On the public citation graph

Dengue‐Specific T Cell Responses in Peripheral Blood Mononuclear Cells Obtained prior to Secondary Dengue Virus Infections in Thai Schoolchildren

0 signed · 159 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/jlb.61.3.338openalex-snapshot
Cytokine production by dengue virus antigen-responsive human T lymphocytes in vitro examined using a double immunocytochemical technique
inferredcites →https://doi.org/10.1006/viro.1997.8925openalex-snapshot
Definition of an Epitope on NS3 Recognized by Human CD4+Cytotoxic T Lymphocyte Clones Cross-Reactive for Dengue Virus Types 2, 3, and 4
inferredcites →https://doi.org/10.1006/viro.1999.9656openalex-snapshot
Immunopathogenesis of Dengue Hemorrhagic Fever
inferredcites →https://doi.org/10.1007/978-3-642-78530-6_6openalex-snapshot
Cytotoxic T Lymphocytes in Dengue Virus Infection
inferredcites →https://doi.org/10.1007/978-3-7091-9326-6_7openalex-snapshot
Immunopathologic mechanisms of dengue hemorrhagic fever and dengue shock syndrome
inferredcites →https://doi.org/10.1016/s0031-3025(16)34854-1openalex-snapshot
Dengue haemorrhagic fever: diagnosis, treatment, prevention and control
inferredcites →https://doi.org/10.1084/jem.170.3.763openalex-snapshot
Dengue virus-specific human T cell clones. Serotype crossreactive proliferation, interferon gamma production, and cytotoxic activity.
inferredcites →https://doi.org/10.1086/314680openalex-snapshot
Early Immune Activation in Acute Dengue Illness Is Related to Development of Plasma Leakage and Disease Severity
inferredcites →https://doi.org/10.1086/315072openalex-snapshot
Early CD69 Expression on Peripheral Blood Lymphocytes from Children with Dengue Hemorrhagic Fever
inferredcites →https://doi.org/10.1086/315215openalex-snapshot
Dengue Viremia Titer, Antibody Response Pattern, and Virus Serotype Correlate with Disease Severity
inferredcites →https://doi.org/10.1086/340365openalex-snapshot
Differing Influences of Virus Burden and Immune Activation on Disease Severity in Secondary Dengue‐3 Virus Infections
inferredcites →https://doi.org/10.1086/517807openalex-snapshot
Pathophysiologic and Prognostic Role of Cytokines in Dengue Hemorrhagic Fever
inferredcites →https://doi.org/10.1089/aid.1990.6.993openalex-snapshot
Antibody-Enhanced Infection of Monocytes as the Pathogenetic Mechanism for Severe Dengue Illness
inferredcites →https://doi.org/10.1089/vim.1993.6.143openalex-snapshot
Dengue Virus-Specific, Human CD4 + Cytotoxic T Lymphocytes Generated in Short-Term Culture
inferredcites →https://doi.org/10.1093/clinids/11.supplement_4.s830openalex-snapshot
Antibody, Macrophages, Dengue Virus Infection, Shock, and Hemorrhage: A Pathogenetic Cascade
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a113932openalex-snapshot
RISK FACTORS IN DENGUE SHOCK SYNDROME: A PROSPECTIVE EPIDEMIOLOGIC STUDY IN RAYONG, THAILAND
inferredcites →https://doi.org/10.1099/0022-1317-76-9-2243openalex-snapshot
Flavivirus-cross-reactive, HLA-DR15-restricted epitope on NS3 recognized by human CD4+ CD8- cytotoxic T lymphocyte clones
inferredcites →https://doi.org/10.1126/science.3277268openalex-snapshot
Pathogenesis of Dengue: Challenges to Molecular Biology
inferredcites →https://doi.org/10.1128/cmr.11.3.480openalex-snapshot
Dengue and Dengue Hemorrhagic Fever
inferredcites →https://doi.org/10.1128/jvi.62.11.3928-3933.1988openalex-snapshot
Gamma interferon augments Fc gamma receptor-mediated dengue virus infection of human monocytic cells
inferredcites →https://doi.org/10.1128/jvi.65.4.1823-1828.1991openalex-snapshot
Dengue virus-specific, human CD4+ CD8- cytotoxic T-cell clones: multiple patterns of virus cross-reactivity recognized by NS3-specific T-cell clones
inferredcites →https://doi.org/10.1128/jvi.67.10.5962-5967.1993openalex-snapshot
Dengue virus-specific human CD4+ T-lymphocyte responses in a recipient of an experimental live-attenuated dengue virus type 1 vaccine: bulk culture proliferation, clonal analysis, and precursor frequency determination
inferredcites →https://doi.org/10.1128/jvi.67.10.6285-6288.1993openalex-snapshot
Definition of an HLA-DPw2-restricted epitope on NS3, recognized by a dengue virus serotype-cross-reactive human CD4+ CD8- cytotoxic T-cell clone
inferredcites →https://doi.org/10.1128/jvi.70.1.141-147.1996openalex-snapshot
Identification of two epitopes on the dengue 4 virus capsid protein recognized by a serotype-specific and a panel of serotype-cross-reactive human CD4+ cytotoxic T-lymphocyte clones
inferredcites →https://doi.org/10.1128/jvi.73.5.3623-3629.1999openalex-snapshot
Bystander Target Cell Lysis and Cytokine Production by Dengue Virus-Specific Human CD4+Cytotoxic T-Lymphocyte Clones
inferredcites →https://doi.org/10.1128/jvi.75.8.3501-3508.2001openalex-snapshot
Human Dendritic Cells Are Activated by Dengue Virus Infection: Enhancement by Gamma Interferon and Implications for Disease Pathogenesis
inferredcites →https://doi.org/10.1172/jci113911openalex-snapshot
Human T cell responses to dengue virus antigens. Proliferative responses and interferon gamma production.
inferredcites →https://doi.org/10.1172/jci115457openalex-snapshot
Activation of T lymphocytes in dengue virus infections. High levels of soluble interleukin 2 receptor, soluble CD4, soluble CD8, interleukin 2, and interferon-gamma in sera of children with dengue.
inferredcites →https://doi.org/10.4049/jimmunol.154.3.1287openalex-snapshot
Dengue virus-specific, HLA-B35-restricted, human CD8+ cytotoxic T lymphocyte (CTL) clones. Recognition of NS3 amino acids 500 to 508 by CTL clones of two different serotype specificities.
inferredcites →https://doi.org/10.4269/ajtmh.1958.7.561openalex-snapshot
Techniques for Hemagglutination and Hemagglutination-Inhibition with Arthropod-Borne Viruses
inferredcites →https://doi.org/10.4269/ajtmh.1988.38.172openalex-snapshot
A Prospective Study of Dengue Infections in Bangkok
inferredcites →https://doi.org/10.4269/ajtmh.1989.40.418openalex-snapshot
An Enzyme-Linked Immunosorbent Assay to Characterize Dengue Infections Where Dengue and Japanese Encephalitis Co-Circulate
inferredcites →https://doi.org/10.4269/ajtmh.1993.48.222openalex-snapshot
High Levels of Interferon Alpha in the Sera of Children with Dengue Virus Infection
inferredcites →https://doi.org/10.4269/ajtmh.1993.48.324openalex-snapshot
Serum Levels of Tumor Necrosis Factor-α (TNF-α), Interleukin-6 (IL-6), and Interleukin-1β (IL-1β) in Dengue-Infected Patients

What points at this work

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

inferred← citeshttps://doi.org/10.5281/zenodo.816331openalex-extracted
Host-Virus Interactions In Dengue Infection Indicate Targets For Detection And Therapeutic Interventions
inferred← citeshttps://doi.org/10.1002/eji.200737699openalex-snapshot
Preservation of a critical epitope core region is associated with the high degree of flaviviral cross‐reactivity exhibited by a dengue‐specific CD4+ T cell clone
inferred← citeshttps://doi.org/10.1002/jmv.21051openalex-snapshot
Monocytes, but not T or B cells, are the principal target cells for dengue virus (DV) infection among human peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1002/jmv.25561openalex-snapshot
Significance of RANTES‐CCR5 axis and linked downstream immunomodulation in Dengue pathogenesis: A study from Guwahati, India
inferred← citeshttps://doi.org/10.1002/rmv.2577openalex-snapshot
Role of Gut Microbiota in Dengue
inferred← citeshttps://doi.org/10.1007/978-1-4899-7448-8_15openalex-snapshot
Flaviviruses: Dengue
inferred← citeshttps://doi.org/10.1007/978-1-4939-8567-8_14openalex-snapshot
Cultured ELISpot Assay to Investigate Dengue Virus Specific T-Cell Responses
inferred← citeshttps://doi.org/10.1007/978-1-4939-9544-8_15-1openalex-snapshot
Flaviviruses: Dengue
inferred← citeshttps://doi.org/10.1007/978-3-642-02215-9_7openalex-snapshot
Cellular Immunology of Sequential Dengue Virus Infection and its Role in Disease Pathogenesis
inferred← citeshttps://doi.org/10.1007/s00281-017-0625-1openalex-snapshot
Immune-mediated cytokine storm and its role in severe dengue
inferred← citeshttps://doi.org/10.1007/s00705-023-05814-6openalex-snapshot
Angiotensin II and dengue
inferred← citeshttps://doi.org/10.1007/s11262-014-1087-3openalex-snapshot
Recombinant dengue 2 virus NS3 protein conserves structural antigenic and immunological properties relevant for dengue vaccine design
inferred← citeshttps://doi.org/10.1007/s11306-023-02011-zopenalex-snapshot
Integrated clinical and metabolomic analysis of dengue infection shows molecular signatures associated with host-pathogen interaction in different phases of the disease
inferred← citeshttps://doi.org/10.1007/s40475-013-0009-0openalex-snapshot
Immunopathogenesis versus Protection in Dengue Virus Infections
inferred← citeshttps://doi.org/10.1016/b978-0-12-801078-5.00013-3openalex-snapshot
Viruses Responsible for Hemorrhagic Fevers
inferred← citeshttps://doi.org/10.1016/b978-0-443-06839-3.00153-3openalex-snapshot
Flaviviruses (Yellow Fever, Dengue, Dengue Hemorrhagic Fever, Japanese Encephalitis, West Nile Encephalitis, St. Louis Encephalitis, Tick-Borne Encephalitis)
inferred← citeshttps://doi.org/10.1016/b978-0-443-15283-2.00009-9openalex-snapshot
Role of cytokines in Dengue infection
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4801-3.00155-7openalex-snapshot
Flaviviruses (Dengue, Yellow Fever, Japanese Encephalitis, West Nile Encephalitis, St. Louis Encephalitis, Tick-Borne Encephalitis, Kyasanur Forest Disease, Alkhurma Hemorrhagic Fever, Zika)
inferred← citeshttps://doi.org/10.1016/j.ajpath.2013.02.027openalex-snapshot
Inflammatory and Innate Immune Responses in Dengue Infection
inferred← citeshttps://doi.org/10.1016/j.amepre.2015.09.006openalex-snapshot
Trials and Tribulations on the Path to Developing a Dengue Vaccine
inferred← citeshttps://doi.org/10.1016/j.antiviral.2008.06.010openalex-snapshot
Mouse models of dengue virus infection and disease
inferred← citeshttps://doi.org/10.1016/j.antiviral.2012.04.006openalex-snapshot
Serotype specificity of recombinant fusion protein containing domain III and capsid protein of dengue virus 2
inferred← citeshttps://doi.org/10.1016/j.chom.2016.12.010openalex-snapshot
Mapping and Role of the CD8 + T Cell Response During Primary Zika Virus Infection in Mice
inferred← citeshttps://doi.org/10.1016/j.coviro.2018.03.004openalex-snapshot
The use of longitudinal cohorts for studies of dengue viral pathogenesis and protection
inferred← citeshttps://doi.org/10.1016/j.cyto.2015.03.021openalex-snapshot
Association of combinations of interleukin-10 and pro-inflammatory cytokine gene polymorphisms with dengue hemorrhagic fever
inferred← citeshttps://doi.org/10.1016/j.femsim.2004.11.012openalex-snapshot
Altered T helper 1 reaction but not increase of virus load in patients with dengue hemorrhagic fever
inferred← citeshttps://doi.org/10.1016/j.humimm.2010.08.004openalex-snapshot
Tumor necrosis factor–alpha, transforming growth factor–β1, and interleukin-10 gene polymorphisms: implication in protection or susceptibility to dengue hemorrhagic fever
inferred← citeshttps://doi.org/10.1016/j.humimm.2013.01.027openalex-snapshot
Association of HLA-DRB1 and TNF genotypes with dengue hemorrhagic fever
inferred← citeshttps://doi.org/10.1016/j.jaut.2017.04.008openalex-snapshot
Original antigenic sin: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.jcv.2018.09.020openalex-snapshot
CD4 T cell responses to flaviviruses
inferred← citeshttps://doi.org/10.1016/j.meegid.2018.04.032openalex-snapshot
Understanding dengue virus evolution to support epidemic surveillance and counter-measure development
inferred← citeshttps://doi.org/10.1016/j.micinf.2007.03.012openalex-snapshot
Characterization of humoral and cellular immune responses in cynomolgus macaques upon primary and subsequent heterologous infections with dengue viruses
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2010.08.024openalex-snapshot
Monthly district level risk of dengue occurrences in Sakon Nakhon Province, Thailand
inferred← citeshttps://doi.org/10.1016/j.trstmh.2007.06.019openalex-snapshot
Different clinical and laboratory manifestations between dengue haemorrhagic fever and dengue fever with bleeding tendency
inferred← citeshttps://doi.org/10.1016/j.vaccine.2006.03.066openalex-snapshot
Innate and adaptive cellular immunity in flavivirus-naïve human recipients of a live-attenuated dengue serotype 3 vaccine produced in Vero cells (VDV3)
inferred← citeshttps://doi.org/10.1016/j.vaccine.2007.02.079openalex-snapshot
Scientific consultation on immunological correlates of protection induced by dengue vaccines
inferred← citeshttps://doi.org/10.1016/j.vaccine.2008.08.019openalex-snapshot
Cell-mediated immunity induced by chimeric tetravalent dengue vaccine in naive or flavivirus-primed subjects
inferred← citeshttps://doi.org/10.1016/j.vaccine.2008.10.086openalex-snapshot
Scientific consultation on cell mediated immunity (CMI) in dengue and dengue vaccine development
inferred← citeshttps://doi.org/10.1016/j.vaccine.2009.09.098openalex-snapshot
Preclinical and clinical development of YFV 17D-based chimeric vaccines against dengue, West Nile and Japanese encephalitis viruses
inferred← citeshttps://doi.org/10.1016/j.vaccine.2011.03.038openalex-snapshot
A human challenge model for dengue infection reveals a possible protective role for sustained interferon gamma levels during the acute phase of illness
inferred← citeshttps://doi.org/10.1016/j.vaccine.2011.06.094openalex-snapshot
From research to phase III: Preclinical, industrial and clinical development of the Sanofi Pasteur tetravalent dengue vaccine
inferred← citeshttps://doi.org/10.1016/j.vaccine.2011.07.022openalex-snapshot
The pathogenesis of dengue
inferred← citeshttps://doi.org/10.1016/j.vaccine.2013.07.082openalex-snapshot
A model international partnership for community-based research on vaccine-preventable diseases: The Kamphaeng Phet-AFRIMS Virology Research Unit (KAVRU)
inferred← citeshttps://doi.org/10.1016/j.vaccine.2015.05.095openalex-snapshot
Trials and tribulations on the path to developing a dengue vaccine
inferred← citeshttps://doi.org/10.1016/j.vaccine.2015.09.104openalex-snapshot
Analysis of cell-mediated immune responses in support of dengue vaccine development efforts
inferred← citeshttps://doi.org/10.1016/j.vetimm.2005.10.003openalex-snapshot
Replication of West Nile virus in equine peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1016/s0065-3527(03)60010-2openalex-snapshot
Immunology and Immunopathogenesis of Dengue Disease
inferred← citeshttps://doi.org/10.1016/s0958-1669(03)00061-2openalex-snapshot
Vaccines for the prevention of neglected diseases — dengue fever
inferred← citeshttps://doi.org/10.1016/s1473-3099(09)70254-3openalex-snapshot
Progress towards a dengue vaccine
inferred← citeshttps://doi.org/10.1038/nri3014openalex-snapshot
Immunity to dengue virus: a tale of original antigenic sin and tropical cytokine storms
inferred← citeshttps://doi.org/10.1038/s41590-018-0210-3openalex-snapshot
The immune response against flaviviruses
inferred← citeshttps://doi.org/10.1038/s41590-023-01654-3openalex-snapshot
Global and cell type-specific immunological hallmarks of severe dengue progression identified via a systems immunology approach
inferred← citeshttps://doi.org/10.1038/s41598-019-56381-3openalex-snapshot
Impaired production of immune mediators in dengue virus type 2-infected mononuclear cells of adults with end stage renal disease
inferred← citeshttps://doi.org/10.1038/sj.icb.7100008openalex-snapshot
Of cascades and perfect storms: the immunopathogenesis of dengue haemorrhagic fever‐dengue shock syndrome (DHF/DSS)
inferred← citeshttps://doi.org/10.1080/17460441.2020.1718099openalex-snapshot
What translatable knowledge from dengue vaccine design can we pass onto future anti-parasitic vaccine development?
inferred← citeshttps://doi.org/10.1080/22221751.2019.1685913openalex-snapshot
Dengue haemorrhagic fever: a job done via exosomes?
inferred← citeshttps://doi.org/10.1086/381768openalex-snapshot
Impaired T Helper 1 Function of Nonstructural Protein 3–Specific T Cells in Japanese Patients with Encephalitis with Neurological Sequelae
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1086/526790openalex-snapshot
Cross‐Reactive Memory CD8+T Cells Alter the Immune Response to Heterologous Secondary Dengue Virus Infections in Mice in a Sequence‐Specific Manner
inferred← citeshttps://doi.org/10.1086/596507openalex-snapshot
Patterns of Gene Transcript Abundance in the Blood of Children with Severe or Uncomplicated Dengue Highlight Differences in Disease Evolution and Host Response to Dengue Virus Infection
inferred← citeshttps://doi.org/10.1089/vim.2010.0034openalex-snapshot
Differential In Vivo Clearance and Response to Secondary Heterologous Infections by H2 b -Restricted Dengue Virus-Specific CD8 + T Cells
inferred← citeshttps://doi.org/10.1093/infdis/jir012openalex-snapshot
Intracellular Cytokine Production by Dengue Virus–specific T cells Correlates with Subclinical Secondary Infection
inferred← citeshttps://doi.org/10.1097/01.qco.0000244047.31135.faopenalex-snapshot
Immunopathological mechanisms in dengue and dengue hemorrhagic fever
inferred← citeshttps://doi.org/10.1101/2022.12.11.519930openalex-snapshot
Global and cell type-specific immunological hallmarks of severe dengue progression
inferred← citeshttps://doi.org/10.1109/tbme.2019.2897285openalex-snapshot
Severe Dengue Prognosis Using Human Genome Data and Machine Learning
inferred← citeshttps://doi.org/10.1111/eva.12554openalex-snapshot
Challenges in dengue research: A computational perspective
inferred← citeshttps://doi.org/10.1111/imm.12863openalex-snapshot
Regulatory T‐cells in acute dengue viral infection
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2009.05055.xopenalex-snapshot
T Lymphocyte Responses to Heterologous Secondary Dengue Virus Infections
inferred← citeshttps://doi.org/10.1128/cmr.00035-09openalex-snapshot
Dengue Virus Pathogenesis: an Integrated View
inferred← citeshttps://doi.org/10.1128/jvi.00313-07openalex-snapshot
Dengue Virus (DV) Replication in Monocyte-Derived Macrophages Is Not Affected by Tumor Necrosis Factor Alpha (TNF-α), and DV Infection Induces Altered Responsiveness to TNF-α Stimulation
inferred← citeshttps://doi.org/10.1128/jvi.01568-07openalex-snapshot
Primary Human Splenic Macrophages, but Not T or B Cells, Are the Principal Target Cells for Dengue Virus Infection In Vitro
inferred← citeshttps://doi.org/10.1128/jvi.02575-06openalex-snapshot
Both Virus and Tumor Necrosis Factor Alpha Are Critical for Endothelium Damage in a Mouse Model of Dengue Virus-Induced Hemorrhage
inferred← citeshttps://doi.org/10.1128/jvi.79.5.2900-2909.2005openalex-snapshot
Cellular and Humoral Immunity following Snow Mountain Virus Challenge
inferred← citeshttps://doi.org/10.1128/msphere.00671-19openalex-snapshot
Cell-Mediated Immunity Generated in Response to a Purified Inactivated Vaccine for Dengue Virus Type 1
inferred← citeshttps://doi.org/10.1142/9781848162297_0008openalex-snapshot
Elimination of Infection
inferred← citeshttps://doi.org/10.1146/annurev-immunol-031210-101315openalex-snapshot
Immune Response to Dengue Virus and Prospects for a Vaccine
inferred← citeshttps://doi.org/10.1146/annurev-immunol-042617-053142openalex-snapshot
Immune Response to Dengue and Zika
inferred← citeshttps://doi.org/10.1155/2013/648475openalex-snapshot
HLA-B*44 Is Associated with Dengue Severity Caused by DENV-3 in a Brazilian Population
inferred← citeshttps://doi.org/10.1155/2013/843469openalex-snapshot
The Battle between Infection and Host Immune Responses of Dengue Virus and Its Implication in Dengue Disease Pathogenesis
inferred← citeshttps://doi.org/10.11606/d.17.2010.tde-26082010-152600openalex-snapshot
Avaliação de um modelo animal para estudo da infecção pelo vírus da dengue
inferred← citeshttps://doi.org/10.11606/d.42.2012.tde-03082012-083441openalex-snapshot
Análise das respostas adaptativas quando um antígeno do vírus da dengue é direcionado para duas populações distintas de células dendríticas.
inferred← citeshttps://doi.org/10.1172/jci.insight.94500openalex-snapshot
Dengue vaccine–induced CD8+ T cell immunity confers protection in the context of enhancing, interfering maternal antibodies
inferred← citeshttps://doi.org/10.1172/jci21512openalex-snapshot
Dengue: defining protective versus pathologic immunity
inferred← citeshttps://doi.org/10.1177/14703203261485159openalex-snapshot
Severe dengue evolution in obesity: Possible role of angiotensin II
inferred← citeshttps://doi.org/10.1186/1471-2172-11-47openalex-snapshot
Bystander T cells in human immune responses to dengue antigens
inferred← citeshttps://doi.org/10.1186/1471-2334-10-356openalex-snapshot
Acute dengue virus 2 infection in Gabonese patients is associated with an early innate immune response, including strong interferon alpha production
inferred← citeshttps://doi.org/10.1186/1471-2334-8-86openalex-snapshot
Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
inferred← citeshttps://doi.org/10.13028/7n2k-2n29openalex-snapshot
CD8+ T Cell Serotype-Cross-Reactivity is a Predominant Feature of Dengue Virus Infections in Humans: A Dissertation
inferred← citeshttps://doi.org/10.13028/m27g7sopenalex-snapshot
CD8+ T Cell and NK Responses to a Novel Dengue Epitope: A Possible Role for KIR3DL1 in Dengue Pathogenesis: A Dissertation
inferred← citeshttps://doi.org/10.13028/s0dv-7754openalex-snapshot
Serotype Cross-Reactive CD8+ T Cell Response to Heterologous Secondary Dengue Virus Infections in Humans: a Dissertation
inferred← citeshttps://doi.org/10.13028/t0x5-az54openalex-snapshot
Cross-Reactive Memory CD4+ and CD8+ T Cells Alter the Immune Response to Heterologous Secondary Dengue Virus Infections in Mice: A Dissertation
inferred← citeshttps://doi.org/10.1371/journal.pntd.0001449openalex-snapshot
IFN-γ Production Depends on IL-12 and IL-18 Combined Action and Mediates Host Resistance to Dengue Virus Infection in a Nitric Oxide-Dependent Manner
inferred← citeshttps://doi.org/10.1371/journal.pntd.0006975openalex-snapshot
Protective versus pathologic pre-exposure cytokine profiles in dengue virus infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0007892openalex-snapshot
Gene Expression Profiling during Early Acute Febrile Stage of Dengue Infection Can Predict the Disease Outcome
inferred← citeshttps://doi.org/10.1371/journal.pone.0140545openalex-snapshot
Human CD4+ T Helper Cell Responses after Tick-Borne Encephalitis Vaccination and Infection
inferred← citeshttps://doi.org/10.1586/14760584.2013.815412openalex-snapshot
Dengue vaccines: recent developments, ongoing challenges and current candidates
inferred← citeshttps://doi.org/10.1586/14760584.2016.1116949openalex-snapshot
Immune correlates for dengue vaccine development
inferred← citeshttps://doi.org/10.1586/14787210.3.5.689openalex-snapshot
Dengue: translating scientific progress into workable solutions
inferred← citeshttps://doi.org/10.1586/17474086.2015.1071186openalex-snapshot
Infectious complications in children with acute lymphoblastic leukemia treated in low-middle-income countries
inferred← citeshttps://doi.org/10.1590/s0074-02762012000100007openalex-snapshot
Profile of circulating levels of IL-1Ra, CXCL10/IP-10, CCL4/MIP-1β and CCL2/MCP-1 in dengue fever and parvovirosis
inferred← citeshttps://doi.org/10.17533/udea.iatreia.09openalex-snapshot
Inmunopatología del dengue: importancia y participación de los monocitos y sus subpoblaciones
inferred← citeshttps://doi.org/10.2217/fmb.13.171openalex-snapshot
Elucidating the Role of T cells in Protection Against and Pathogenesis of Dengue Virus Infections
inferred← citeshttps://doi.org/10.32657/10356/155246openalex-snapshot
Role of glycolysis in myeloid cells during dengue infection
inferred← citeshttps://doi.org/10.3389/fcimb.2022.887729openalex-snapshot
Mucosal Vaccination: A Promising Alternative Against Flaviviruses
inferred← citeshttps://doi.org/10.3389/fimmu.2014.00093openalex-snapshot
T-Cell Immunity to Infection with Dengue Virus in Humans
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01316openalex-snapshot
Cross-Reactive T Cell Immunity to Dengue and Zika Viruses: New Insights Into Vaccine Development
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01359openalex-snapshot
Longitudinal Analysis of Memory B and T Cell Responses to Dengue Virus in a 5-Year Prospective Cohort Study in Thailand
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01522openalex-snapshot
T Cell Responses Induced by DNA Vaccines Based on the DENV2 E and NS1 Proteins in Mice: Importance in Protection and Immunodominant Epitope Identification
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00513openalex-snapshot
Virus-Induced T Cell-Mediated Heterologous Immunity and Vaccine Development
inferred← citeshttps://doi.org/10.3389/fimmu.2021.710300openalex-snapshot
Longitudinal Analysis of Dengue Virus–Specific Memory T Cell Responses and Their Association With Clinical Outcome in Subsequent DENV Infection
inferred← citeshttps://doi.org/10.3390/covid3090089openalex-snapshot
Biology and Behavior of Severe Acute Respiratory Syndrome Coronavirus Contagion with Emphasis on Treatment Strategies, Risk Assessment, and Resilience
inferred← citeshttps://doi.org/10.3390/microorganisms7090296openalex-snapshot
Contemporary Strategies and Current Trends in Designing Antiviral Drugs against Dengue Fever via Targeting Host-Based Approaches
inferred← citeshttps://doi.org/10.3390/pathogens12111362openalex-snapshot
Viremia and Inflammatory Cytokines in Dengue: Interleukin-2 as a Biomarker of Infection, and Interferon-α and -γ as Markers of Primary versus Secondary Infection
inferred← citeshttps://doi.org/10.3390/pathogens9060470openalex-snapshot
Adaptive Immunity to Dengue Virus: Slippery Slope or Solid Ground for Rational Vaccine Design?
inferred← citeshttps://doi.org/10.3390/v9060159openalex-snapshot
Garlic Organosulfur Compounds Reduce Inflammation and Oxidative Stress during Dengue Virus Infection
inferred← citeshttps://doi.org/10.3390/vaccines7010011openalex-snapshot
T-Cell Response to Viral Hemorrhagic Fevers
inferred← citeshttps://doi.org/10.3390/vaccines7040203openalex-snapshot
Considering Genomic and Immunological Correlates of Protection for a Dengue Intervention
inferred← citeshttps://doi.org/10.4049/jimmunol.1600846openalex-snapshot
A Role for Human Skin Mast Cells in Dengue Virus Infection and Systemic Spread
inferred← citeshttps://doi.org/10.4049/jimmunol.175.4.2676openalex-snapshot
Altered Cytokine Responses of Dengue-Specific CD4+ T Cells to Heterologous Serotypes
inferred← citeshttps://doi.org/10.4103/ajim.ajim_96_21openalex-snapshot
Original Antigenic Sin in Dengue - Hoskins Effect
inferred← citeshttps://doi.org/10.4161/hv.25562openalex-snapshot
Persistence of Th1/Tc1 responses one year after tetravalent dengue vaccination in adults and adolescents in Singapore
inferred← citeshttps://doi.org/10.4269/ajtmh.2009.80.656openalex-snapshot
Comparison of Two Active Surveillance Programs for the Detection of Clinical Dengue Cases in Iquitos, Peru
inferred← citeshttps://doi.org/10.5123/s2176-62232011000200008openalex-snapshot
Desenvolvimento de uma vacina tetravalente contra dengue
inferred← citeshttps://doi.org/10.70675/84773006z54bez4906zb40dzc0f24aaeb05aopenalex-snapshot
Contribution à la caractérisation moléculaire et cellulaire des chimères YF-17D / Dengue dans le cadre du développement préclinique du vaccin Dengvaxia®
inferred← citeshttps://doi.org/10.70675/bf5a816fz6c11z48f0z93d2z08f03ee2c8a0openalex-snapshot
Le Syndrome de choc de dengue, approches clinique et in vitro
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.