Investigation of an Mpox Outbreak Affecting Many Vaccinated Persons in Chicago, Illinois-March 2023-June 2023.
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Faherty Emily A G, Holly Taylor, Ogale Yasmin P, Spencer Hillary, Becht Ashley M, Crisler Gordon, Wasz Michael, Stonehouse Patrick, Barbian Hannah J, Zelinski Christy, Kittner Alyse, Foulkes Dorothy, Anderson Kendall W, Evans Tiffany, Nicolae Lavinia, Staton Amber, Hardnett Carla, Townsend Michael B, Carson William C, Satheshkumar Panayampalli S, Hutson Christina L, Gigante Crystal M, Quilter Laura A S, Gorman Susan, Borah Brian, Black Stephanie R, Pacilli Massimo, Kern David, Kerins Janna, McCollum Andrea M, Rao Agam K, Tabidze Irina
Аннотация
METHODS: We interviewed patients and reviewed medical records to assess demographic, behavioral, and clinical characteristics; mpox vaccine status; and vaccine administration routes. We evaluated serum antibody levels after infection and compared patient viral genomes with MPXV sequences in available databases. We discussed potential vaccine compromise with partners who manufactured, handled, and administered the vaccine associated with breakthrough infections.
RESULTS: During 18 March-27 June 2023, we identified 49 mpox cases; 57% of these mpox patients were FV. FV patients received both JYNNEOS doses subcutaneously (57%), intradermally (7%), or via heterologous administration (36%). FV patients had more median sex partners (3; interquartile range [IQR] = 1-4) versus not fully vaccinated patients (1; IQR = 1-2). Thirty-six of 37 sequenced specimens belonged to lineage B.1.20 of clade IIb MPXV, which did not demonstrate any amino acid changes relative to B.1, the predominant lineage from May 2022. Vaccinated patients demonstrated expected humoral antibody responses; none were hospitalized. No vaccine storage excursions were identified. Approximately 63% of people at risk for mpox in Chicago were FV during this period.
CONCLUSIONS: Our investigation indicated that cases were likely due to frequent behaviors associated with mpox transmission, even with relatively high vaccine effectiveness and vaccine coverage. Cases after vaccination might occur in similar populations.