Residual Antigen Presentation after Influenza Virus Infection Affects CD8 T Cell Activation and Migration

Immunity

Volumn 24, Issue 4, 2006, Pages 439-449

  Zammit, David J ^a   Turner, Damian L ^a   Klonowski, Kimberly D ^a   Lefrançois, Leo ^a   Cauley, Linda S ^a  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

CELLIMMUNO; MICROBIO

Indexed keywords

VIRUS ANTIGEN;

AIRWAY; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIGEN PRESENTATION; ARTICLE; CD8+ T LYMPHOCYTE; CELL MIGRATION; CELL POPULATION; FEMALE; INFLUENZA; INFLUENZA VIRUS; LYMPH NODE; MOUSE; NONHUMAN; PRIORITY JOURNAL; T LYMPHOCYTE ACTIVATION;

ANIMALS; ANTIGEN PRESENTATION; CD8-POSITIVE T-LYMPHOCYTES; CELL MOVEMENT; DISEASE MODELS, ANIMAL; FEMALE; FLOW CYTOMETRY; INFLUENZA A VIRUS; LUNG; LYMPH NODES; LYMPHOCYTE ACTIVATION; MEDIASTINUM; MICE; MICE, CONGENIC; MICE, INBRED C57BL; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; VIRUS DISEASES;

EID: 33645971304     PISSN: 10747613     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.immuni.2006.01.015     Document Type: Article

References (51)

1. Aronsson F., Karlsson H., Ljunggren H.G., and Kristensson K. Persistence of the influenza A/WSN/33 virus RNA at midbrain levels of immunodefective mice. J. Neurovirol. 7 (2001) 117-124
2. Aronsson F., Lannebo C., Paucar M., Brask J., Kristensson K., and Karlsson H. Persistence of viral RNA in the brain of offspring to mice infected with influenza A/WSN/33 virus during pregnancy. J. Neurovirol. 8 (2002) 353-357
3. Chang J., and Braciale T.J. Respiratory syncytial virus infection suppresses lung CD8+ T-cell effector activity and peripheral CD8+ T-cell memory in the respiratory tract. Nat. Med. 8 (2002) 54-60
4. Dahl M.E., Dabbagh K., Liggitt D., Kim S., and Lewis D.B. Viral-induced T helper type 1 responses enhance allergic disease by effects on lung dendritic cells. Nat. Immunol. 5 (2004) 337-343
5. Daly K., Nguyen P., Woodland D.L., and Blackman M.A. Immunodominance of major histocompatibility complex class I-restricted influenza virus epitopes can be influenced by the T-cell receptor repertoire. J. Virol. 69 (1995) 7416-7422
6. Doherty P.C., Topham D.J., and Tripp R.A. Establishment and persistence of virus-specific CD4+ and CD8+ T cell memory. Immunol. Rev. 150 (1996) 23-44
7. Donskoy E., and Goldschneider I. Thymocytopoiesis is maintained by blood-borne precursors throughout postnatal life. A study in parabiotic mice. J. Immunol. 148 (1992) 1604-1612
8. Ely K.H., Cauley L.S., Roberts A.D., Brennan J.W., Cookenham T., and Woodland D.L. Nonspecific recruitment of memory CD8(+) T cells to the lung airways during respiratory virus infections. J. Immunol. 170 (2003) 1423-1429
9. Ely K.H., Roberts A.D., and Woodland D.L. Cutting edge: effector memory CD8+ T cells in the lung airways retain the potential to mediate recall responses. J. Immunol. 171 (2003) 3338-3342
10. Ely K.H., Cookenham T., Roberts A.D., and Woodland D.L. Memory T cell populations in the lung airways are maintained by continual recruitment. J. Immunol. 176 (2006) 537-543
11. Flynn K.J., Belz G.T., Altman J.D., Ahmed R., Woodland D.L., and Doherty P.C. Virus-specific CD8(+) T cells in primary and secondary influenza pneumonia. Immunity 8 (1998) 683-691
12. Gray D. A role for antigen in the maintenance of immunological memory. Nat. Rev. Immunol. 2 (2002) 60-65
13. Hamilton-Easton A., and Eichelberger M. Virus-specific antigen presentation by different subsets of cells from lung and mediastinal lymph node tissues of influenza virus-infected mice. J. Virol. 69 (1995) 6359-6366
14. Hogan R.J., Usherwood E.J., Zhong W., Roberts A.A., Dutton R.W., Harmsen A.G., and Woodland D.L. Activated antigen-specific CD8+ T cells persist in the lungs following recovery from respiratory virus infections. J. Immunol. 166 (2001) 1813-1822
15. Hogan R.J., Zhong W.M., Usherwood E.J., Cookenham T., Roberts A.D., and Woodland D.L. Protection from respiratory virus infections can be mediated by antigen-specific CD4(+) T cells that persist in the lungs. J. Exp. Med. 193 (2001) 981-986
16. Hogquist K.A., Jameson S.C., Heath W.R., Howard J.L., Bevan M.J., and Carbone F.R. T cell receptor antagonist peptides induce positive selection. Cell 76 (1994) 17-27
17. Huster K.M., Busch V., Schiemann M., Linkemann K., Kerksiek K.M., Wagner H., and Busch D.H. Selective expression of IL-7 receptor on memory T cells identifies early CD40L-dependent generation of distinct CD8+ memory T cell subsets. Proc. Natl. Acad. Sci. USA 101 (2004) 5610-5615
18. Jelly-Gibbs D.M., Brown D.M., Dibble J.P., Haynes L., Eaton S.M., and Swain S.L. Unexpected prolonged presentation of influenza antigens promotes CD4 T cell memory generation. J. Exp. Med. 202 (2005) 697-706
19. Julia V., Hessel E.M., Malherbe L., Glaichenhaus N., O'Garra A., and Coffman R.L. A restricted subset of dendritic cells captures airborne antigens and remains able to activate specific T cells long after antigen exposure. Immunity 16 (2002) 271-283
20. Kaech S.M., Tan J.T., Wherry E.J., Konieczny B.T., Surh C.D., and Ahmed R. Selective expression of the interleukin 7 receptor identifies effector CD8 T cells that give rise to long-lived memory cells. Nat. Immunol. 4 (2003) 1191-1198
21. Khanna K.M., Bonneau R.H., Kinchington P.R., and Hendricks R.L. Herpes simplex virus-specific memory CD8+ T cells are selectively activated and retained in latently infected sensory ganglia. Immunity 18 (2003) 593-603
22. Klonowski K.D., Williams K.J., Marzo A.L., Blair D.A., Lingenheld E.G., and Lefrancois L. Dynamics of blood-borne CD8 memory T cell migration in vivo. Immunity 20 (2004) 551-562
23. Kranzer K., Bauer M., Lipford G.B., Heeg K., Wagner H., and Lang R. CpG-oligodeoxynucleotides enhance T-cell receptor-triggered interferon-gamma production and up-regulation of CD69 via induction of antigen-presenting cell-derived interferon type I and interleukin-12. Immunology 99 (2000) 170-178
24. Kundig T.M., Bachmann M.F., Oehen S., Hoffmann U.W., Simard J.J., Kalberer C.P., Pircher H., Ohashi P.S., Hengartner H., and Zinkernagel R.M. On the role of antigen in maintaining cytotoxic T-cell memory. Proc. Natl. Acad. Sci. USA 93 (1996) 9716-9723
25. Lang K.S., Recher M., Navarini A.A., Harris N.L., Lohning M., Junt T., Probst H.C., Hengartner H., and Zinkernagel R.M. Inverse correlation between IL-7 receptor expression and CD8 T cell exhaustion during persistent antigen stimulation. Eur. J. Immunol. 35 (2005) 738-745
26. Liang S., Mozdzanowska K., Palladino G., and Gerhard W. Heterosubtypic immunity to influenza type A virus in mice. Effector mechanisms and their longevity. J. Immunol. 152 (1994) 1653-1661
27. Lyons A.B., and Parish C.R. Determination of lymphocyte division by flow cytometry. J. Immunol. Methods 171 (1994) 131-137
28. Marshall D.R., Turner S.J., Belz G.T., Wingo S., Andreansky S., Sangster M.Y., Riberdy J.M., Liu T., Tan M., and Doherty P.C. Measuring the diaspora for virus-specific CD8+ T cells. Proc. Natl. Acad. Sci. USA 98 (2001) 6313-6318
29. Masopust D., Vezys V., Usherwood E.J., Cauley L.S., Olson S., Marzo A.L., Ward R.L., Woodland D.L., and Lefrancois L. Activated primary and memory CD8 T cells migrate to nonlymphoid tissues regardless of site of activation or tissue of origin. J. Immunol. 172 (2004) 4875-4882
30. Moskophidis D., and Kioussis D. Contribution of virus-specific CD8+ cytotoxic T cells to virus clearance or pathologic manifestations of influenza virus infection in a T cell receptor transgenic mouse model. J. Exp. Med. 188 (1998) 223-232
31. Nguyen H.H., Moldoveanu Z., Novak M.J., van Ginkel F.W., Ban E., Kiyono H., Mcghee J.R., and Mestecky J. Heterosubtypic immunity to lethal influenza A virus infection is associated with virus-specific CD8(+) cytotoxic T lymphocyte responses induced in mucosa-associated tissues. Virology 254 (1999) 50-60
32. Nguyen H.H., van Ginkel F.W., Vu H.L., Mcghee J.R., and Mestecky J. Heterosubtypic immunity to influenza A virus infection requires B cells but not CD8+ cytotoxic T lymphocytes. J. Infect. Dis. 183 (2001) 368-376
33. Ostler T., and Ehl S. Pulmonary T cells induced by respiratory syncytial virus are functional and can make an important contribution to long-lived protective immunity. Eur. J. Immunol. 32 (2002) 2562-2569
34. Ostler T., Hussell T., Surh C.D., Openshaw P., and Ehl S. Long-term persistence and reactivation of T cell memory in the lung of mice infected with respiratory syncytial virus. Eur. J. Immunol. 31 (2001) 2574-2582
35. Pope C., Kim S.K., Marzo A., Masopust D., Williams K., Jiang J., Shen H., and Lefrancois L. Organ-specific regulation of the CD8 T cell response to Listeria monocytogenes infection. J. Immunol. 166 (2001) 3402-3409
36. Ray S.J., Franki S.N., Pierce R.H., Dimitrova S., Koteliansky V., Sprague A.G., Doherty P.C., De Fougerolles A.R., and Topham D.J. The collagen binding alpha1beta1 integrin VLA-1 regulates CD8 T cell-mediated immune protection against heterologous influenza infection. Immunity 20 (2004) 167-179
37. Redmond W.L., and Sherman L.A. Peripheral tolerance of CD8 T lymphocytes. Immunity 22 (2005) 275-284
38. Schluns K.S., Kieper W.C., Jameson S.C., and Lefrancois L. Interleukin-7 mediates the homeostasis of naive and memory CD8 T cells in vivo. Nat. Immunol. 1 (2000) 426-432
39. Schwartz D.A., Quinn T.J., Thorne P.S., Sayeed S., Yi A.K., and Krieg A.M. CpG motifs in bacterial DNA cause inflammation in the lower respiratory tract. J. Clin. Invest. 100 (1997) 68-73
40. Stephens R., Randolph D.A., Huang G., Holtzman M.J., and Chaplin D.D. Antigen-nonspecific recruitment of Th2 cells to the lung as a mechanism for viral infection-induced allergic asthma. J. Immunol. 169 (2002) 5458-5467
41. Sun S., and Sprent J. Role of type I interferons in T cell activation induced by CpG DNA. Curr. Top. Microbiol. Immunol. 247 (2000) 107-117
42. Topham D.J., Tripp R.A., and Doherty P.C. CD8+ T cells clear influenza virus by perforin or Fas-dependent processes. J. Immunol. 159 (1997) 5197-5200
43. Topham D.J., Castrucci M.R., Wingo F.S., Belz G.T., and Doherty P.C. The role of antigen in the localization of naive, acutely activated, and memory CD8(+) T cells to the lung during influenza pneumonia. J. Immunol. 167 (2001) 6983-6990
44. Townsend A.R., and Skehel J.J. The influenza A virus nucleoprotein gene controls the induction of both subtype specific and cross-reactive cytotoxic T cells. J. Exp. Med. 160 (1984) 552-563
45. Townsend A.R., Rothbard J., Gotch F.M., Bahadur G., Wraith D., and McMichael A.J. The epitopes of influenza nucleoprotein recognized by cytotoxic T lymphocytes can be defined with short synthetic peptides. Cell 44 (1986) 959-968
46. Webby R.J., Andreansky S., Stambas J., Rehg J.E., Webster R.G., Doherty P.C., and Turner S.J. Protection and compensation in the influenza virus-specific CD8+ T cell response. Proc. Natl. Acad. Sci. USA 100 (2003) 7235-7240
47. Woodland D.L., Ely K.H., Crowe S.R., Tighe M., Brennan J.W., Harmsen A.G., and Cauley L.S. Antiviral memory T-cell responses in the lung. Microbes Infect. 4 (2002) 1091-1098
48. Yamamoto N., Suzuki S., Shirai A., Suzuki M., Nakazawa M., Nagashima Y., and Okubo T. Dendritic cells are associated with augmentation of antigen sensitization by influenza A virus infection in mice. Eur. J. Immunol. 30 (2000) 316-326
49. Yewdell J.W., and Haeryfar S.M. Understanding presentation of viral antigens to CD8+ T cells in vivo: the key to rational vaccine design. Annu. Rev. Immunol. 23 (2005) 651-682
50. Zammit D.J., Cauley L.S., Pham Q.M., and Lefrancois L. Dendritic cells maximize the memory CD8 T cell response to infection. Immunity 22 (2005) 561-570
51. Zinkernagel R.M. On differences between immunity and immunological memory. Curr. Opin. Immunol. 14 (2002) 523-536