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      Thymic stromal lymphopoietin expression is increased in asthmatic airways and correlates with expression of Th2-attracting chemokines and disease severity.

      The Journal of Immunology Author Choice
      Adult, Aged, Asthma, immunology, pathology, physiopathology, Cell Movement, Chemokine CCL1, Chemokine CCL17, Chemokine CCL22, Chemokine CXCL10, Chemokine CXCL11, Chemokines, CC, biosynthesis, genetics, Chemokines, CXC, Cytokines, Humans, Middle Aged, RNA, Messenger, Receptors, Chemokine, Respiratory Mucosa, metabolism, Severity of Illness Index, Stromal Cells, Th1 Cells, Th2 Cells, Thymus Gland, Up-Regulation

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          Abstract

          Thymic stromal lymphopoietin (TSLP) is said to increase expression of chemokines attracting Th2 T cells. We hypothesized that asthma is characterized by elevated bronchial mucosal expression of TSLP and Th2-attracting, but not Th1-attracting, chemokines as compared with controls, with selective accumulation of cells bearing receptors for these chemokines. We used in situ hybridization and immunohistochemistry to examine the expression and cellular provenance of TSLP, Th2-attracting (thymus and activation-regulated chemokine (TARC)/CCL17, macrophage-derived chemokine (MDC)/CCL22, I-309/CCL1) and Th1-attracting (IFN-gamma-inducible protein 10 (IP-10)/CXCL10, IFN-inducible T cell alpha-chemoattractant (I-TAC)/CXCL11) chemokines and expression of their receptors CCR4, CCR8, and CXCR3 in bronchial biopsies from 20 asthmatics and 15 normal controls. The numbers of cells within the bronchial epithelium and submucosa expressing mRNA for TSLP, TARC/CCL17, MDC/CCL22, and IP-10/CXCL10, but not I-TAC/CXCL11 and I-309/CCL1, were significantly increased in asthmatics as compared with controls (p

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