1. Investigation of an Mpox Outbreak Affecting Many Vaccinated Persons in Chicago, Illinois-March 2023-June 2023.
- Author
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Faherty EAG, Holly T, Ogale YP, Spencer H, Becht AM, Crisler G, Wasz M, Stonehouse P, Barbian HJ, Zelinski C, Kittner A, Foulkes D, Anderson KW, Evans T, Nicolae L, Staton A, Hardnett C, Townsend MB, Carson WC, Satheshkumar PS, Hutson CL, Gigante CM, Quilter LAS, Gorman S, Borah B, Black SR, Pacilli M, Kern D, Kerins J, McCollum AM, Rao AK, and Tabidze I
- Subjects
- Humans, Chicago epidemiology, Female, Male, Adult, Middle Aged, Young Adult, Antibodies, Viral blood, Aged, Adolescent, Viral Vaccines immunology, Viral Vaccines administration & dosage, Genome, Viral, Disease Outbreaks, Vaccination, Mpox (monkeypox) epidemiology
- Abstract
Background: After months of few mpox cases, an increase in cases was reported in Chicago during May 2023, predominantly among fully vaccinated (FV) patients. We investigated the outbreak scope, differences between vaccinated and unvaccinated patients, and hypotheses for monkeypox virus (MPXV) infection after vaccination., 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., Competing Interests: Potential conflicts of interest. The authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed., (Published by Oxford University Press on behalf of Infectious Diseases Society of America 2024.)
- Published
- 2024
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