Chimeric immune receptor T cells bypass class I requirements and recognize multiple cell types relevant in HIV-1 infection

Virology

Volumn 306, Issue 2, 2003, Pages 371-375

  Severino, Michael E ^a   Sarkis, Phuong Thi Nguyen ^a   Walker, Bruce D ^a   Yang, Otto O ^b  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b UCLA MEDICAL CENTER   (United States)

Author keywords

Cellular immunity; Chimeric immune receptors; CTL; Gene therapy; HIV 1; Immune escape; Immunotherapy

Indexed keywords

CD4 ANTIGEN; GLYCOPROTEIN GP 120; T LYMPHOCYTE RECEPTOR;

ANTIVIRAL ACTIVITY; ARTICLE; CELL IMMORTALIZATION; CELL SURFACE; CELL TYPE; CELLULAR IMMUNITY; CONTROLLED STUDY; CYTOTOXIC T LYMPHOCYTE; DENDRITIC CELL; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; MONOCYTE; PRIORITY JOURNAL; VIRUS REPLICATION;

ANTIGENS, CD3; CD4-POSITIVE T-LYMPHOCYTES; CELL LINE; DENDRITIC CELLS; GENE THERAPY; HISTOCOMPATIBILITY ANTIGENS CLASS I; HIV INFECTIONS; HIV-1; HUMANS; IMMUNITY, CELLULAR; IMMUNOTHERAPY; MONOCYTES; RECEPTORS, IMMUNOLOGIC; RECOMBINANT FUSION PROTEINS; T-LYMPHOCYTES, CYTOTOXIC; TRANSDUCTION, GENETIC; VIRUS REPLICATION;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0037440955     PISSN: 00426822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0042-6822(02)00055-7     Document Type: Article

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