All Stories

  1. Editorial: Unraveling the long-term effects of COVID-19
  2. Exposure of dogs to influenza A and B viruses
  3. Pseudotyped virus-based platform and structural analysis reveal potential cross-reactivity sites between influenza C and D viruses
  4. Development of an ELISA-Based Pulldown Approach for Functional Analysis of Antigen-Specific Antibodies
  5. Host enzymes activate influenza D virus
  6. A Safer and Better Test for Detecting Influenza D in Cattle
  7. Development of an ELISA-Based Pulldown Approach for Functional Analysis of Antigen-Specific Antibodies
  8. Novel Antibody-Based Nasal Spray for Flu Prevention
  9. Molecular pathogenesis—Part B
  10. Limited evidence for exposure of horses in the United Kingdom to influenza D virus
  11. Efficacy and potential human and economic impact of a broadly protective betacoronavirus vaccine
  12. Serological evidence of SARS-CoV-2 infection in red and fallow deer in Great Britain.
  13. Dipeptidase 1 is a functional receptor for a porcine coronavirus
  14. A Novel dual Influenza virus and SARS-CoV-2 neutralisation assay
  15. Immunogenicity and Efficacy of Digitally Immune Optimised H1N1 Vaccine Candidates in Swine and Murine Animal Models
  16. Divergent antibody-mediated population immunity to H5, H7 and H9 subtype potential pandemic influenza viruses
  17. Natural infection and vaccination interact to shape Fc-mediated immunity against SARS-CoV-2
  18. Investigating factors driving shifts in subtype dominance within H5Nx clade 2.3.4.4b high pathogenicity avian influenza viruses
  19. Differential modulation of SARS-CoV-2 infection by complement factor H and properdin
  20. Cross-Neutralizing Monoclonal Antibodies with Broad Activity Against Human and Bat-Derived SARS-Related Coronaviruses
  21. Development and optimisation of Influenza C and Influenza D pseudotyped viruses
  22. Quantitative characterisation of extracellular vesicles designed to decoy or compete with SARS-CoV-2 reveals differential mode of action across variants of concern and highlights the diversity of Omicron
  23. SARS-CoV-2 and its S protein activate the ability of the infected cells to escape immune attack
  24. Computationally designed haemagglutinin with nanocage plug-and-display elicits pan-H5 influenza vaccine responses
  25. Development of bivalent RBD adapted COVID-19 vaccines for broad sarbecovirus immunity
  26. Development and optimisation of Influenza C and Influenza D pseudotyped viruses
  27. Enhanced variant neutralization through glycan masking of SARS-CoV-2 XBB1.5 RBD
  28. Compartmentalised mucosal and blood immunity to SARS-CoV-2 is associated with high seroprevalence before the Delta wave in Africa
  29. Digitally Immune-Optimised Next-Generation Influenza Vaccine Provides Cross-Clade Protection Against Emerging H5Nx Viruses
  30. Investigating Factors Driving Shifts in Subtype Dominance within H5Nx Clade 2.3.4.4b High-Pathogenicity Avian Influenza viruses
  31. Intranasal administration of a panreactive influenza antibody reveals Fc-independent mode of protection
  32. Digitally Immune-Optimised Next-Generation Influenza H5Nx Vaccination Provides Protection with Broad Cross-Clade Neutralisation Against Global Threats
  33. Alternative splicing expands the antiviral IFITM repertoire in Chinese rufous horseshoe bats
  34. Cellular sialoglycans are differentially required for endosomal and cell-surface entry of SARS-CoV-2 in lung cell lines
  35. Greater preservation of SARS‐CoV‐2 neutralising antibody responses following the ChAdOx1‐S (AZD1222) vaccine compared with mRNA vaccines in haematopoietic cell transplant recipients
  36. Digitally immune optimised haemagglutinin with nanocage plug-and-display elicits broadly neutralising pan-H5 influenza subtype vaccine responses
  37. Serological analysis in humans in Malaysian Borneo suggests prior exposure to H5 avian influenza near migratory shorebird habitats
  38. Validation of a Lassa virus functional neutralisation assay.
  39. Compartmentalised mucosal and blood immunity to SARS-CoV-2 associated with high seroprevalence before Delta wave in Africa
  40. A Transgenic Mouse With a Humanized B-Cell Repertoire Mounts an Antibody Response to Influenza Infection and Vaccination
  41. Antigenic sin and multiple breakthrough infections drive converging evolution of COVID-19 neutralizing responses
  42. Immune signature in vaccinated versus non-vaccinated aged people with COVID-19 pneumonia
  43. Conference Report: LPMHealthcare Emerging Viruses 2023 (EVOX23): Pandemics—Learning from the Past and Present to Prepare for the Future
  44. Immune signature in vaccinated versus non-vaccinated aged people with COVID-19 pneumonia
  45. Centenarians, semi and supercentenarians, COVID-19 and Spanish flu: a serological assessment to gain insight into the resilience of older centenarians to COVID-19
  46. Cellular sialoglycans are differentially required for endosomal and cell-surface entry of SARS-CoV-2
  47. Evaluation of monkeypox‐ and vaccinia‐virus neutralizing antibodies before and after smallpox vaccination: A sero‐epidemiological study
  48.  A validate and standardized pseudotyped microneutralization assay as a safe and powerful tool to measure LASSA neutralising antibodies for vaccine development and comparison
  49. Centenarians, Semi and Supercentenarians, COVID-19 and Spanish Flu: a serological assessment to gain insight into the resilience of older centenarians to COVID- 19
  50. A structure-function analysis shows SARS-CoV-2 BA.2.86 balances antibody escape and ACE2 affinity
  51. Mapping the interaction sites of human and avian influenza A viruses and complement factor H
  52. Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection
  53. The SARS-CoV-2 neutralizing antibody response to SD1 and its evasion by BA.2.86
  54. B cell maturation restored ancestral germlines to control Omicron BA.2.86
  55. The antiviral potential of the antiandrogen enzalutamide and the viral‐androgen signaling interplay in seasonal coronaviruses
  56. A pan-influenza monoclonal antibody neutralizes H5 strains and prophylactically protects through intranasal administration
  57. Immunological insights into COVID-19 in Southern Nigeria
  58. Studying longitudinal neutralising antibody levels against Equid herpesvirus 1 in experimentally infected horses using a novel pseudotype based assay
  59. Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection
  60. Alternative splicing expands the antiviral IFITM repertoire in Chinese horseshoe bats
  61. The antiviral potential of the antiandrogen enzalutamide and the viral-androgen interplay in seasonal coronaviruses
  62. Serological evidence of virus infection in Eidolon helvum fruit bats: implications for bushmeat consumption in Nigeria
  63. Pseudotyped Viruses As a Molecular Tool to Monitor Humoral Immune Responses Against SARS-CoV-2 Via Neutralization Assay
  64. A computationally designed antigen eliciting broad humoral responses against SARS-CoV-2 and related sarbecoviruses
  65. Virus neutralisation assays using pseudotype vs wildtype viruses
  66. Mapping the interaction sites of Influenza A viruses and human complement Factor H
  67. Capture and inactivation of viral particles from bioaerosols by electrostatic precipitation
  68. 52 Human factor H and properdin modulate SARS-CoV-2 infection in a complement-independent manner
  69. Immunogenicity of a silica nanoparticle-based SARS-CoV-2 vaccine in mice
  70. Human complement Factor H and Properdin act as soluble pattern recognition receptors and differentially modulate SARS-CoV-2 Infection
  71. Serological evidence of high pathogenicity virus infection inEidolon helvumfruit bats in Nigeria
  72. Complement Activation-Independent Attenuation of SARS-CoV-2 Infection by C1q and C4b-Binding Protein
  73. 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
  74. Isolation of a pair of potent broadly neutralizing mAb binding to RBD and SD1 domains of SARS-CoV-2
  75. Rapid escape of new SARS-CoV-2 Omicron variants from BA.2 directed antibody responses.
  76. Differential T-cell and Antibody Responses induced by mRNA versus adenoviral vectored COVID-19 vaccines in Patients with Immunodeficiencies
  77. Glycan masking of a non-neutralising epitope enhances neutralising antibodies targeting the RBD of SARS-CoV-2 and its variants
  78. Efficient Viral Capture and Inactivation from Bioaerosols Using Electrostatic Precipitation
  79. Pseudotyped Viruses for Influenza
  80. Efficient Viral Capture and Inactivation From Bioaerosols Using Electrostatic Precipitation
  81. Studying Longitudinal Neutralising Antibody Levels Against Equid Herpesvirus 1 in Experimentally Infected Horses Using a Novel Pseudotype Based Assay
  82. 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
  83. Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria
  84. Application and comparison of lyophilisation protocols to enhance stable long-term storage of filovirus pseudotypes for use in antibody neutralisation tests
  85. 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
  86. A delicate balance between antibody evasion and ACE2 affinity for Omicron BA.2.75
  87. SARS-CoV-2 Vaccine Immunogenicity in Patients with Gastrointestinal Cancer Receiving Systemic Anti-Cancer Therapy
  88. Vaccination and protective immunity to SARS-CoV-2 omicron variants in people with immunodeficiencies
  89. Persistent but dysfunctional mucosal SARS-CoV-2-specific IgA and low lung IL-1β associate with COVID-19 fatal outcome: A cross-sectional analysis
  90. Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
  91. Author Correction: Isolation of infectious Lloviu virus from Schreiber’s bats in Hungary
  92. Antibody correlates of protection from SARS-CoV-2 reinfection prior to vaccination: a nested case-control within the SIREN study
  93. Quantitative, multiplexed, targeted proteomics for ascertaining variant specific SARS-CoV-2 antibody response
  94. Human surfactant protein D facilitates SARS-CoV-2 pseudotype binding and entry in DC-SIGN expressing cells, and downregulates spike protein induced inflammation
  95. Author Correction: SARS-CoV-2 evolution during treatment of chronic infection
  96. Author Correction: Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies
  97. Human seasonal coronavirus neutralisation and COVID‐19 severity
  98. Immune boosting by B.1.1.529 ( Omicron) depends on previous SARS-CoV-2 exposure
  99. Antibody escape of SARS-CoV-2 Omicron BA.4 and BA.5 from vaccine and BA.1 serum
  100. 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
  101. Use of Equine Herpesvirus 1 glycoprotein pseudotyped lentiviral particles for the development of serological tests and assessment of lyophilisation for transport and storage
  102. Fatal COVID-19 outcomes are associated with an antibody response targeting epitopes shared with endemic coronaviruses
  103. Further antibody escape by Omicron BA.4 and BA.5 from vaccine and BA.1 serum
  104. Broad-spectrum CRISPR-mediated inhibition of SARS-CoV-2 variants and endemic coronaviruses in vitro
  105. Human Surfactant Protein D Facilitates SARS-CoV-2 Pseudotype Binding and Entry in DC-SIGN Expressing Cells, and Downregulates Spike protein Induced Inflammation
  106. Application and comparison of lyophilisation protocols to enhance stable long-term storage of filovirus pseudotypes for use in antibody neutralisation tests
  107. Pseudotyped Bat Coronavirus RaTG13 is efficiently neutralised by convalescent sera from SARS-CoV-2 infected patients
  108. Potent cross-reactive antibodies following Omicron breakthrough in vaccinees
  109. Isolation of infectious Lloviu virus from Schreiber’s bats in Hungary
  110. 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
  111. SARS-CoV-2 vaccination elicits unconventional IgM specific responses in naïve and previously COVID-19-infected individuals
  112. Durable T-cellular and humoral responses in SARS-CoV-2 hospitalized and community patients
  113. HLA‐DR polymorphism in SARS‐CoV‐2 infection and susceptibility to symptomatic COVID‐19
  114. Lung directed antibody gene transfer confers protection against SARS-CoV-2 infection
  115. AutoPlate: Rapid Dose-Response Curve Analysis for Biological Assays
  116. Gene delivery of a single,structurally engineered Coronavirus vaccine antigen elicits SARS-CoV-2 Omicron and pan-Sarbecovirus neutralisation
  117. Different decay of antibody response and VOC sensitivity in naïve and previously infected subjects at 15 weeks following vaccination with BNT162b2
  118. The antibody response to SARS-CoV-2 Beta underscores the antigenic distance to other variants
  119. Omicron-B.1.1.529 leads to widespread escape from neutralizing antibody responses
  120. Analysis of Serological Biomarkers of SARS-CoV-2 Infection in Convalescent Samples From Severe, Moderate and Mild COVID-19 Cases
  121. Pre-existing polymerase-specific T cells expand in abortive seronegative SARS-CoV-2
  122. Profiling Antibody Response Patterns in COVID-19: Spike S1-Reactive IgA Signature in the Evolution of SARS-CoV-2 Infection
  123. Amino acid substitutions in the H5N1 avian influenza haemagglutinin alter pH of fusion and receptor binding to promote a highly pathogenic phenotype in chickens
  124. Endemic Seasonal Coronavirus Neutralisation and COVID-19 severity
  125. Influenza A (N1-N9) and Influenza B (B/Vic and B/Yam) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine design
  126. Evaluation of a pseudotype virus neutralisation test for measurement of equine influenza virus (EIV) antibody responses induced by vaccination and experimental infection
  127. Generation of EHV‐1 pseudotype virus for cell tropism studies and virus‐neutralising assays
  128. Pseudotyped Bat Coronavirus RaTG13 is efficiently neutralised by convalescent sera from SARS-CoV-2 infected Patients
  129. Coronavirus Pseudotypes for All Circulating Human Coronaviruses for Quantification of Cross-Neutralizing Antibody Responses
  130. Reservoir host studies of Lloviu virus: first isolation, sequencing and serology in Schreiber’s bats in Europe
  131. Exploiting Pan Influenza A and Pan Influenza B Pseudotype Libraries for Efficient Vaccine Antigen Selection
  132. Blood transcriptional biomarkers of acute viral infection for detection of pre-symptomatic SARS-CoV-2 infection: a nested, case-control diagnostic accuracy study
  133. Pre-existing polymerase-specific T cells expand in abortive seronegative SARS-CoV-2 infection
  134. Detection of serum cross-reactive antibodies and memory response to SARS-CoV-2 in pre-pandemic and post-COVID-19 convalescent samples
  135. 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
  136. Feasibility for SARS-CoV-2 Tests in the Hospital: An Exposure Analysis of Critical Control Points Approach
  137. Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
  138. Paucity and discordance of neutralising antibody responses to SARS-CoV-2 VOCs in vaccinated immunodeficient patients and health-care workers in the UK
  139. Measuring SARS-CoV-2 VOC neutralisation
  140. Development of Lentiviral Vectors Pseudotyped With Influenza B Hemagglutinins: Application in Vaccine Immunogenicity, mAb Potency, and Sero-Surveillance Studies
  141. Establishing correlates of immunity for SARS-CoV-2
  142. Synthetic influenza viruses from all A and B subtypes for vaccine testing
  143. Fatal COVID-19 outcomes are associated with an antibody response targeting epitopes shared with endemic coronaviruses
  144. Single Pfizer shot protects prior infected against variants.
  145. Comparison of Serological Assays for the Detection of SARS-CoV-2 Antibodies
  146. Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies
  147. Using safe mimic viruses to study antibody responses after COVID infection or vaccination
  148. SARS-CoV-2 evolution during treatment of chronic infection
  149. Nanobodies mapped to cross-reactive and divergent epitopes on A(H7N9) influenza hemagglutinin using yeast display
  150. Extremely potent human monoclonal antibodies from COVID-19 convalescent patients
  151. The antigenic anatomy of SARS-CoV-2 receptor binding domain
  152. Correlation of Influenza B Haemagglutination Inhibiton, Single-Radial Haemolysis and Pseudotype-Based Microneutralisation Assays for Immunogenicity Testing of Seasonal Vaccines
  153. SARS-CoV-2 B.1.1.7 sensitivity to mRNA vaccine-elicited, convalescent and monoclonal antibodies
  154. C4b Binding Protein Acts as an Innate Immune Effector Against Influenza A Virus
  155. SARS-CoV-2 Vaccination Elicits Unconventional IgM Specific Responses in Naïve and Previously COVID19-Infected Individuals
  156. Fatal COVID-19 Outcomes are Associated with an Antibody Response Targeting Epitopes Shared with Endemic Coronaviruses
  157. Production, Titration, Neutralisation, Storage and Lyophilisation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Lentiviral Pseudotypes
  158. Discordant neutralizing antibody and T cell responses in asymptomatic and mild SARS-CoV-2 infection
  159. 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
  160. Neutralising antibodies in Spike mediated SARS-CoV-2 adaptation
  161. Development of immunohistochemistry and in situ hybridisation for the detection of SARS-CoV and SARS-CoV-2 in formalin-fixed paraffin-embedded specimens
  162. Longitudinal observation and decline of neutralizing antibody responses in the three months following SARS-CoV-2 infection in humans
  163. Detection of neutralising antibodies to SARS-CoV-2 to determine population exposure in Scottish blood donors between March and May 2020
  164. Healthcare workers with mild / asymptomatic SARS-CoV-2 infection show T cell responses and neutralising antibodies after the first wave
  165. Characterisation of SARS-CoV-2 Lentiviral Pseudotypes and Correlation between Pseudotype-Based Neutralisation Assays and Live Virus-Based Micro Neutralisation Assays
  166. Combined Point-of-Care Nucleic Acid and Antibody Testing for SARS-CoV-2 following Emergence of D614G Spike Variant
  167. Potent anti-SARS-CoV-2 Antibody Responses are Associated with Better Prognosis in Hospital Inpatient COVID-19 Disease
  168. Evaluation of a Pseudotyped Virus Neutralisation Test for the Measurement of Equine Influenza Virus-Neutralising Antibody Responses Induced by Vaccination and Infection
  169. Longitudinal evaluation and decline of antibody responses in SARS-CoV-2 infection
  170. Influenza D pseudotyped lentiviruses: production, neutralisation assay and serological surveillance
  171. Tropism and neutralisation studies on bat influenza H17N10
  172. Generation of Equine Herpesvirus type 1 glycoprotein pseudotyped lentiviral particles for use as a tool for tropism and diagnostic studies
  173. Combined point of care SARS-CoV-2 nucleic acid and antibody testing in suspected moderate to severe COVID-19 disease
  174. Feasibility for SARS-CoV-2 Tests in the Hospital: An Exposure Analysis of Critical Control Points Approach
  175. Protection From Influenza by Intramuscular Gene Vector Delivery of a Broadly Neutralizing Nanobody Does Not Depend on Antibody Dependent Cellular Cytotoxicity
  176. 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
  177. Detection of neutralising antibodies to SARS coronavirus 2 to determine population exposure in Scottish blood donors between March and May 2020
  178. ­­­The Antigenic Anatomy of SARS-CoV-2 Receptor Binding Domain
  179. A Promising MERS Vaccine for Camels
  180. Entry of the bat influenza H17N10 virus into mammalian cells is enabled by the MHC class II HLA-DR receptor
  181. Generation, lyophilisation and epitope modification of high titre filovirus pseudotyped lentiviruses for use in antibody neutralisation assays and ELISA
  182. Identification of Broad-Spectrum Antiviral Compounds by Targeting Viral Entry
  183. Cross-Reactive and Lineage-Specific Single Domain Antibodies against Influenza B Hemagglutinin
  184. Generation, lyophilisation and epitope modification of high titre filovirus pseudotyped lentiviruses for use in antibody neutralisation assays
  185. The bat influenza H17N10 is neutralized by broadly-neutralizing monoclonal antibodies and its neuraminidase facilitates viral egress
  186. The MHC class-II HLA-DR receptor mediates bat influenza A-like H17N10 virus entry into mammalian cells
  187. The bat influenza H17N10 can be neutralized by broadly-neutralizing monoclonal antibodies and its neuraminidase can facilitate viral egress.
  188. Development and use of Lentiviral Vectors Pseudotyped with Influenza B Haemagglutinins: application to vaccine immunogenicity, mAb potency and sero-surveillance studies
  189. Cross-Protective Immune Responses Induced by Sequential Influenza Virus Infection and by Sequential Vaccination With Inactivated Influenza Vaccines
  190. A naturally protective epitope of limited variability as an influenza vaccine target
  191. Production of lentiviral vectors pseudotyped with influenza neuraminidase (NA) v1 (protocols.io.rkkd4uw)
  192. Cross-protective immune responses induced by sequential influenza virus infection and by sequential vaccination with inactivated influenza vaccines
  193. Integrase Defective Lentiviral Vector as a Vaccine Platform for Delivering Influenza Antigens
  194. How to measure neutralising antibodies with pseudotypes - a practical guide.
  195. Measuring the level of antibodies against influenza neuraminidase.
  196. Measuring the antibody response against influenza neuraminidase
  197. An epitope of limited variability as a novel influenza vaccine target
  198. The Use of Hyperimmune Chicken Reference Sera Is Not Appropriate for the Validation of Influenza Pseudotype Neutralization Assays
  199. The use of hyperimmune chicken reference sera is not appropriate for the validation of influenza pseudotype neutralization assays
  200. Novel Bivalent Viral-Vectored Vaccines Induce Potent Humoral and Cellular Immune Responses Conferring Protection against Stringent Influenza A Virus Challenge
  201. Four potential vaccines developed against MERS-CoV tested in mice
  202. Chimeric influenza haemagglutinins: Generation and use in pseudotype neutralization assays
  203. Production of SARS coronavirus virus mimics for measurement of protective antibody levels.
  204. The Optimisation of Pseudotyped Viruses for the Characterisation of Immune Responses to Equine Influenza Virus
  205. Exploiting viral pseudotypes for emerging virus research
  206. The contribution of specific haemagglutinin mutations to equine influenza vaccine breakdown
  207. Optimisation of equine influenza pseudotyped virus production
  208. Stalking influenza by vaccination with pre-fusion headless HA mini-stem
  209. Induction of broad immunity by thermostabilised vaccines incorporated in dissolvable microneedles using novel fabrication methods
  210. 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
  211. Who are the Viral Pseudotype Unit, and what do they do ?
  212. Technical considerations for the generation of novel pseudotyped viruses
  213. Ebolavirus: pseudotypes, libraries and standards
  214. Structures of complexes formed by H5 influenza hemagglutinin with a potent broadly neutralizing human monoclonal antibody
  215. Hemagglutinin Sequence Conservation Guided Stem Immunogen Design from Influenza A H3 Subtype
  216. Taking viral pseudotypes out of the laboratory and into the clinic.
  217. The use of pseudotypes to study viruses, virus sero-epidemiology and vaccination
  218. The application of pseudotypes to influenza pandemic preparedness
  219. Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
  220. What are influenza pseudotypes and how can they be used ?
  221. Antiviral therapies against Ebola and other emerging viral diseases using existing medicines that block virus entry
  222. Cross-reactive immunity against influenza viruses in children and adults following 2009 pandemic H1N1 infection
  223. Antiviral therapies against Ebola and other emerging viral diseases using existing medicines that block virus entry
  224. An optimised method for the production of MERS-CoV spike expressing viral pseudotypes
  225. Freeze-drying pseudotype viruses for serology in resource-poor laboratories
  226. Dramatic Potentiation of the Antiviral Activity of HIV Antibodies by Cholesterol Conjugation
  227. Influenza vaccine serology
  228. Influenza hemagglutinin stem-fragment immunogen elicits broadly neutralizing antibodies and confers heterologous protection
  229. Detection of antibodies against H5 and H7 strains in birds: evaluation of influenza pseudovirus particle neutralization tests
  230. Multiplex Evaluation of Influenza Neutralizing Antibodies with Potential Applicability to In-Field Serological Studies
  231. Discordant Correlation between Serological Assays Observed When Measuring Heterosubtypic Responses against Avian Influenza H5 and H7 Viruses in Unexposed Individuals
  232. Chicken Interferon-Inducible Transmembrane Protein 3 Restricts Influenza Viruses and LyssavirusesIn Vitro
  233. Comparative Serological Assays for the Study of H5 and H7 Avian Influenza Viruses
  234. Current progress with serological assays for exotic emerging/re-emerging viruses
  235. Improved adjuvanting of seasonal influenza vaccines: Preclinical studies of MVA‐NP+M1 coadministration with inactivated influenza vaccine
  236. 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
  237. 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
  238. The production and development of H7 Influenza virus pseudotypes for the study of humoral responses against avian viruses
  239. The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes
  240. The use of equine influenza pseudotypes for serological screening
  241. A Neutralizing Antibody Selected from Plasma Cells That Binds to Group 1 and Group 2 Influenza A Hemagglutinins
  242. 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
  243. Faculty Opinions recommendation of Llama-derived single domain antibodies to build multivalent, superpotent and broadened neutralizing anti-viral molecules.
  244. Llama-Derived Single Domain Antibodies to Build Multivalent, Superpotent and Broadened Neutralizing Anti-Viral Molecules
  245. Nanobodies With In Vitro Neutralizing Activity Protect Mice Against H5N1 Influenza Virus Infection
  246. Adjuvant-Free Immunization with Hemagglutinin-Fc Fusion Proteins as an Approach to Influenza Vaccines
  247. Virus neutralising activity of African fruit bat (Eidolon helvum) sera against emerging lyssaviruses
  248. Heterosubtypic neutralizing antibodies are produced by individuals immunized with a seasonal influenza vaccine
  249. Investigating original antigenic sin responses to H5N1 influenza viruses (92.19)
  250. The Use of Retroviral Pseudotypes for the Measurement of Antibody Responses to SARS Coronavirus
  251. Pseudoparticle neutralization is a reliable assay to measure immunity and cross-reactivity to H5N1 influenza viruses
  252. Human monoclonal antibodies in single chain fragment variable format with potent neutralization activity against influenza virus H5N1
  253. Neutralizing monoclonal antibodies to different clades of Influenza A H5N1 viruses
  254. Retroviral Pseudotypes
  255. T Cell Responses to Whole SARS Coronavirus in Humans
  256. In vitro evaluation of neuraminidase inhibitors using the neuraminidase-dependent release assay of hemagglutinin-pseudotyped viruses
  257. Investigating antibody neutralization of lyssaviruses using lentiviral pseudotypes: a cross-species comparison
  258. Type I feline coronavirus spike glycoprotein fails to recognize aminopeptidase N as a functional receptor on feline cell lines
  259. A sensitive retroviral pseudotype assay for influenza H5N1‐neutralizing antibodies
  260. The distribution of the endogenous retroviruses HERV-K113 and HERV-K115 in health and disease
  261. Longitudinally Profiling Neutralizing Antibody Response to SARS Coronavirus with Pseudotypes
  262. Enhancement of humoral immune responses to a human cytomegalovirus DNA vaccine: Adjuvant effects of aluminum phosphate and CpG oligodeoxynucleotides
  263. DNA vaccines against cytomegalovirus: current progress
  264. Distinct Mitochondrial and Cytosolic Enzymes Mediate Trypanothione-dependent Peroxide Metabolism in Trypanosoma cruzi
  265. Overexpression of superoxide dismutase in Trypanosoma cruzi results in increased sensitivity to the trypanocidal agents gentian violet and benznidazole
  266. Cloning of an Fe-superoxide dismutase gene homologue from Trypanosoma cruzi