• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

口服细菌裂解物刺激人体产生免疫球蛋白。

Immunoglobulin production in man stimulated by an orally administered bacterial lysate.

作者信息

Puigdollers J M, Serna G R, Hernandez del Rey I, Barruffet M T, Torroella J J

出版信息

Respiration. 1980;40(3):142-9. doi: 10.1159/000194264.

DOI:10.1159/000194264
PMID:7003667
Abstract

The concentrations of secretory immunoglobulins in the saliva, and of immunoglobulin in the serum, have been measured by the radial immunodiffusion method in 12 healthy volunteers, before and after oral administration of Broncho-Vaxom which is a lysate of bacteria that usually cause infection in the upper respiratory tract. The mean concentration of secretory IgA in the saliva was increased by over 100% after the 10-day administration of the product. This increase was statistically significant between the 20th and 33rd day after the beginning of the treatment (p < 0.05). It fell to a normal level after a month in 4 subjects who received one treatment course only. In 8 subjects who received a second treatment course beginning 1 month after termination of the first course, the high concentration of IgAs in the saliva persisted for at least 3 months. A significant increase in the serum concentrations of IgG of about 50% and of IgM of at least 100% above the initial level was observed in the treated subjects in the time between day 35 and 5 months after the beginning of the experiment (p < 0.05).

摘要

采用放射免疫扩散法,对12名健康志愿者口服Broncho-Vaxom(一种通常引起上呼吸道感染的细菌裂解物)前后唾液中分泌型免疫球蛋白和血清中免疫球蛋白的浓度进行了测定。在服用该产品10天后,唾液中分泌型IgA的平均浓度增加了100%以上。这种增加在治疗开始后的第20天至第33天之间具有统计学意义(p<0.05)。仅接受一个疗程治疗的4名受试者在一个月后降至正常水平。在8名在第一个疗程结束后1个月开始接受第二个疗程治疗的受试者中,唾液中高浓度的IgA持续了至少3个月。在实验开始后的第35天至5个月期间,治疗组受试者血清中IgG浓度显著增加约50%,IgM浓度至少比初始水平增加100%(p<0.05)。

相似文献

1
Immunoglobulin production in man stimulated by an orally administered bacterial lysate.口服细菌裂解物刺激人体产生免疫球蛋白。
Respiration. 1980;40(3):142-9. doi: 10.1159/000194264.
2
[Assessment of salivary IgA titer in children with recurrent respiratory infections treated with polyvalent oral vaccine. A controlled study].[用多价口服疫苗治疗复发性呼吸道感染儿童的唾液免疫球蛋白A滴度评估。一项对照研究]
Minerva Pediatr. 1988 Jun;40(6):355-60.
3
Naturally occurring immune response against bacteria commonly involved in upper respiratory tract infections: analysis of the antigen-specific salivary IgA levels.针对上呼吸道感染中常见细菌的天然免疫反应:抗原特异性唾液IgA水平分析
Immunol Lett. 2003 Mar 3;86(1):85-91. doi: 10.1016/s0165-2478(02)00290-0.
4
Salivary immunoglobulin A production in chronic bronchitis patients given an orally administered bacterial extract.给予口服细菌提取物的慢性支气管炎患者唾液免疫球蛋白A的产生情况
Respiration. 1993;60(6):313-8. doi: 10.1159/000196228.
5
Systemic immunization with pneumococcal polysaccharide vaccine induces a predominant IgA2 response of peripheral blood lymphocytes and increases of both serum and secretory anti-pneumococcal antibodies.用肺炎球菌多糖疫苗进行全身免疫可诱导外周血淋巴细胞产生主要的IgA2应答,并增加血清和分泌型抗肺炎球菌抗体。
J Immunol. 1988 Jun 1;140(11):3793-800.
6
Immune response in the lungs following oral immunization with bacterial lysates of respiratory pathogens.用呼吸道病原体细菌裂解物进行口服免疫后肺部的免疫反应。
Clin Diagn Lab Immunol. 1994 Mar;1(2):150-4. doi: 10.1128/cdli.1.2.150-154.1994.
7
Attempted induction of interferon by bacterial vaccines in allergic and nonallergic humans.尝试通过细菌疫苗在过敏和非过敏人群中诱导干扰素。
Ann Allergy. 1974 Feb;32(2):70-2.
8
Trial of an oral antigen in upper respiratory tract infections in two Bristol schools.
Practitioner. 1974 Nov;213(1277):720-6.
9
Specific immune response in the respiratory tract after administration of an oral polyvalent bacterial vaccine.口服多价细菌疫苗后呼吸道中的特异性免疫反应。
Infect Immun. 1983 Feb;39(2):491-6. doi: 10.1128/iai.39.2.491-496.1983.
10
Efficacy of a "mixed bacterial vaccine" in prophylaxis of acute respiratory infections: possible role of interferon.一种“混合细菌疫苗”在预防急性呼吸道感染中的疗效:干扰素的可能作用。
Am J Epidemiol. 1974 May;99(5):347-59. doi: 10.1093/oxfordjournals.aje.a121620.

引用本文的文献

1
Human vaccine candidates for infections caused by : A systematic review.针对由……引起的感染的人类候选疫苗:一项系统综述。
Health Sci Rep. 2024 Sep 10;7(9):e70061. doi: 10.1002/hsr2.70061. eCollection 2024 Sep.
2
Clinical and Immunological Benefits of OM-85 Bacterial Lysate in Patients with Allergic Rhinitis, Asthma, and COPD and Recurrent Respiratory Infections.OM-85细菌溶解产物对过敏性鼻炎、哮喘、慢性阻塞性肺疾病及反复呼吸道感染患者的临床和免疫学益处
Lung. 2016 Aug;194(4):687-97. doi: 10.1007/s00408-016-9880-5. Epub 2016 Apr 27.
3
Prospective, randomized comparison of OM-85 BV and a prophylactic antibiotic in children with recurrent infections and immunoglobulin A and/or G subclass deficiency.
OM-85 BV与预防性抗生素在复发性感染及免疫球蛋白A和/或G亚类缺乏儿童中的前瞻性随机对照研究。
Curr Ther Res Clin Exp. 2003 Sep;64(8):600-15. doi: 10.1016/j.curtheres.2003.09.008.
4
OM85-BV induced the productions of IL-1β, IL-6, and TNF-α via TLR4- and TLR2-mediated ERK1/2/NF-κB pathway in RAW264.7 cells.OM85-BV通过RAW264.7细胞中TLR4和TLR2介导的ERK1/2/NF-κB途径诱导IL-1β、IL-6和TNF-α的产生。
J Interferon Cytokine Res. 2014 Jul;34(7):526-36. doi: 10.1089/jir.2013.0077. Epub 2014 Mar 7.
5
Prevention of respiratory tract infections with bacterial lysate OM-85 bronchomunal in children and adults: a state of the art.使用细菌溶解产物OM-85防治儿童和成人呼吸道感染:最新进展
Multidiscip Respir Med. 2013 May 22;8(1):33. doi: 10.1186/2049-6958-8-33.
6
Prevention of infection in immunosuppressive patients with autoimmune nephrosis by using an immunostimulating bacterial lysate Broncho-vaxom.免疫刺激细菌裂解物 Broncho-vaxom 预防自身免疫性肾病免疫抑制患者感染。
Hum Vaccin Immunother. 2012 Dec 1;8(12):1802-7. doi: 10.4161/hv.21874. Epub 2012 Aug 24.
7
Sublingual therapeutic immunization with a polyvalent bacterial preparation in patients with recurrent respiratory infections: immunomodulatory effect on antigen-specific memory CD4+ T cells and impact on clinical outcome.舌下免疫治疗复发性呼吸道感染患者的多价细菌制剂:对抗原特异性记忆 CD4+T 细胞的免疫调节作用及其对临床结果的影响。
Clin Exp Immunol. 2011 Apr;164(1):100–7. doi: 10.1111/j.1365-2249.2011.04320.x.
8
[Not Available].[未提供]。
Clin Drug Investig. 1997;13(2):76-84. doi: 10.2165/00044011-199713020-00003.
9
Prevention of recurrent rhinopharyngitis in at-risk children in France: a cost-effectiveness model for a nonspecific immunostimulating bacterial extract (OM-85 BV).法国高危儿童复发性鼻咽炎的预防:非特异性免疫刺激细菌提取物(OM-85 BV)的成本效益模型
Pharmacoeconomics. 2003;21(14):1053-68. doi: 10.2165/00019053-200321140-00005.
10
Specific immune response in the respiratory tract after administration of an oral polyvalent bacterial vaccine.口服多价细菌疫苗后呼吸道中的特异性免疫反应。
Infect Immun. 1983 Feb;39(2):491-6. doi: 10.1128/iai.39.2.491-496.1983.