Detection of spontaneous and antigen-induced human interleukin-4 responses in vitro: comparison of ELISPOT, a novel ELISA and real-time RT-PCR

被引:68
作者
Ekerfelt, C [1 ]
Ernerudh, J
Jenmalm, MC
机构
[1] Linkoping Univ Hosp, Fac Hlth Sci, Clin Res Ctr, S-58185 Linkoping, Sweden
[2] Linkoping Univ Hosp, Fac Hlth Sci, Dept Hlth & Environm, Div Clin Immunol, S-58185 Linkoping, Sweden
[3] Linkoping Univ Hosp, Fac Hlth Sci, Dept Hlth & Environm, Div Paediat, S-58185 Linkoping, Sweden
关键词
IL-4; ELISPOT; ELISA; real-time PCR; pregnancy; atopy;
D O I
10.1016/S0022-1759(01)00520-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-4 (IL-4) is an important T-helper cell type 2 (Th2) cytokine in man, driving Th2 polarisation and exerting the most antagonistic effects to the Th1 cytokine interferon-gamma (IFN-gamma). Nevertheless, few data on spontaneous and antigen-specific secretion of IL-4 in man are available, mainly due to difficulties in the detection of IL-4, In this study, we compared three assays that can detect antigen-induced IL-4 responses; ELISPOT, ELISA after blocking the IL-4 receptor during cell culture, and real-time reverse transcription polymerase chain reaction (RT-PCR). Spontaneous, antigen- and allergen-induced responses were analysed in peripheral blood mononuclear cells from three groups with different secretion patterns for IL-4: atopic individuals, nonatopic individuals and pregnant women. ELISPOT displayed the highest sensitivity and was the only assay that could detect spontaneous secretion of IL-4 in all analysed samples. The IL-4 receptor blocking ELISA was considered best for the detection of in vitro antigen- and allergen-induced responses, since the results obtained from the ELISPOT and real-time RT-PCR displayed lower specificity, possibly because of seemingly aberrant IL-4 responses in the group of pregnant women. The real-time RT-PCR for detection of IL-4 mRNA proved to be sensitive, but expression of IL-4 mRNA was not correlated with the secretion of IL-4. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:55 / 67
页数:13
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