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本文引用的文献

1
Progress Toward Polio Eradication - Worldwide, January 2019-June 2021.迈向消灭脊灰的进展——全球,2019 年 1 月至 2021 年 6 月。
MMWR Morb Mortal Wkly Rep. 2021 Aug 27;70(34):1129-1135. doi: 10.15585/mmwr.mm7034a1.
2
Poliovirus excretion among children with primary immune deficiency in Pakistan: a pilot surveillance study protocol.巴基斯坦原发性免疫缺陷儿童中脊髓灰质炎病毒的排泄情况:一项试点监测研究方案。
BMJ Open. 2021 Jul 28;11(7):e045904. doi: 10.1136/bmjopen-2020-045904.
3
Update on Immunodeficiency-Associated Vaccine-Derived Polioviruses - Worldwide, July 2018-December 2019.免疫缺陷相关疫苗衍生脊灰病毒最新情况 - 全球,2018 年 7 月至 2019 年 12 月。
MMWR Morb Mortal Wkly Rep. 2020 Jul 17;69(28):913-917. doi: 10.15585/mmwr.mm6928a4.
4
New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data.免疫缺陷相关疫苗衍生脊髓灰质炎病毒感染的病理生理学新见解;对超过 50 年数据的系统回顾。
Vaccine. 2018 Mar 20;36(13):1711-1719. doi: 10.1016/j.vaccine.2018.02.059. Epub 2018 Feb 23.
5
Vaccine-derived poliovirus surveillance in China during 2001-2013: the potential challenge for maintaining polio free status.2001 - 2013年中国疫苗衍生脊髓灰质炎病毒监测:维持无脊髓灰质炎状态面临的潜在挑战
BMC Infect Dis. 2017 Dec 2;17(1):742. doi: 10.1186/s12879-017-2849-z.
6
Poliovirus Excretion in Children with Primary Immunodeficiency Disorders, India.印度原发性免疫缺陷疾病患儿中的脊髓灰质炎病毒排泄情况。
Emerg Infect Dis. 2017 Oct;23(10):1664-1670. doi: 10.3201/eid2310.170724.
7
Completing Polio Eradication: The Case for Antiviral Drugs.实现脊髓灰质炎根除:抗病毒药物的作用
J Infect Dis. 2017 Feb 1;215(3):333-334. doi: 10.1093/infdis/jiw547.
8
BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies.BCG 疫苗接种在严重联合免疫缺陷患者中的应用:并发症、风险和疫苗接种政策。
J Allergy Clin Immunol. 2014 Apr;133(4):1134-41. doi: 10.1016/j.jaci.2014.02.028.
9
Severe axillary lymphadenitis after BCG vaccination: alert for primary immunodeficiencies.卡介苗接种后严重腋窝淋巴结炎:原发性免疫缺陷症的警示。
J Microbiol Immunol Infect. 2010 Dec;43(6):530-7. doi: 10.1016/S1684-1182(10)60082-5.

2022 年中国重庆一名严重原发性免疫缺陷疾病儿童中检出一株高度分化的 3 型疫苗衍生脊髓灰质炎病毒。

Detection of a Highly Divergent Type 3 Vaccine-Derived Poliovirus in a Child with a Severe Primary Immunodeficiency Disorder - Chongqing, China, 2022.

出版信息

MMWR Morb Mortal Wkly Rep. 2022 Sep 9;71(36):1148-1150. doi: 10.15585/mmwr.mm7136a2.

DOI:10.15585/mmwr.mm7136a2
PMID:36074738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9470223/
Abstract

Oral poliovirus vaccine (OPV) has proven to be highly effective in the global effort to eradicate poliomyelitis because of its ability to induce both humoral and intestinal immunity, ease of administration, and low cost (1). Sabin-strain OPV contains live attenuated virus and induces immunity by replicating in the intestinal tract, triggering an immune response that clears the vaccine virus. However, among undervaccinated communities and persons with immunodeficiency, OPV mutations that arise during prolonged replication can result in the emergence of genetically divergent, neurovirulent vaccine-derived polioviruses (VDPVs). In addition, OPV has resulted in rare cases of vaccine-associated paralytic poliomyelitis (VAPP) among vaccine recipients or their close contacts (1). Identification of circulating polioviruses relies on surveillance of acute flaccid paralysis (AFP) and environmental surveillance of wastewater (i.e., sewage). In 2022, type 3 VDPV (VDPV3) was detected in stool specimens from an infant with primary immunodeficiency disorder (PID) through a pilot surveillance program to identify VDPVs in children with PIDs. Integrated AFP, environmental, and immunodeficiency-associated VDPV (iVDPV) surveillance is critical to detecting and containing all polioviruses and achieving the goal of global polio eradication.

摘要

口服脊髓灰质炎疫苗(OPV)因其能够诱导体液和肠道免疫、易于管理和成本低廉,已被证明在全球消灭脊髓灰质炎的努力中非常有效 (1)。沙宾株 OPV 含有活减毒病毒,通过在肠道内复制诱导免疫,引发清除疫苗病毒的免疫反应。然而,在疫苗接种不足的社区和免疫功能低下的人群中,OPV 复制过程中出现的突变可导致具有遗传差异、神经毒力的疫苗衍生脊髓灰质炎病毒(VDPV)的出现。此外,OPV 还导致疫苗接种者或其密切接触者中出现罕见的疫苗相关麻痹性脊髓灰质炎(VAPP)病例 (1)。循环脊髓灰质炎病毒的鉴定依赖于急性弛缓性麻痹 (AFP) 的监测和废水(即污水)的环境监测。2022 年,通过一项针对原发性免疫缺陷病 (PID) 儿童中 VDPV 的试点监测计划,在一名 PID 婴儿的粪便标本中检测到了 3 型 VDPV(VDPV3)。综合 AFP、环境和与免疫缺陷相关的 VDPV (iVDPV) 监测对于发现和控制所有脊髓灰质炎病毒以及实现全球消灭脊髓灰质炎的目标至关重要。