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

被引:29
作者
Hale, C
Bartholomew, M
Taylor, V
Stables, J
Topley, P
Tite, J
机构
[1] WELLCOME RES LABS,MOLEC IMMUNOL GRP,BECKENHAM BR3 3BS,KENT,ENGLAND
[2] WELLCOME RES LABS,EXPT BIOL GRP,DIV BIOL,BECKENHAM BR3 3BS,KENT,ENGLAND
关键词
D O I
10.1111/j.1365-2567.1996.tb00003.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:183 / 190
页数:8
相关论文
共 13 条
[1]   CD59, AN LY-6-LIKE PROTEIN EXPRESSED IN HUMAN LYMPHOID-CELLS, REGULATES THE ACTION OF THE COMPLEMENT MEMBRANE ATTACK COMPLEX ON HOMOLOGOUS CELLS [J].
DAVIES, A ;
SIMMONS, DL ;
HALE, G ;
HARRISON, RA ;
TIGHE, H ;
LACHMANN, PJ ;
WALDMANN, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) :637-654
[2]  
DECKERT M, 1992, J IMMUNOL, V148, P672
[3]  
DYER MJS, 1989, BLOOD, V73, P1431
[4]   THE CAMPATH-1 ANTIGEN (CDW52) [J].
HALE, G ;
XIA, MQ ;
TIGHE, HP ;
DYER, MJS ;
WALDMANN, H .
TISSUE ANTIGENS, 1990, 35 (03) :118-127
[5]   HUMANIZED MONOCLONAL-ANTIBODY THERAPY FOR RHEUMATOID-ARTHRITIS [J].
ISAACS, JD ;
WATTS, RA ;
HAZLEMAN, BL ;
HALE, G ;
KEOGAN, MT ;
COBBOLD, SP ;
WALDMANN, H .
LANCET, 1992, 340 (8822) :748-752
[6]   A MAJOR MESSENGER-RNA OF THE HUMAN EPIDIDYMAL PRINCIPAL CELLS, HE5, ENCODES THE LEUKOCYTE DIFFERENTIATION CDW52 ANTIGEN PEPTIDE BACKBONE [J].
KIRCHHOFF, C ;
KRULL, N ;
PERA, I ;
IVELL, R .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1993, 34 (01) :8-15
[7]   BIOSYNTHESIS OF GLYCOSYLPHOSPHATIDYLINOSITOL (GPI)-ANCHORED MEMBRANE-PROTEINS IN INTACT-CELLS - SPECIFIC AMINO-ACID-REQUIREMENTS ADJACENT TO THE SITE OF CLEAVAGE AND GPI ATTACHMENT [J].
KODUKULA, K ;
GERBER, LD ;
AMTHAUER, R ;
BRINK, L ;
UDENFRIEND, S .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :657-664
[8]   INHIBITION OF COMPLEMENT ACTIVATION ON THE SURFACE OF CELLS AFTER INCORPORATION OF DECAY-ACCELERATING FACTOR (DAF) INTO THEIR MEMBRANES [J].
MEDOF, ME ;
KINOSHITA, T ;
NUSSENZWEIG, V .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (05) :1558-1578
[9]   FUSION OF SEQUENCE ELEMENTS FROM NONANCHORED PROTEINS TO GENERATE A FULLY FUNCTIONAL SIGNAL FOR GLYCOPHOSPHATIDYLINOSITOL MEMBRANE ANCHOR ATTACHMENT [J].
MORAN, P ;
CARAS, IW .
JOURNAL OF CELL BIOLOGY, 1991, 115 (06) :1595-1600
[10]  
SHENOYSCARIA AM, 1992, J IMMUNOL, V149, P3535