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Increase in CD23(+) B cells in infants with bronchiolitis is accompanied by appearance of ige and igg4 antibodies specific for respiratory syncytial virus (CROSBI ID 78078)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Rabatić, Sabina ; Gagro, Alenka ; Lokar Kolbas, Renata ; Kršulović-Hrešić, Vilka ; Vrtar, Zvonimir ; Popow Kraupp, Therese ; Draženović, Vladimir ; Mlinarić-Galinović, Gordana Increase in CD23(+) B cells in infants with bronchiolitis is accompanied by appearance of ige and igg4 antibodies specific for respiratory syncytial virus // The Journal of infectious diseases, 175 (1997), 1; 32-37-x

Podaci o odgovornosti

Rabatić, Sabina ; Gagro, Alenka ; Lokar Kolbas, Renata ; Kršulović-Hrešić, Vilka ; Vrtar, Zvonimir ; Popow Kraupp, Therese ; Draženović, Vladimir ; Mlinarić-Galinović, Gordana

engleski

Increase in CD23(+) B cells in infants with bronchiolitis is accompanied by appearance of ige and igg4 antibodies specific for respiratory syncytial virus

Infection with respiratory syncytial virus (RSV) may induce asthma-like symptoms and RSV-specific IgE in infected infants as a result of Th2-like response to RSV. The effect of RSV infection on the expression of B cell antigens CD21 and CD23, putative participants in Th2 responses, was investigated. Samples from bronchiolitic infants (n = 19) were tested by three-color immunofluorescence flow cytometry during the acute phase of infection and 4-6 weeks later. In 6 of 10 RSV-positive infants, the percentage of CD23(+) B cells was higher than in 9 RSV-negative children and in controls. Both CD21(+) and CD21(-) B cells exhibited a higher percentage of CD23. The group with increased expression of CD23 antigen had RSV-specific IgE and IgG4 antibodies. These findings corroborate the hypothesis that RSV could provoke a Th2-type response, but the relationship between CD23 antigen and RSV infection must be determined.

human lymphocytes-b.; increased expression; allergic-asthma; responses

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Podaci o izdanju

175 (1)

1997.

32-37-x

objavljeno

0022-1899

Povezanost rada

Temeljne medicinske znanosti, Kliničke medicinske znanosti

Indeksiranost