共 117 条
Cellular immune therapy for chronic lymphocytic leukemia
被引:29
作者:

Kater, Arnon P.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Amsterdam, Acad Med Ctr, Dept Hematol, NL-1105 AZ Amsterdam, Netherlands

van Oers, Marinus H. J.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Amsterdam, Acad Med Ctr, Dept Hematol, NL-1105 AZ Amsterdam, Netherlands

Kipps, Thomas J.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Amsterdam, Acad Med Ctr, Dept Hematol, NL-1105 AZ Amsterdam, Netherlands
机构:
[1] Univ Amsterdam, Acad Med Ctr, Dept Hematol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Calif San Diego, Moores Canc Ctr, San Diego, CA 92103 USA
来源:
关键词:
D O I:
10.1182/blood-2007-01-068932
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Although chemotherapy can induce complete responses in patients with chronic lymphocytic leukemia (CLL), it is not considered curative. Treated patients generally develop recurrent disease requiring additional therapy, which can cause worsening immune dysfunction, myelosuppression, and selection for chemotherapy-resistant leukemia-cell subclones. Cellular immune therapy promises to mitigate these complications and potentially provide for curative treatment. Most experience with this is in the use of allogeneic hematopoietic stem-cell transplantation (allo-HSCT), in which graft-versus-leukemia (GVL) effects can be observed and shown responsible for. long-term disease-free survival. However, use of allo-HSCT for CLL is limited because of the lack of suitable donors and the treatment-related morbidity/mortality for elderly patients, who constitute the majority at risk for developing this disease. The GVL effect, however, suggests there are specific CLL-associated antigens that could be targeted in autologous cellular immune therapy. Effective strategies for this will have to overcome the disease-related acquired immune deficiency and the capacity of the leukemia-cell to induce T-cell tolerance, thereby compromising the activity of even conventional vaccines in patients with this disease. We will discuss the different strategies being developed to overcome these limitations that might provide for effective cellular immune therapy of CLL.
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页码:2811 / 2818
页数:8
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机构: Fdn Santa Lucia, IRCCS, Biochem & Mol Biol Lab, I-00179 Rome, Italy

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Candi, E
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机构: Fdn Santa Lucia, IRCCS, Biochem & Mol Biol Lab, I-00179 Rome, Italy
[79]
PEPTIDES NATURALLY PRESENTED BY MHC CLASS-I MOLECULES
[J].
RAMMENSEE, HG
;
FALK, K
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ROTZSCHKE, O
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ANNUAL REVIEW OF IMMUNOLOGY,
1993, 11
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RAMMENSEE, HG
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机构: Max-Planck-Inst. für Biologie, Abteilung Immungenetik

FALK, K
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机构: Max-Planck-Inst. für Biologie, Abteilung Immungenetik

ROTZSCHKE, O
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机构: Max-Planck-Inst. für Biologie, Abteilung Immungenetik
[80]
ACTIVATED T-CELLS INDUCE EXPRESSION OF B7/BB1 ON NORMAL OR LEUKEMIC B-CELLS THROUGH A CD40-DEPENDENT SIGNAL
[J].
RANHEIM, EA
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KIPPS, TJ
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JOURNAL OF EXPERIMENTAL MEDICINE,
1993, 177 (04)
:925-935

RANHEIM, EA
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机构:
UNIV CALIF SAN DIEGO, DEPT MED, 9500 GILMAN DR, LA JOLLA, CA 92093 USA UNIV CALIF SAN DIEGO, DEPT MED, 9500 GILMAN DR, LA JOLLA, CA 92093 USA

KIPPS, TJ
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UNIV CALIF SAN DIEGO, DEPT MED, 9500 GILMAN DR, LA JOLLA, CA 92093 USA UNIV CALIF SAN DIEGO, DEPT MED, 9500 GILMAN DR, LA JOLLA, CA 92093 USA