Deflazacort protects against late‐phase but not early‐phase reactions induced by the allergen‐specific conjunctival provocation test

The protective effects of deflazacort against the inflammation that follows the conjunctival provocation test (CPT) by specific allergen were assessed in 24 patients with rhinoconjunctivitis caused by Parietaria judaica in a double‐blind study. After a screening CPT, patients were randomized into fo...

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Veröffentlicht in:Allergy (Copenhagen) 1993-08, Vol.48 (6), p.421-430
Hauptverfasser: Ciprandi, G., Buscaglia, S., Pesce, G. P., Iudice, A., Bagnasco, M., Canonica, G. W.
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container_end_page 430
container_issue 6
container_start_page 421
container_title Allergy (Copenhagen)
container_volume 48
creator Ciprandi, G.
Buscaglia, S.
Pesce, G. P.
Iudice, A.
Bagnasco, M.
Canonica, G. W.
description The protective effects of deflazacort against the inflammation that follows the conjunctival provocation test (CPT) by specific allergen were assessed in 24 patients with rhinoconjunctivitis caused by Parietaria judaica in a double‐blind study. After a screening CPT, patients were randomized into four treatment groups, each being given deflazacort (oral tablets) at 6, 30, and 60 mg once daily, or matching placebo, for 3 d, outside the pollen season. Clinical evaluation (itching, hyperemia, lacrimation, and swelling of eyelids) and cytologic assessment (number of inflammatory cells in conjunctival scraping and evaluation of ICAM (intercellular adhesion molecule)‐1/CD54 expression on epithelial cells) were performed at base line, 30 min (early‐phase reaction (EPR), 6 h and 24 h (late‐phase reaction (LPR)) after specific CPT, and before and after treatment. Neither the EPR clinical reactions nor the EPR total number of inflammatory cells was modified by deflazacort. However, the LPR clinical effects were significantly reduced by deflazacort at 30 or 60mg/d (P
doi_str_mv 10.1111/j.1398-9995.1993.tb00740.x
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P. ; Iudice, A. ; Bagnasco, M. ; Canonica, G. W.</creator><creatorcontrib>Ciprandi, G. ; Buscaglia, S. ; Pesce, G. P. ; Iudice, A. ; Bagnasco, M. ; Canonica, G. W.</creatorcontrib><description>The protective effects of deflazacort against the inflammation that follows the conjunctival provocation test (CPT) by specific allergen were assessed in 24 patients with rhinoconjunctivitis caused by Parietaria judaica in a double‐blind study. After a screening CPT, patients were randomized into four treatment groups, each being given deflazacort (oral tablets) at 6, 30, and 60 mg once daily, or matching placebo, for 3 d, outside the pollen season. Clinical evaluation (itching, hyperemia, lacrimation, and swelling of eyelids) and cytologic assessment (number of inflammatory cells in conjunctival scraping and evaluation of ICAM (intercellular adhesion molecule)‐1/CD54 expression on epithelial cells) were performed at base line, 30 min (early‐phase reaction (EPR), 6 h and 24 h (late‐phase reaction (LPR)) after specific CPT, and before and after treatment. Neither the EPR clinical reactions nor the EPR total number of inflammatory cells was modified by deflazacort. However, the LPR clinical effects were significantly reduced by deflazacort at 30 or 60mg/d (P&lt;0.01), as compared with placebo. The total number of inflammatory cells during LPR was significantly reduced by deflazacort at 30 or 60 nig/d ((P&lt;0.01), as compared with placebo. Furthermore, CD54 expression was significantly reduced by deflazacort at 30 or 60 mg/d both in the EPR ((P&lt;0.01) and LPR ((P&lt;0.01), as compared with placebo. None of the studied indicators were modified at the 6 mg/d dose. 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P.</creatorcontrib><creatorcontrib>Iudice, A.</creatorcontrib><creatorcontrib>Bagnasco, M.</creatorcontrib><creatorcontrib>Canonica, G. W.</creatorcontrib><title>Deflazacort protects against late‐phase but not early‐phase reactions induced by the allergen‐specific conjunctival provocation test</title><title>Allergy (Copenhagen)</title><addtitle>Allergy</addtitle><description>The protective effects of deflazacort against the inflammation that follows the conjunctival provocation test (CPT) by specific allergen were assessed in 24 patients with rhinoconjunctivitis caused by Parietaria judaica in a double‐blind study. After a screening CPT, patients were randomized into four treatment groups, each being given deflazacort (oral tablets) at 6, 30, and 60 mg once daily, or matching placebo, for 3 d, outside the pollen season. Clinical evaluation (itching, hyperemia, lacrimation, and swelling of eyelids) and cytologic assessment (number of inflammatory cells in conjunctival scraping and evaluation of ICAM (intercellular adhesion molecule)‐1/CD54 expression on epithelial cells) were performed at base line, 30 min (early‐phase reaction (EPR), 6 h and 24 h (late‐phase reaction (LPR)) after specific CPT, and before and after treatment. Neither the EPR clinical reactions nor the EPR total number of inflammatory cells was modified by deflazacort. However, the LPR clinical effects were significantly reduced by deflazacort at 30 or 60mg/d (P&lt;0.01), as compared with placebo. The total number of inflammatory cells during LPR was significantly reduced by deflazacort at 30 or 60 nig/d ((P&lt;0.01), as compared with placebo. Furthermore, CD54 expression was significantly reduced by deflazacort at 30 or 60 mg/d both in the EPR ((P&lt;0.01) and LPR ((P&lt;0.01), as compared with placebo. None of the studied indicators were modified at the 6 mg/d dose. 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W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deflazacort protects against late‐phase but not early‐phase reactions induced by the allergen‐specific conjunctival provocation test</atitle><jtitle>Allergy (Copenhagen)</jtitle><addtitle>Allergy</addtitle><date>1993-08</date><risdate>1993</risdate><volume>48</volume><issue>6</issue><spage>421</spage><epage>430</epage><pages>421-430</pages><issn>0105-4538</issn><eissn>1398-9995</eissn><abstract>The protective effects of deflazacort against the inflammation that follows the conjunctival provocation test (CPT) by specific allergen were assessed in 24 patients with rhinoconjunctivitis caused by Parietaria judaica in a double‐blind study. After a screening CPT, patients were randomized into four treatment groups, each being given deflazacort (oral tablets) at 6, 30, and 60 mg once daily, or matching placebo, for 3 d, outside the pollen season. Clinical evaluation (itching, hyperemia, lacrimation, and swelling of eyelids) and cytologic assessment (number of inflammatory cells in conjunctival scraping and evaluation of ICAM (intercellular adhesion molecule)‐1/CD54 expression on epithelial cells) were performed at base line, 30 min (early‐phase reaction (EPR), 6 h and 24 h (late‐phase reaction (LPR)) after specific CPT, and before and after treatment. Neither the EPR clinical reactions nor the EPR total number of inflammatory cells was modified by deflazacort. However, the LPR clinical effects were significantly reduced by deflazacort at 30 or 60mg/d (P&lt;0.01), as compared with placebo. The total number of inflammatory cells during LPR was significantly reduced by deflazacort at 30 or 60 nig/d ((P&lt;0.01), as compared with placebo. Furthermore, CD54 expression was significantly reduced by deflazacort at 30 or 60 mg/d both in the EPR ((P&lt;0.01) and LPR ((P&lt;0.01), as compared with placebo. None of the studied indicators were modified at the 6 mg/d dose. This study shows that deflazacort has a highly protective action against clinical and cellular LPR effects induced by the specific CPT, In addition, deflazacort markedly reduces CD54 expression on the conjunctival epithelium during both EPR and LPR.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>7902021</pmid><doi>10.1111/j.1398-9995.1993.tb00740.x</doi><tpages>10</tpages></addata></record>
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subjects Adolescent
Adult
Allergens - administration & dosage
Allergens - adverse effects
Anti-Inflammatory Agents - therapeutic use
Antigens, CD - biosynthesis
CD54 (ICAM‐I (intercellular adhesion molecule‐1)
Cell Adhesion Molecules - biosynthesis
conjunctival provocation test
Conjunctivitis, Allergic - complications
Conjunctivitis, Allergic - immunology
Conjunctivitis, Allergic - pathology
Conjunctivitis, Allergic - prevention & control
deflazacort
Double-Blind Method
early‐phase reaction
Epithelium - metabolism
Epithelium - pathology
Female
Humans
inflammatory response
Intercellular Adhesion Molecule-1
late‐phase reaction
Male
Middle Aged
Parietaria judaica
Pregnenediones - therapeutic use
Rhinitis, Allergic, Perennial - complications
Rhinitis, Allergic, Perennial - immunology
Rhinitis, Allergic, Perennial - pathology
Rhinitis, Allergic, Perennial - prevention & control
Time Factors
title Deflazacort protects against late‐phase but not early‐phase reactions induced by the allergen‐specific conjunctival provocation test
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