Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Med Virol ; 96(6): e29728, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38860589

ABSTRACT

Since May 2022, several countries outside of Africa experienced multiple clusters of monkeypox virus (MPXV)-associated disease. In the present study, anti-MPXV and anti-vaccinia virus (VACV) neutralizing antibody responses were evaluated in two cohorts of subjects from the general Italian population (one half born before the WHO-recommended end of smallpox vaccination in 1980, the other half born after). Higher titers (either against MPXV or VACV) were observed in the cohort of individuals born before the interruption of VACV vaccination. An association between VACV and MPXV antibody levels was observed, suggesting that the smallpox vaccination may confer some degree of cross-protection against MPXV infection. Results from this study highlight low levels of immunity toward the assessed Orthopoxviruses, especially in young adults, advocating the introduction of a VACV- or MPXV-specific vaccine in case of resurgence of monkeypox disease outbreaks.


Subject(s)
Antibodies, Neutralizing , Antibodies, Viral , Monkeypox virus , Smallpox Vaccine , Vaccination , Vaccinia virus , Humans , Antibodies, Neutralizing/blood , Antibodies, Neutralizing/immunology , Antibodies, Viral/blood , Male , Adult , Female , Smallpox Vaccine/immunology , Smallpox Vaccine/administration & dosage , Italy/epidemiology , Monkeypox virus/immunology , Young Adult , Seroepidemiologic Studies , Middle Aged , Vaccinia virus/immunology , Mpox (monkeypox)/epidemiology , Mpox (monkeypox)/immunology , Adolescent , Smallpox/prevention & control , Smallpox/immunology , Smallpox/epidemiology , Cross Protection/immunology , Aged , Cohort Studies , Child
2.
Front Public Health ; 11: 1195674, 2023.
Article in English | MEDLINE | ID: mdl-37415699

ABSTRACT

Introduction: In early to mid-2022, an unexpected outbreak of Monkeypox virus infections occurred outside the African endemic regions. Vaccines originally developed in the past to protect against smallpox are one of the available countermeasures to prevent and protect against Orthopoxvirus infections. To date, there are few studies on the cross-reactivity of neutralizing antibodies elicited by previous vaccinia virus-based vaccination and/or Monkeypox virus infection. The aim of this study was to evaluate a possible approach to performing Monkeypox and vaccinia live-virus microneutralization assays in which the read-out is based on the production of cytopathic effect in the cell monolayer. Methods: Given the complexity of Orthopoxviruses, the microneutralization assay was performed in such a way as to uncover a potential role of complement, with and without the addition of an external source of Baby Rabbit Complement. A set of human serum samples from individuals who had been naturally infected with Monkeypox virus and individuals who may have and not have undergone vaccinia virus vaccinations, was used to evaluate the performance, sensitivity, and specificity of the assay. Results and conclusions: The results of the present study confirm the presence and cross-reactivity of antibodies elicited by vaccinia-based vaccines, which proved able to neutralize the Monkeypox virus in the presence of an external source of complement.


Subject(s)
Mpox (monkeypox) , Smallpox Vaccine , Vaccinia , Humans , Vaccinia virus , Mpox (monkeypox)/prevention & control , Antibodies, Viral , Monkeypox virus , Antibodies, Neutralizing , Vaccination
SELECTION OF CITATIONS
SEARCH DETAIL
...