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Lymphoid microenvironment in the gut for immunoglobulin A and inflammation
Author(s) -
Chin Robert,
Wang Jing,
Fu YangXin
Publication year - 2003
Publication title -
immunological reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.839
H-Index - 223
eISSN - 1600-065X
pISSN - 0105-2896
DOI - 10.1034/j.1600-065x.2003.00066.x
Subject(s) - biology , lymphotoxin , chemokine , lamina propria , immunology , lymphotoxin beta receptor , inflammation , stroma , microbiology and biotechnology , cxcl13 , lymphatic system , cytokine , chemokine receptor , genetics , immunohistochemistry , epithelium
Summary: Signaling through lymphotoxin β receptor (LTβR) initiates the unfolding of a host of developmental programs ranging from the organogenesis of lymph nodes and Peyer's patches (PPs) to the coordination of splenic microarchitecture. While investigating an alternative pathway to immunoglobulin A (IgA) production, it was uncovered that LTβR signaling in the lamina propria (LP) stroma orchestrates the coordinated expression of key chemokines and adhesion molecules, creation of a cytokine milieu, and stroma development that facilitates robust IgA production independent of secondary lymphoid structures. Simultaneously, this same infrastructure can be commandeered by autoreactive T cells to organize both the acute destruction of the intestinal mucosa and chronic intestinal inflammation via the ligands for LTβR. The ability to modulate LTβR signaling may alternatively permit the suppression of autoimmune responses and augmentation of gut defenses.