• 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

相似文献

1
Safety and clinical efficacy of human rabies immunoglobulin in post exposure prophylaxis for category III animal exposures.人用狂犬病免疫球蛋白在 III 类动物暴露后预防中的安全性和临床疗效。
Hum Vaccin Immunother. 2022 Nov 30;18(5):2081024. doi: 10.1080/21645515.2022.2081024. Epub 2022 Jun 10.
2
Comparison of a Novel Human Rabies Monoclonal Antibody to Human Rabies Immunoglobulin for Postexposure Prophylaxis: A Phase 2/3, Randomized, Single-Blind, Noninferiority, Controlled Study.新型人用狂犬病单抗与狂犬病免疫球蛋白用于狂犬病暴露后预防的比较:一项 2/3 期、随机、单盲、非劣效、对照研究。
Clin Infect Dis. 2018 Jan 18;66(3):387-395. doi: 10.1093/cid/cix791.
3
Defining the volume of rabies immunoglobulins/ rabies monoclonal antibodies requirement for wound infiltration of category III animal exposures - an exploratory study.定义狂犬病免疫球蛋白/狂犬病单克隆抗体在 III 类动物接触伤口浸润中的用量需求 - 一项探索性研究。
Hum Vaccin Immunother. 2021 Dec 2;17(12):5355-5360. doi: 10.1080/21645515.2021.2013079. Epub 2022 Jan 21.
4
A phase 2b, Randomized, double blinded comparison of the safety and efficacy of the monoclonal antibody mixture SYN023 and human rabies immune globulin in patients exposed to rabies.一项 2b 期、随机、双盲比较 SYN023 单克隆抗体混合物和人狂犬病免疫球蛋白在狂犬病暴露患者中的安全性和疗效的研究。
Vaccine. 2024 Sep 17;42(22):126018. doi: 10.1016/j.vaccine.2024.05.066. Epub 2024 Jun 4.
5
Comparing recombinant human rabies monoclonal antibody (ormutivimab) with human rabies immunoglobulin (HRIG) for postexposure prophylaxis: A phase III, randomized, double-blind, non-inferiority trial.比较重组人狂犬病单克隆抗体(ormutivimab)与人狂犬病免疫球蛋白(HRIG)用于暴露后预防:一项 III 期、随机、双盲、非劣效性试验。
Int J Infect Dis. 2023 Sep;134:53-62. doi: 10.1016/j.ijid.2023.05.017. Epub 2023 May 19.
6
Time of administration of rabies immunoglobulins and adequacy of antibody response upon post-exposure prophylaxis: a descriptive retrospective study in Belgium.狂犬病免疫球蛋白给药时间和暴露后预防的抗体反应充足性:比利时的一项描述性回顾性研究。
Acta Clin Belg. 2021 Apr;76(2):91-97. doi: 10.1080/17843286.2019.1662993. Epub 2019 Sep 4.
7
Safety and efficacy results of simulated post-exposure prophylaxis with human immune globulin (HRIG; KEDRAB) co-administered with active vaccine in healthy subjects: a comparative phase 2/3 trial.在健康受试者中,人免疫球蛋白(HRIG;凯德瑞)与活性疫苗联合使用进行模拟暴露后预防的安全性和有效性结果:一项2/3期对照试验。
Hum Vaccin Immunother. 2020;16(2):452-459. doi: 10.1080/21645515.2019.1656967. Epub 2019 Sep 24.
8
A randomized non-inferiority clinical study to assess post-exposure prophylaxis by a new purified vero cell rabies vaccine (Rabivax-S) administered by intramuscular and intradermal routes.一项随机非劣效性临床研究,旨在评估通过肌肉注射和皮内注射新型纯化Vero细胞狂犬病疫苗(Rabivax-S)进行暴露后预防的效果。
Vaccine. 2016 Sep 14;34(40):4820-6. doi: 10.1016/j.vaccine.2016.08.005. Epub 2016 Aug 21.
9
Shortening intradermal rabies post-exposure prophylaxis regimens to 1 week: Results from a phase III clinical trial in children, adolescents and adults.缩短皮内狂犬病暴露后预防方案至 1 周:儿童、青少年和成人 III 期临床试验结果。
PLoS Negl Trop Dis. 2018 Jun 6;12(6):e0006340. doi: 10.1371/journal.pntd.0006340. eCollection 2018 Jun.
10
Safety and immunogenicity of rabies vaccine as 4 - dose Essen Intramuscular regimen for post exposure prophylaxis: A non - randomized, comparative controlled study.狂犬病疫苗作为暴露后预防的 4 剂 Essen 肌内注射方案的安全性和免疫原性:一项非随机、对照的比较研究。
Hum Vaccin Immunother. 2021 Aug 3;17(8):2554-2559. doi: 10.1080/21645515.2021.1883388. Epub 2021 Feb 23.

引用本文的文献

1
Demographic, temporal, and spatial analysis of human animal bite cases in Mymensingh District, Bangladesh.孟加拉国迈门辛区人类动物咬伤病例的人口统计学、时间和空间分析。
PLoS Negl Trop Dis. 2025 Jun 9;19(6):e0012204. doi: 10.1371/journal.pntd.0012204. eCollection 2025 Jun.
2
A prospective study on safety and clinical efficacy of rabies biologicals in paediatric patients with category III animal exposure.狂犬病生物制品在Ⅲ级动物暴露儿科患者中的安全性和临床疗效的前瞻性研究。
Clin Exp Vaccine Res. 2025 Jan;14(1):59-66. doi: 10.7774/cevr.2025.14.e1. Epub 2025 Jan 13.
3
Safety Evaluation of the Novel Cocktail of Monoclonal Antibodies for Postexposure Prophylaxis in Category III Animal Exposures.新型单克隆抗体鸡尾酒疗法用于Ⅲ类动物暴露后预防的安全性评估。
J Glob Infect Dis. 2024 Oct 18;16(4):140-144. doi: 10.4103/jgid.jgid_71_24. eCollection 2024 Oct-Dec.
4
Epidemiology, transmission dynamics, risk factors, and future directions of rabies in the Arabian Peninsula using one health approach: a review.采用一体化健康方法对阿拉伯半岛狂犬病的流行病学、传播动力学、风险因素及未来方向的综述
Eur J Public Health. 2025 Jan 1;35(Supplement_1):i14-i22. doi: 10.1093/eurpub/ckae164.
5
Safety assessment of the world's first novel cocktail of two monoclonal antibodies in WHO category-III animal-bite patients.全球首款两种单克隆抗体新型鸡尾酒疗法用于世界卫生组织III类动物咬伤患者的安全性评估。
J Family Med Prim Care. 2024 Oct;13(10):4493-4498. doi: 10.4103/jfmpc.jfmpc_377_24. Epub 2024 Oct 18.
6
Post-Marketing Surveillance of the World's First Novel Cocktail of Rabies Monoclonal Antibodies: TwinRab™ in Real \-World Setting.全球首款狂犬病单克隆抗体新型鸡尾酒疗法TwinRab™在真实世界环境中的上市后监测
Indian J Community Med. 2024 Mar-Apr;49(2):443-447. doi: 10.4103/ijcm.ijcm_562_23. Epub 2024 Mar 7.
7
Tracking lethal threat: in-depth review of rabies.追踪致命威胁:狂犬病深度综述。
Open Vet J. 2023 Nov;13(11):1385-1399. doi: 10.5455/OVJ.2023.v13.i11.1. Epub 2023 Nov 30.
8
Pediatric Long Bone Fractures After Dog Bites: A Case Series and Systematic Review.犬咬伤后儿童长骨骨折:病例系列与系统评价
Cureus. 2023 Oct 17;15(10):e47230. doi: 10.7759/cureus.47230. eCollection 2023 Oct.

本文引用的文献

1
Defining the volume of rabies immunoglobulins/ rabies monoclonal antibodies requirement for wound infiltration of category III animal exposures - an exploratory study.定义狂犬病免疫球蛋白/狂犬病单克隆抗体在 III 类动物接触伤口浸润中的用量需求 - 一项探索性研究。
Hum Vaccin Immunother. 2021 Dec 2;17(12):5355-5360. doi: 10.1080/21645515.2021.2013079. Epub 2022 Jan 21.
2
Safety and efficacy of rabies immunoglobulin in pediatric patients with suspected exposure.疑似暴露后儿童患者使用狂犬病免疫球蛋白的安全性和有效性。
Hum Vaccin Immunother. 2021 Jul 3;17(7):2090-2096. doi: 10.1080/21645515.2020.1854000. Epub 2021 Feb 9.
3
RABIES IMMUNOGLOBULIN: Brief history and recent experiences in Côte d'Ivoire.狂犬病免疫球蛋白:科特迪瓦的简要历史和近期经验。
Acta Trop. 2020 Nov;211:105629. doi: 10.1016/j.actatropica.2020.105629. Epub 2020 Jul 11.
4
A Phase 3, Randomized, Open-label, Noninferiority Trial Evaluating Anti-Rabies Monoclonal Antibody Cocktail (TwinrabTM) Against Human Rabies Immunoglobulin (HRIG).一项评估抗狂犬病单克隆抗体鸡尾酒(TwinrabTM)与狂犬病免疫球蛋白(HRIG)的 3 期、随机、开放标签、非劣效性试验。
Clin Infect Dis. 2021 Nov 2;73(9):e2722-e2728. doi: 10.1093/cid/ciaa779.
5
Facilities and services of postexposure prophylaxis in anti-rabies clinics: A national assessment in India.狂犬病暴露后预防诊所的设施和服务:印度的全国评估。
Indian J Public Health. 2019 Sep;63(Supplement):S26-S30. doi: 10.4103/ijph.IJPH_367_19.
6
Safety and efficacy results of simulated post-exposure prophylaxis with human immune globulin (HRIG; KEDRAB) co-administered with active vaccine in healthy subjects: a comparative phase 2/3 trial.在健康受试者中,人免疫球蛋白(HRIG;凯德瑞)与活性疫苗联合使用进行模拟暴露后预防的安全性和有效性结果:一项2/3期对照试验。
Hum Vaccin Immunother. 2020;16(2):452-459. doi: 10.1080/21645515.2019.1656967. Epub 2019 Sep 24.
7
Four Thousand Years of Concepts Relating to Rabies in Animals and Humans, Its Prevention and Its Cure.四千年来关于动物和人类狂犬病的概念、预防及治疗
Trop Med Infect Dis. 2017 Mar 24;2(2):5. doi: 10.3390/tropicalmed2020005.
8
Comparison of a Novel Human Rabies Monoclonal Antibody to Human Rabies Immunoglobulin for Postexposure Prophylaxis: A Phase 2/3, Randomized, Single-Blind, Noninferiority, Controlled Study.新型人用狂犬病单抗与狂犬病免疫球蛋白用于狂犬病暴露后预防的比较:一项 2/3 期、随机、单盲、非劣效、对照研究。
Clin Infect Dis. 2018 Jan 18;66(3):387-395. doi: 10.1093/cid/cix791.
9
Public Health Weekly Reports for MAY 18, 1945.1945年5月18日公共卫生周报
Public Health Rep (1896). 1945 May 18;60(20):545-576.
10
Re-evaluating the burden of rabies in Africa and Asia.重新评估非洲和亚洲的狂犬病负担。
Bull World Health Organ. 2005 May;83(5):360-8. Epub 2005 Jun 24.

人用狂犬病免疫球蛋白在 III 类动物暴露后预防中的安全性和临床疗效。

Safety and clinical efficacy of human rabies immunoglobulin in post exposure prophylaxis for category III animal exposures.

机构信息

Department of Community Medicine, Kempegowda Institute of Medical Sciences, Bangalore, India.

Department of Community Medicine, Bangalore Medical College & Research Institute, Bangalore, India.

出版信息

Hum Vaccin Immunother. 2022 Nov 30;18(5):2081024. doi: 10.1080/21645515.2022.2081024. Epub 2022 Jun 10.

DOI:10.1080/21645515.2022.2081024
PMID:35687876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9621008/
Abstract

The human rabies immunoglobulin (HRIG) is a life-saving immune biological essential for all category III animal exposures. It provides neutralizing antibodies at the site of exposure until the body can produce vaccine-mediated antibodies. We conducted this study to determine the safety and clinical efficacy of an HRIG being used presently for post-exposure prophylaxis (PEP) and to strengthen the existing evidence for its further usage. We conducted a prospective cohort study in 123 subjects with category III animal exposures at the KIMS Hospital and Research Center, Bangalore, India. Post-exposure prophylaxis (PEP) with wound toilet, a single application of HRIG, and a full course of anti-rabies vaccination were provided to all the study subjects. The volume of HRIG was calculated according to the body weight, and all the wounds were infiltrated as was anatomically feasible. All the study subjects were followed up for immediate and delayed adverse events (AE), both local and systemic. Subsequently, all the subjects were followed up for 6 months to demonstrate the clinical efficacy of PEP. The incidence of AEs was 11.4% including local pain, erythema, itching, headache, body ache, fever, and malaise. All AEs were mild and subsided without any complications. All the study subjects were healthy and alive after 6 months following the administration of HRIG, along with a full course of anti-rabies vaccine. Our study provides evidence of safety and clinical efficacy of HRIG for category III animal exposures and supports its continued usage.

摘要

人用狂犬病免疫球蛋白(HRIG)是所有 III 类动物暴露后救命的免疫生物制剂。它在暴露部位提供中和抗体,直到身体产生疫苗介导的抗体。我们进行这项研究是为了确定目前用于暴露后预防(PEP)的 HRIG 的安全性和临床疗效,并为其进一步使用提供现有证据。我们在印度班加罗尔的 KIMS 医院和研究中心对 123 名 III 类动物暴露的受试者进行了前瞻性队列研究。所有研究对象均接受了伤口清洗、单次 HRIG 应用和全程狂犬病疫苗接种的 PEP。根据体重计算 HRIG 的用量,所有伤口均进行了浸润,尽可能做到解剖上可行。所有研究对象均进行了即时和延迟不良事件(AE)的随访,包括局部和全身。随后,所有研究对象均进行了 6 个月的随访,以证明 PEP 的临床疗效。AE 的发生率为 11.4%,包括局部疼痛、红斑、瘙痒、头痛、全身疼痛、发热和不适。所有 AE 均为轻度,无需任何并发症即可消退。所有研究对象在接受 HRIG 和全程狂犬病疫苗接种后 6 个月均健康存活。我们的研究为 III 类动物暴露后 HRIG 的安全性和临床疗效提供了证据,并支持其继续使用。