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CD4 T-Cell Subsets in Malaria: TH1/TH2 Revisited

https://doi.org/10.3389/fimmu.2014.00671

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

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The immune response to Plasmodium chabaudi malaria in interleukin‐4‐deficient mice

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IL‐6: Regulator of Treg/Th17 balance

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Type I interferons suppress CD4+ T‐cell‐dependent parasite control during blood‐stage Plasmodium infection

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Type I interferon potentiates T ‐cell receptor mediated induction of IL ‐10‐producing CD 4+ T cells

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T‐bet modulates the antibody response and immune protection during murine malaria

inferredcites →https://doi.org/10.1006/expr.1996.0108openalex-snapshot

Plasmodium yoelii:Peptide Immunization Induces Protective CD4+T Cells against a Previously Unrecognized Cryptic Epitope of the Circumsporozoite Protein

inferredcites →https://doi.org/10.1006/expr.1996.0111openalex-snapshot

Plasmodium chabaudi chabaudi:Differential Susceptibility of Gene-Targeted Mice Deficient in IL-10 to an Erythrocytic-Stage Infection

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Whole-Genome Analysis of Plasmodium spp. Utilizing a New Agilent Technologies DNA Microarray Platform

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Life Cycles and Morphology

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Development of experimental cerebral malaria is independent of IL-23 and IL-17

inferredcites →https://doi.org/10.1016/j.celrep.2013.11.002openalex-snapshot

PD-1 Dependent Exhaustion of CD8+ T Cells Drives Chronic Malaria

inferredcites →https://doi.org/10.1016/j.chom.2009.01.004openalex-snapshot

Host-Parasite Interactions Revealed by Plasmodium falciparum Metabolomics

inferredcites →https://doi.org/10.1016/j.chom.2010.01.008openalex-snapshot

Eating at the Table of Another: Metabolomics of Host-Parasite Interactions

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Helper T cell diversity and plasticity

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Malaria antigen-mediated enhancement of interleukin-21 responses of peripheral blood mononuclear cells in African adults

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Differential role of T regulatory and Th17 in Swiss mice infected with Plasmodium berghei ANKA and Plasmodium yoelii

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Classical CD11c+ dendritic cells, not plasmacytoid dendritic cells, induce T cell responses to Plasmodium chabaudi malaria

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Functional and Epigenetic Studies Reveal Multistep Differentiation and Plasticity of In Vitro-Generated and In Vivo-Derived Follicular T Helper Cells

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Human Circulating PD-1+CXCR3−CXCR5+ Memory Tfh Cells Are Highly Functional and Correlate with Broadly Neutralizing HIV Antibody Responses

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The contribution of Plasmodium chabaudi to our understanding of malaria

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Systems immunology of human malaria

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Signal transduction pathways and transcriptional regulation in the control of Th17 differentiation

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Plasmodium falciparum apical membrane antigen 1 vaccine elicits multifunctional CD4 cytokine-producing and memory T cells

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The Roles of Cytokines Produced in the Immune Response to the Erythrocytic Stages of Mouse Malarias

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Insights into the immunopathogenesis of malaria using mouse models

inferredcites →https://doi.org/10.1038/gene.2013.20openalex-snapshot

Unique transcriptional profile of liver-resident memory CD8+ T cells induced by immunization with malaria sporozoites

inferredcites →https://doi.org/10.1038/nature10957openalex-snapshot

Pathogen-induced human TH17 cells produce IFN-γ or IL-10 and are regulated by IL-1β

inferredcites →https://doi.org/10.1038/ni.1767openalex-snapshot

Production of interleukin 22 but not interleukin 17 by a subset of human skin-homing memory T cells

inferredcites →https://doi.org/10.1038/ni.1770openalex-snapshot

Identification of a human helper T cell population that has abundant production of interleukin 22 and is distinct from TH-17, TH1 and TH2 cells

inferredcites →https://doi.org/10.1038/ni.1899openalex-snapshot

Effector T cell plasticity: flexibility in the face of changing circumstances

inferredcites →https://doi.org/10.1038/ni.2025openalex-snapshot

Border patrol: regulation of immunity, inflammation and tissue homeostasis at barrier surfaces by IL-22

inferredcites →https://doi.org/10.1038/ni.2180openalex-snapshot

Therapeutic blockade of PD-L1 and LAG-3 rapidly clears established blood-stage Plasmodium infection

inferredcites →https://doi.org/10.1038/ni1539openalex-snapshot

TGF-β and IL-6 drive the production of IL-17 and IL-10 by T cells and restrain TH-17 cell–mediated pathology

inferredcites →https://doi.org/10.1038/nm.3109openalex-snapshot

Inadequate T follicular cell help impairs B cell immunity during HIV infection

inferredcites →https://doi.org/10.1038/nm0202-166openalex-snapshot

IL-4-secreting CD4+ T cells are crucial to the development of CD8+ T-cell responses against malaria liver stages

inferredcites →https://doi.org/10.1038/nm1009openalex-snapshot

A CD4+ T-cell immune response to a conserved epitope in the circumsporozoite protein correlates with protection from natural Plasmodium falciparum infection and disease

inferredcites →https://doi.org/10.1038/nm1592openalex-snapshot

Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major

inferredcites →https://doi.org/10.1038/nm1628openalex-snapshot

CD8+ T lymphocytes protective against malaria liver stages are primed in skin-draining lymph nodes

inferredcites →https://doi.org/10.1038/nprot.2006.69openalex-snapshot

Real-time in vivo imaging of transgenic bioluminescent blood stages of rodent malaria parasites in mice

inferredcites →https://doi.org/10.1038/nri2097openalex-snapshot

TH1 cells control themselves by producing interleukin-10

inferredcites →https://doi.org/10.1038/nri2274openalex-snapshot

T-cell quality in memory and protection: implications for vaccine design

inferredcites →https://doi.org/10.1038/nrmicro3111openalex-snapshot

Looking under the skin: the first steps in malarial infection and immunity

inferredcites →https://doi.org/10.1038/sj.gene.6364214openalex-snapshot

Investigation of malaria susceptibility determinants in the IFNG/IL26/IL22 genomic region

inferredcites →https://doi.org/10.1038/sj.icb.7100040openalex-snapshot

Intravascular infiltrates and organ‐specific inflammation in malaria pathogenesis

inferredcites →https://doi.org/10.1038/srep03549openalex-snapshot

Pre-erythrocytic antibody profiles induced by controlled human malaria infections in healthy volunteers under chloroquine prophylaxis

inferredcites →https://doi.org/10.1073/pnas.0806727105openalex-snapshot

Blood-stage Plasmodium infection induces CD8 + T lymphocytes to parasite-expressed antigens, largely regulated by CD8α + dendritic cells

inferredcites →https://doi.org/10.1073/pnas.1001323107openalex-snapshot

A prospective analysis of the Ab response to Plasmodium falciparum before and after a malaria season by protein microarray

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In vivo imaging of CD8 + T cell-mediated elimination of malaria liver stages

inferredcites →https://doi.org/10.1073/pnas.87.14.5484openalex-snapshot

Production by activated human T cells of interleukin 4 but not interferon-gamma is associated with elevated levels of serum antibodies to activating malaria antigens.

inferredcites →https://doi.org/10.1084/jem.20052450openalex-snapshot

Malaria infection changes the ability of splenic dendritic cell populations to stimulate antigen-specific T cells

inferredcites →https://doi.org/10.1093/infdis/jiu293openalex-snapshot

Cytotoxic Markers Associate With Protection Against Malaria in Human Volunteers Immunized With Plasmodium falciparum Sporozoites

inferredcites →https://doi.org/10.1093/infdis/jiu354openalex-snapshot

Memory B-Cell and Antibody Responses Induced by Plasmodium falciparum Sporozoite Immunization

inferredcites →https://doi.org/10.1093/intimm/1.4.416openalex-snapshot

Frequencies of CD4+ T cells reactive with Plasmodium chabaudi chabaudi: distinct response kinetics for cells with Th1 and Th2 characteristics during infection

inferredcites →https://doi.org/10.1098/rsob.120157openalex-snapshot

Plasticity within the αβ+CD4+T-cell lineage: when, how and what for?

inferredcites →https://doi.org/10.1111/imr.12029openalex-snapshot

Metabolic control of the Treg/Th17 axis

inferredcites →https://doi.org/10.1111/j.1365-2249.1993.tb05951.xopenalex-snapshot

Differential induction of helper T cell subsets during blood-stagePlasmodium chabaudiAS infection in resistant and susceptible mice

inferredcites →https://doi.org/10.1111/j.1365-2567.2010.03363.xopenalex-snapshot

Phenotypic and functional profiling of malaria-induced CD8 and CD4 T cells during blood-stage infection with Plasmodium yoelii

inferredcites →https://doi.org/10.1111/j.1600-065x.1989.tb00553.xopenalex-snapshot

The Response of CD4+ T Cells to Plasmodium chabaudi chabaudi

inferredcites →https://doi.org/10.1126/science.162.3849.123openalex-snapshot

Interferon Induced by Plasmodium berghei

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Class II-Restricted Protective Immunity Induced by Malaria Sporozoites

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Full-Length Plasmodium falciparum Circumsporozoite Protein Administered with Long-Chain Poly(I·C) or the Toll-Like Receptor 4 Agonist Glucopyranosyl Lipid Adjuvant-Stable Emulsion Elicits Potent Antibody and CD4+T Cell Immunity and Protection in Mice

inferredcites →https://doi.org/10.1128/iai.58.11.3671-3678.1990openalex-snapshot

Role of gamma interferon during infection with Plasmodium chabaudi chabaudi

inferredcites →https://doi.org/10.1128/iai.68.8.4399-4406.2000openalex-snapshot

Central Role of Endogenous Gamma Interferon in Protective Immunity against Blood-Stage Plasmodium chabaudi AS Infection

inferredcites →https://doi.org/10.1146/annurev-immunol-031210-101400openalex-snapshot

Follicular Helper CD4 T Cells (T FH )

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TH1 and TH2 Cells: Different Patterns of Lymphokine Secretion Lead to Different Functional Properties

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Type I IFN signaling in CD8– DCs impairs Th1-dependent malaria immunity

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Malaria-specific transgenic CD4+ T cells protect immunodeficient mice from lethal infection and demonstrate requirement for a protective threshold of antibody production for parasite clearance

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HIV nonprogressors preferentially maintain highly functional HIV-specific CD8+ T cells

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Interferon-γ—central mediator of protective immune responses against the pre-erythrocytic and blood stage of malaria

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CD4+ T Cells Modulate Expansion and Survival but Not Functional Properties of Effector and Memory CD8+ T Cells Induced by Malaria Sporozoites

inferredcites →https://doi.org/10.1371/journal.pone.0028432openalex-snapshot

Type I IFN Promotes IL-10 Production from T Cells to Suppress Th17 Cells and Th17-Associated Autoimmune Inflammation

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Phenotypic and Functional Profiling of CD4 T Cell Compartment in Distinct Populations of Healthy Adults with Different Antigenic Exposure

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IL-10 from CD4+CD25−Foxp3−CD127− Adaptive Regulatory T Cells Modulates Parasite Clearance and Pathology during Malaria Infection

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Distinct Roles for FOXP3+ and FOXP3− CD4+ T Cells in Regulating Cellular Immunity to Uncomplicated and Severe Plasmodium falciparum Malaria

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Effector Memory Th1 CD4 T Cells Are Maintained in a Mouse Model of Chronic Malaria

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IFNγ/IL-10 Co-producing Cells Dominate the CD4 Response to Malaria in Highly Exposed Children

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Exposure-Dependent Control of Malaria-Induced Inflammation in Children

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Metabolomics in the fight against malaria

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Interleukin-21 is associated with IgG1 and IgG3 antibodies to erythrocyte-binding antigen-175 peptide 4 of Plasmodium falciparum in Gabonese children with acute falciparum malaria.

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IL-22 Protects Against Liver Pathology and Lethality of an Experimental Blood-Stage Malaria Infection

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Filarial Infection Suppresses Malaria-Specific Multifunctional Th1 and Th17 Responses in Malaria and Filarial Coinfections

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MHC Class II Tetramers

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IL-27 Promotes IL-10 Production by Effector Th1 CD4+ T Cells: A Critical Mechanism for Protection from Severe Immunopathology during Malaria Infection

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IFN-γ–Producing CD4+ T Cells Promote Experimental Cerebral Malaria by Modulating CD8+ T Cell Accumulation within the Brain

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Chronic Exposure to Plasmodium falciparum Is Associated with Phenotypic Evidence of B and T Cell Exhaustion

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The Transcription Factor T-bet Regulates Parasitemia and Promotes Pathogenesis during Plasmodium berghei ANKA Murine Malaria

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IFN-γ–Induced Priming Maintains Long-Term Strain-Transcending Immunity against Blood-Stage Plasmodium chabaudi Malaria

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Production of IL 2 and IFN-gamma by T cells from malaria patients in response to Plasmodium falciparum or erythrocyte antigens in vitro.

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Role of IFN-gamma in lethal and nonlethal malaria in susceptible and resistant murine hosts.

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T and B cell responses of Plasmodium falciparum malaria-immune individuals to synthetic peptides corresponding to sequences in different regions of the P. falciparum antigen Pf155/RESA.

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Effector functions of circumsporozoite peptide-primed CD4+ T cell clones against Plasmodium yoelii liver stages

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IFN-α and IL-10 Induce the Differentiation of Human Type 1 T Regulatory Cells

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Type I IFN Negatively Regulates CD8+ T Cell Responses through IL-10-Producing CD4+ T Regulatory 1 Cells

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

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inferred← citeshttps://doi.org/10.1016/j.vaccine.2024.02.070openalex-snapshot

Non-clinical toxicity and immunogenicity evaluation of a Plasmodium vivax malaria vaccine using Poly-ICLC (Hiltonol®) as adjuvant

inferred← citeshttps://doi.org/10.1017/s0031182015001092openalex-snapshot

Examining cellular immune responses to inform development of a blood-stage malaria vaccine

inferred← citeshttps://doi.org/10.1017/s0031182016001694openalex-snapshot

The role of chemokines and their receptors during protist parasite infections

inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.4c00460openalex-snapshot

Modular Display of Plasmodium yoelii Circumsporozoite Surface Protein and Merozoite Surface Protein-1 on Norovirus-like Particles

inferred← citeshttps://doi.org/10.1038/cddis.2015.112openalex-snapshot

PD-1 and Tim-3 pathways are associated with regulatory CD8+ T-cell function in decidua and maintenance of normal pregnancy

inferred← citeshttps://doi.org/10.1038/nm.4395openalex-snapshot

Regulatory T cells impede acute and long-term immunity to blood-stage malaria through CTLA-4

inferred← citeshttps://doi.org/10.1038/s41420-020-00363-2openalex-snapshot

Mesenchymal stem cells protect against malaria pathogenesis by reprogramming erythropoiesis in the bone marrow

inferred← citeshttps://doi.org/10.1038/s41421-024-00681-0openalex-snapshot

Specialized Tfh cell subsets driving type-1 and type-2 humoral responses in lymphoid tissue

inferred← citeshttps://doi.org/10.1038/s41467-023-42235-0openalex-snapshot

Gut Bacteroides act in a microbial consortium to cause susceptibility to severe malaria

inferred← citeshttps://doi.org/10.1038/s41577-019-0158-zopenalex-snapshot

T cell-mediated immunity to malaria

inferred← citeshttps://doi.org/10.1038/s41598-017-09099-zopenalex-snapshot

Longitudinal study of changes in γδ T cells and CD4+ T cells upon asymptomatic malaria infection in Indonesian children

inferred← citeshttps://doi.org/10.1038/s41598-017-10776-2openalex-snapshot

Mechanism of splenic cell death and host mortality in a Plasmodium yoelii malaria model

inferred← citeshttps://doi.org/10.1038/s41598-018-22659-1openalex-snapshot

Differential expression pattern of co-inhibitory molecules on CD4+ T cells in uncomplicated versus complicated malaria

inferred← citeshttps://doi.org/10.1038/s41598-018-33599-1openalex-snapshot

Detection of host pathways universally inhibited after Plasmodium yoelii infection for immune intervention

inferred← citeshttps://doi.org/10.1038/s41598-022-05344-2openalex-snapshot

Bacillus subtilis spores as delivery system for nasal Plasmodium falciparum circumsporozoite surface protein immunization in a murine model

inferred← citeshttps://doi.org/10.1038/s41598-025-90473-7openalex-snapshot

The differential effect of Interferon-gamma on acute kidney injury and parasitemia in experimental malaria

inferred← citeshttps://doi.org/10.1038/srep34527openalex-snapshot

A chimeric protein-based malaria vaccine candidate induces robust T cell responses against Plasmodium vivax MSP119

inferred← citeshttps://doi.org/10.1039/c9fo02376copenalex-snapshot

Effect of transglutaminase cross-linking on the allergenicity of tofu based on a BALB/c mouse model

inferred← citeshttps://doi.org/10.1080/08830185.2024.2336539openalex-snapshot

Cerebral malaria pathogenesis: Dissecting the role of CD4 + and CD8 + T-cells as major effectors in disease pathology

inferred← citeshttps://doi.org/10.1080/21505594.2020.1726569openalex-snapshot

Balancing in a black box: Potential immunomodulatory roles for TGF-β signaling during blood-stage malaria

inferred← citeshttps://doi.org/10.1080/22221751.2025.2552783openalex-snapshot

Conserved multiepitopes in Plasmodium falciparum STEVORs enable rational design of a fusion antigen vaccine construct with broad immunogenicity

inferred← citeshttps://doi.org/10.1084/jem.20201313openalex-snapshot

How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein

inferred← citeshttps://doi.org/10.1096/fj.202401237ropenalex-snapshot

Myeloid‐derived suppressor cells inhibit responses of T follicular helper cells during experimental Plasmodium yoelii infection

inferred← citeshttps://doi.org/10.1101/074971openalex-snapshot

Temporal mixture modelling of single-cell RNA-seq data resolves a CD4 + T cell fate bifurcation

inferred← citeshttps://doi.org/10.1101/2020.12.17.423374openalex-snapshot

The dynamic landscape of parasitaemia dependent intestinal microbiota shifting at species level and the correlated gut transcriptome during Plasmodium yoelii infection

inferred← citeshttps://doi.org/10.1101/2023.04.17.537202openalex-snapshot

The impact of innate immunity on malaria parasite infection dynamics

inferred← citeshttps://doi.org/10.1101/501957openalex-snapshot

Profiling gene expression of the host response to a Plasmodium vivax irradiated sporozoite immunization and infectious challenge

inferred← citeshttps://doi.org/10.1111/1440-1681.12699openalex-snapshot

Decreased percentage of NKG 2D+ NK cells in patients with incident onset of Type 1 Diabetes

inferred← citeshttps://doi.org/10.1111/imr.12814openalex-snapshot

Deciphering host immunity to malaria using systems immunology

inferred← citeshttps://doi.org/10.1111/pim.12220openalex-snapshot

Administration of naloxone in combination with recombinantPlasmodium vivax AMA ‐1 in BALB /c mice induces mixed Th1/Th2 immune responses

inferred← citeshttps://doi.org/10.1111/pim.12441openalex-snapshot

Antecedent Nippostrongylus infection alters the lung immune response to Plasmodium berghei

inferred← citeshttps://doi.org/10.1111/pim.12723openalex-snapshot

Combinatorial Tim‐3 and PD‐1 activity sustains antigen‐specific Th1 cell numbers during blood‐stage malaria

inferred← citeshttps://doi.org/10.1111/pim.12763openalex-snapshot

Host‐pathogen interaction in the tissue environment during Plasmodium blood‐stage infection

inferred← citeshttps://doi.org/10.1111/pim.70045openalex-snapshot

Immune Modulation by Plasmodium yoelii : Insights From Lethal and Non‐Lethal Strains

inferred← citeshttps://doi.org/10.1111/tan.13196openalex-snapshot

The role of HLA‐G in parasitic diseases

inferred← citeshttps://doi.org/10.1126/sciadv.aaw6957openalex-snapshot

A single-nucleotide polymorphism in a Plasmodium berghei ApiAP2 transcription factor alters the development of host immunity

inferred← citeshttps://doi.org/10.1126/sciimmunol.aal2192openalex-snapshot

Single-cell RNA-seq and computational analysis using temporal mixture modeling resolves T H 1/T FH fate bifurcation in malaria

inferred← citeshttps://doi.org/10.1126/sciimmunol.aau6085openalex-snapshot

Structure and function of the immune system in the spleen

inferred← citeshttps://doi.org/10.1126/sciimmunol.ads2957openalex-snapshot

Clone tracking through repeated malaria identifies high-fidelity memory CD4 T cell responses

inferred← citeshttps://doi.org/10.1128/iai.00157-16openalex-snapshot

Chemically Attenuated Blood-Stage Plasmodium yoelii Parasites Induce Long-Lived and Strain-Transcending Protection

inferred← citeshttps://doi.org/10.1128/iai.00345-24openalex-snapshot

Synergistic blockade of TIGIT and PD-L1 increases type-1 inflammation and improves parasite control during murine blood-stage Plasmodium yoelii non-lethal infection

inferred← citeshttps://doi.org/10.1128/iai.01100-15openalex-snapshot

Parasite-Specific CD4 + IFN-γ + IL-10 + T Cells Distribute within Both Lymphoid and Nonlymphoid Compartments and Are Controlled Systemically by Interleukin-27 and ICOS during Blood-Stage Malaria Infection

inferred← citeshttps://doi.org/10.1134/s2079086424601273openalex-snapshot

Monoclonal Antibodies to a Variable Fragment of the T-Cell Receptor—At the Service of Science and Medicine

inferred← citeshttps://doi.org/10.1155/2016/2926436openalex-snapshot

Dendritic Cells and Their Multiple Roles during Malaria Infection

inferred← citeshttps://doi.org/10.1155/2019/3741294openalex-snapshot

Prevalence of Malaria and TB Coinfection at a National Tuberculosis Treatment Centre in Uganda

inferred← citeshttps://doi.org/10.1155/2019/9264217openalex-snapshot

Immunogenic Evaluation of Ribosomal P-Protein Antigen P0, P1, and P2 and Pentameric Protein Complex P0-(P1-P2)2ofPlasmodium falciparumin a Mouse Model

inferred← citeshttps://doi.org/10.1155/2022/1267841openalex-snapshot

Pyrroloquinoline Quinone Administration Alleviates Allergic Airway Inflammation in Mice by Regulating the JAK-STAT Signaling Pathway

inferred← citeshttps://doi.org/10.1155/2022/5886687openalex-snapshot

Computational Clues of Immunogenic Hotspots in Plasmodium falciparum Erythrocytic Stage Vaccine Candidate Antigens: In Silico Approach

inferred← citeshttps://doi.org/10.1155/jotm/3879562openalex-snapshot

Hepatitis B Vaccine Nonresponse and Associated Risk Factors: Insights From a Cohort Study

inferred← citeshttps://doi.org/10.11606/t.42.2017.tde-14072017-144533openalex-snapshot

Análise do papel de genes bir no processo adaptativo ao hospedeiro e desenvolvimento de proteolipossomos para potencial uso vacinal com foco em reinvasão sanguinea de Plasmodium.

inferred← citeshttps://doi.org/10.11606/t.42.2019.tde-02102019-143339openalex-snapshot

Importância do receptor p2x7 no controle da população de células T auxiliares foliculares e na produção de anticorpos específicos durante a malária causada por >i /i< e >i

inferred← citeshttps://doi.org/10.11606/t.9.2021.tde-06072021-102151openalex-snapshot

Caracterização imunológica da formulação vacinal baseada em VLP (>i /i<) da Proteína Circumsporozoíta de >i /i<

inferred← citeshttps://doi.org/10.1186/s12865-020-00391-8openalex-snapshot

Adaptive immune responses mediated age-related Plasmodium yoelii 17XL and 17XNL infections in 4 and 8-week-old BALB/c mice

inferred← citeshttps://doi.org/10.1186/s12866-022-02480-7openalex-snapshot

A comprehensive study of epitopes and immune reactivity among Plasmodium species

inferred← citeshttps://doi.org/10.1186/s12936-016-1471-7openalex-snapshot

Plasma levels of Galectin-9 reflect disease severity in malaria infection

inferred← citeshttps://doi.org/10.1186/s12936-017-1781-4openalex-snapshot

A novel in vitro model reveals distinctive modulatory roles of Plasmodium falciparum and Plasmodium vivax on naïve cell-mediated immunity

inferred← citeshttps://doi.org/10.1186/s12936-020-3129-8openalex-snapshot

Moringa oleifera treatment increases Tbet expression in CD4+ T cells and remediates immune defects of malnutrition in Plasmodium chabaudi-infected mice

inferred← citeshttps://doi.org/10.1186/s13071-015-0940-0openalex-snapshot

L-Arginine supplementation in mice enhances NO production in spleen cells and inhibits Plasmodium yoelii transmission in mosquitoes

inferred← citeshttps://doi.org/10.1186/s13071-023-05897-9openalex-snapshot

Elicitation of T-cell-derived IFN-γ-dependent immunity by highly conserved Plasmodium ovale curtisi Duffy binding protein domain region II (PocDBP-RII)

inferred← citeshttps://doi.org/10.1186/s13071-024-06144-5openalex-snapshot

Blockage of mechanosensitive Piezo1 channel alleviates the severity of experimental malaria-associated acute lung injury

inferred← citeshttps://doi.org/10.1186/s13071-025-06714-1openalex-snapshot

Cytokine pattern during asymptomatic Anaplasma spp. infections and effect of co-infections by malaria and helminths in schoolchildren of Franceville, southeastern Gabon

inferred← citeshttps://doi.org/10.1186/s13071-026-07439-5openalex-snapshot

The LEF1–LAG3 axis regulates CD4+ T cell function during Plasmodium yoelii NSM infection

inferred← citeshttps://doi.org/10.1245/s10434-015-4923-3openalex-snapshot

A High RORγT/CD3 Ratio is a Strong Prognostic Factor for Postoperative Survival in Advanced Colorectal Cancer: Analysis of Helper T Cell Lymphocytes (Th1, Th2, Th17 and Regulatory T Cells)

inferred← citeshttps://doi.org/10.1371/journal.pntd.0013554openalex-snapshot

Interleukin-10 limits immune-mediated pathology in chronic subclinical plasmodial infection

inferred← citeshttps://doi.org/10.1371/journal.pone.0141141openalex-snapshot

Co-expression of Interleukin-15 Enhances the Protective Immune Responses Induced by Immunization with a Murine Malaria MVA-Based Vaccine Encoding the Circumsporozoite Protein

inferred← citeshttps://doi.org/10.1371/journal.pone.0144654openalex-snapshot

IFN-γ and IL-21 Double Producing T Cells Are Bcl6-Independent and Survive into the Memory Phase in Plasmodium chabaudi Infection

inferred← citeshttps://doi.org/10.1371/journal.pone.0157919openalex-snapshot

Malnutrition in Healthy Individuals Results in Increased Mixed Cytokine Profiles, Altered Neutrophil Subsets and Function

inferred← citeshttps://doi.org/10.1371/journal.pone.0175864openalex-snapshot

CD4 T-cell expression of IFN-γ and IL-17 in pediatric malarial anemia

inferred← citeshttps://doi.org/10.1371/journal.ppat.1006484openalex-snapshot

T follicular helper cells regulate the activation of B lymphocytes and antibody production during Plasmodium vivax infection

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009122openalex-snapshot

Etiology of lactic acidosis in malaria

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009288openalex-snapshot

Extrafollicular CD4 T cell-derived IL-10 functions rapidly and transiently to support anti-Plasmodium humoral immunity

inferred← citeshttps://doi.org/10.1371/journal.ppat.1010282openalex-snapshot

Systems analysis of immune responses to attenuated P. falciparum malaria sporozoite vaccination reveals excessive inflammatory signatures correlating with impaired immunity

inferred← citeshttps://doi.org/10.1371/journal.ppat.1011665openalex-snapshot

Mechanistic insights into the interaction between the host gut microbiome and malaria

inferred← citeshttps://doi.org/10.15252/emmm.202317713openalex-snapshot

IL‐27 produced during acute malaria infection regulates Plasmodium‐specific memory CD4+ T cells

inferred← citeshttps://doi.org/10.15406/ppij.2018.06.00155openalex-snapshot

Antibodies, prophylaxis, transmission

inferred← citeshttps://doi.org/10.15698/mic2021.09.759openalex-snapshot

Understanding the pathogenesis of infectious diseases by single-cell RNA sequencing

inferred← citeshttps://doi.org/10.15761/crt.1000270openalex-snapshot

Unravelling the controversies surrounding host immune response to helminth and malaria parasites

inferred← citeshttps://doi.org/10.1615/plasmamed.2021038540openalex-snapshot

Growth Comparison between Lymphocyte BW5147 T Cells and EL4 T Cells Using Atmospheric Oxygen Plasma Irradiation

inferred← citeshttps://doi.org/10.21203/rs.3.rs-122131/v1openalex-snapshot

The Dynamic Landscape of Parasitaemia Dependent Intestinal Microbiota Shifting at Species Level and the Correlated Gut Transcriptome During Plasmodium Yoelii Infection

inferred← citeshttps://doi.org/10.2174/9789815079609123010010openalex-snapshot

A Time Travel with Anti-Malarial Drugs: Then, Now and Beyond

inferred← citeshttps://doi.org/10.25904/1912/3001openalex-snapshot

Novel Approaches to Whole Parasite Blood-Stage Malaria Vaccine Development

inferred← citeshttps://doi.org/10.3168/jds.2021-20260openalex-snapshot

Effects of enzymatic hydrolysis on the allergenicity of natural cow milk based on a BALB/c mouse model

inferred← citeshttps://doi.org/10.32657/10220/48099openalex-snapshot

Modulation of adaptive and innate immune responses by myeloid cells during malaria

inferred← citeshttps://doi.org/10.32657/10356/72534openalex-snapshot

Control of Plasmodium falciparum infection by human natural killer cells

inferred← citeshttps://doi.org/10.3389/fcimb.2019.00322openalex-snapshot

Activation of Mast Cells Promote Plasmodium berghei ANKA Infection in Murine Model

inferred← citeshttps://doi.org/10.3389/fcimb.2020.610121openalex-snapshot

Accelerator or Brake: Immune Regulators in Malaria

inferred← citeshttps://doi.org/10.3389/fcimb.2021.685239openalex-snapshot

Lessons Learned for Pathogenesis, Immunology, and Disease of Erythrocytic Parasites: Plasmodium and Babesia

inferred← citeshttps://doi.org/10.3389/fcimb.2021.788546openalex-snapshot

Properties and Roles of γδT Cells in Plasmodium yoelii nigeriensis NSM Infected C57BL/6 Mice

inferred← citeshttps://doi.org/10.3389/fcimb.2022.968325openalex-snapshot

Testosterone induces sexual dimorphism during infection with Plasmodium berghei ANKA

inferred← citeshttps://doi.org/10.3389/fimmu.2015.00198openalex-snapshot

CD4+ T Cell Differentiation in Infection: Amendments to the Th1/Th2 Axiom

inferred← citeshttps://doi.org/10.3389/fimmu.2016.00517openalex-snapshot

Visceral Leishmaniasis Patients Display Altered Composition and Maturity of Neutrophils as well as Impaired Neutrophil Effector Functions

inferred← citeshttps://doi.org/10.3389/fimmu.2017.00027openalex-snapshot

The Deubiquitinating Enzyme Cylindromatosis Dampens CD8+ T Cell Responses and Is a Critical Factor for Experimental Cerebral Malaria and Blood–Brain Barrier Damage

inferred← citeshttps://doi.org/10.3389/fimmu.2017.01333openalex-snapshot

Conventional CD11chigh Dendritic Cells Are Important for T Cell Priming during the Initial Phase of Plasmodium yoelii Infection, but Are Dispensable at Later Time Points

inferred← citeshttps://doi.org/10.3389/fimmu.2018.02579openalex-snapshot

The Influence of Parasite Infections on Host Immunity to Co-infection With Other Pathogens

inferred← citeshttps://doi.org/10.3389/fimmu.2019.00135openalex-snapshot

Induction of Plasmodium-Specific Immune Responses Using Liposome-Based Vaccines

inferred← citeshttps://doi.org/10.3389/fimmu.2019.01225openalex-snapshot

T Cell-Specific Overexpression of Acid Sphingomyelinase Results in Elevated T Cell Activation and Reduced Parasitemia During Plasmodium yoelii Infection

inferred← citeshttps://doi.org/10.3389/fimmu.2020.575103openalex-snapshot

Evolutionarily Selected Overexpression of the Cytokine BAFF Enhances Mucosal Immune Response Against P. falciparum

inferred← citeshttps://doi.org/10.3389/fimmu.2021.642585openalex-snapshot

Attenuated T Cell Responses Are Associated With the Blockade of Cerebral Malaria Development by YOP1-Deficient Plasmodium berghei ANKA

inferred← citeshttps://doi.org/10.3389/fimmu.2022.1005332openalex-snapshot

Process development and preclinical evaluation of a major Plasmodium falciparum blood stage vaccine candidate, Cysteine-Rich Protective Antigen (CyRPA)

inferred← citeshttps://doi.org/10.3389/fimmu.2022.971392openalex-snapshot

Perturbations in the T cell receptor β repertoire during malaria infection in children: A preliminary study

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1140426openalex-snapshot

P2RX7 signaling drives the differentiation of Th1 cells through metabolic reprogramming for aerobic glycolysis

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1171176openalex-snapshot

The impact of innate immunity on malaria parasite infection dynamics in rodent models

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1179314openalex-snapshot

Immunogenomic profile at baseline predicts host susceptibility to clinical malaria

inferred← citeshttps://doi.org/10.3389/fimmu.2025.1607201openalex-snapshot

Red pulp macrophages clear parasites, while marginal metallophilic and marginal zone macrophages support CD4+ T cell activation during Plasmodium yoelii infection

inferred← citeshttps://doi.org/10.3389/fmicb.2016.00982openalex-snapshot

Malaria-Cutaneous Leishmaniasis Co-infection: Influence on Disease Outcomes and Immune Response

inferred← citeshttps://doi.org/10.3389/fmicb.2023.1046002openalex-snapshot

Current understanding of the immune potential of B-cell subsets in malarial pathogenesis

inferred← citeshttps://doi.org/10.3389/fphar.2024.1484934openalex-snapshot

Impact on parasitemia, survival time and pro-inflammatory immune response in mice infected with Plasmodium berghei treated with Eleutherine plicata

inferred← citeshttps://doi.org/10.3390/ani13213376openalex-snapshot

Rhodotorula mucilaginosa ZTHY2 Attenuates Cyclophosphamide-Induced Immunosuppression in Mice

inferred← citeshttps://doi.org/10.3390/foods13081206openalex-snapshot

Transglutaminase-Cross-Linked Tofu Suppressed Soybean-Induced Allergic Reactions by Enhancing Intestinal Mucosa Immune Tolerance

inferred← citeshttps://doi.org/10.3390/ijms21041402openalex-snapshot

β2 Integrins—Multi-Functional Leukocyte Receptors in Health and Disease

inferred← citeshttps://doi.org/10.3390/molecules28062527openalex-snapshot

Natural Plasmodium falciparum Infection Stimulates Human Antibodies to MSP1 Epitopes Identified in Mice Infection Models upon Non-Natural Modified Peptidomimetic Vaccination

inferred← citeshttps://doi.org/10.3390/pathogens12010049openalex-snapshot

Mouse Models for Mycobacterium tuberculosis Pathogenesis: Show and Do Not Tell

inferred← citeshttps://doi.org/10.3390/pathogens14010071openalex-snapshot

Targeting T-Cell Activation for Malaria Immunotherapy: Scoping Review

inferred← citeshttps://doi.org/10.3390/vaccines14050423openalex-snapshot

Cellular Immune Response and T Cell Epitope Mapping of Plasmodium falciparum Chimeric Vaccine Candidate GMZ2.6c and Its Components (MSP-3, GLURP and Pfs48/45) in Individuals Naturally Exposed to Malaria in Brazilian Amazon

inferred← citeshttps://doi.org/10.3390/vaccines8020190openalex-snapshot

Protective Malaria Vaccine in Mice Based on the Plasmodium vivax Circumsporozoite Protein Fused with the Mumps Nucleocapsid Protein

inferred← citeshttps://doi.org/10.3390/vaccines9101072openalex-snapshot

Plasmodium falciparum Malaria Vaccines and Vaccine Adjuvants

inferred← citeshttps://doi.org/10.37349/ei.2024.00134openalex-snapshot

Entrance to the multifaceted world of CD4+ T cell subsets

inferred← citeshttps://doi.org/10.3923/ajbs.2023.636.669openalex-snapshot

Molecular and Epigenetics Mechanisms for the Immune Control of Plasmodium Parasites Infection: A Comprehensive Review

inferred← citeshttps://doi.org/10.4049/jimmunol.1701316openalex-snapshot

Recent Insights into CD4+ Th Cell Differentiation in Malaria

inferred← citeshttps://doi.org/10.4049/jimmunol.2200899openalex-snapshot

CD4 T Cell–Dependent and –Independent Roles for IFN-γ in Blood-Stage Malaria

inferred← citeshttps://doi.org/10.48112/bcs.v1i2.97openalex-snapshot

Is Laps of Time Since Malaria Elimination a Factor in COVID-19 Mortality?

inferred← citeshttps://doi.org/10.51200/bjms.v12i3.1158openalex-snapshot

Role of Immunopathology in Clinical Course of Malaria: A Review

inferred← citeshttps://doi.org/10.5772/intechopen.97045openalex-snapshot

Regulation of T-reg/Th-17 Balance: One Step Closer Towards Immunotherapy Against Malaria Infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.26675453openalex-snapshot

Additional file 1 of Blockage of mechanosensitive Piezo1 channel alleviates the severity of experimental malaria-associated acute lung injury

inferred← citeshttps://doi.org/10.70675/579dde47zf123z4b30z8dbaz9284bc6d464bopenalex-snapshot

Impact des infections helminthiques sur la réponse immune anti-plasmodiale et sur l'infection palustre chez les enfants du sud-Bénin

inferred← citeshttps://doi.org/10.70675/5ec1f53bzca32z4533za8f3z3ff14e7322beopenalex-snapshot

Étude de l'expression de l'interleukine 34 et de son rôle tolérogène dans la peau en conditions inflammatoires

inferred← citeshttps://doi.org/10.7554/elife.77975openalex-snapshot

The acid ceramidase/ceramide axis controls parasitemia in Plasmodium yoelii-infected mice by regulating erythropoiesis

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