenza monoclonal antibody neutralizes H5 strains and prophylactically protects through intranasal administration
  8. Immunological insights into COVID-19 in Southern Nigeria
  9. Studying longitudinal neutralising antibody levels against Equid herpesvirus 1 in experimentally infected horses using a novel pseudotype based assay
  10. Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection
  11. Alternative splicing expands the antiviral IFITM repertoire in Chinese horseshoe bats
  12. The antiviral potential of the antiandrogen enzalutamide and the viral-androgen interplay in seasonal coronaviruses
  13. Serological evidence of virus infection in Eidolon helvum fruit bats: implications for bushmeat consumption in Nigeria
  14. Pseudotyped Viruses As a Molecular Tool to Monitor Humoral Immune Responses Against SARS-CoV-2 Via Neutralization Assay
  15. A computationally designed antigen eliciting broad humoral responses against SARS-CoV-2 and related sarbecoviruses
  16. Virus neutralisation assays using pseudotype vs wildtype viruses
  17. Capture and inactivation of viral particles from bioaerosols by electrostatic precipitation
  18. 52 Human factor H and properdin modulate SARS-CoV-2 infection in a complement-independent manner
  19. Immunogenicity of a silica nanoparticle-based SARS-CoV-2 vaccine in mice
  20. Human complement Factor H and Properdin act as soluble pattern recognition receptors and differentially modulate SARS-CoV-2 Infection
  21. Serological evidence of high pathogenicity virus infection inEidolon helvumfruit bats in Nigeria
  22. Complement Activation-Independent Attenuation of SARS-CoV-2 Infection by C1q and C4b-Binding Protein
  23. Novel intranasal vaccine targeting SARS-CoV-2 receptor binding domain to mucosal microfold cells and adjuvanted with TLR3 agonist Riboxxim™ elicits strong antibody and T-cell responses in mice
  24. Isolation of a pair of potent broadly neutralizing mAb binding to RBD and SD1 domains of SARS-CoV-2
  25. Rapid escape of new SARS-CoV-2 Omicron variants from BA.2 directed antibody responses.
  26. Differential T-cell and Antibody Responses induced by mRNA versus adenoviral vectored COVID-19 vaccines in Patients with Immunodeficiencies
  27. Glycan masking of a non-neutralising epitope enhances neutralising antibodies targeting the RBD of SARS-CoV-2 and its variants
  28. Efficient Viral Capture and Inactivation from Bioaerosols Using Electrostatic Precipitation
  29. Pseudotyped Viruses for Influenza
  30. Efficient Viral Capture and Inactivation From Bioaerosols Using Electrostatic Precipitation
  31. Studying Longitudinal Neutralising Antibody Levels Against Equid Herpesvirus 1 in Experimentally Infected Horses Using a Novel Pseudotype Based Assay
  32. Analysis of Antibody Neutralisation Activity against SARS-CoV-2 Variants and Seasonal Human Coronaviruses NL63, HKU1, and 229E Induced by Three Different COVID-19 Vaccine Platforms
  33. Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
  34. Application and comparison of lyophilisation protocols to enhance stable long-term storage of filovirus pseudotypes for use in antibody neutralisation tests
  35. A delicate balance between antibody evasion and ACE2 affinity for Omicron BA.2.75
  36. SARS-CoV-2 Vaccine Immunogenicity in Patients with Gastrointestinal Cancer Receiving Systemic Anti-Cancer Therapy
  37. Vaccination and protective immunity to SARS-CoV-2 omicron variants in people with immunodeficiencies
  38. Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
  39. Antibody correlates of protection from SARS-CoV-2 reinfection prior to vaccination: a nested case-control within the SIREN study
  40. Quantitative, multiplexed, targeted proteomics for ascertaining variant specific SARS-CoV-2 antibody response
  41. Human surfactant protein D facilitates SARS-CoV-2 pseudotype binding and entry in DC-SIGN expressing cells, and downregulates spike protein induced inflammation
  42. Human seasonal coronavirus neutralisation and COVID‐19 severity
  43. Immune boosting by B.1.1.529 ( Omicron) depends on previous SARS-CoV-2 exposure
  44. Antibody escape of SARS-CoV-2 Omicron BA.4 and BA.5 from vaccine and BA.1 serum
  45. Comparison of lentiviral and vesicular stomatitis virus core SARS-CoV-2 pseudotypes and generation of a stable cell line for use in antibody neutralisation assays
  46. Use of Equine Herpesvirus 1 glycoprotein pseudotyped lentiviral particles for the development of serological tests and assessment of lyophilisation for transport and storage
  47. Fatal COVID-19 outcomes are associated with an antibody response targeting epitopes shared with endemic coronaviruses
  48. Further antibody escape by Omicron BA.4 and BA.5 from vaccine and BA.1 serum
  49. Broad-spectrum CRISPR-mediated inhibition of SARS-CoV-2 variants and endemic coronaviruses in vitro
  50. Human Surfactant Protein D Facilitates SARS-CoV-2 Pseudotype Binding and Entry in DC-SIGN Expressing Cells, and Downregulates Spike protein Induced Inflammation
  51. Application and comparison of lyophilisation protocols to enhance stable long-term storage of filovirus pseudotypes for use in antibody neutralisation tests
  52. Pseudotyped Bat Coronavirus RaTG13 is efficiently neutralised by convalescent sera from SARS-CoV-2 infected patients
  53. Potent cross-reactive antibodies following Omicron breakthrough in vaccinees
  54. Isolation of infectious Lloviu virus from Schreiber’s bats in Hungary
  55. Neutralisation Hierarchy of SARS-CoV-2 Variants of Concern Using Standardised, Quantitative Neutralisation Assays Reveals a Correlation With Disease Severity; Towards Deciphering Protective Antibody Thresholds
  56. SARS-CoV-2 vaccination elicits unconventional IgM specific responses in naïve and previously COVID-19-infected individuals
  57. Durable T-cellular and humoral responses in SARS-CoV-2 hospitalized and community patients
  58. HLA‐DR polymorphism in SARS‐CoV‐2 infection and susceptibility to symptomatic COVID‐19
  59. Lung directed antibody gene transfer confers protection against SARS-CoV-2 infection
  60. AutoPlate: Rapid Dose-Response Curve Analysis for Biological Assays
  61. Gene delivery of a single,structurally engineered Coronavirus vaccine antigen elicits SARS-CoV-2 Omicron and pan-Sarbecovirus neutralisation
  62. Different decay of antibody response and VOC sensitivity in naïve and previously infected subjects at 15 weeks following vaccination with BNT162b2
  63. The antibody response to SARS-CoV-2 Beta underscores the antigenic distance to other variants
  64. Analysis of Serological Biomarkers of SARS-CoV-2 Infection in Convalescent Samples From Severe, Moderate and Mild COVID-19 Cases
  65. Pre-existing polymerase-specific T cells expand in abortive seronegative SARS-CoV-2
  66. Profiling Antibody Response Patterns in COVID-19: Spike S1-Reactive IgA Signature in the Evolution of SARS-CoV-2 Infection
  67. Amino acid substitutions in the H5N1 avian influenza haemagglutinin alter pH of fusion and receptor binding to promote a highly pathogenic phenotype in chickens
  68. Endemic Seasonal Coronavirus Neutralisation and COVID-19 severity
  69. Influenza A (N1-N9) and Influenza B (B/Vic and B/Yam) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine design
  70. Evaluation of a pseudotype virus neutralisation test for measurement of equine influenza virus (EIV) antibody responses induced by vaccination and experimental infection
  71. Generation of EHV‐1 pseudotype virus for cell tropism studies and virus‐neutralising assays
  72. Pseudotyped Bat Coronavirus RaTG13 is efficiently neutralised by convalescent sera from SARS-CoV-2 infected Patients
  73. Coronavirus Pseudotypes for All Circulating Human Coronaviruses for Quantification of Cross-Neutralizing Antibody Responses
  74. Reservoir host studies of Lloviu virus: first isolation, sequencing and serology in Schreiber’s bats in Europe
  75. Exploiting Pan Influenza A and Pan Influenza B Pseudotype Libraries for Efficient Vaccine Antigen Selection
  76. Blood transcriptional biomarkers of acute viral infection for detection of pre-symptomatic SARS-CoV-2 infection: a nested, case-control diagnostic accuracy study
  77. Detection of serum cross-reactive antibodies and memory response to SARS-CoV-2 in pre-pandemic and post-COVID-19 convalescent samples
  78. Breadth of neutralising antibody responses to SARS-CoV-2 variants of concern is augmented by vaccination following prior infection: studies in UK healthcare workers and immunodeficient patients
  79. Feasibility for SARS-CoV-2 Tests in the Hospital: An Exposure Analysis of Critical Control Points Approach
  80. Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
  81. Paucity and discordance of neutralising antibody responses to SARS-CoV-2 VOCs in vaccinated immunodeficient patients and health-care workers in the UK
  82. Measuring SARS-CoV-2 VOC neutralisation
  83. Development of Lentiviral Vectors Pseudotyped With Influenza B Hemagglutinins: Application in Vaccine Immunogenicity, mAb Potency, and Sero-Surveillance Studies
  84. Establishing correlates of immunity for SARS-CoV-2
  85. Synthetic influenza viruses from all A and B subtypes for vaccine testing
  86. Fatal COVID-19 outcomes are associated with an antibody response targeting epitopes shared with endemic coronaviruses
  87. Single Pfizer shot protects prior infected against variants.
  88. Comparison of Serological Assays for the Detection of SARS-CoV-2 Antibodies
  89. Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies
  90. Using safe mimic viruses to study antibody responses after COVID infection or vaccination
  91. SARS-CoV-2 evolution during treatment of chronic infection
  92. Nanobodies mapped to cross-reactive and divergent epitopes on A(H7N9) influenza hemagglutinin using yeast display
  93. Extremely potent human monoclonal antibodies from COVID-19 convalescent patients
  94. The antigenic anatomy of SARS-CoV-2 receptor binding domain
  95. Correlation of Influenza B Haemagglutination Inhibiton, Single-Radial Haemolysis and Pseudotype-Based Microneutralisation Assays for Immunogenicity Testing of Seasonal Vaccines
  96. SARS-CoV-2 B.1.1.7 sensitivity to mRNA vaccine-elicited, convalescent and monoclonal antibodies
  97. C4b Binding Protein Acts as an Innate Immune Effector Against Influenza A Virus
  98. SARS-CoV-2 Vaccination Elicits Unconventional IgM Specific Responses in Naïve and Previously COVID19-Infected Individuals
  99. Fatal COVID-19 Outcomes are Associated with an Antibody Response Targeting Epitopes Shared with Endemic Coronaviruses
  100. Production, Titration, Neutralisation, Storage and Lyophilisation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Lentiviral Pseudotypes
  101. Discordant neutralizing antibody and T cell responses in asymptomatic and mild SARS-CoV-2 infection
  102. Convalescent plasma therapy for the treatment of patients with COVID ‐19: Assessment of methods available for antibody detection and their correlation with neutralising antibody levels
  103. Neutralising antibodies in Spike mediated SARS-CoV-2 adaptation
  104. Development of immunohistochemistry and in situ hybridisation for the detection of SARS-CoV and SARS-CoV-2 in formalin-fixed paraffin-embedded specimens
  105. Longitudinal observation and decline of neutralizing antibody responses in the three months following SARS-CoV-2 infection in humans
  106. Detection of neutralising antibodies to SARS-CoV-2 to determine population exposure in Scottish blood donors between March and May 2020
  107. Healthcare workers with mild / asymptomatic SARS-CoV-2 infection show T cell responses and neutralising antibodies after the first wave
  108. Characterisation of SARS-CoV-2 Lentiviral Pseudotypes and Correlation between Pseudotype-Based Neutralisation Assays and Live Virus-Based Micro Neutralisation Assays
  109. Combined Point-of-Care Nucleic Acid and Antibody Testing for SARS-CoV-2 following Emergence of D614G Spike Variant
  110. Potent anti-SARS-CoV-2 Antibody Responses are Associated with Better Prognosis in Hospital Inpatient COVID-19 Disease
  111. Evaluation of a Pseudotyped Virus Neutralisation Test for the Measurement of Equine Influenza Virus-Neutralising Antibody Responses Induced by Vaccination and Infection
  112. Longitudinal evaluation and decline of antibody responses in SARS-CoV-2 infection
  113. Influenza D pseudotyped lentiviruses: production, neutralisation assay and serological surveillance
  114. Tropism and neutralisation studies on bat influenza H17N10
  115. Generation of Equine Herpesvirus type 1 glycoprotein pseudotyped lentiviral particles for use as a tool for tropism and diagnostic studies
  116. Combined point of care SARS-CoV-2 nucleic acid and antibody testing in suspected moderate to severe COVID-19 disease
  117. Feasibility for SARS-CoV-2 Tests in the Hospital: An Exposure Analysis of Critical Control Points Approach
  118. Protection From Influenza by Intramuscular Gene Vector Delivery of a Broadly Neutralizing Nanobody Does Not Depend on Antibody Dependent Cellular Cytotoxicity
  119. Convalescent plasma therapy for the treatment of patients with COVID-19: Assessment of methods available for antibody detection and their correlation with neutralising antibody levels
  120. Detection of neutralising antibodies to SARS coronavirus 2 to determine population exposure in Scottish blood donors between March and May 2020
  121. A Promising MERS Vaccine for Camels
  122. Entry of the bat influenza H17N10 virus into mammalian cells is enabled by the MHC class II HLA-DR receptor
  123. Generation, lyophilisation and epitope modification of high titre filovirus pseudotyped lentiviruses for use in antibody neutralisation assays and ELISA
  124. Identification of Broad-Spectrum Antiviral Compounds by Targeting Viral Entry
  125. Cross-Reactive and Lineage-Specific Single Domain Antibodies against Influenza B Hemagglutinin
  126. Generation, lyophilisation and epitope modification of high titre filovirus pseudotyped lentiviruses for use in antibody neutralisation assays
  127. The bat influenza H17N10 is neutralized by broadly-neutralizing monoclonal antibodies and its neuraminidase facilitates viral egress
  128. The MHC class-II HLA-DR receptor mediates bat influenza A-like H17N10 virus entry into mammalian cells
  129. The bat influenza H17N10 can be neutralized by broadly-neutralizing monoclonal antibodies and its neuraminidase can facilitate viral egress.
  130. Development and use of Lentiviral Vectors Pseudotyped with Influenza B Haemagglutinins: application to vaccine immunogenicity, mAb potency and sero-surveillance studies
  131. Cross-Protective Immune Responses Induced by Sequential Influenza Virus Infection and by Sequential Vaccination With Inactivated Influenza Vaccines
  132. A naturally protective epitope of limited variability as an influenza vaccine target
  133. Production of lentiviral vectors pseudotyped with influenza neuraminidase (NA) v1 (protocols.io.rkkd4uw)
  134. Cross-protective immune responses induced by sequential influenza virus infection and by sequential vaccination with inactivated influenza vaccines
  135. Integrase Defective Lentiviral Vector as a Vaccine Platform for Delivering Influenza Antigens
  136. How to measure neutralising antibodies with pseudotypes - a practical guide.
  137. Measuring the level of antibodies against influenza neuraminidase.
  138. Measuring the antibody response against influenza neuraminidase
  139. An epitope of limited variability as a novel influenza vaccine target
  140. The Use of Hyperimmune Chicken Reference Sera Is Not Appropriate for the Validation of Influenza Pseudotype Neutralization Assays
  141. The use of hyperimmune chicken reference sera is not appropriate for the validation of influenza pseudotype neutralization assays
  142. Novel Bivalent Viral-Vectored Vaccines Induce Potent Humoral and Cellular Immune Responses Conferring Protection against Stringent Influenza A Virus Challenge
  143. Four potential vaccines developed against MERS-CoV tested in mice
  144. Chimeric influenza haemagglutinins: Generation and use in pseudotype neutralization assays
  145. Production of SARS coronavirus virus mimics for measurement of protective antibody levels.
  146. The Optimisation of Pseudotyped Viruses for the Characterisation of Immune Responses to Equine Influenza Virus
  147. Exploiting viral pseudotypes for emerging virus research
  148. The contribution of specific haemagglutinin mutations to equine influenza vaccine breakdown
  149. Optimisation of equine influenza pseudotyped virus production
  150. Stalking influenza by vaccination with pre-fusion headless HA mini-stem
  151. Induction of broad immunity by thermostabilised vaccines incorporated in dissolvable microneedles using novel fabrication methods
  152. Activation of cross-reactive mucosal T and B cell responses in human nasopharynx-associated lymphoid tissue in vitro by Modified Vaccinia Ankara-vectored influenza vaccines
  153. Who are the Viral Pseudotype Unit, and what do they do ?
  154. Technical considerations for the generation of novel pseudotyped viruses
  155. Ebolavirus: pseudotypes, libraries and standards
  156. Structures of complexes formed by H5 influenza hemagglutinin with a potent broadly neutralizing human monoclonal antibody
  157. Hemagglutinin Sequence Conservation Guided Stem Immunogen Design from Influenza A H3 Subtype
  158. Taking viral pseudotypes out of the laboratory and into the clinic.
  159. The use of pseudotypes to study viruses, virus sero-epidemiology and vaccination
  160. The application of pseudotypes to influenza pandemic preparedness
  161. Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
  162. What are influenza pseudotypes and how can they be used ?
  163. Antiviral therapies against Ebola and other emerging viral diseases using existing medicines that block virus entry
  164. Cross-reactive immunity against influenza viruses in children and adults following 2009 pandemic H1N1 infection
  165. Antiviral therapies against Ebola and other emerging viral diseases using existing medicines that block virus entry
  166. An optimised method for the production of MERS-CoV spike expressing viral pseudotypes
  167. Freeze-drying pseudotype viruses for serology in resource-poor laboratories
  168. Dramatic Potentiation of the Antiviral Activity of HIV Antibodies by Cholesterol Conjugation
  169. Influenza vaccine serology
  170. Influenza hemagglutinin stem-fragment immunogen elicits broadly neutralizing antibodies and confers heterologous protection
  171. Detection of antibodies against H5 and H7 strains in birds: evaluation of influenza pseudovirus particle neutralization tests
  172. Multiplex Evaluation of Influenza Neutralizing Antibodies with Potential Applicability to In-Field Serological Studies
  173. Discordant Correlation between Serological Assays Observed When Measuring Heterosubtypic Responses against Avian Influenza H5 and H7 Viruses in Unexposed Individuals
  174. Chicken Interferon-Inducible Transmembrane Protein 3 Restricts Influenza Viruses and LyssavirusesIn Vitro
  175. Comparative Serological Assays for the Study of H5 and H7 Avian Influenza Viruses
  176. Current progress with serological assays for exotic emerging/re-emerging viruses
  177. Improved adjuvanting of seasonal influenza vaccines: Preclinical studies of MVA‐NP+M1 coadministration with inactivated influenza vaccine
  178. Mutations in haemagglutinin that affect receptor binding and pH stability increase replication of a PR8 influenza virus with H5 HA in the upper respiratory tract of ferrets and may contribute to transmissibility
  179. Infection with 2009 H1N1 Influenza Virus Primes for Immunological Memory in Human Nose-Associated Lymphoid Tissue, Offering Cross-Reactive Immunity to H1N1 and Avian H5N1 Viruses
  180. The production and development of H7 Influenza virus pseudotypes for the study of humoral responses against avian viruses
  181. The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes
  182. The use of equine influenza pseudotypes for serological screening
  183. A Neutralizing Antibody Selected from Plasma Cells That Binds to Group 1 and Group 2 Influenza A Hemagglutinins
  184. Antigenic Drift in H5N1 Avian Influenza Virus in Poultry Is Driven by Mutations in Major Antigenic Sites of the Hemagglutinin Molecule Analogous to Those for Human Influenza Virus
  185. Faculty Opinions recommendation of Llama-derived single domain antibodies to build multivalent, superpotent and broadened neutralizing anti-viral molecules.
  186. Llama-Derived Single Domain Antibodies to Build Multivalent, Superpotent and Broadened Neutralizing Anti-Viral Molecules
  187. Nanobodies With In Vitro Neutralizing Activity Protect Mice Against H5N1 Influenza Virus Infection
  188. Adjuvant-Free Immunization with Hemagglutinin-Fc Fusion Proteins as an Approach to Influenza Vaccines
  189. Virus neutralising activity of African fruit bat (Eidolon helvum) sera against emerging lyssaviruses
  190. Heterosubtypic neutralizing antibodies are produced by individuals immunized with a seasonal influenza vaccine
  191. Investigating original antigenic sin responses to H5N1 influenza viruses (92.19)
  192. The Use of Retroviral Pseudotypes for the Measurement of Antibody Responses to SARS Coronavirus
  193. Pseudoparticle neutralization is a reliable assay to measure immunity and cross-reactivity to H5N1 influenza viruses
  194. Human monoclonal antibodies in single chain fragment variable format with potent neutralization activity against influenza virus H5N1
  195. Neutralizing monoclonal antibodies to different clades of Influenza A H5N1 viruses
  196. Retroviral Pseudotypes
  197. T Cell Responses to Whole SARS Coronavirus in Humans
  198. In vitro evaluation of neuraminidase inhibitors using the neuraminidase-dependent release assay of hemagglutinin-pseudotyped viruses
  199. Investigating antibody neutralization of lyssaviruses using lentiviral pseudotypes: a cross-species comparison
  200. Type I feline coronavirus spike glycoprotein fails to recognize aminopeptidase N as a functional receptor on feline cell lines
  201. A sensitive retroviral pseudotype assay for influenza H5N1‐neutralizing antibodies
  202. The distribution of the endogenous retroviruses HERV-K113 and HERV-K115 in health and disease
  203. Longitudinally Profiling Neutralizing Antibody Response to SARS Coronavirus with Pseudotypes
  204. Enhancement of humoral immune responses to a human cytomegalovirus DNA vaccine: Adjuvant effects of aluminum phosphate and CpG oligodeoxynucleotides
  205. DNA vaccines against cytomegalovirus: current progress
  206. Distinct Mitochondrial and Cytosolic Enzymes Mediate Trypanothione-dependent Peroxide Metabolism in Trypanosoma cruzi
  207. Overexpression of superoxide dismutase in Trypanosoma cruzi results in increased sensitivity to the trypanocidal agents gentian violet and benznidazole
  208. Cloning of an Fe-superoxide dismutase gene homologue from Trypanosoma cruzi