Respiratory syncytial virus-specific CD8+ memory T cell responses in elderly persons

被引:90
作者
de Bree, GJ
Heidema, J
van Leeuwen, EMM
van Bleek, GM
Jonkers, RE
Jansen, HM
van Lier, RAW
Out, TA
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Expt Immunol, NL-1100 DE Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Pulmonol, NL-1100 DE Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Div Nephrol & Clin Immunol & Rheumatol, NL-1100 DE Amsterdam, Netherlands
[4] Univ Utrecht, Wilhelmina Childrens Ctr, Univ Med Ctr, Div Pediat, Utrecht, Netherlands
关键词
D O I
10.1086/429695
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. We investigated respiratory syncytial virus (RSV)-specific CD8(+) memory T cell responses in healthy control participants (n = 31) and in patients with chronic obstructive pulmonary disease (COPD) n = 9), with respect to frequency, memory phenotype, and proliferative requirements. Methods. The properties of RSV-specific CD8(+) T cells were analyzed by use of RSV tetramers. The proliferative requirements of RSV-specific CD8(+) T cells were analyzed by culture of peripheral-blood mononuclear cells with RSV peptide in combination with distinct cytokines. Results. RSV-specific CD8(+) memory T cells showed a high level of expression of CD27 and interleukin-7R alpha and a low level of expression of CCR7. In the healthy participants, the frequency of RSV tetramer(+) CD8(+) T cells was significantly lower than the frequency of influenza virus A ( FLU) tetramer(+) CD8(+) T cells (P = .0001). In contrast to FLU tetramer+ CD8(+) T cells, we could detect RSV tetramer(+) CD8(+) T cells in the subgroup of elderly healthy participants ( age, >= 55 years) and in the patients with COPD only after in vitro expansion. Expanded RSV-specific T cells produced interferon-gamma and granzyme B. Conclusion. We provide evidence that a pool of functional RSV- specific CD8(+) memory T cells persists in the peripheral blood of healthy individuals and patients with COPD. Low numbers of RSV- specific memory T cells in the elderly and in patients with COPD may explain the increased susceptibility to RSV infection in these populations.
引用
收藏
页码:1710 / 1718
页数:9
相关论文
共 31 条
[1]   Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections [J].
Appay, V ;
Dunbar, PR ;
Callan, M ;
Klenerman, P ;
Gillespie, GMA ;
Papagno, L ;
Ogg, GS ;
King, A ;
Lechner, F ;
Spina, CA ;
Little, S ;
Havlir, DV ;
Richman, DD ;
Gruener, N ;
Pape, G ;
Waters, A ;
Easterbrook, P ;
Salio, M ;
Cerundolo, V ;
McMichael, AJ ;
Rowland-Jones, SL .
NATURE MEDICINE, 2002, 8 (04) :379-385
[2]   Constitutive CD27/CD70 interaction induces expansion of effector-type T cells and results in IFNγ-mediated B cell depletion [J].
Arens, R ;
Tesselaar, K ;
Baars, PA ;
van Schijndel, GMW ;
Hendriks, J ;
Pals, ST ;
Krimpenfort, P ;
Borst, J ;
van Oers, MHJ ;
van Lier, RAW .
IMMUNITY, 2001, 15 (05) :801-812
[3]   HLA class I-restricted cytotoxic T-cell epitopes of the respiratory syncytial virus fusion protein [J].
Brandenburg, AH ;
de Waal, L ;
Timmerman, HH ;
Hoogerhout, P ;
de Swart, RL ;
Osterhaus, ADME .
JOURNAL OF VIROLOGY, 2000, 74 (21) :10240-10244
[4]  
Brandenburg AH, 2000, J MED VIROL, V62, P267, DOI 10.1002/1096-9071(200010)62:2&lt
[5]  
267::AID-JMV20&gt
[6]  
3.0.CO
[7]  
2-8
[8]   CYTO-TOXIC T-CELLS CLEAR VIRUS BUT AUGMENT LUNG PATHOLOGY IN MICE INFECTED WITH RESPIRATORY SYNCYTIAL VIRUS [J].
CANNON, MJ ;
OPENSHAW, PJM ;
ASKONAS, BA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :1163-1168
[9]   HUMAN CYTOTOXIC T-CELLS STIMULATED BY ANTIGEN ON DENDRITIC CELLS RECOGNIZE THE N, SH, F, M, 22K, AND 1B PROTEINS OF RESPIRATORY SYNCYTIAL VIRUS [J].
CHERRIE, AH ;
ANDERSON, K ;
WERTZ, GW ;
OPENSHAW, PJM .
JOURNAL OF VIROLOGY, 1992, 66 (04) :2102-2110
[10]   Age-related impaired type 1 T cell responses to influenza: Reduced activation ex vivo, decreased expansion in CTL culture in vitro, and blunted response to influenza vaccination in vivo in the elderly [J].
Deng, YP ;
Jing, Y ;
Campbell, AE ;
Gravenstein, S .
JOURNAL OF IMMUNOLOGY, 2004, 172 (06) :3437-3446