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Clinical presentation, viral shedding, and neutralizing antibody responses of mpox cases in South Korea: Single center experience.
Chin, BumSik; Um, Jihye; Kim, Min-Kyung; Kim, Hyang Su; Yim, Hong Soon; Cho, Hyee Jin; Lim, So Yun; Kim, Yeonjae; Jeon, Jaehyun; Park, Jun-Sun.
Afiliação
  • Chin B; Division of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul, South Korea.
  • Um J; Public Health Research Institute, National Medical Center, Seoul, South Korea; Department of Public Health, Korea University Graduate School, Seoul, South Korea.
  • Kim MK; Division of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul, South Korea.
  • Kim HS; Public Health Research Institute, National Medical Center, Seoul, South Korea.
  • Yim HS; Public Health Research Institute, National Medical Center, Seoul, South Korea.
  • Cho HJ; Department of Internal Medicine, National Medical Center, Seoul, South Korea.
  • Lim SY; Division of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul, South Korea.
  • Kim Y; Division of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul, South Korea.
  • Jeon J; Division of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul, South Korea.
  • Park JS; Public Health Research Institute, National Medical Center, Seoul, South Korea. Electronic address: junsunpark@nmc.or.kr.
J Clin Virol ; 173: 105692, 2024 08.
Article em En | MEDLINE | ID: mdl-38830304
ABSTRACT

BACKGROUND:

A global mpox outbreak occurred in 2022, and a domestic outbreak started in South Korea in April 2023. This study aimed to evaluate the clinical characteristics, viral shedding, and immune response of mpox in South Korea.

METHODS:

Patients hospitalized with mpox in the National Medical Center between September 2022 and June 2023 were included in this study. Oropharyngeal (OP), anogenital lesion (AL), and skin lesion (SL) swabs and blood samples were collected, and monkeypox virus (MPXV) DNA using real-time polymerase chain reaction (RT-PCR) and culture assays were performed. Neutralizing antibodies (NAbs) against MPXV A.2.1, B.1.1, and B.1.3 were detected using plaque reduction neutralization tests.

RESULTS:

Eighteen patients were enrolled, of whom 17 (94.4 %) were male, with a median (IQR) age of 32.5 (24-51) years. While nine (50 %) were HIV-infected individuals, none of them revealed CD4+ counts less than 200 cells/µL. MPXV DNA was detected in 87.3 % and 82.7 % of patient's ALs and SLs, respectively, until 2 weeks after symptom onset. While MPXV was isolated for up to 15 days in all three sample types, the culture positivity decreased to 53.8 % and 42.9 % in ALs and SLs after 10 days, respectively, and 28.6 % and 22.2 %, respectively, after 2 weeks from symptom onset. The NAb titers against MPXV A.2.1 were significantly lower than those against B.1.1 and B.1.3.

CONCLUSIONS:

Infectious MPXV was isolated from various anatomical sites up to 15 days after symptom onset. The MPXV NAb response was varied among different lineages, and this implies limited cross-lineage protection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eliminação de Partículas Virais / Anticorpos Neutralizantes / Anticorpos Antivirais Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eliminação de Partículas Virais / Anticorpos Neutralizantes / Anticorpos Antivirais Idioma: En Ano de publicação: 2024 Tipo de documento: Article