The Role of Animal Models in the Study of Hematopoietic Stem Cell Transplantation and GvHD: A Historical Overview

被引:36
作者
Boieri, Margherita [1 ,2 ]
Shah, Pranali [3 ]
Dressel, Ralf [3 ]
Inngjerdingen, Marit [1 ,2 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Dept Mol Med, Oslo, Norway
[2] Oslo Univ Hosp, Dept Immunol, Oslo, Norway
[3] Univ Med Ctr Gottingen, Inst Cellular & Mol Immunol, Gottingen, Germany
关键词
animal models; HSCT; aGvHD; cGvHD; pathophysiology; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; REGULATORY T-CELLS; MESENCHYMAL STROMAL CELLS; ANTIGEN-PRESENTING CELLS; TOTAL-BODY IRRADIATION; MINOR HISTOCOMPATIBILITY BARRIERS; IDIOPATHIC PNEUMONIA SYNDROME; NECROSIS-FACTOR-ALPHA; SKIN EXPLANT MODEL;
D O I
10.3389/fimmu.2016.00333
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bone marrow transplantation (BMT) is the only therapeutic option for many hematological malignancies, but its applicability is limited by life-threatening complications, such as graft-versus-host disease (GvHD). The last decades have seen great advances in the understanding of BMT and its related complications; in particular GvHD. Animal models are beneficial to study complex diseases, as they allow dissecting the contribution of single components in the development of the disease. Most of the current knowledge on the therapeutic mechanisms of BMT derives from studies in animal models. Parallel to BMT, the understanding of the pathophysiology of GvHD, as well as the development of new treatment regimens, has also been supported by studies in animal models. Pre-clinical experimentation is the basis for deep understanding and successful improvements of clinical applications. In this review, we retrace the history of BMT and GvHD by describing how the studies in animal models have paved the way to the many advances in the field. We also describe how animal models contributed to the understanding of GvHD pathophysiology and how they are fundamental for the discovery of new treatments.
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页数:20
相关论文
共 292 条
[1]   Inhibition of platelet-derived growth factor signaling attenuates pulmonary fibrosis [J].
Abdollahi, A ;
Li, ML ;
Ping, G ;
Plathow, C ;
Domhan, S ;
Kiessling, F ;
Lee, LB ;
McMahon, G ;
Gröne, HJ ;
Lipson, KE ;
Huber, PE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (06) :925-935
[2]   Co-infusion of donor bone marrow with host mesenchymal stem cells treats GVHD and promotes vascularized skin allograft survival in rats [J].
Aksu, Ali Emre ;
Horibe, Elaine ;
Sacks, Justin ;
Ikeguchi, Ryosuke ;
Breitinger, Jeremy ;
Scozio, Merissa ;
Unadkat, Jignesh ;
Feili-Hariri, Maryam .
CLINICAL IMMUNOLOGY, 2008, 127 (03) :348-358
[3]   Xenogeneic Graft-versus-Host-Disease in NOD-scid IL-2Rγnull Mice Display a T-Effector Memory Phenotype [J].
Ali, Niwa ;
Flutter, Barry ;
Rodriguez, Robert Sanchez ;
Sharif-Paghaleh, Ehsan ;
Barber, Linda D. ;
Lombardi, Giovanna ;
Nestle, Frank O. .
PLOS ONE, 2012, 7 (08)
[4]  
ALLISON AC, 1971, LANCET, V2, P135
[5]   A PHASE-I PHASE-II STUDY EVALUATING THE MURINE ANTI-IL-2 RECEPTOR ANTIBODY-2A3 FOR TREATMENT OF ACUTE GRAFT-VERSUS-HOST DISEASE [J].
ANASETTI, C ;
MARTIN, PJ ;
HANSEN, JA ;
APPELBAUM, FR ;
BEATTY, PG ;
DONEY, K ;
HARKONEN, S ;
JACKSON, A ;
REICHERT, T ;
STEWART, P ;
STORB, R ;
SULLIVAN, KM ;
THOMAS, ED ;
WARNER, N ;
WITHERSPOON, RP .
TRANSPLANTATION, 1990, 50 (01) :49-54
[6]   Distinct roles for donor- and host-derived antigen-presenting cells and costimulatory molecules in murine chronic graft-versus-host disease: requirements depend on target organ [J].
Anderson, BE ;
McNiff, JM ;
Jain, D ;
Blazar, BR ;
Shlomchik, WD ;
Shlomchik, MJ .
BLOOD, 2005, 105 (05) :2227-2234
[7]   Memory CD4+ T cells do not induce graft-versus-host disease [J].
Anderson, BE ;
McNiff, J ;
Yan, J ;
Doyle, H ;
Mamula, M ;
Shlomchik, MJ ;
Shlomchik, WD .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (01) :101-108
[8]   A phase I/II double-blind, placebo-controlled study of recombinant human interleukin-11 for mucositis and acute GVHD prevention in allogeneic stem cell transplantation [J].
Antin, JH ;
Lee, SJ ;
Neuberg, D ;
Alyea, E ;
Soiffer, RJ ;
Sonis, S ;
Ferrara, JLM .
BONE MARROW TRANSPLANTATION, 2002, 29 (05) :373-377
[9]   An essential role for IFN-γ in regulation of alloreactive CD8 T cells following allogeneic hematopoietic cell transplantation [J].
Asavaroengchai, Wannee ;
Wang, Hui ;
Wang, Shumei ;
Wang, Lan ;
Bronson, Roderick ;
Sykes, Megan ;
Yang, Yong-Guang .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2007, 13 (01) :46-55
[10]   Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota [J].
Atarashi, Koji ;
Tanoue, Takeshi ;
Oshima, Kenshiro ;
Suda, Wataru ;
Nagano, Yuji ;
Nishikawa, Hiroyoshi ;
Fukuda, Shinji ;
Saito, Takuro ;
Narushima, Seiko ;
Hase, Koji ;
Kim, Sangwan ;
Fritz, Joelle V. ;
Wilmes, Paul ;
Ueha, Satoshi ;
Matsushima, Kouji ;
Ohno, Hiroshi ;
Olle, Bernat ;
Sakaguchi, Shimon ;
Taniguchi, Tadatsugu ;
Morita, Hidetoshi ;
Hattori, Masahira ;
Honda, Kenya .
NATURE, 2013, 500 (7461) :232-+