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The use of labeled fusion protein for detection of B19 parvovirus IgM antibodies by an immunocapture test.

作者信息

Morinet F, Courouce A M, Galibert F, Perol Y

机构信息

Hôpital Saint-Louis, Université Paris VII, Service de Bactériologie-Virologie, France.

出版信息

J Virol Methods. 1991 Apr;32(1):21-30. doi: 10.1016/0166-0934(91)90181-x.

DOI:10.1016/0166-0934(91)90181-x
PMID:1648571
Abstract

A new anti-B19 IgM ELISA was developed taking advantage of antibody-capture with biotinylated fusion protein as antigen. Specificity was examined using serum IgM antibody positive for rubella, hepatitis B core antigen, cytomegalovirus and Epstein-Barr virus as well as with sera positive for rheumatoid factors or antinuclear antibodies. The specificity was found to be 96%. Of one hundred serum samples compared using the new ELISA or the standard MACRIA tests for the presence of B19 IgM, 88 gave the same results. Fifty-three were negative and 35 were positive. Six sera were ELISA-negative MACRIA-positive, and six MACRIA-negative ELISA-positive. Thus, the ELISA gave 90% agreement with MACRIA. In a clinical study with 725 sera from suspected B19 infections, 161 (22%) were found positive by ELISA. The positive sera were from patients suffering from arthritis (35%), rash (35%), acute or chronic erythroblastopenia (21%), pancytopenia (5%), vascular purpura (2%) and lymphadenopathy (2%). A series of serum specimens obtained from two-B19 infected individuals were also studied. The IgM antibody became undetectable after four months.

摘要

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