Severe acute respiratory syndrome coronavirus 2 seroprevalence and longitudinal antibody response following natural infection in pregnancy: A prospective cohort study.

Severe acute respiratory syndrome coronavirus 2 seroprevalence and longitudinal antibody response following natural infection in pregnancy: A prospective cohort study.
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DOI:
10.1177/17455057231190955
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发表时间:
2023-01
期刊:
影响因子:
2.4
通讯作者:
Lacourse, Sylvia M.
Lacourse, Sylvia M.
中科院分区:
其他
文献类型:
--
作者:
Drake, Alison L.;Escudero, Jaclyn N.;Aurelio, Morgan C.;Wetzler, Erica A.;Ellington, Sascha R.;Zapata, Lauren B.;Galang, Romeo R.;Snead, Margaret C.;Yamamoto, Krissy;Salerno, Carol C.;Richardson, Barbra A.;Greninger, Alexander L.;Kachikis, Alisa B.;Englund, Janet A.;Lacourse, Sylvia M.

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产前护理提供了独特的机会,以评估严重急性呼吸系统综合征冠状病毒2血清阳性率和抗体反应持续时间后,自然感染在怀孕期间检测;经胎盘抗体转移可能会告知围产期和新生儿的保护。我们估计血清阳性率和持久性抗体自然感染(抗核衣壳免疫球蛋白G)在孕妇中,并评估经胎盘转移效率。我们进行了一项横断面研究来测量严重急性呼吸综合征冠状病毒2型血清阳性率,并进行了一项前瞻性队列研究来纵向测量抗核衣壳免疫球蛋白G反应和母体来源的抗核衣壳抗体的经胎盘转移。我们于2020年12月9日至2021年6月19日在华盛顿的西雅图对孕妇进行了抗核衣壳免疫球蛋白G血清阳性率研究筛查。我们在2020年12月9日至2022年8月9日的前瞻性队列中招募了血清阳性率研究中的抗核衣壳免疫球蛋白G阳性患者,或通过病历确定的逆转录聚合酶链反应阳性或抗原阳性结果。在横断面研究(N = 1284)中,5%(N = 65)的严重急性呼吸综合征冠状病毒2型抗核衣壳免疫球蛋白G检测阳性,包括39例(60%)既往无阳性逆转录聚合酶链反应结果和42例(65%)无症状。在前瞻性队列研究中(共N = 107例; N = 65例来自血清阳性率研究),86例(N = 80%)在妊娠期间具有抗核衣壳免疫球蛋白G阳性结果。在63名有分娩样本和既往抗核衣壳阳性结果的参与者中,29名(46%)分娩时抗核衣壳免疫球蛋白G阴性。剩余的34个抗核衣壳免疫球蛋白G阳性分娩时配对的脐带血,19(56%)有有效的经胎盘抗核衣壳免疫球蛋白G抗体转移。从首次抗核衣壳免疫球蛋白G阳性到低于阳性抗体阈值的中位时间为19周,且既往逆转录聚合酶链反应阳性状态无差异。母体来源的严重急性呼吸综合征冠状病毒2抗体自然感染可能会在分娩前减弱。建议孕妇接种疫苗,以减少严重疾病并保护婴儿。
Antenatal care provides unique opportunities to assess severe acute respiratory syndrome coronavirus 2 seroprevalence and antibody response duration after natural infection detected during pregnancy; transplacental antibody transfer may inform peripartum and neonatal protection. We estimated seroprevalence and durability of antibodies from natural infection (anti-nucleocapsid immunoglobulin G) among pregnant people, and evaluated transplacental transfer efficiency. We conducted a cross-sectional study to measure severe acute respiratory syndrome coronavirus 2 seroprevalence, and a prospective cohort study to longitudinally measure anti-nucleocapsid immunoglobulin G responses and transplacental transfer of maternally derived anti-nucleocapsid antibodies. We screened pregnant people for the seroprevalence study between 9 December 2020 and 19 June 2021 for anti-nucleocapsid immunoglobulin G in Seattle, Washington. We enrolled anti-nucleocapsid immunoglobulin G positive people from the seroprevalence study or identified through medical records with positive reverse transcription polymerase chain reaction or antigen positive results in a prospective cohort between 9 December 2020 and 9 August 2022. In the cross-sectional study (N = 1284), 5% (N = 65) tested severe acute respiratory syndrome coronavirus 2 anti-nucleocapsid immunoglobulin G positive, including 39 (60%) without prior positive reverse transcription polymerase chain reaction results and 42 (65%) without symptoms. In the prospective cohort study (N = 107 total; N = 65 from the seroprevalence study), 86 (N = 80%) had anti-nucleocapsid immunoglobulin G positive results during pregnancy. Among 63 participants with delivery samples and prior anti-nucleocapsid positive results, 29 (46%) were anti-nucleocapsid immunoglobulin G negative by delivery. Of 34 remaining anti-nucleocapsid immunoglobulin G positive at delivery with paired cord blood, 19 (56%) had efficient transplacental anti-nucleocapsid immunoglobulin G antibody transfer. Median time from first anti-nucleocapsid immunoglobulin G positive to below positive antibody threshold was 19 weeks and did not differ by prior positive reverse transcription polymerase chain reaction status. Maternally derived severe acute respiratory syndrome coronavirus 2 antibodies to natural infection may wane before delivery. Vaccines are recommended for pregnant persons to reduce severe illness and confer protection to infants.
DOI: 10.1016/j.jcv.2021.104765
发表时间: 2021-03
期刊: Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
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