Department of Community Medicine, Kempegowda Institute of Medical Sciences, Bangalore, India.
Department of Community Medicine, Bangalore Medical College & Research Institute, Bangalore, India.
Hum Vaccin Immunother. 2022 Nov 30;18(5):2081024. doi: 10.1080/21645515.2022.2081024. Epub 2022 Jun 10.
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.
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。