2008
DOI: 10.1111/j.1600-0897.2008.00606.x
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ORIGINAL ARTICLE: Developmental Delay and Other Anomalies in the Offspring from Hens Immunized Against Soluble and Foreign Chick Embryo Antigens

Abstract: If pathogenic activity by these isoantibodies can be shown to occur naturally in humans, as has been postulated, it could account for some miscarriage, developmental delay, fetal and perinatal death and birth defects of currently unknown etiology.

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Cited by 4 publications
(3 citation statements)
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“…This is the first published report of histopathological lesions induced by fEIA isoantibodies . The macroscopic study of all descendants from hens immunized with chicken embryo extract (a total of 81 chick embryos) and control hens [66 embryos] led Rodríguez‐Burgos and Juárez to state the following: ‘By applying the statistical analysis to the different subgroups from experimental and [control] embryos, classified according to the displayed anomalies, we obtained the following results: monsters and malformations 8 / 81 and [3 / 66] (there were no significant differences); intraovo growth retardation (IOGR) and (delayed development: DD) 14/81 and [4 / 66] ( P = 0.063); DD and (IOGR) 34 / 81 and [1/66] ( P = 0.017); died by functional anomalies and digested embryos 10 / 81 and [4 / 66] ( P = 0.037); survived more than a week with anomalies 3 / 10 and [0 / 8] ( P = 0.004). Finally, birds without anomalies (normals) were 21 / 81 and [46/66] ( P ≤ 0.001)’.…”
Section: Introductionmentioning
confidence: 99%
“…This is the first published report of histopathological lesions induced by fEIA isoantibodies . The macroscopic study of all descendants from hens immunized with chicken embryo extract (a total of 81 chick embryos) and control hens [66 embryos] led Rodríguez‐Burgos and Juárez to state the following: ‘By applying the statistical analysis to the different subgroups from experimental and [control] embryos, classified according to the displayed anomalies, we obtained the following results: monsters and malformations 8 / 81 and [3 / 66] (there were no significant differences); intraovo growth retardation (IOGR) and (delayed development: DD) 14/81 and [4 / 66] ( P = 0.063); DD and (IOGR) 34 / 81 and [1/66] ( P = 0.017); died by functional anomalies and digested embryos 10 / 81 and [4 / 66] ( P = 0.037); survived more than a week with anomalies 3 / 10 and [0 / 8] ( P = 0.004). Finally, birds without anomalies (normals) were 21 / 81 and [46/66] ( P ≤ 0.001)’.…”
Section: Introductionmentioning
confidence: 99%
“…12 Previous research has suggested that immune mechanisms may play a critical role in the development of human congenital defects. 13 IL-27 is a novel heterodimeric cytokine that consists of IL-27p28 and Epstein-Barr virus-induced gene 3 (EBI3). [14][15][16] IL-27, with its gene located on chromosome 16 (16p11), is a new IL-12 family member.…”
mentioning
confidence: 99%
“…In addition, there are a large number of cytokines involved in embryogenesis 12 . Previous research has suggested that immune mechanisms may play a critical role in the development of human congenital defects 13 …”
mentioning
confidence: 99%