Immune markers of disease severity and treatment response in pediatric acquired aplastic anemia

被引:16
作者
Sutton, Kathryn S.
Shereck, Evan B.
Nemecek, Eneida R.
Kurre, Peter
机构
[1] Oregon Hlth & Sci Univ, Oregon Stem Cell Ctr, Pape Family Pediat Res Inst, Dept Pediat, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Oregon Stem Cell Ctr, Pape Family Pediat Res Inst, Dept Cell & Dev Biol, Portland, OR 97239 USA
关键词
aplastic anemia; immunosuppression; PNH clones; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; BONE-MARROW; MINOR POPULATION; ANTITHYMOCYTE GLOBULIN; IMMUNOSUPPRESSIVE THERAPY; T-CELLS; CHILDREN; CLONES; CYCLOSPORINE; DEFICIENT;
D O I
10.1002/pbc.24247
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background To investigate the immune status among pediatric patients with aplastic anemia (AA) and explore PNH-status, T-regulatory and NK-cell frequency as potential markers of clinical response. Methods Data were retrospectively analyzed from twenty-six patients diagnosed with AA. PNH populations, T- and NK-subsets were determined via flow cytometry. Results At diagnosis, 9/23 patients with severe AA (SAA) versus 1/3 with moderate AA (MAA) were PNHpos. Among PNHpos patients treated with ATG based immunosuppression, 2/6 had a complete response (CR), while 4/6 had a partial response (PR), similarly 2/6 PNHneg patients had a CR and 4/6 had a PR. Lymphocyte subset immunophenotyping revealed that T-regulatory cells represented 7.2% of total lymphocytes at diagnosis. Their frequency varied with disease severity (5.5% for SAA and 14.1% for MAA) and response (8.9% for CR and 1.5% for PR), generally increasing following therapy with IST (14.6%). The NK cell frequency was not substantially different based on disease severity or response. Conclusions Neither PNH cell populations, nor NK cell frequency corresponded with disease severity or response. T-regulatory cell frequency, although not statistically significant given the small sample size, corresponded with both severity and response, indicating potential utility as a prognostic tool. Pediatr Blood Cancer 2013; 60: 455-460. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:455 / 460
页数:6
相关论文
共 39 条
  • [21] Naturally arising Foxp3-expressing CD25+ CD4+ regulatory T cells in immunological tolerance to self and non-self
    Sakaguchi, S
    [J]. NATURE IMMUNOLOGY, 2005, 6 (04) : 345 - 352
  • [22] Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long-term observation follow-up
    Saracco, Paola
    Quarello, Paola
    Iori, Anna Paola
    Zecca, Marco
    Longoni, Daniela
    Svahn, Johanna
    Varotto, Stefania
    Del Vecchio, Gian Carlo
    Dufour, Carlo
    Ramenghi, Ugo
    Bacigalupo, Andrea
    Locasciulli, Anna
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2008, 140 (02) : 197 - 205
  • [23] Paroxysmal nocturnal hemoglobinuria clones in severe aplastic anemia patients treated with horse anti-thymocyte globulin plus cyclosporine
    Scheinberg, Phillip
    Marte, Michael
    Nunez, Olga
    Young, Neal S.
    [J]. HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2010, 95 (07): : 1075 - 1080
  • [24] Long-Term Outcome of Pediatric Patients with Severe Aplastic Anemia Treated with Antithymocyte Globulin and Cyclosporine
    Scheinberg, Phillip
    Wu, Colin O.
    Nunez, Olga
    Young, Neal S.
    [J]. JOURNAL OF PEDIATRICS, 2008, 153 (06) : 814 - 819
  • [25] Predicting response to immunosuppressive therapy and survival in severe aplastic anaemia
    Scheinberg, Phillip
    Wu, Colin O.
    Nunez, Olga
    Young, Neal S.
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2009, 144 (02) : 206 - 216
  • [26] Deficient CD4+ CD25+ FOXP3+ T regulatory cells in acquired aplastic anemia
    Solomou, Elena E.
    Rezvani, Katayoun
    Mielke, Stephan
    Malide, Daniela
    Keyvanfar, Keyvan
    Visconte, Valeria
    Kajigaya, Sachiko
    Barrett, A. John
    Young, Neal S.
    [J]. BLOOD, 2007, 110 (05) : 1603 - 1606
  • [27] Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia
    Sugimori, C
    Chuhjo, T
    Feng, XM
    Yamazaki, H
    Takami, A
    Teramura, M
    Mizoguchi, H
    Omine, M
    Nakao, S
    [J]. BLOOD, 2006, 107 (04) : 1308 - 1314
  • [28] Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure
    Sugimori, Chiharu
    Mochizuki, Kanako
    Qi, Zhirong
    Sugimori, Naomi
    Ishiyama, Ken
    Kondo, Yukio
    Yamazaki, Hirohito
    Takami, Akiyoshi
    Okumura, Hirokazu
    Nakao, Shinji
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2009, 147 (01) : 102 - 112
  • [29] DEFICIENCY OF THE GPI ANCHOR CAUSED BY A SOMATIC MUTATION OF THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
    TAKEDA, J
    MIYATA, T
    KAWAGOE, K
    IIDA, Y
    ENDO, Y
    FUJITA, T
    TAKAHASHI, M
    KITANI, T
    KINOSHITA, T
    [J]. CELL, 1993, 73 (04) : 703 - 711
  • [30] Paroxysmal nocturnal haemoglobinuria clones in children with acquired aplastic anaemia: a prospective single centre study
    Timeus, Fabio
    Crescenzio, Nicoletta
    Lorenzati, Anna
    Doria, Alessandra
    Foglia, Luiselda
    Pagliano, Sara
    Quarello, Paola
    Ramenghi, Ugo
    Saracco, Paola
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2010, 150 (04) : 483 - 485