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Protective Efficacy of VP1-Specific Neutralizing Antibody Associated with a Reduction of Viral Load and Pro-Inflammatory Cytokines in Human SCARB2-Transgenic Mice

https://doi.org/10.1371/journal.pone.0069858

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1 of the 43 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1002/14651858.cd004883.pub2 (notice 2010-09-08).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/14651858.cd004883.pub2openalex-snapshot

Immunoglobulin treatment for respiratory syncytial virus infection

inferredcites →https://doi.org/10.1006/viro.1995.1450openalex-snapshot

Molecular Comparison of Coxsackie A Virus Serotypes

inferredcites →https://doi.org/10.1007/bf01317855openalex-snapshot

Neurovirulence in cynomolgus monkeys of enterovirus 71 isolated from a patient with hand, foot and mouth disease

inferredcites →https://doi.org/10.1007/s004310000640openalex-snapshot

Prophylaxis of intravenous immunoglobulin and acyclovir in perinatal varicella

inferredcites →https://doi.org/10.1016/0022-510x(94)00261-lopenalex-snapshot

A case of protracted coxsackie virus meningoencephalitis in a marginally immunodeficient child treated successfully with intravenous immunoglobulin

inferredcites →https://doi.org/10.1016/j.jcv.2006.05.009openalex-snapshot

Modulation of cytokine production by intravenous immunoglobulin in patients with enterovirus 71-associated brainstem encephalitis

inferredcites →https://doi.org/10.1016/j.jviromet.2011.01.016openalex-snapshot

Detection, characterization and quantitation of Coxsackievirus A16 using polyclonal antibodies against recombinant capsid subunit proteins

inferredcites →https://doi.org/10.1016/j.jviromet.2011.02.003openalex-snapshot

Generation of murine monoclonal antibodies which cross-neutralize human enterovirus genogroup B isolates

inferredcites →https://doi.org/10.1016/j.jviromet.2012.09.024openalex-snapshot

Characterization of enterovirus 71 capsids using subunit protein-specific polyclonal antibodies

inferredcites →https://doi.org/10.1016/j.micinf.2007.06.002openalex-snapshot

Passive protection against lethal enterovirus 71 infection in newborn mice by neutralizing antibodies elicited by a synthetic peptide

inferredcites →https://doi.org/10.1016/j.vaccine.2004.05.037openalex-snapshot

Optimization of microcarrier cell culture process for the inactivated enterovirus type 71 vaccine development

inferredcites →https://doi.org/10.1016/j.vaccine.2006.06.083openalex-snapshot

High immunogenic enterovirus 71 strain and its production using serum-free microcarrier Vero cell culture

inferredcites →https://doi.org/10.1016/s0022-3476(98)70155-6openalex-snapshot

Fatal enterovirus 71 encephalomyelitis

inferredcites →https://doi.org/10.1016/s0264-410x(01)00385-1openalex-snapshot

Protection against lethal enterovirus 71 infection in newborn mice by passive immunization with subunit VP1 vaccines and inactivated virus

inferredcites →https://doi.org/10.1016/s0887-8994(98)00087-3openalex-snapshot

Outbreak of severe neurologic involvement associated with enterovirus 71 infection

inferredcites →https://doi.org/10.1038/nm.1992openalex-snapshot

Scavenger receptor B2 is a cellular receptor for enterovirus 71

inferredcites →https://doi.org/10.1038/nrmicro1343openalex-snapshot

Coronavirus infection of the central nervous system: host–virus stand-off

inferredcites →https://doi.org/10.1056/nejm199909233411301openalex-snapshot

An Epidemic of Enterovirus 71 Infection in Taiwan

inferredcites →https://doi.org/10.1080/080352502760069016openalex-snapshot

Different proinflammatory reactions in fatal and non-fatal enterovirus 71 infections: implications for early recognition and therapy

inferredcites →https://doi.org/10.1086/318454openalex-snapshot

Neurological Manifestations of Enterovirus 71 Infection in Children during an Outbreak of Hand, Foot, and Mouth Disease in Western Australia

inferredcites →https://doi.org/10.1086/345905openalex-snapshot

Proinflammatory Cytokine Reactions in Enterovirus 71 Infections of the Central Nervous System

inferredcites →https://doi.org/10.1086/376998openalex-snapshot

Pathogenesis of Enterovirus 71 Brainstem Encephalitis in Pediatric Patients: Roles of Cytokines and Cellular Immune Activation in Patients with Pulmonary Edema

inferredcites →https://doi.org/10.1086/520149openalex-snapshot

Clinical Spectrum of Enterovirus 71 Infection in Children in Southern Taiwan, with an Emphasis on Neurological Complications

inferredcites →https://doi.org/10.1086/591462openalex-snapshot

Acute Chemokine Response in the Blood and Cerebrospinal Fluid of Children with Enterovirus 71–Associated Brainstem Encephalitis

inferredcites →https://doi.org/10.1097/nen.0b013e31817713e7openalex-snapshot

Pathologic Characterization of a Murine Model of Human Enterovirus 71 Encephalomyelitis

inferredcites →https://doi.org/10.1099/vir.0.19423-0openalex-snapshot

A murine oral enterovirus 71 infection model with central nervous system involvement

inferredcites →https://doi.org/10.1099/vir.0.79883-0openalex-snapshot

Differential localization of neurons susceptible to enterovirus 71 and poliovirus type 1 in the central nervous system of cynomolgus monkeys after intravenous inoculation

inferredcites →https://doi.org/10.1099/vir.0.81195-0openalex-snapshot

Type I interferons protect mice against enterovirus 71 infection

inferredcites →https://doi.org/10.1099/vir.0.81925-0openalex-snapshot

A humanized murine monoclonal antibody protects mice either before or after challenge with virulent Venezuelan equine encephalomyelitis virus

inferredcites →https://doi.org/10.1128/jcm.00630-09openalex-snapshot

Reemergence of Enterovirus 71 in 2008 in Taiwan: Dynamics of Genetic and Antigenic Evolution from 1998 to 2008

inferredcites →https://doi.org/10.1128/jcm.35.6.1373-1377.1997openalex-snapshot

A new PCR-based seroneutralization assay in cell culture for diagnosis of hepatitis E

inferredcites →https://doi.org/10.1128/jvi.01779-10openalex-snapshot

Sustained High Levels of Interleukin-6 Contribute to the Pathogenesis of Enterovirus 71 in a Neonate Mouse Model

inferredcites →https://doi.org/10.1128/jvi.06103-11openalex-snapshot

A Non-Mouse-Adapted Enterovirus 71 (EV71) Strain Exhibits Neurotropism, Causing Neurological Manifestations in a Novel Mouse Model of EV71 Infection

inferredcites →https://doi.org/10.1128/jvi.73.12.9969-9975.1999openalex-snapshot

Molecular Epidemiology and Evolution of Enterovirus 71 Strains Isolated from 1970 to 1998

inferredcites →https://doi.org/10.1128/jvi.78.15.7916-7924.2004openalex-snapshot

A Mouse-Adapted Enterovirus 71 Strain Causes Neurological Disease in Mice after Oral Infection

inferredcites →https://doi.org/10.1155/2012/831282openalex-snapshot

Immunological Evaluation and Comparison of Different EV71 Vaccine Candidates

inferredcites →https://doi.org/10.1161/circresaha.108.192179openalex-snapshot

CXCL10 Inhibits Viral Replication Through Recruitment of Natural Killer Cells in Coxsackievirus B3-Induced Myocarditis

inferredcites →https://doi.org/10.1186/1743-422x-7-47openalex-snapshot

The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments

inferredcites →https://doi.org/10.1371/journal.pone.0030507openalex-snapshot

Human SCARB2-Mediated Entry and Endocytosis of EV71

inferredcites →https://doi.org/10.1371/journal.pone.0057591openalex-snapshot

Human SCARB2 Transgenic Mice as an Infectious Animal Model for Enterovirus 71

inferredcites →https://doi.org/10.2217/fmb.11.40openalex-snapshot

Viral Myocarditis: Potential Defense Mechanisms Within The Cardiomyocyte Against Virus Infection

inferredcites →https://doi.org/10.3201/eid0903.020285openalex-snapshot

Enterovirus 71 Outbreaks, Taiwan: Occurrence and Recognition

inferredcites →https://doi.org/10.4049/jimmunol.141.10.3606openalex-snapshot

Protection of mice against Japanese encephalitis virus by passive administration with monoclonal antibodies.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4019249openalex-extracted

Exploring Molecular Moieties on Carbonized Polymer Dots from Flavonoid Glycosides with Activity Against Enterovirus A71

inferred← citeshttps://doi.org/10.1002/rmv.2322openalex-snapshot

Does enterovirus 71 urge for effective vaccine control strategies? Challenges and current opinion

inferred← citeshttps://doi.org/10.1016/j.antiviral.2016.04.015openalex-snapshot

A monoclonal antibody to ameliorate central nervous system infection and improve survival in a murine model of human Enterovirus-A71 encephalomyelitis

inferred← citeshttps://doi.org/10.1016/j.jcv.2013.11.007openalex-snapshot

Detection and identification of viral pathogens in patients with hand, foot, and mouth disease by multilocus PCR, reverse-transcription PCR and electrospray ionization mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104210openalex-snapshot

Acarbose, as a potential drug, effectively blocked the dynamic metastasis of EV71 from the intestine to the whole body

inferred← citeshttps://doi.org/10.1016/j.vaccine.2014.06.062openalex-snapshot

Coxsackievirus A 16 infection does not interfere with the specific immune response induced by an enterovirus 71 inactivated vaccine in rhesus monkeys

inferred← citeshttps://doi.org/10.1016/j.vaccine.2014.08.064openalex-snapshot

Prospect and challenges for the development of multivalent vaccines against hand, foot and mouth diseases

inferred← citeshttps://doi.org/10.1038/s41598-018-28281-5openalex-snapshot

A CpG-adjuvanted intranasal enterovirus 71 vaccine elicits mucosal and systemic immune responses and protects human SCARB2-transgenic mice against lethal challenge

inferred← citeshttps://doi.org/10.1080/17460441.2021.1965987openalex-snapshot

Novel strategies for the development of hand, foot, and mouth disease vaccines and antiviral therapies

inferred← citeshttps://doi.org/10.1080/21645515.2015.1049780openalex-snapshot

Is a multivalent hand, foot, and mouth disease vaccine feasible?

inferred← citeshttps://doi.org/10.1093/cid/ciu852openalex-snapshot

Review of Enterovirus 71 Vaccines

inferred← citeshttps://doi.org/10.1111/bpa.12279openalex-snapshot

Understanding Enterovirus 71 Neuropathogenesis and Its Impact on Other Neurotropic Enteroviruses

inferred← citeshttps://doi.org/10.1155/2014/670506openalex-snapshot

Immunogenicity Studies of Bivalent Inactivated Virions of EV71/CVA16 Formulated with Submicron Emulsion Systems

inferred← citeshttps://doi.org/10.1186/1423-0127-21-31openalex-snapshot

Animal models of enterovirus 71 infection: applications and limitations

inferred← citeshttps://doi.org/10.1371/journal.pntd.0003692openalex-snapshot

Recombinant Adeno-Vaccine Expressing Enterovirus 71-Like Particles against Hand, Foot, and Mouth Disease

inferred← citeshttps://doi.org/10.1586/14787210.2014.895666openalex-snapshot

Update of enterovirus 71 infection: epidemiology, pathogenesis and vaccine

inferred← citeshttps://doi.org/10.3389/fmicb.2020.01105openalex-snapshot

Remdesivir (GS-5734) Impedes Enterovirus Replication Through Viral RNA Synthesis Inhibition

inferred← citeshttps://doi.org/10.3390/pathogens10050625openalex-snapshot

Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study

inferred← citeshttps://doi.org/10.3390/v10120674openalex-snapshot

Immunocompetent and Immunodeficient Mouse Models for Enterovirus 71 Pathogenesis and Therapy

inferred← citeshttps://doi.org/10.3390/v15040932openalex-snapshot

Human SCARB2 Acts as a Cellular Associator for Helping Coxsackieviruses A10 Infection

inferred← citeshttps://doi.org/10.3892/etm.2015.2405openalex-snapshot

Coxsackievirus A16 infection stimulates imbalances of T cells in children

inferred← citeshttps://doi.org/10.7774/cevr.2017.6.1.4openalex-snapshot

Enterovirus 71 infection and vaccines

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