PMID- 16176400 OWN - NLM STAT- MEDLINE DCOM- 20060406 LR - 20080528 IS - 0905-6157 (Print) IS - 0905-6157 (Linking) VI - 16 IP - 6 DP - 2005 Sep TI - Three-year follow-up of clinical and inflammation parameters in children monosensitized to mites undergoing sub-lingual immunotherapy. PG - 519-26 AB - Parallel follow-up of clinical and inflammatory markers during sub-lingual immunotherapy (SLIT) is highly beneficial. Twenty-four children (age 4-16) monosensitized to house dust mite were randomized to receive either active or placebo SLIT for 1 yr in a double-blind placebo controlled design (Marcucci et al., Allergy 2003: 58: 657-62). Thereafter, for 2 yr they all received active treatment. Symptom scores for rhinitis, asthma, and drug usage were daily recorded. Eosinophil cationic protein (ECP) and tryptase in sputum and nasal secretions, serum and nasal mite-specific immunoglobulin E (IgE) were recorded before treatment and at 10-12 months intervals. Nasal ECP and nasal tryptase after specific nasal provocation tests were significantly reduced as compared to baseline values (p = 0.0043 and 0.0195, respectively) in the third year of active treatment. None of the other inflammatory parameters was increased. In placebo treated patients all these parameters tended to decrease only after switching to active treatment. Clinical scores did not improve in treated vs. placebo patients in the double-blind placebo-controlled phase of the study. In both cohorts a clinical benefit was observed as intra-group score reduction as compared to baseline. A significant difference was reached in patients treated for 2 yr for rhinitis and asthma (p = 0.0009 and 0.0019, respectively) but not for drug usage and in patients treated for 3 yr for rhinitis, asthma, and drug usage (p = 0.0105, 0.0048, and 0.02, respectively). SLIT in children monosensitized to mites reverted the spontaneous increase in nasal IgE and in local parameters of allergic inflammation. These outcomes were followed by a consolidated clinical improvement in the second and third year of treatment. FAU - Marcucci, F AU - Marcucci F AD - Clinica Pediatrica, University of Perugia, Italy. FAU - Sensi, L AU - Sensi L FAU - Di Cara, G AU - Di Cara G FAU - Salvatori, S AU - Salvatori S FAU - Bernini, M AU - Bernini M FAU - Pecora, S AU - Pecora S FAU - Burastero, S E AU - Burastero SE LA - eng PT - Journal Article PT - Randomized Controlled Trial PL - England TA - Pediatr Allergy Immunol JT - Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology JID - 9106718 RN - 0 (Anti-Asthmatic Agents) RN - 0 (Histamine H1 Antagonists) RN - 0 (Inflammation Mediators) RN - 37341-29-0 (Immunoglobulin E) RN - EC 3.1.27.- (Eosinophil Cationic Protein) RN - EC 3.1.27.- (RNASE3 protein, human) RN - EC 3.4.21.- (Serine Endopeptidases) RN - EC 3.4.21.59 (Tryptases) SB - IM EIN - Pediatr Allergy Immunol. 2006 Jun;17(4):318 CIN - Pediatr Allergy Immunol. 2006 Jun;17(4):315; author reply 316-7. PMID: 16771788 MH - Administration, Sublingual MH - Adolescent MH - Animals MH - Anti-Asthmatic Agents/*administration & dosage MH - Antibody Specificity MH - Asthma/drug therapy/*immunology/metabolism MH - Child MH - Child Welfare MH - Child, Preschool MH - *Desensitization, Immunologic MH - Double-Blind Method MH - Eosinophil Cationic Protein/immunology/metabolism MH - Follow-Up Studies MH - Histamine H1 Antagonists/*administration & dosage MH - Humans MH - *Immunization MH - Immunoglobulin E/blood MH - Inflammation Mediators/blood/*immunology MH - Pyroglyphidae/drug effects/*immunology MH - Rhinitis, Allergic, Perennial/drug therapy/*immunology/metabolism MH - Serine Endopeptidases/immunology/metabolism MH - Tryptases EDAT- 2005/09/24 09:00 MHDA- 2006/04/07 09:00 CRDT- 2005/09/24 09:00 PHST- 2005/09/24 09:00 [pubmed] PHST- 2006/04/07 09:00 [medline] PHST- 2005/09/24 09:00 [entrez] AID - PAI301 [pii] AID - 10.1111/j.1399-3038.2005.00301.x [doi] PST - ppublish SO - Pediatr Allergy Immunol. 2005 Sep;16(6):519-26. doi: 10.1111/j.1399-3038.2005.00301.x.