Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method
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Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method
Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method
解放军医学杂志(英文版)1987年第1期 页码:46-48
Affiliations:
1. Department of Microbiology Fourth Military Medical College
2. ,Xi’an
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纸质出版:1987
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Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method[J]. 解放军医学杂志(英文版), 1987,(1):46-48.
[1]徐志凯,汪美先,姜绍谆,马文煜,王海涛.Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method[J].Journal of Medical Colleges of PLA,1987(01):46-48.
Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method[J]. 解放军医学杂志(英文版), 1987,(1):46-48.DOI:
[1]徐志凯,汪美先,姜绍谆,马文煜,王海涛.Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method[J].Journal of Medical Colleges of PLA,1987(01):46-48.DOI:
Detections of HFRS Virus Antigen and Antibody by a McAb ELISA Indirect Sandwich Method
摘要
Abstract
<正> An ELISA indirect sandwich method using monoclonal antibodies(McAb)against hem-orrhagic fever with renal syndrome(HFRS)virus has been developed fordetections of HFRS virus antigen and specific antibody.Dynamic changes of HFRS virusantigens in the cells infected and their culture supernatants were observed by indirectfluorescence-antibody technique(IFAT)and ELISA separately.It was shown that HFRSvirus antigens in the cells and in the supernatants peaked separately 8 days and 14 daysafter infection.A hundred and seventy-nine brain and lung specimens of suckling miceinfected were examined by ELISA and IFAT.The positive rates were 72.1% and 68.2%
respectively.Furthermore
the IgM antibodies of 121 sera from HFRS patients wereexamined by ELISA and IFAT.The positive rates were 90.1% and 83.5% respectively.The IgG antibodies of 178 sera from HFRS patients were also examined by the twomethods
and both of the positive rates were 89.3%.The antibody titer measured byELISA was higher than the titer by IFAT.The above results suggest that the ELISA is aspecific and sensitive method and can be used for early diagnosis
epidemiologicalsurveillance and etiological study of HFRS.
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