PMID- 15836753 OWN - NLM STAT- MEDLINE DCOM- 20050711 LR - 20131121 IS - 0954-7894 (Print) IS - 0954-7894 (Linking) VI - 35 IP - 4 DP - 2005 Apr TI - Increased responsiveness of basophils of patients with chronic urticaria to sera but hypo-responsiveness to other stimuli. PG - 456-60 AB - BACKGROUND: Although it has been shown that basophils from patients with chronic ordinary urticaria (CU) are less responsive than normal basophils when stimulated with anti-IgE, very few studies have examined the response of those cells to alternative stimuli. OBJECTIVE: To compare releasability between basophils from healthy donors and patients with CU. METHODS: We examined the response of IL-3-treated basophils from healthy donors, atopic controls and CU patients to anti-IgE, monocyte chemoattractant protein-1 (MCP-1), bradykinin, C5a and to sera obtained from other urticaria patients and normal controls. We also compared the response of basophils from CU patients whose sera activate normal basophils (autoimmune CU) from those who do not (idiopathic CU). RESULTS: Basophils of CU patients release significantly less histamine than basophils of normal controls when stimulated with anti-IgE, and to a lesser degree with C5a. No differences were observed when basophils from patients were incubated with Bradykinin or MCP-1. However, when basophils of CU patients were incubated with sera from other CU patients or even normal sera, we found significantly higher histamine release compared with the response of basophils from normal donors. We could not distinguish responsiveness of basophils of patients with chronic autoimmune urticaria from patients with chronic idiopathic urticaria. CONCLUSION: Basophils of patients with chronic idiopathic urticaria and chronic autoimmune urticaria are hypo-responsive to anti-IgE and C5a, normally responsive to MCP-1 or bradykinin, and hyper-responsive to serum. The serum factor to which a response has not yet been identified; however, basophils of patients with chronic urticaria, in general, appear to have abnormal regulation of signaling pathways. FAU - Luquin, E AU - Luquin E AD - Department of Allergy and Clinical Immunology, Clinica Universitaria, Universidad de Navarra, Pamplona, Spain. FAU - Kaplan, A P AU - Kaplan AP FAU - Ferrer, M AU - Ferrer M LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Clin Exp Allergy JT - Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology JID - 8906443 RN - 0 (Antibodies, Anti-Idiotypic) RN - 0 (Autoantibodies) RN - 0 (Chemokine CCL2) RN - 37341-29-0 (Immunoglobulin E) RN - 80295-54-1 (Complement C5a) RN - S8TIM42R2W (Bradykinin) SB - IM MH - Antibodies, Anti-Idiotypic/immunology MH - Autoantibodies/immunology MH - Basophils/*immunology MH - Bradykinin/immunology MH - Cells, Cultured MH - Chemokine CCL2/immunology MH - Chronic Disease MH - Complement C5a/immunology MH - Histamine Release/immunology MH - Humans MH - Immunoglobulin E/immunology MH - Urticaria/*immunology EDAT- 2005/04/20 09:00 MHDA- 2005/07/12 09:00 CRDT- 2005/04/20 09:00 PHST- 2005/04/20 09:00 [pubmed] PHST- 2005/07/12 09:00 [medline] PHST- 2005/04/20 09:00 [entrez] AID - CEA2212 [pii] AID - 10.1111/j.1365-2222.2005.02212.x [doi] PST - ppublish SO - Clin Exp Allergy. 2005 Apr;35(4):456-60. doi: 10.1111/j.1365-2222.2005.02212.x.