Respiratory syncytial virus predisposes mice to augmented allergic airway responses via IL-13-mediated mechanisms

被引:127
作者
Lukacs, NW
Tekkanat, KK
Berlin, A
Hogaboam, CM
Miller, A
Evanoff, H
Lincoln, P
Maassab, H
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Pediat, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, Ann Arbor, MI 48109 USA
关键词
D O I
10.4049/jimmunol.167.2.1060
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 development of severe childhood asthma may be influenced by several factors including environmental and infectious stimuli. The causal relationship between infectious viral responses, such as respiratory syncytial virus (RSV), and severe asthma during early childhood is unclear. In these studies, the ability for an initial RSV infection to exacerbate and promote a more severe asthmatic-type response was investigated by combining established murine models of disease. We examined the ability of RSV to induce exacerbation of allergic disease over a relatively long period, leading to development of severe airway responses including airway inflammation and hyperreactivity. The preferential production of IL-13 during a primary RSV infection appears to play a critical role for the exacerbation of cockroach allergen-induced disease. The depletion of IL-13 during RSV infections inhibited the exacerbation and acceleration of severe allergen-induced airway hyperreactivity. This was indicated by decreases in airway hyperreactivity and changes in lung chemokine production. These data suggest that the airway responses during asthma can be greatly affected by a previous RSV infection, even when infection occurs before allergen sensitization. Overall, infection of the airways with RSV can induce an IL-13-dependent change in airway function and promotes an environment that contributes to the development of severe allergic asthmatic responses.
引用
收藏
页码:1060 / 1065
页数:6
相关论文
共 47 条
[41]   The incidence of respiratory tract infection in adults requiring hospitalization for asthma [J].
Teichtahl, H ;
Buckmaster, N ;
Pertnikovs, E .
CHEST, 1997, 112 (03) :591-596
[42]   IL-13-induced airway hyperreactivity during respiratory syncytial virus infection is STAT6 dependent [J].
Tekkanat, KK ;
Maassab, HF ;
Cho, DS ;
Lai, JJ ;
John, A ;
Berlin, A ;
Kaplan, MH ;
Lukacs, NW .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :3542-3548
[43]  
TEKKANAT KK, IN PRESS AM J PATHOL
[44]   RSV AND CHRONIC ASTHMA [J].
WELLIVER, RC .
LANCET, 1995, 346 (8978) :789-790
[45]   Interleukin-13: Central mediator of allergic asthma [J].
Wills-Karp, M ;
Luyimbazi, J ;
Xu, XY ;
Schofield, B ;
Neben, TY ;
Karp, CL ;
Donaldson, DD .
SCIENCE, 1998, 282 (5397) :2258-2261
[46]   PURIFIED INTERLEUKIN-5 SUPPORTS THE TERMINAL DIFFERENTIATION AND PROLIFERATION OF MURINE EOSINOPHILIC PRECURSORS [J].
YAMAGUCHI, Y ;
SUDA, T ;
SUDA, J ;
EGUCHI, M ;
MIURA, Y ;
HARADA, N ;
TOMINAGA, A ;
TAKATSU, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (01) :43-56
[47]   Pulmonary expression of interleukin-13 causes inflammation, mucus hypersecretion, subepithelial fibrosis, physiologic abnormalities, and eotaxin production [J].
Zhou, Z ;
Homer, RJ ;
Wang, ZD ;
Chen, QS ;
Geba, GP ;
Wang, JM ;
Zhang, Y ;
Elias, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (06) :779-788