133 results match your criteria: "Dana-Faber Cancer Institute[Affiliation]"
FASEB J
July 1991
Dana-Faber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115.
The immunodeficiency virus type 1 is a complex retrovirus. In addition to genes that specify the proteins of the virus particle and the replicative enzymes common to all retroviruses, HIV-1 specifies at least six additional proteins that regulate the virus life cycle. Two of these regulatory genes, tat and rev, specify proteins essential for replication.
View Article and Find Full Text PDFCell Immunol
October 1990
Division of Pediatric Oncology, Dana-Faber Cancer Institute, Boston, Massachusetts.
Various investigators have examined the relationship between tumor cell susceptibility to natural killer (NK) cell lysis and the expression of HLA class I antigens on the tumor cell. There is controversy as to whether or not an inverse relationship exists, and if so, the basis of the relationship between these two phenomena remains undefined. To address these questions, the genomic clones for two HLA antigens were transfected into the erythroleukemia cell line K562, a cell line that is used as the standard to assess human NK and major histocompatibility complex (MHC) nonrestricted cytolysis.
View Article and Find Full Text PDFAnn Intern Med
February 1990
Dana-Faber Cancer Institute, Boston, Massachusetts.
Study Objective: To study the activity of continuous infusion cisplatin, 5-fluorouracil, and high-dose leucovorin (PFL) as induction chemotherapy in patients with previously untreated, advanced squamous cell carcinoma of the head and neck.
Design: Nonrandomized, prospective trial.
Setting: A comprehensive cancer center.
Cancer Res
February 1990
Division of Pediatric Oncology, Dana-Faber Cancer Institute, Boston, Massachusetts 02115.
Cellular density in culture has profound effects on major histocompatibility complex (MHC) class I antigen expression in BALB/c-3T3 cells. Cells which have been confluent for greater than 24 h demonstrate a 2- to 6-fold increase in MHC class I antigen expression compared to subconfluent cells. These density-associated changes in MHC class I antigen expression occur both in untransformed and in v-mos or v-rasKi-transformed cells.
View Article and Find Full Text PDFCancer Res
November 1988
Dana-Faber Cancer Institute, Boston, Massachusetts 02115.
In an attempt to develop better combination therapies for use with local radiation, the interaction between bleomycin and hyperthermia +/- radiation was studied in the FSaIIC tumor system. In cells exposed in vitro to bleomycin at 37 degrees C and at pH 7.40, the drug was substantially more toxic toward normally oxygenated than hypoxic cells.
View Article and Find Full Text PDFJ Exp Med
August 1988
Division of Tumor Virology, Dana-Faber Cancer Institute, Boston, Massachusetts.
A subpopulation of the CD3+ peripheral T lymphocytes express the TCR-gamma/delta complex. Three distinct TCR-gamma forms that differ in size and in the ability to form a disulfide bridge with the TCR-delta subunit have been described. In this study we analyze the structural difference between the non-disulfide-linked 55-kD and 40-kD TCR-gamma chains.
View Article and Find Full Text PDFVaccine
April 1988
Dana-Faber Cancer Institute, Harvard Medical School, Boston.
Anti-idiotypic antibodies which carry the internal image of a foreign antigen, i.e. so-called Ab2 beta antibodies, have been successfully used as vaccines to pathogens, as tools to isolate cellular receptors or as reagents in cancer therapy.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 1988
Division of Tumor Immunology, Dana-Faber Cancer Institute, Boston, MA.
The B1 (CD20) molecule is a Mr 33,000 phosphoprotein on the surface of human B lymphocytes that may serve a central role in the humoral immune response by regulating B-cell proliferation and differentiation. In this report, a cDNA clone that encodes the B1 molecule was isolated and the amino acid sequence of B1 was determined. B-cell-specific cDNA clones were selected from a human tonsillar cDNA library by differential hybridization with labeled cDNA derived from either size-fractionated B-cell mRNA or size-fractionated T-cell mRNA.
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