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Significant control of Zika infection in macaques depends on the elapsing time after dengue exposure

https://doi.org/10.1101/625293
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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/eji.201243229openalex-snapshot
IL‐22 modulates IL‐17A production and controls inflammation and tissue damage in experimental dengue infection
inferredcites →https://doi.org/10.1002/jmv.23758openalex-snapshot
Immunopathogenesis of dengue hemorrhagic fever: Contribution to the study of human liver lesions
inferredcites →https://doi.org/10.1016/j.bjid.2016.05.001openalex-snapshot
Zika virus infection, a new public health challenge
inferredcites →https://doi.org/10.1016/j.immuni.2008.02.020openalex-snapshot
Human Effector and Memory CD8+ T Cell Responses to Smallpox and Yellow Fever Vaccines
inferredcites →https://doi.org/10.1016/s0140-6736(16)00562-6openalex-snapshot
Guillain-Barré Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study
inferredcites →https://doi.org/10.1016/s0140-6736(16)00644-9openalex-snapshot
Acute myelitis due to Zika virus infection
inferredcites →https://doi.org/10.1016/s0923-2516(97)88364-1openalex-snapshot
The impact of dengue haemorrhagic fever on liver function
inferredcites →https://doi.org/10.1016/s1473-3099(17)30697-7openalex-snapshot
Zika virus and microcephaly: where do we go from here?
inferredcites →https://doi.org/10.1038/44385openalex-snapshot
Two subsets of memory T lymphocytes with distinct homing potentials and effector functions
inferredcites →https://doi.org/10.1038/emi.2017.42openalex-snapshot
Humoral cross-reactivity between Zika and dengue viruses: implications for protection and pathology
inferredcites →https://doi.org/10.1038/labinvest.2008.70openalex-snapshot
Liver injury caused by antibodies against dengue virus nonstructural protein 1 in a murine model
inferredcites →https://doi.org/10.1038/labinvest.2009.83openalex-snapshot
Hepatic damage associated with dengue-2 virus replication in liver cells of BALB/c mice
inferredcites →https://doi.org/10.1038/ncomms12204openalex-snapshot
A rhesus macaque model of Asian-lineage Zika virus infection
inferredcites →https://doi.org/10.1038/ncomms15674openalex-snapshot
Zika virus pathogenesis in rhesus macaques is unaffected by pre-existing immunity to dengue virus
inferredcites →https://doi.org/10.1038/ni.3515openalex-snapshot
Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with zika virus
inferredcites →https://doi.org/10.1038/nm.2612openalex-snapshot
Preexisting influenza-specific CD4+ T cells correlate with disease protection against influenza challenge in humans
inferredcites →https://doi.org/10.1038/nm887openalex-snapshot
Original antigenic sin and apoptosis in the pathogenesis of dengue hemorrhagic fever
inferredcites →https://doi.org/10.1038/nmicrobiol.2017.36openalex-snapshot
Identification of Zika virus epitopes reveals immunodominant and protective roles for dengue virus cross-reactive CD8+ T cells
inferredcites →https://doi.org/10.1038/nri778openalex-snapshot
Effector and memory T-cell differentiation: implications for vaccine development
inferredcites →https://doi.org/10.1038/s41467-017-01669-zopenalex-snapshot
Dengue virus-reactive CD8+ T cells mediate cross-protection against subsequent Zika virus challenge
inferredcites →https://doi.org/10.1038/s41467-018-05458-0openalex-snapshot
Cross-reactive Dengue virus-specific CD8+ T cells protect against Zika virus during pregnancy
inferredcites →https://doi.org/10.1056/nejmc1602964openalex-snapshot
Zika Virus Associated with Meningoencephalitis
inferredcites →https://doi.org/10.1056/nejmc1603618openalex-snapshot
Uveitis Associated with Zika Virus Infection
inferredcites →https://doi.org/10.1056/nejmc1604449openalex-snapshot
Evidence of Sexual Transmission of Zika Virus
inferredcites →https://doi.org/10.1056/nejmoa1602412openalex-snapshot
Zika Virus Infection in Pregnant Women in Rio de Janeiro
inferredcites →https://doi.org/10.1073/pnas.1010867107openalex-snapshot
Immunodominant T-cell responses to dengue virus NS3 are associated with DHF
inferredcites →https://doi.org/10.1073/pnas.1505956112openalex-snapshot
Dengue virus infection elicits highly polarized CX3CR1 + cytotoxic CD4 + T cells associated with protective immunity
inferredcites →https://doi.org/10.1073/pnas.1607931113openalex-snapshot
Human antibody responses after dengue virus infection are highly cross-reactive to Zika virus
inferredcites →https://doi.org/10.1086/382280openalex-snapshot
Relationship of Preexisting Dengue Virus (DV) Neutralizing Antibody Levels to Viremia and Severity of Disease in a Prospective Cohort Study of DV Infection in Thailand
inferredcites →https://doi.org/10.1086/590117openalex-snapshot
Dengue in Vietnamese Infants—Results of Infection‐Enhancement Assays Correlate with Age‐Related Disease Epidemiology, and Cellular Immune Responses Correlate with Disease Severity
inferredcites →https://doi.org/10.1089/jir.2017.0106openalex-snapshot
T Cell Immunity to Zika and Dengue Viral Infections
inferredcites →https://doi.org/10.1093/cid/ciw476openalex-snapshot
Zika Virus Infection Associated With Severe Thrombocytopenia
inferredcites →https://doi.org/10.1093/cid/ciw692openalex-snapshot
Male-to-Female Sexual Transmission of Zika Virus—United States, January–April 2016
inferredcites →https://doi.org/10.1093/cid/cix732openalex-snapshot
Innate, T-, and B-Cell Responses in Acute Human Zika Patients
inferredcites →https://doi.org/10.1093/infdis/jir012openalex-snapshot
Intracellular Cytokine Production by Dengue Virus–specific T cells Correlates with Subclinical Secondary Infection
inferredcites →https://doi.org/10.1093/infdis/jit436openalex-snapshot
A Shorter Time Interval Between First and Second Dengue Infections Is Associated With Protection From Clinical Illness in a School-based Cohort in Thailand
inferredcites →https://doi.org/10.1093/infdis/jix513openalex-snapshot
Humoral Immune Responses Against Zika Virus Infection and the Importance of Preexisting Flavivirus Immunity
inferredcites →https://doi.org/10.1093/infdis/jix540openalex-snapshot
Nonhuman Primate Models of Zika Virus Infection, Immunity, and Therapeutic Development
inferredcites →https://doi.org/10.1093/infdis/jiy164openalex-snapshot
Longitudinal Analysis of Antibody Cross-neutralization Following Zika Virus and Dengue Virus Infection in Asia and the Americas
inferredcites →https://doi.org/10.1101/621094openalex-snapshot
Time elapsed between Zika and dengue virus infections affects antibody and T cell responses
inferredcites →https://doi.org/10.1111/j.1600-065x.2010.00926.xopenalex-snapshot
Generation of effector CD8 + T cells and their conversion to memory T cells
inferredcites →https://doi.org/10.1126/science.290.5489.92openalex-snapshot
Dynamics of T Lymphocyte Responses: Intermediates, Effectors, and Memory Cells
inferredcites →https://doi.org/10.1126/science.aaf8505openalex-snapshot
Specificity, cross-reactivity, and function of antibodies elicited by Zika virus infection
inferredcites →https://doi.org/10.1126/science.aav6618openalex-snapshot
Impact of preexisting dengue immunity on Zika virus emergence in a dengue endemic region
inferredcites →https://doi.org/10.1126/sciimmunol.aan6809openalex-snapshot
Zika virus activates de novo and cross-reactive memory B cell responses in dengue-experienced donors
inferredcites →https://doi.org/10.1128/jvi.01461-13openalex-snapshot
Cytokine-Dependent Induction of CD4+T cells with Cytotoxic Potential during Influenza Virus Infection
inferredcites →https://doi.org/10.1128/jvi.01469-17openalex-snapshot
Prior Dengue Virus Exposure Shapes T Cell Immunity to Zika Virus in Humans
inferredcites →https://doi.org/10.1128/jvi.02223-14openalex-snapshot
Kinetic and Phenotypic Analysis of CD8 + T Cell Responses after Priming with Alphavirus Replicons and Homologous or Heterologous Booster Immunizations
inferredcites →https://doi.org/10.1128/jvi.03203-15openalex-snapshot
B Cell Responses during Secondary Dengue Virus Infection Are Dominated by Highly Cross-Reactive, Memory-Derived Plasmablasts
inferredcites →https://doi.org/10.1128/jvi.06075-11openalex-snapshot
Rapid and Massive Virus-Specific Plasmablast Responses during Acute Dengue Virus Infection in Humans
inferredcites →https://doi.org/10.1128/mbio.01123-16openalex-snapshot
Dengue Virus Envelope Dimer Epitope Monoclonal Antibodies Isolated from Dengue Patients Are Protective against Zika Virus
inferredcites →https://doi.org/10.1186/s12879-016-1656-2openalex-snapshot
Patterns and causes of liver involvement in acute dengue infection
inferredcites →https://doi.org/10.1186/s13256-017-1510-1openalex-snapshot
Dengue hemorrhagic fever complicated with acute liver failure: a case report
inferredcites →https://doi.org/10.1371/journal.pmed.1002726openalex-snapshot
Prior dengue virus infection and risk of Zika: A pediatric cohort in Nicaragua
inferredcites →https://doi.org/10.1371/journal.pntd.0001676openalex-snapshot
Clinical Relevance and Discriminatory Value of Elevated Liver Aminotransferase Levels for Dengue Severity
inferredcites →https://doi.org/10.1371/journal.pntd.0002357openalex-snapshot
Symptomatic Versus Inapparent Outcome in Repeat Dengue Virus Infections Is Influenced by the Time Interval between Infections and Study Year
inferredcites →https://doi.org/10.1371/journal.pntd.0004536openalex-snapshot
Maternal Antibody-Mediated Disease Enhancement in Type I Interferon-Deficient Mice Leads to Lethal Disease Associated with Liver Damage
inferredcites →https://doi.org/10.1371/journal.pntd.0005168openalex-snapshot
Heterologous Protection against Asian Zika Virus Challenge in Rhesus Macaques
inferredcites →https://doi.org/10.1371/journal.pntd.0007060openalex-snapshot
Does prior dengue virus exposure worsen clinical outcomes of Zika virus infection? A systematic review, pooled analysis and lessons learned
inferredcites →https://doi.org/10.1371/journal.pone.0046292openalex-snapshot
Intrahepatic Infiltrating NK and CD8 T Cells Cause Liver Cell Death in Different Phases of Dengue Virus Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1006219openalex-snapshot
Zika Virus infection of rhesus macaques leads to viral persistence in multiple tissues
inferredcites →https://doi.org/10.1371/journal.ppat.1006317openalex-snapshot
Correction: Zika Virus infection of rhesus macaques leads to viral persistence in multiple tissues
inferredcites →https://doi.org/10.1371/journal.ppat.1006487openalex-snapshot
Impact of prior flavivirus immunity on Zika virus infection in rhesus macaques
inferredcites →https://doi.org/10.1371/journal.ppat.1007237openalex-snapshot
CD4+T cells mediate protection against Zika associated severe disease in a mouse model of infection
inferredcites →https://doi.org/10.15585/mmwr.mm6534e3openalex-snapshot
Hearing Loss in Infants with Microcephaly and Evidence of Congenital Zika Virus Infection — Brazil, November 2015–May 2016
inferredcites →https://doi.org/10.1590/s1020-49892002000400003openalex-snapshot
Enhanced severity of secondary dengue-2 infections: death rates in 1981 and 1997 Cuban outbreaks
inferredcites →https://doi.org/10.1590/s1413-86702004000200006openalex-snapshot
Aminotransferase changes and acute hepatitis in patients with dengue fever: analysis of 1,585 cases
inferredcites →https://doi.org/10.2105/ajph.2016.303113openalex-snapshot
The Epidemic of Zika Virus–Related Microcephaly in Brazil: Detection, Control, Etiology, and Future Scenarios
inferredcites →https://doi.org/10.2807/1560-7917.es.2016.21.16.30205openalex-snapshot
Zika virus detection in cerebrospinal fluid from two patients with encephalopathy, Martinique, February 2016
inferredcites →https://doi.org/10.3201/eid1408.080287openalex-snapshot
Genetic and Serologic Properties of Zika Virus Associated with an Epidemic, Yap State, Micronesia, 2007
inferredcites →https://doi.org/10.3201/eid2102.141363openalex-snapshot
Potential Sexual Transmission of Zika Virus
inferredcites →https://doi.org/10.3201/eid2305.161630openalex-snapshot
Lack of Durable Cross-Neutralizing Antibodies Against Zika Virus from Dengue Virus Infection
inferredcites →https://doi.org/10.3389/fimmu.2016.00218openalex-snapshot
The Cellular Bases of Antibody Responses during Dengue Virus Infection
inferredcites →https://doi.org/10.3389/fimmu.2016.00531openalex-snapshot
Cytotoxic CD4 T Cells: Differentiation, Function, and Application to Dengue Virus Infection
inferredcites →https://doi.org/10.3389/fimmu.2018.02862openalex-snapshot
Cytokine-Mediated Tissue Injury in Non-human Primate Models of Viral Infections
inferredcites →https://doi.org/10.4049/jimmunol.168.11.5959openalex-snapshot
T Cell Responses to an HLA-B*07-Restricted Epitope on the Dengue NS3 Protein Correlate with Disease Severity
inferredcites →https://doi.org/10.4049/jimmunol.176.6.3821openalex-snapshot
T Cell Responses in Dengue Hemorrhagic Fever: Are Cross-Reactive T Cells Suboptimal?
inferredcites →https://doi.org/10.4269/ajtmh.1988.38.411openalex-snapshot
Evidence That Maternal Dengue Antibodies Are Important in the Development of Dengue Hemorrhagic Fever in Infants
inferredcites →https://doi.org/10.7326/m16-0332openalex-snapshot
Emergence of Congenital Zika Syndrome: Viewpoint From the Front Lines

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

inferred← citeshttps://doi.org/10.1038/s41467-019-12295-2openalex-snapshot
Time elapsed between Zika and dengue virus infections affects antibody and T cell responses
inferred← citeshttps://doi.org/10.1101/621094openalex-snapshot
Time elapsed between Zika and dengue virus infections affects antibody and T cell responses
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