ABNORMAL NASAL GLANDULAR SECRETION IN RECURRENT SINUSITIS

被引:43
作者
JENEY, EVM [1 ]
RAPHAEL, GD [1 ]
MEREDITH, SD [1 ]
KALINER, MA [1 ]
机构
[1] NIAID,CLIN INVEST LAB,ALLERG DIS SECT,9000 ROCKVILLE PIKE,BLDG 10,11C205,BETHESDA,MD 20892
关键词
D O I
10.1016/S0091-6749(05)80117-4
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Recurrent sinusitis (RS) is a very common clinical problem for which no underlying cause can generally be ascertained. We examined nasal mucosal responses in 14 patients with RS to determine if a relative deficiency in secretion of glandular antimicrobial factors might play a role. Twenty-four subjects with no history of sinusitis were studied concurrently as normal control (NC) subjects. RS was defined by two or more episodes of acute sinusitis per year for 2 or more years. After provocation with 25 mg of methacholine or 1 mg of histamine, nasal washings were analyzed for total proteins: the plasma protein albumin, IgG, and nonsecretory IgA (nsIgA), and the glandular proteins secretory IgA (sIgA), lactoferrin (LFN), and lysozyme (LZM). Although baseline secretions in patients with RS were relatively enriched with LFN and LZM as compared to that of secretions in NC subjects, patients with RS had a blunted cholinergic response with decreased secretion of albumin, IgG, nsIgA, sIgA, and LZM. Histamine responses were equivalent in both patients with RS and NC subjects. After 4 to 12 months of medical treatment, the abnormal cholinergic responses improved on repeat methacholine challenge in all eight subjects with RS rechallenged. Thus, patients with RS have a reversible reduction in nasal mucosal secretory responses to cholinergic stimulation. Since glandular secretions are rich in antimicrobial factors, such as LFN, LZM, and sIgA, it appears possible that the inability to secrete glandular proteins normally may predispose to recurrent infections. © 1990 Mosby-Year Book, Inc.
引用
收藏
页码:10 / 18
页数:9
相关论文
共 29 条
[1]  
ABRAHAM SN, 1985, ADV HOST DEFENSE MEC, V4, P63
[2]  
BALLOW M, 1987, INVEST OPHTH VIS SCI, V28, P543
[3]   IMMUNOGLOBULINS IN MAXILLARY SINUS SECRETION [J].
CARENFELT, C ;
LUNDBERG, C ;
KARLEN, K .
ACTA OTO-LARYNGOLOGICA, 1976, 82 (1-2) :123-130
[4]   ROLE OF LOCAL GAS COMPOSITION IN PATHOGENESIS OF MAXILLARY SINUS EMPYEMA [J].
CARENFELT, C ;
LUNDBERG, C .
ACTA OTO-LARYNGOLOGICA, 1978, 85 (1-2) :116-121
[5]   MAXILLARY SINUSITIS - EFFECTS OF TREATMENT ON LOCAL ANTIBACTERIAL DEFENCE [J].
CARENFELT, C .
ACTA OTO-LARYNGOLOGICA, 1977, 84 (5-6) :440-445
[6]   ACQUIRED CILIARY DEFECTS IN NASAL EPITHELIUM OF CHILDREN WITH ACUTE VIRAL UPPER RESPIRATORY-INFECTIONS [J].
CARSON, JL ;
COLLIER, AM ;
HU, SCS .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (08) :463-468
[8]   EXPERIMENTAL ACUTE SINUSITIS IN RABBITS - A BACTERIOLOGICAL AND HISTOLOGICAL STUDY [J].
JOHANSSON, P ;
KUMLIEN, J ;
CARLSOO, B ;
DRETTNER, B ;
NORD, CE .
ACTA OTO-LARYNGOLOGICA, 1988, 105 (3-4) :357-366
[9]  
KENNEDY DW, 1985, ARCH OTOLARYNGOL, V111, P576
[10]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265