Normalizing the environment recapitulates adult human immune traits in laboratory mice

被引:820
作者
Beura, Lalit K. [1 ]
Hamilton, Sara E. [2 ]
Bi, Kevin [3 ,4 ]
Schenkel, Jason M. [1 ]
Odumade, Oludare A. [2 ,6 ]
Casey, Kerry A. [1 ,7 ]
Thompson, Emily A. [1 ]
Fraser, Kathryn A. [1 ]
Rosato, Pamela C. [1 ]
Filali-Mouhim, Ali [5 ]
Sekaly, Rafick P. [5 ]
Jenkins, Marc K. [1 ]
Vezys, Vaiva [1 ]
Haining, W. Nicholas [3 ,4 ]
Jameson, Stephen C. [2 ]
Masopust, David [1 ]
机构
[1] Univ Minnesota, Dept Microbiol & Immunol, Ctr Immunol, Minneapolis, MN 55414 USA
[2] Univ Minnesota, Dept Lab Med & Pathol, Ctr Immunol, Minneapolis, MN 55414 USA
[3] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[4] Childrens Hosp, Pediat Hematol & Oncol, 300 Longwood Ave, Boston, MA 02115 USA
[5] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[6] Univ Calif San Diego, Rady Childrens Hosp, Dept Pediat, San Diego, CA 92123 USA
[7] MedImmune LLC, Dept Resp Inflammat & Autoimmun, Gaithersburg, MD 20878 USA
基金
美国国家卫生研究院;
关键词
CD8(+) T-CELLS; BARR-VIRUS INFECTION; MEMORY; MOUSE; TRANSLATION; EXPRESSION; GENERATION; MODELS; LOST; GUT;
D O I
10.1038/nature17655
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Our current understanding of immunology was largely defined in laboratory mice, partly because they are inbred and genetically homogeneous, can be genetically manipulated, allow kinetic tissue analyses to be carried out from the onset of disease, and permit the use of tractable disease models. Comparably reductionist experiments are neither technically nor ethically possible in humans. However, there is growing concern that laboratory mice do not reflect relevant aspects of the human immune system, which may account for failures to translate disease treatments from bench to bedside(1-8). Laboratory mice live in abnormally hygienic specific pathogen free (SPF) barrier facilities. Here we show that standard laboratory mouse husbandry has profound effects on the immune system and that environmental changes produce mice with immune systems closer to those of adult humans. Laboratory mice-like newborn, but not adult, humans-lack effector-differentiated and mucosally distributed memory T cells. These cell populations were present in free-living barn populations of feral mice and pet store mice with diverse microbial experience, and were induced in laboratory mice after co-housing with pet store mice, suggesting that the environment is involved in the induction of these cells. Altering the living conditions of mice profoundly affected the cellular composition of the innate and adaptive immune systems, resulted in global changes in blood cell gene expression to patterns that more closely reflected the immune signatures of adult humans rather than neonates, altered resistance to infection, and influenced T-cell differentiation in response to a de novo viral infection. These data highlight the effects of environment on the basal immune state and response to infection and suggest that restoring physiological microbial exposure in laboratory mice could provide a relevant tool for modelling immunological events in free- living organisms, including humans.
引用
收藏
页码:512 / +
页数:12
相关论文
共 42 条
[1]
Heterologous immunity: an overlooked barrier to tolerance [J].
Adams, AB ;
Pearson, TC ;
Larsen, CP .
IMMUNOLOGICAL REVIEWS, 2003, 196 (01) :147-160
[2]
Intravascular staining for discrimination of vascular and tissue leukocytes [J].
Anderson, Kristin G. ;
Mayer-Barber, Katrin ;
Sung, Heungsup ;
Beura, Lalit ;
James, Britnie R. ;
Taylor, Justin J. ;
Qunaj, Lindor ;
Griffith, Thomas S. ;
Vezys, Vaiva ;
Barber, Daniel L. ;
Masopust, David .
NATURE PROTOCOLS, 2014, 9 (01) :209-222
[3]
Behavioral, Virologic, and Immunologic Factors Associated With Acquisition and Severity of Primary Epstein-Barr Virus Infection in University Students [J].
Balfour, Henry H., Jr. ;
Odumade, Oludare A. ;
Schmeling, David O. ;
Mullan, Beth D. ;
Ed, Julie A. ;
Knight, Jennifer A. ;
Vezina, Heather E. ;
Thomas, William ;
Hogquist, Kristin A. .
JOURNAL OF INFECTIOUS DISEASES, 2013, 207 (01) :80-88
[4]
Lymphocytic choriomeningitis virus persistence promotes effector-like memory differentiation and enhances mucosal T cell distribution [J].
Beura, Lalit K. ;
Anderson, Kristin G. ;
Schenkel, Jason M. ;
Locquiao, Jeremiah J. ;
Fraser, Kathryn A. ;
Vezys, Vaiva ;
Pepper, Marion ;
Masopust, David .
JOURNAL OF LEUKOCYTE BIOLOGY, 2015, 97 (02) :217-225
[5]
The Virome in Host Health and Disease [J].
Cadwell, Ken .
IMMUNITY, 2015, 42 (05) :805-813
[6]
GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists [J].
Eden, Eran ;
Navon, Roy ;
Steinfeld, Israel ;
Lipson, Doron ;
Yakhini, Zohar .
BMC BIOINFORMATICS, 2009, 10
[7]
Compendium of Immune Signatures Identifies Conserved and Species-Specific Biology in Response to Inflammation [J].
Godec, Jernej ;
Tan, Yan ;
Liberzon, Arthur ;
Tamayo, Pablo ;
Bhattacharya, Sanchita ;
Butte, Atul J. ;
Mesirov, Jill P. ;
Haining, W. Nicholas .
IMMUNITY, 2016, 44 (01) :194-206
[8]
Inhibiting the Mammalian Target of Rapamycin Blocks the Development of Experimental Cerebral Malaria [J].
Gordon, Emile B. ;
Hart, Geoffrey T. ;
Tran, Tuan M. ;
Waisberg, Michael ;
Akkaya, Munir ;
Skinner, Jeff ;
Zinoecker, Severin ;
Pena, Mirna ;
Yazew, Takele ;
Qi, Chen-Feng ;
Miller, Louis H. ;
Pierce, Susan K. .
MBIO, 2015, 6 (03)
[9]
IL-2 Complex Treatment Can Protect Naive Mice from Bacterial and Viral Infection [J].
Hamilton, Sara E. ;
Schenkel, Jason M. ;
Akue, Adovi D. ;
Jameson, Stephen C. .
JOURNAL OF IMMUNOLOGY, 2010, 185 (11) :6584-6590
[10]
The generation of protective memory-like CD8+ T cells during homeostatic proliferation requires CD4+ T cells [J].
Hamilton, SE ;
Wolkers, MC ;
Schoenberger, SP ;
Jameson, SC .
NATURE IMMUNOLOGY, 2006, 7 (05) :475-481