摘要:
BTCD-hu2 chimeric mice for assaying the pathogenesis of human disease and efficacy and toxicity of disease treatments have been developed by implantation of human fetal thymus and human fetal liver tissue under the kidney capsule of T- and B-cell deficient mice, by engraftment of human fetal bone marrow cells into T- and B-cell deficient mice and combinations of both. The resulting chimeric mice contain human T-cells, human monocytes or combinations thereof in sufficient quantity in the mouse peripheral lymphoid compartment to support HIV-1 infection following intraperitoneal inoculation of HIV-1 into the mouse.
摘要:
The present disclosure relates to a method of modulating one or more genetically modified cells, e.g., chimeric antigen receptor (CAR)-expressing cells, ex vivo and/or in vivo.
摘要:
Polypeptides, nucleic acids, and compositions thereof are provided that include a targeting moiety. The polypeptides, nucleic acids, and compositions that comprise them, can be used in methods to treat subjects, to alter CAR-expressing cells in subjects who may suffer from a disease such as a cancer or a pathogen.
摘要:
Compositions and methods to increase the in vivo capacity of CD8+ T cells to kill HIV-infected and reactivated latent HIV-infected T cells (LHITC) to functionally cure HIV infection or improve the clinical course. Compositions and methods to increase the in vivo capacity of CD8+ T cells to kill CMV or CMV -infected cells are also provided.
摘要:
This invention provides methods for treating subjects infected with human immunodeficiency virus (HIV) which comprise administering to the subjects a radiolabeled antibody or agent effective to kill HIV infected cells, where the antibody or agent is specific for a HIV envelope glycoprotein. The invention also provides compositions and methods for making compositions of radiolabeled antibodies or agents to HIV envelope glycoproteins for treatment of HIV infection.