Search results (24)
« Back to PublicationsEx vivo model of functioning human lymph node reveals role for innate lymphocytes and stroma in response to vaccine adjuvant.
Journal article
Fergusson JR. et al, (2025), Cell Rep, 44
sparagine availability controls germinal center B cell homeostasis.
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Yazicioglu YF. et al, (2024), Sci Immunol, 9
n HLA-E-targeted TCR bispecific molecule redirects T cell immunity against Mycobacterium tuberculosis.
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Paterson RL. et al, (2024), Proc Natl Acad Sci U S A, 121
Emulsion and liposome-based adjuvanted R21 vaccine formulations mediate protection against malaria through distinct immune mechanisms.
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Reinke S. et al, (2023), Cell Rep Med, 4
Steroid-resistant human inflammatory ILC2s are marked by CD45RO and elevated in type 2 respiratory diseases.
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van der Ploeg EK. et al, (2021), Sci Immunol, 6
Immune-Mobilizing Monoclonal T Cell Receptors Mediate Specific and Rapid Elimination of Hepatitis B-Infected Cells.
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Fergusson JR. et al, (2020), Hepatology, 72, 1528 - 1540
High MDR-1 expression by MAIT cells confers resistance to cytotoxic but not immunosuppressive MDR-1 substrates.
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Fergusson JR. et al, (2018), Clin Exp Immunol, 194, 180 - 191
Human Innate Lymphoid Cell Subsets Possess Tissue-Type Based Heterogeneity in Phenotype and Frequency.
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Simoni Y. et al, (2018), Immunity, 48
Maturing Human CD127+ CCR7+ PDL1+ Dendritic Cells Express AIRE in the Absence of Tissue Restricted Antigens.
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Fergusson JR. et al, (2018), Front Immunol, 9
Human Innate Lymphoid Cell Subsets Possess Tissue-Type Based Heterogeneity in Phenotype and Frequency.
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Simoni Y. et al, (2017), Immunity, 46, 148 - 161
Shared and Distinct Phenotypes and Functions of Human CD161++ Vα7.2+ T Cell Subsets.
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Kurioka A. et al, (2017), Front Immunol, 8
CD161(int)CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut.
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Fergusson JR. et al, (2016), Mucosal Immunol, 9, 401 - 413
Prostaglandin D2 and leukotriene E4 synergize to stimulate diverse TH2 functions and TH2 cell/neutrophil crosstalk.
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Xue L. et al, (2015), J Allergy Clin Immunol, 135
MAIT cells are licensed through granzyme exchange to kill bacterially sensitized targets.
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Kurioka A. et al, (2015), Mucosal Immunol, 8, 429 - 440