Cytokine response after severe respiratory syncytial virus bronchiolitis in early life.
Cytokine response after severe respiratory syncytial virus bronchiolitis in early life.
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DOI:
10.1016/j.jaci.2008.07.010
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发表时间:
2008-10
影响因子:
14.2
通讯作者:
Bacharier, Leonard B.
中科院分区:
文献类型:
--
作者:
Castro, Mario;Schweiger, Toni;Yin-DeClue, Huiquing;Ramkumar, Thiruvamoor P.;Christie, Chandrika;Zheng, Jie;Cohen, Rebecca;Schechtman, Kenneth B.;Strunk, Robert;Bacharier, Leonard B.
Immune response following viral infection usually involves Th1-mediated response; however, severe respiratory syncytial virus (RSV) infection appears to be associated with the development of asthma, a Th2-predominant phenotype. To understand the early and subsequent immunologic response to a serious RSV infection in children over time. 206 previously healthy infants hospitalized with severe RSV bronchiolitis were enrolled in a prospective cohort called the RSV Bronchiolitis in Early Life (RBEL) study. Peripheral blood T cells were obtained immediately following RSV infection and at 2, 4 and 6 years of age, stimulated with PMA and ionomycin, and analyzed for interleukin (IL)-2, -4, and - 13 and interferon-γ (IFN-γ) by flow cytometry and real time PCR. 48% (n=97) of the children developed asthma (physician-diagnosed) and 48% (n=97) had eczema by age 6. 32% (n=48 of 150) developed allergic sensitization by 3 yrs of age. Children with asthma had lower IL-13 expression at 6 yrs of age than those without (p=0.001). IFN-γ, IL-2 and -4 levels did not differ by asthma or eczema status during follow-up (all p>0.05). Allergic sensitization was not associated with differences in cytokine levels during follow-up (all p>0.05). Severe RSV infection early in life is associated with a high incidence of asthma and eczema. Contrary to expectations, subsequent immunologic development in those who developed asthma, eczema or allergic sensitization was not associated with a Th2 phenotype in the peripheral blood.
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DOI:
10.1097/01.asn.0000071514.36428.61
发表时间:
2003-07-01
影响因子:
13.6
作者:
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通讯作者:
MacDougall, IC
DOI:
10.1164/rccm.200210-1148oc
发表时间:
2003-09-15
影响因子:
24.7
作者:
Legg, JP;Hussain, IR;Warner, JO
通讯作者:
Warner, JO
影响因子:
3.8
作者:
Overbergh, L;Valckx, D;Mathieu, C
通讯作者:
Mathieu, C
影响因子:
4.3
作者:
Chipeta, J;Komada, Y;Sakurai, M
通讯作者:
Sakurai, M
DOI:
10.1084/jem.20040035
发表时间:
2004-07-05
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
de Heer HJ;Hammad H;Soullié T;Hijdra D;Vos N;Willart MA;Hoogsteden HC;Lambrecht BN
通讯作者:
Lambrecht BN