Multiplexed immunoassays by flow cytometry for diagnosis and surveillance of infectious diseases in resource-poor settings

被引:65
作者
Jani, IV
Janossy, G
Brown, DWG
Mandy, F
机构
[1] UCL Royal Free & Univ Coll Med Sch, Dept Immunol & Mol Pathol, London NW3 2PF, England
[2] Inst Nacl Saude, Dept Immunol, Maputo, Mozambique
[3] Cent Publ Hlth Lab, Enter & Resp Virus Lab, London NW9 5HT, England
[4] Hlth Canada, Ctr Infect Dis Prevent & Control, Populat & Publ Hlth Branch, Bur HIV AIDS & STD,Nalt Lab HIV Immunol, Ottawa, ON K1A 0L2, Canada
关键词
D O I
10.1016/S1473-3099(02)00242-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
An accurate, rapid and cost-effective diagnosis is the cornerstone of efficient clinical and epidemiological management of infections. Here we discuss the relevance of an emerging technology, multiplexed immunoassays read by flow cytometry, for the diagnosis of infectious diseases. In these assays, multiple fluorescent microspheres, conjugated to different antigens or antibodies, constitute the solid phase for detecting antibodies or antigens in biological samples. These assays seem to be more sensitive than traditional immunoassays, have a high throughput capacity, and provide a wide analytical dynamic range. Additionally, they have multiplexing ability-ie, they are capable of measuring multiple antibodies or antigens simultaneously. We discuss four different areas where this technology could make an impact in resource-poor settings: (i) infections causing rash and fever in children; (ii) sero-epidemiological studies on vaccine-preventable diseases; (iii) management of genital ulcers and vaginal discharge; and (iv) screening of infections in blood banking. We predict a widespread use for a new breed of small, affordable, practical flow cytometers as field instruments for replacing ELISA and RIA tests, which will also be capable of doing cellular immunological tests such as CD4+ T-cell enumeration and Plasmodium falciparum detection in whole blood.
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页码:243 / 250
页数:8
相关论文
共 80 条
[1]   Field evaluation of alternative testing strategies for diagnosis and differentiation of HIV-1 and HIV-2 infections in an HIV-1 and HIV-2-prevalent area [J].
Andersson, S ;
daSilva, Z ;
Norrgren, H ;
Dias, F ;
Biberfeld, G .
AIDS, 1997, 11 (15) :1815-1822
[2]  
*ASS GEN MED MED S, 1999, SEX TRANSM INFECT S1, V75, P29
[3]  
Benecky MJ, 1997, CLIN CHEM, V43, P1764
[4]  
Benecky MJ, 1998, CLIN CHEM, V44, P2052
[5]  
Brando B, 2000, CYTOMETRY, V42, P327, DOI 10.1002/1097-0320(20001215)42:6<327::AID-CYTO1000>3.0.CO
[6]  
2-F
[7]   Simultaneous quantitation of 15 cytokines using a multiplexed flow cytometric assay [J].
Carson, RT ;
Vignali, DAA .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 227 (1-2) :41-52
[8]   Diagnostic polymerase chain reaction for donovanosis [J].
Carter, J ;
Bowden, FJ ;
Sriprakash, KS ;
Bastian, I ;
Kemp, DJ .
CLINICAL INFECTIOUS DISEASES, 1999, 28 (05) :1168-1169
[9]   BIOCHEMICAL-DIAGNOSIS OF VAGINITIS - DETERMINATION OF DIAMINES IN VAGINAL FLUID [J].
CHEN, KCS ;
AMSEL, R ;
ESCHENBACH, DA ;
HOLMES, KK .
JOURNAL OF INFECTIOUS DISEASES, 1982, 145 (03) :337-345
[10]   DIAGNOSIS OF CHLAMYDIA-TRACHOMATIS INFECTIONS IN MEN AND WOMEN BY TESTING FIRST-VOID URINE BY LIGASE CHAIN-REACTION [J].
CHERNESKY, MA ;
JANG, D ;
LEE, H ;
BURCZAK, JD ;
HU, H ;
SELLORS, J ;
TOMAZICALLEN, SJ ;
MAHONY, JB .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (11) :2682-2685