Severe, persistent, and fatal T-cell immunodeficiency following therapy for infantile leukemia

被引:11
作者
Geerlinks, Ashley V. [1 ]
Issekutz, Thomas [1 ]
Wahlstrom, Justin T. [2 ]
Sullivan, Kathleen E. [3 ]
Cowan, Morton J. [2 ]
Dvorak, Christopher C. [2 ]
Fernandez, Conrad V. [1 ]
机构
[1] Dalhousie Univ, IWK Hlth Ctr, Dept Pediat, Halifax, NS, Canada
[2] Univ Calif San Francisco, Dept Pediat, Benioff Childrens Hosp, San Francisco, CA USA
[3] Univ Penn, Childrens Hosp Philadelphia, Dept Pediat, Perelman Sch Med, Philadelphia, CA USA
关键词
ALL; death; immunocompromised host; immunodeficiency; infant leukemia; molecular diagnosis and therapy; ACUTE LYMPHOBLASTIC-LEUKEMIA; RECOMBINANT HUMAN INTERLEUKIN-7; CHILDRENS ONCOLOGY GROUP; INDUCTION THERAPY; RECOVERY; DISEASE; CHEMOTHERAPY; HEALTH; RISK; IL-7;
D O I
10.1002/pbc.26108
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We describe five cases of children who completed chemotherapy for infantile acute lymphoblastic leukemia (ALL) and soon after were diagnosed with severe T-cell, non-HIV immunodeficiency, with varying B-cell and NK-cell depletion. There was near absence of CD3(+), CD4(+), and CD8(+) cells. All patients developed multiple, primarily opportunistic infections. Unfortunately, four patients died, although one was successfully treated by hematopoietic stem cell transplantation. These immunodeficiencies appeared to be secondary to intensive infant ALL chemotherapy. Our report highlights the importance of the early consideration of this life-threatening immune complication in patients who received chemotherapy for infantile ALL.
引用
收藏
页码:2046 / 2049
页数:4
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