Literature DB >> 8690449

Recognition of CD52 allelic gene products by CAMPATH-1H antibodies.

C Hale1, M Bartholomew, V Taylor, J Stables, P Topley, J Tite.   

Abstract

Cloning of the CD52 from a B-lymphocyte tumour cDNA library revealed two closely related sequences differing only at two amino acids C-terminal to the proposed point of glycosylphosphatidylinositol (GPI)-linkage. When transfected into CHO cells only one of these sequences gave high-level expression of the antigen recognized by the prototypic anti-CD52 antibody CAMPATH-1 whereas in JURKAT cells good expression levels were obtained with both sequences. Fusion of the sequence from the second sequence to DNA encoding the extracellular domain of CD4 indicated that this sequence was capable of directing GPI linkage. The possible implications for the function of CD52 and serotherapy with anti-CD52 antibodies are discussed.

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Year:  1996        PMID: 8690449      PMCID: PMC1456427          DOI: 10.1111/j.1365-2567.1996.tb00003.x

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  13 in total

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Authors:  M Q Xia; M Tone; L Packman; G Hale; H Waldmann
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Authors:  C Kirchhoff; N Krull; I Pera; R Ivell
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Authors:  P Moran; I W Caras
Journal:  J Cell Biol       Date:  1991-12       Impact factor: 10.539

10.  Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes.

Authors:  M E Medof; T Kinoshita; V Nussenzweig
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7.  Screening and Identification of Key Microenvironment-Related Genes in Non-functioning Pituitary Adenoma.

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9.  Clinical pharmacology of alemtuzumab, an anti-CD52 immunomodulator, in multiple sclerosis.

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  10 in total

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