Enzyme immunoassay for the diagnosis of cat-scratch disease defined by polymerase chain reaction

被引:57
作者
Giladi, M
Kletter, Y
Avidor, B
Metzkor-Cotter, E
Varon, M
Golan, Y
Weinberg, M
Riklis, I
Ephros, M
Slater, L
机构
[1] Tel Aviv Sourasky Med Ctr, Bernard Pridan Lab Mol Biol Infect Dis, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Sourasky Med Ctr, Infect Dis Unit, IL-64239 Tel Aviv, Israel
[3] Tel Aviv Sourasky Med Ctr, Virol Lab, IL-64239 Tel Aviv, Israel
[4] Minist Hlth, Natl Publ Hlth Labs, Tel Aviv, Israel
[5] Carmel Hosp, Dept Pediat, Haifa, Israel
[6] Technion Israel Inst Technol, Fac Med, Haifa, Israel
[7] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Oklahoma City, OK USA
关键词
D O I
10.1086/324162
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Whole-cell immunofluorescent antibody (IFA) tests for detection of anti-Bartonella henselae immunoglobulin (Ig) G are commonly used to diagnose cat-scratch disease (CSD). The need to cultivate B. henselae in Vero cells for antigen preparation and the absence of routinely applied IFA assays for IgM constitute the major disadvantages of this form of test. We describe the results of an enzyme immunoassay (EIA) for IgM and IgG that used N-lauroyl-sarcosine-insoluble outer membrane antigens from agar-grown B. henselae performed in 84 patients with definite CSD (regional lymphadenitis, cat contact, and greater than or equal to1 confirmatory test: polymerase chain reaction, skin test, or B. henselae culture). Although this method has been used as a diagnostic tool in several case reports, it has not previously been evaluated in a large study of definitively proven CSD cases. Results of this study indicate that the EIA described herein can play an important role in the serodiagnosis of CSD, although improvement of the sensitivity, particularly that of the IgM, would be desirable.
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收藏
页码:1852 / 1858
页数:7
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