The role of ICOS and other costimulatory molecules in allergy and asthma

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B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion

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CTLA-4 can function as a negative regulator of T cell activation

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B7/CD28 Costimulation Is Essential for the Homeostasis of the CD4+CD25+ Immunoregulatory T Cells that Control Autoimmune Diabetes

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B7-1 and B7-2 costimulatory molecules activate differentially the Th1/Th2 developmental pathways: Application to autoimmune disease therapy

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ICOS is an inducible T-cell co-stimulator structurally and functionally related to CD28

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ICOS co-stimulatory receptor is essential for T-cell activation and function

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Antigen-specific regulatory T cells develop via the ICOS–ICOS-ligand pathway and inhibit allergen-induced airway hyperreactivity

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ICOS is essential for effective T-helper-cell responses

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CD28 delivers a costimulatory signal involved in antigen-specific IL-2 production by human T cells.

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B7h, a Novel Costimulatory Homolog of B7.1 and B7.2, Is Induced by TNFα

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Mouse Inducible Costimulatory Molecule (ICOS) Expression Is Enhanced by CD28 Costimulation and Regulates Differentiation of CD4+ T Cells

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ICOS is critical for T helper cell–mediated lung mucosal inflammatory responses

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The costimulatory molecule ICOS plays an important role in the immunopathogenesis of EAE

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Costimulation through B7-2 (CD86) Is Required for the Induction of a Lung Mucosal T Helper Cell 2 (TH2) Immune Response and Altered Airway Responsiveness

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OX40 (CD134) Controls Memory T Helper 2 Cells that Drive Lung Inflammation

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Inducible Costimulator Protein (Icos) Controls T Helper Cell Subset Polarization after Virus and Parasite Infection

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A Critical Role for B7/CD28 Costimulation in Experimental Autoimmune Encephalomyelitis: A Comparative Study Using Costimulatory Molecule-Deficient Mice and Monoclonal Antibody Blockade

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A negative regulatory function of B7 revealed in B7-1 transgenic mice

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