TY - JOUR
T1 - Antiviral instruction of bone marrow leukocytes during respiratory viral infections
AU - Hermesh, Tamar
AU - Moltedo, Bruno
AU - Moran, Thomas M.
AU - López, Carolina B.
N1 - Funding Information:
The authors wish to thank Karla Tapia for designing the graphical abstract and for technical support. We also thank Luis Muñoz, Olga Herrera, Sharon Czelusniak, and Madhu Kumar for excellent technical support; the Mount Sinai School of Medicine flow cytometry and the irradiator shared resource facilities for their service. This work was supported by NIH/NIAID grants A1083481 and A1083284 to C.B.L. and grants AI041111 and AI082970 to T.M.M. T.H. designed and executed the experiments and wrote the manuscript. B.M. helped with discussion and execution of experiments. T.M.M. discussed and financed experiments. C.B.L. designed, discussed, and financed experiments and wrote the manuscript.
PY - 2010/5/20
Y1 - 2010/5/20
N2 - Respiratory viral infections trigger a robust inflammatory response in the lung, producing cytokines, chemokines, and growth factors that promote infiltration of effector leukocytes. Whereas the role of chemokines and infiltrating leukocytes in antiviral immunity is well studied, the effect that lung cytokines have on leukocytes in distal hematopoietic and lymphoid tissues and their role in antiviral immunity is unknown. We show that, during infection with influenza or Sendai virus, the lung communicates with the sterile bone marrow, the primary site of hematopoiesis, through type I interferons. While in the bone marrow, leukocytes exposed to type I interferons activate an antiviral transcriptional program and become resistant to infection with different viruses. The protected bone marrow leukocytes are capable of migrating to the infected lung and contribute to virus clearance. These findings show that appropriate instruction of cells during their development in the bone marrow is needed for effective control of infection.
AB - Respiratory viral infections trigger a robust inflammatory response in the lung, producing cytokines, chemokines, and growth factors that promote infiltration of effector leukocytes. Whereas the role of chemokines and infiltrating leukocytes in antiviral immunity is well studied, the effect that lung cytokines have on leukocytes in distal hematopoietic and lymphoid tissues and their role in antiviral immunity is unknown. We show that, during infection with influenza or Sendai virus, the lung communicates with the sterile bone marrow, the primary site of hematopoiesis, through type I interferons. While in the bone marrow, leukocytes exposed to type I interferons activate an antiviral transcriptional program and become resistant to infection with different viruses. The protected bone marrow leukocytes are capable of migrating to the infected lung and contribute to virus clearance. These findings show that appropriate instruction of cells during their development in the bone marrow is needed for effective control of infection.
UR - http://www.scopus.com/inward/record.url?scp=77955290497&partnerID=8YFLogxK
U2 - 10.1016/j.chom.2010.04.006
DO - 10.1016/j.chom.2010.04.006
M3 - Article
C2 - 20478536
AN - SCOPUS:77955290497
SN - 1931-3128
VL - 7
SP - 343
EP - 353
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 5
ER -