Results 11 to 20 of about 182,231 (346)

Cross-Tissue Transcriptomic Analysis of Human Secondary Lymphoid Organ-Residing ILC3s Reveals a Quiescent State in the Absence of Inflammation

open access: yesCell Reports, 2017
A substantial number of human and mouse group 3 innate lymphoid cells (ILC3s) reside in secondary lymphoid organs, yet the phenotype and function of these ILC3s is incompletely understood.
Yotam E. Bar-Ephraim   +12 more
doaj   +2 more sources

Development of Secondary Lymphoid Organs [PDF]

open access: yesAnnual Review of Immunology, 2008
Secondary lymphoid organs develop during embryogenesis or in the first few weeks after birth according to a highly coordinated series of interactions between newly emerging hematopoietic cells and immature mesenchymal or stromal cells. These interactions are orchestrated by homeostatic chemokines, cytokines, and growth factors that attract ...
Troy D, Randall   +2 more
openaire   +3 more sources

Stroma cell priming in enteric lymphoid organ morphogenesis

open access: yesFrontiers in Immunology, 2012
The lymphoid system is equipped with a network of specialized platforms located at strategic sites, which grant strict immune-surveillance and efficient immune responses.
Manuela eFerreira   +2 more
doaj   +2 more sources

CCL21 Expression Pattern of Human Secondary Lymphoid Organ Stroma Is Conserved in Inflammatory Lesions with Lymphoid Neogenesis [PDF]

open access: yesThe American Journal of Pathology, 2007
CCL21 is a homeostatic lymphoid chemokine instrumental in the recruitment and organization of T cells and dendritic cells into lymphoid T areas. In human secondary lymphoid organs (SLOs), CCL21 is produced by cells distributed throughout the T zone, whereas high endothelial venules (HEVs) lack CCL21 mRNA.
Manzo A.   +8 more
openaire   +4 more sources

Cooperating Mechanisms of CXCR5 and CCR7 in Development and Organization of Secondary Lymphoid Organs [PDF]

open access: yesThe Journal of Experimental Medicine, 2003
Homeostatic chemokines participate in the development of secondary lymphoid organs and later on in the functional organization of these tissues. The development of lymph nodes (LNs) and Peyer's patches depends on the recruitment of CD3− CD4+ interleukin (IL)-7Rαhi cells to sites of future organ development.
Ohl, L.   +7 more
openaire   +4 more sources

Secondary lymphoid organ homing phenotype of human myeloid dendritic cells disrupted by an intracellular oral pathogen. [PDF]

open access: yesInfect Immun, 2014
Miles B   +9 more
europepmc   +2 more sources

Identification of a pharyngeal mucosal lymphoid organ in zebrafish and other teleosts: Tonsils in fish?

open access: yesScience Advances, 2023
The constant exposure of the fish branchial cavity to aquatic pathogens causes local mucosal immune responses to be extremely important for their survival.
J. Rességuier   +12 more
semanticscholar   +1 more source

Delivering mRNA to Secondary Lymphoid Tissues by Phosphatidylserine‐Loaded Lipid Nanoparticles

open access: yesAdvanced Healthcare Materials, 2022
Lipid nanoparticles (LNPs) are one of the most successful technologies in messenger RNA (mRNA) delivery. While the liver is the most frequent target for LNP delivery of mRNA, technologies for delivering mRNA molecules to extrahepatic tissues are also ...
Masaki Gomi   +11 more
semanticscholar   +1 more source

Emergence and Evolution of Secondary Lymphoid Organs [PDF]

open access: yesAnnual Review of Cell and Developmental Biology, 2016
For effective adaptive immunity to foreign antigens (Ag), secondary lymphoid organs (SLO) provide the confined environment in which Ag-restricted lymphocytes, with very low precursor frequencies, interact with Ag on Ag-presenting cells (APC). The spleen is the primordial SLO, arising in conjunction with adaptive immunity in early jawed vertebrates. The
Harold R, Neely, Martin F, Flajnik
openaire   +2 more sources

In Silico Analysis of the Longevity and Timeline of Individual Germinal Center Reactions in a Primary Immune Response

open access: yesCells, 2021
Germinal centers (GCs) are transient structures in the secondary lymphoid organs, where B cells undergo affinity maturation to produce high affinity memory and plasma cells.
Theinmozhi Arulraj   +2 more
doaj   +1 more source

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