1988
DOI: 10.1128/jcm.26.4.781-783.1988
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Establishment by enzyme-linked immunosorbent assay of seronegative range for herpes simplex virus and cytomegalovirus antibodies and evaluation of heterologous responses to live varicella vaccine

Abstract: Cord serum samples treated with staphylococcus protein A and an immune affinity column to remove immunoglobulin G were used to establish a seronegative range for herpes simplex virus and cytomegalovirus. No seroconversions or increased heterologous antibody levels to herpes simplex virus or cytomegalovirus were found in live varicella vaccine recipients.

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Cited by 2 publications
(2 citation statements)
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“…The coated plates could be used for up to 3 months. The ELISA method used in our laboratory (8,21), including the assays for CMV and HSV-1 (16) and for VZV (28), has been described in detail elsewhere. The results were expressed as difference of optical density (DOD), which was calculated by subtracting the average optical density of two controls from the average of two antigen values multiplied by a thousand.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The coated plates could be used for up to 3 months. The ELISA method used in our laboratory (8,21), including the assays for CMV and HSV-1 (16) and for VZV (28), has been described in detail elsewhere. The results were expressed as difference of optical density (DOD), which was calculated by subtracting the average optical density of two controls from the average of two antigen values multiplied by a thousand.…”
Section: Methodsmentioning
confidence: 99%
“…Establishment of the seronegative range. The method for determining the seronegative range has been described elsewhere (16). Twenty cord serum samples were treated with protein G (Quik-Sep IgM assay; Isolab, Inc., Akron, Ohio) twice to remove IgG.…”
Section: Methodsmentioning
confidence: 99%