GENE MARKING TO DETERMINE WHETHER AUTOLOGOUS MARROW INFUSION RESTORES LONG-TERM HEMATOPOIESIS IN CANCER-PATIENTS

被引:373
作者
BRENNER, MK
RILL, DR
HOLLADAY, MS
HESLOP, HE
MOEN, RC
BUSCHLE, M
KRANCE, RA
SANTANA, VM
ANDERSON, WF
IHLE, JN
机构
[1] UNIV TENNESSEE, CTR HLTH SCI, COLL MED, DEPT PEDIAT, MEMPHIS, TN 38163 USA
[2] UNIV TENNESSEE, CTR HLTH SCI, COLL MED, DEPT MED, MEMPHIS, TN 38163 USA
[3] GENET THERAPY INC, GAITHERSBURG, MD 20878 USA
[4] USC, SCH MED, LOS ANGELES, CA 90033 USA
[5] ST JUDE CHILDRENS RES HOSP, DEPT BIOCHEM, MEMPHIS, TN 38101 USA
关键词
D O I
10.1016/0140-6736(93)92122-A
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The contribution of infused bone marrow cells to long-term haemopoietic recovery in patients undergoing autologous bone marrow transplantation is unknown. Such information would help to clarify the role of this procedure in cancer therapy and would aid in the development of strategies to reduce the risk of subsequent aplasia. By transferring a neomycin resistance marker gene into the marrow cells of 20 patients before transplantation, we were able to trace the pattern of haemopoietic reconstitution postinfusion. The marker gene was present and expressed in all haemopoietic lineages in vivo in 15 of 18 evaluable patients at 1 month post-transplantation, in 8 of 9 patients at 6 months, and in 5 of 5 at 1 year. The marker has remained detectable for up to 18 months-the duration of our study. Our findings indicate that harvested bone marrow consistently contributes to long-term multilineage recovery of haemopoiesis after autologous marrow transplantation in cancer patients. These results, provide a rationale for the continued exploration of more ablative preparative regimens with single or sequential autologous marrow transplants.
引用
收藏
页码:1134 / 1137
页数:4
相关论文
共 25 条
  • [1] HUMAN GENE-THERAPY
    ANDERSON, WF
    [J]. SCIENCE, 1992, 256 (5058) : 808 - 813
  • [2] EVIDENCE THAT THE PACKAGING SIGNAL OF MOLONEY MURINE LEUKEMIA-VIRUS EXTENDS INTO THE GAG REGION
    BENDER, MA
    PALMER, TD
    GELINAS, RE
    MILLER, AD
    [J]. JOURNAL OF VIROLOGY, 1987, 61 (05) : 1639 - 1646
  • [3] BODINE DM, 1991, EXP HEMATOL, V19, P206
  • [4] EFFECT OF RECOMBINANT HUMAN GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR ON HEMATOPOIETIC RECONSTITUTION AFTER HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS BONE-MARROW TRANSPLANTATION
    BRANDT, SJ
    PETERS, WP
    ATWATER, SK
    KURTZBERG, J
    BOROWITZ, MJ
    JONES, RB
    SHPALL, EJ
    BAST, RC
    GILBERT, CJ
    OETTE, DH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (14) : 869 - 876
  • [5] GENE-MARKING TO TRACE ORIGIN OF RELAPSE AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION
    BRENNER, MK
    RILL, DR
    MOEN, RC
    KRANCE, RA
    MIRRO, J
    ANDERSON, WF
    IHLE, JN
    [J]. LANCET, 1993, 341 (8837) : 85 - 86
  • [6] SUCCESSFUL TREATMENT OF ACUTE MYELOID-LEUKEMIA BEYOND 1ST REMISSION WITH AUTOLOGOUS BONE-MARROW TRANSPLANTATION USING BUSULFAN CYCLOPHOSPHAMIDE AND UNPURGED MARROW - THE BRITISH-AUTOGRAFT-GROUP EXPERIENCE
    CHOPRA, R
    GOLDSTONE, AH
    MCMILLAN, AK
    POWLES, R
    SMITH, AG
    PRENTICE, HG
    REID, C
    MARCUS, R
    BELL, A
    MILLIGAN, D
    MCCARTHY, D
    MORGENSTERN, G
    BARNARD, D
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (10) : 1840 - 1847
  • [7] EKHTERAE D, 1990, BLOOD, V75, P365
  • [8] GALE RP, 1989, LANCET, V2, P315
  • [9] GIANNI AM, 1989, LANCET, V2, P580
  • [10] GRAHAMPOLE J, 1991, BLOOD, V78, P1607