Introduction Ac quired immunodeficiency syndrome (AIDS) is the first Human Retrovirus. It neither curable nor vaccinable, is the most contagious disease to the human being. Many scientists are trying to develop a vacc...Introduction Ac quired immunodeficiency syndrome (AIDS) is the first Human Retrovirus. It neither curable nor vaccinable, is the most contagious disease to the human being. Many scientists are trying to develop a vaccine against the simian AIDS (SAIDS) from monkey to prevent the AIDS. Raji cell line, one of myeloma cells, is usally used to test the isolation and toxcity of SAIDS. Ten percent fetal bovine serum (FBS) is necessary for the suspension culture of Raji cell, which is easily affected by mycoplasma. Therefore, a展开更多
To investigate the phenotypic knockout of HIV-1 chemokine coreceptor CXCR4 and CCR5 by intrakines and its inhibitory effect on HIV-1 infection. Primary human PBLs were transduced with the recombinant vector pLNCX-R-K-...To investigate the phenotypic knockout of HIV-1 chemokine coreceptor CXCR4 and CCR5 by intrakines and its inhibitory effect on HIV-1 infection. Primary human PBLs were transduced with the recombinant vector pLNCX-R-K-S-K followed by anti-NGFR/anti-IgG-magnetic bead method selection and FCM detection. The transduced PBI.S were infected with DP1 HFV-1 virus thereafter envelope-mediated syncytium formation and p24 detection were carried out to study the blockage of HIV-1 infection by co-inactivation of CCR5 and CXCR4. pLNCX-R-K-S-K -transduced PBLs were isolated with an anti-NGFR/anti-IgG-magnetic bead method. After isolation, about 70% of the PBI.S were posi- tive for the NGFR marker. When the transduced PBLs were infected with DP1 HIV-1 virus, envelop-mediated syncytium for- mation was almost completely inhibited by pLNCX-R-K-S-K transfection. Also, p24 antigen was very low in the cultures of pLNCX-R-K-S-K transduced PBLs. pLNCX-R-K-S-K transduction inhibited the produc- tion of DP1 p24 antigen by 15%, 43% and 19% on days 4, 7 and 10 respectively. The lymphocytes with the phenotypic knockout of CCR5 and CXCR4 could protect primary human PBLs from DP1 HIV-1 virus infection.展开更多
文摘Introduction Ac quired immunodeficiency syndrome (AIDS) is the first Human Retrovirus. It neither curable nor vaccinable, is the most contagious disease to the human being. Many scientists are trying to develop a vaccine against the simian AIDS (SAIDS) from monkey to prevent the AIDS. Raji cell line, one of myeloma cells, is usally used to test the isolation and toxcity of SAIDS. Ten percent fetal bovine serum (FBS) is necessary for the suspension culture of Raji cell, which is easily affected by mycoplasma. Therefore, a
文摘To investigate the phenotypic knockout of HIV-1 chemokine coreceptor CXCR4 and CCR5 by intrakines and its inhibitory effect on HIV-1 infection. Primary human PBLs were transduced with the recombinant vector pLNCX-R-K-S-K followed by anti-NGFR/anti-IgG-magnetic bead method selection and FCM detection. The transduced PBI.S were infected with DP1 HFV-1 virus thereafter envelope-mediated syncytium formation and p24 detection were carried out to study the blockage of HIV-1 infection by co-inactivation of CCR5 and CXCR4. pLNCX-R-K-S-K -transduced PBLs were isolated with an anti-NGFR/anti-IgG-magnetic bead method. After isolation, about 70% of the PBI.S were posi- tive for the NGFR marker. When the transduced PBLs were infected with DP1 HIV-1 virus, envelop-mediated syncytium for- mation was almost completely inhibited by pLNCX-R-K-S-K transfection. Also, p24 antigen was very low in the cultures of pLNCX-R-K-S-K transduced PBLs. pLNCX-R-K-S-K transduction inhibited the produc- tion of DP1 p24 antigen by 15%, 43% and 19% on days 4, 7 and 10 respectively. The lymphocytes with the phenotypic knockout of CCR5 and CXCR4 could protect primary human PBLs from DP1 HIV-1 virus infection.