BB-10010 - AN ACTIVE VARIANT OF HUMAN MACROPHAGE INFLAMMATORY PROTEIN-1-ALPHA WITH IMPROVED PHARMACEUTICAL PROPERTIES

被引:61
作者
HUNTER, MG
BAWDEN, L
BROTHERTON, D
CRAIG, S
CRIBBES, S
CZAPLEWSKI, LG
DEXTER, TM
DRUMMOND, AH
GEARING, AH
HEYWORTH, CM
LORD, BI
MCCOURT, M
VARLEY, PG
WOOD, LM
EDWARDS, RM
LEWIS, PJ
机构
[1] SYSTEMIX INC,PALO ALTO,CA
[2] CHRISTIE HOSP NATL HLTH SERV TRUST,CANC RES INST,CRC,DEPT EXPTL HAEMATOL,MANCHESTER,LANCS,ENGLAND
关键词
D O I
10.1182/blood.V86.12.4400.bloodjournal86124400
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The stem cell inhibitor, macrophage inflammatory protein-1 alpha (MIP-1 alpha) or LD78, protects multipotent hematopoietic progenitors in murine models from the cytotoxic effects of chemotherapy. Clinical use of human MIP-1 alpha during chemotherapy could therefore lead to faster hematologic recovery and may allow dose intensification. We have also shown that human MIP-1 alpha causes the rapid mobilization of hematopoietic cells, suggesting an additional clinical use in peripheral blood stem cell transplantation. However, the clinical evaluation of human MIP-1 alpha is complicated by its tendency to associate and form high molecular weight polymers. We have produced a variant of rhMIP-1 alpha, BE-10010, carrying a single amino acid substitution of Asp26 > Ala, with a reduced tendency to form large polymers at physiologic pH and ionic strength. This greatly increases its solubility, facilitating its production and clinical formulation. We confirmed the potency of BE-10010 as a human MIP-1 alpha-like agonist in receptor binding, calcium mobilization, inhibition of colony formation, and thymidine suicide assays. The myeloprotective activity of BE-10010 was shown in a murine model of repeated chemotherapy using hydroxyurea. BE-10010 is therefore an ideal variant with which to evaluate the therapeutic potential of recombinant human MIP-1 alpha. (C) 1995 by The American Society of Hematology.
引用
收藏
页码:4400 / 4408
页数:9
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