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DOI 10.1155/2012/974067

Медицинская библиотека · Clinical & developmental immunology · 2011

Immune modulation in primary vaccinia virus zoonotic human infections.

Silva Gomes Juliana Assis, de Araújo Fernanda Fortes, de Souza Trindade Giliane, Quinan Bárbara Resende, Drumond Betânia Paiva, Ferreira Jaqueline Maria Siqueira, Mota Bruno Eduardo Fernandes, Nogueira Maurício Lacerda, Kroon Erna Geessien, Santos Abrahão Jônatas, Côrrea-Oliveira Rodrigo, da Fonseca Flávio Guimarães

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

In 2010, the WHO celebrated the 30th anniversary of the smallpox eradication. Ironically, infections caused by viruses related to smallpox are being increasingly reported worldwide, including Monkeypox, Cowpox, and Vaccinia virus (VACV). Little is known about the human immunological responses elicited during acute infections caused by orthopoxviruses. We have followed VACV zoonotic outbreaks taking place in Brazil and analyzed cellular immune responses in patients acutely infected by VACV. Results indicated that these patients show a biased immune modulation when compared to noninfected controls. Amounts of B cells are low and less activated in infected patients. Although present, T CD4(+) cells are also less activated when compared to noninfected individuals, and so are monocytes/macrophages. Similar results were obtained when Balb/C mice were experimentally infected with a VACV sample isolated during the zoonotic outbreaks. Taking together, the data suggest that zoonotic VACVs modulate specific immune cell compartments during an acute infection in humans.

Для цитирования: Silva Gomes Juliana Assis, de Araújo Fernanda Fortes, de Souza Trindade Giliane, Quinan Bárbara Resende, Drumond Betânia Paiva, Ferreira Jaqueline Maria Siqueira, Mota Bruno Eduardo Fernandes, Nogueira Maurício Lacerda, Kroon Erna Geessien, Santos Abrahão Jônatas, Côrrea-Oliveira Rodrigo, da Fonseca Flávio Guimarães. Immune modulation in primary vaccinia virus zoonotic human infections.. Clinical & developmental immunology. 2011. DOI: 10.1155/2012/974067.

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