Immunity to Respiratory Viruses

被引:194
作者
Kohlmeier, Jacob E. [1 ]
Woodland, David L. [1 ]
机构
[1] Trudeau Inst Inc, Saranac Lake, NY 12983 USA
关键词
lung; T cell; memory; influenza; CD8(+) T-CELLS; INFLUENZA-A-VIRUS; PLASMACYTOID DENDRITIC CELLS; TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; MEMORY B-CELLS; CUTTING EDGE; SYNCYTIAL-VIRUS; RIG-I; LYMPHOID-TISSUE;
D O I
10.1146/annurev.immunol.021908.132625
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The respiratory tract is characterized by an extensive surface area that is in direct contact with the environment, posing a significant problem for effective immune surveillance. Yet most respiratory pathogens are quickly recognized and controlled by a coordinated response involving the innate and adaptive arms of the immune system. The investigation of pulmonary immunity to respiratory viruses during a primary infection has demonstrated that Multiple innate and adaptive immune mechanisms are necessary for efficient antiviral responses, and the inhibition of any single mechanism can have disastrous consequences for the host. Furthermore, the investigation of recall responses in the lung has shown that protection from a secondary challenge infection is a complex and elegant process that occurs in distinct stages. In this review, we discuss recent advances that describe the roles of individual components during primary and secondary responses to respiratory virus infections and how these discoveries have added to our understanding of antiviral immunity in the lung.
引用
收藏
页码:61 / 82
页数:22
相关论文
共 143 条
[1]   Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[2]   Mouse type IIFN-producing cells are immature APCs with plasmacytoid morphology [J].
Asselin-Paturel, C ;
Boonstra, A ;
Dalod, M ;
Durand, I ;
Yessaad, N ;
Dezutter-Dambuyant, C ;
Vicari, A ;
O'Garra, A ;
Biron, C ;
Brière, F ;
Trinchieri, G .
NATURE IMMUNOLOGY, 2001, 2 (12) :1144-1150
[3]   Recall proliferation potential of memory CD8+ T cells and antiviral protection [J].
Bachmann, MF ;
Wolint, P ;
Schwarz, K ;
Oxenius, A .
JOURNAL OF IMMUNOLOGY, 2005, 175 (07) :4677-4685
[4]  
BACHMANN MF, 1994, J IMMUNOL, V153, P3386
[5]   CD8+ T cell contraction is controlled by early inflammation [J].
Badovinac, VP ;
Porter, BB ;
Harty, JT .
NATURE IMMUNOLOGY, 2004, 5 (08) :809-817
[6]   Accelerated CD8+ T-cell memory and prime-boost response after dendritic-cell vaccination [J].
Badovinac, VP ;
Messingham, KAN ;
Jabbari, A ;
Haring, JS ;
Harty, JT .
NATURE MEDICINE, 2005, 11 (07) :748-756
[7]   Endogenous naive CD8+ T cell precursor frequency regulates primary and memory responses to infection [J].
Bar, Joshua J. ;
Khanna, Kamal M. ;
Lefrancois, Leo .
IMMUNITY, 2008, 28 (06) :859-869
[8]   B-1 and B-2 cell-derived immunoglobulin M antibodies are nonredundant components of the protective response to influenza virus infection [J].
Baumgarth, N ;
Herman, OC ;
Jager, GC ;
Brown, LE ;
Herzenberg, LA ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :271-280
[9]   Bone marrow is a preferred site for homeostatic proliferation of memory CD8 T cells [J].
Becker, TC ;
Coley, SM ;
Wherry, EJ ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2005, 174 (03) :1269-1273
[10]   Distinct migrating and nonmigrating dendritic cell populations are involved in MHC class I-restricted antigen presentation after lung infection with virus [J].
Belz, GT ;
Smith, CM ;
Kleinert, L ;
Reading, P ;
Brooks, A ;
Shortman, K ;
Carbone, FR ;
Heath, WR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (23) :8670-8675