1998
DOI: 10.1046/j.1365-2222.1998.00424.x
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Role of CD28/B7 co‐stimulation in airway T helper 2 (TH2) immune responses in asthma

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Cited by 4 publications
(2 citation statements)
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“…There is increasing evidence that AR or asthma, chronic airway inflammatory diseases characterized by reversible airway obstruction, hyper‐reactivity and lymphocyte/eosinophil recruitment are driven and maintained by chronically activated T cells with a T‐helper 2 (Th2) phenotype. These T cells promote the activation and recruitment of B cells and regulate the Ig class switch to the development of antigen‐specific IgE responses [35–38]. We previously reported that a majority of the CD4 + T cells in the nasal mucosa of allergic rhinitics co‐expressed the CD45RO surface molecule, and a predominant proportion of CD4 + T cells in the nasal epithelium were CD45RO + (memory T cells) [39].…”
Section: Discussionmentioning
confidence: 99%
“…There is increasing evidence that AR or asthma, chronic airway inflammatory diseases characterized by reversible airway obstruction, hyper‐reactivity and lymphocyte/eosinophil recruitment are driven and maintained by chronically activated T cells with a T‐helper 2 (Th2) phenotype. These T cells promote the activation and recruitment of B cells and regulate the Ig class switch to the development of antigen‐specific IgE responses [35–38]. We previously reported that a majority of the CD4 + T cells in the nasal mucosa of allergic rhinitics co‐expressed the CD45RO surface molecule, and a predominant proportion of CD4 + T cells in the nasal epithelium were CD45RO + (memory T cells) [39].…”
Section: Discussionmentioning
confidence: 99%
“…However, Vβ8a-positive cells are not identical with the IL-4 producers, since our measurements of intracellular cytokines reveal that IL-4 production does not increase in parallel with Vβ8a increase. The differentiation of cytokine-producing Th cells is influenced by antigen affinity for the T cell receptor as well as co-stimulation signals like CD28 and CD86 [30]. Tao et al [31]suggest that naive CD4 T cells are receptive to CD28-dependent IL-4 production only if they receive a weak T cell receptor signal.…”
Section: Discussionmentioning
confidence: 99%