T cell activation pathways: B7, LFA-3, and ICAM-1 shape unique T cell profiles
AG Wingren, E Parra, M Varga… - Critical Reviews™ in …, 2017 - dl.begellhouse.com
AG Wingren, E Parra, M Varga, T Kalland, HO Sjogren, G Hedlund, M Dohlsten
Critical Reviews™ in Immunology, 2017•dl.begellhouse.comTwo signals are required for induction of cell proliferation and cytokine production in resting
T cells. Occupancy of the T cell receptor by antigen/MHC complexes delivers the first signal
to the T cell, while the second signal is provided by interaction with costimulatory ligands on
APC. CD2, LFA-1, and CD28 are the major costimulatory and adhesive molecules on T cells
and bind to the LFA-3, ICAM-1 and B7 ligands, respectively, on APC. LFA-3 plays a central
role for naive and memory T helper cells during the early phase of an immune response …
T cells. Occupancy of the T cell receptor by antigen/MHC complexes delivers the first signal
to the T cell, while the second signal is provided by interaction with costimulatory ligands on
APC. CD2, LFA-1, and CD28 are the major costimulatory and adhesive molecules on T cells
and bind to the LFA-3, ICAM-1 and B7 ligands, respectively, on APC. LFA-3 plays a central
role for naive and memory T helper cells during the early phase of an immune response …
Abstract
Two signals are required for induction of cell proliferation and cytokine production in resting T cells. Occupancy of the T cell receptor by antigen/MHC complexes delivers the first signal to the T cell, while the second signal is provided by interaction with costimulatory ligands on APC. CD2, LFA-1, and CD28 are the major costimulatory and adhesive molecules on T cells and bind to the LFA-3, ICAM-1 and B7 ligands, respectively, on APC. LFA-3 plays a central role for naive and memory T helper cells during the early phase of an immune response. The LFA-3/CD2 pathway initiates strong antigen-independent cell adhesion, substantial expansion of naive T helper cells, and induction of large amounts of IFN-γ in memory cells.
