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References from Malaria durably disrupts macrophage-to-macrophage crosstalk in the spleen. Local targets link to admitted publications; unresolved targets remain external evidence.
Structure and function of the immune system in the spleen
10.1126/sciimmunol.aau6085 · 2019 · External reference
Establishment and maintenance of the macrophage niche
10.1016/j.immuni.2020.02.015 · 2020 · External reference
Reticular fibroblasts expressing the transcription factor WT1 define a stromal niche that maintains and replenishes splenic red pulp macrophages
10.1016/j.immuni.2020.06.008 · 2020 · External reference
Circuit design features of a stable two-cell system
10.1016/j.cell.2018.01.015 · 2018 · External reference
Targeting circulating labile heme as a defense strategy against malaria
10.26508/lsa.202302276 · 2024 · External reference
The Cryo-EM structure of human CD163 bound to haptoglobin-hemoglobin reveals molecular mechanisms of hemoglobin scavenging
10.1038/s41467-024-55171-4 · 2024 · External reference
Renal control of life-threatening malarial anemia
10.1016/j.celrep.2023.112057 · 2023 · External reference
CD163+ red pulp macrophages interact with marginal metallophilic macrophages during blood-stage malaria to maintain splenic architecture
10.1016/j.immuni.2026.07.006 · 2026 · External reference
Red pulp macrophages in the human spleen are a distinct cell population with a unique expression of Fc-γ receptors
10.1182/bloodadvances.2017015008 · 2018 · External reference
Distribution of nerve fibers and nerve-immune cell association in mouse spleen revealed by immunofluorescent staining
10.1038/s41598-020-66619-0 · 2020 · External reference
