Treatment of Familial Hemophagocytic Lymphohistiocytosis with Third-Party Mesenchymal Stromal Cells

被引:15
作者
Mougiakakos, Dimitrios [1 ,2 ]
Machaczka, Maciej [3 ]
Jitschin, Regina [2 ]
Klimkowska, Monika [4 ]
Entesarian, Miriam [5 ]
Bryceson, Yenan T. [6 ]
Henter, Jan-Inge [5 ]
Sander, Birgitta [7 ]
Le Blanc, Katarina [2 ]
机构
[1] Univ Erlangen Nurnberg, Dept Internal Med 5, D-91054 Erlangen, Germany
[2] Huddinge Univ Hosp, Karolinska Inst, Div Clin Immunol, Stockholm, Sweden
[3] Karolinska Univ, Huddinge Hosp, Karolinska Inst,Dept Med Huddinge, Div Haematol, Stockholm, Sweden
[4] Karolinska Univ, Huddinge Hosp, Dept Clin Pathol & Cytol, Stockholm, Sweden
[5] Karolinska Univ, Hosp Solna, Karolinska Inst,Childhood Canc Res Unit, Dept Womens & Childrens Hlth, Stockholm, Sweden
[6] Karolinska Univ, Huddinge Hosp, Karolinska Inst,Ctr Infect Med, Dept Med, Stockholm, Sweden
[7] Karolinska Univ, Huddinge Hosp, Karolinska Inst,Dept Lab Med, Div Pathol, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
VERSUS-HOST-DISEASE; STEM-CELLS; MULTIPOTENT; THERAPY; MONOCYTE;
D O I
10.1089/scd.2012.0214
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stromal cells (MSCs) represent an attractive tool for cellular therapies on grounds of their immunomodulatory and regenerative properties. Here, we report the first case of familial hemophagocytic lymphohistiocytosis (FHL) treated with MSCs. This rare autosomal recessive disorder is characterized by hyperinflammation that results from a failure of natural control mechanisms to terminate immune responses. Crosstalk between innate (macrophages) and adaptive (T cells) immunity is heavily altered. Immuno-chemotherapy is only temporarily effective in the control of FHL, and the outcome is usually fatal unless the patient undergoes allogeneic stem cell transplantation. Our hypothesis was that the application of MSCs could be effective in the treatment of FHL, since MSCs possess a broad repertoire of immunomodulating mechanisms impacting both innate and adaptive immunity pathways. In fact, the adoptive transfer of third-party MSCs transiently controlled the extreme immunological deterioration in the described patient who was otherwise not responsive to standard treatment, including repetitive chemotherapy. If these transient effects of MSCs can be confirmed in future-controlled clinical trials, adoptive MSC therapy could represent a salvage agent in FHL acting as a bridge to definitive treatment with stem cell transplantation.
引用
收藏
页码:3147 / 3151
页数:5
相关论文
共 23 条
[11]   Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells [J].
Le Blanc, K ;
Rasmusson, I ;
Sundberg, B ;
Götherström, C ;
Hassan, M ;
Uzunel, M ;
Ringdén, O .
LANCET, 2004, 363 (9419) :1439-1441
[12]   Multipotent mesenchymal stromal cells and the innate immune system [J].
Le Blanc, Katarina ;
Mougiakakos, Dimitrios .
NATURE REVIEWS IMMUNOLOGY, 2012, 12 (05) :383-U17
[13]   Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease:: a phase II study [J].
LeBlanc, Katarina ;
Frassoni, Francesco ;
Ball, Lynne ;
Locatelli, Franco ;
Roelofs, Helene ;
Lewis, Ian ;
Lanino, Edoardo ;
Sundberg, Berit ;
Bernardo, Maria Ester ;
Remberger, Mats ;
Dini, Giorgio ;
Egeler, R. Maarten ;
Bacigalupo, Andrea ;
Fibbe, Willem ;
Ringden, Olle .
LANCET, 2008, 371 (9624) :1579-1586
[14]   Activating receptors promote NK cell expansion for maintenance, IL-10 production, and CD8 T cell regulation during viral infection [J].
Lee, Seung-Hwan ;
Kim, Kwang-Sin ;
Fodil-Cornu, Nassima ;
Vidal, Silvia M. ;
Biron, Christine A. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (10) :2235-2251
[15]   Interleukin-15 and the regulation of lymphoid homeostasis [J].
Lodolce, J ;
Burkett, P ;
Koka, R ;
Boone, D ;
Chien, M ;
Chan, F ;
Madonia, M ;
Chai, S ;
Ma, A .
MOLECULAR IMMUNOLOGY, 2002, 39 (09) :537-544
[16]   Alemtuzumab treatment for hemophagocytic lymphohistiocytosis [J].
Machaczka, Maciej ;
Vaktnas, Johan ;
Chiang, Samuel C. C. ;
Bryceson, Yenan T. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2010, 7 (10) :1-1
[17]   Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4 [J].
Menager, Mickael M. ;
Menasche, Gael ;
Romao, Maryse ;
Knapnougel, Perrine ;
Ho, Chen-Hsuan ;
Garfa, Meriem ;
Raposo, Graca ;
Feldmann, Jerome ;
Fischer, Alain ;
de Saint Basile, Genevieve .
NATURE IMMUNOLOGY, 2007, 8 (03) :257-267
[18]   Bone marrow stromal cells attenuate sepsis via prostaglandin E2-dependent reprogramming of host macrophages to increase their interleukin-10 production [J].
Nemeth, Krisztian ;
Leelahavanichkul, Asada ;
Yuen, Peter S. T. ;
Mayer, Balazs ;
Parmelee, Alissa ;
Doi, Kent ;
Robey, Pamela G. ;
Leelahavanichkul, Kantima ;
Koller, Beverly H. ;
Brown, Jared M. ;
Hu, Xuzhen ;
Jelinek, Ivett ;
Star, Robert A. ;
Mezey, Eva .
NATURE MEDICINE, 2009, 15 (01) :42-49
[19]   Increased serum levels of interferon-γ-inducible protein 10 and monokine induced by gamma interferon in patients with haemophagocytic lymphohistiocytosis [J].
Takada, H ;
Takahata, Y ;
Nomura, A ;
Ohga, S ;
Mizuno, Y ;
Hara, T .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 133 (03) :448-453
[20]   Increased serum monocyte chemoattractant protein-1 macrophage inflammatory protein-1β, and interleukin-8 concentrations in hemophagocytic lymphohistiocytosis [J].
Tamura, Kazushi ;
Kanazawa, Takashi ;
Tsukada, Shota ;
Kobayashi, Tohru ;
Kawamura, Machiko ;
Morikawa, Akihiro .
PEDIATRIC BLOOD & CANCER, 2008, 51 (05) :662-668