INHIBITION OF HIV-1 INFECTION INVITRO BY MURINE MONOCLONAL ANTI-P24 ANTIBODIES

被引:8
作者
FRANKE, L
GRUNOW, R
MEISSNER, K
PORSTMANN, T
VONBAEHR, R
机构
[1] Department of Medical Immunology, Medical School (Charité), Humboldt University, Berlin
关键词
CD4; HIV-1; IMMUNOFLUORESCENCE; P24; REVERSE TRANSCRIPTASE; VIRUS REPLICATION;
D O I
10.1002/jmv.1890370212
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Murine monoclonal antibodies (Mabs) to the major core protein p24 of the human immunodeficiency virus type 1 (HIV-1) were tested for their ability to inhibit the replication and spread of the virus in permanent cell cultures (Molt4/8, K37, H9) and in the culture of II-2 stimulated T cells of healthy donors. After addition of ascitic fluid containing monoclonal anti-p24 antibodies or purified anti-p24 antibodies or the respective control to co-cultures of infected and non-infected cells, HIV-1 replication was evaluated by determining the percentage of infected cells and the activity of reverse transcriptase (RT) in cell-free supernatant. In addition, the supernatant's infectivity was determined. FACS analysis demonstrated p24 antigen in about 40% of unfixed HIV-1 infected cells at the cell membrane. Monoclonal anti-p24 antibodies of different epitope specificity added to the cells but not to the virus delayed the spread of HIV-1 infection in permanent cell culture. Furthermore, anti-p24 Mabs inhibited the release of RT-active virus particles by HIV-1 infected cell lines or II-2 stimulated T-lymphocytes, respectively, up to 60%. The mode of action of anti-p24 antibodies after HIV-1 infection is discussed on the basis of the data obtained.
引用
收藏
页码:137 / 142
页数:6
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