Bronchoalveolar lavage cell pattern from healthy human lung
Bronchoalveolar lavage cell pattern from healthy human lung
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DOI:
10.1111/j.1365-2249.2011.04529.x
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发表时间:
2012-03-01
影响因子:
4.6
通讯作者:
van Velzen-Blad, H.
中科院分区:
文献类型:
--
作者:
Heron, M.;Grutters, J. C.;van Velzen-Blad, H.
Bronchoalveolar lavage (BAL) is widely accepted as a key diagnostic procedure in interstitial lung diseases (ILD). We performed a study to obtain reference intervals of differential cell patterns in BAL fluid with special attention to the origin of lavage fluid, e.g. bronchial/alveolar, to atopy and smoking status and to age of the healthy people. We performed bronchoalveolar lavage in 55 healthy subjects with known atopy status (age: 18-64 years, non-smokers/smokers: 34/21) and determined differential cell counts and lymphocyte subsets in BAL fluid and blood. Moreover, in a subgroup of non-smoking healthy individuals we measured the expression of the regulatory T cell marker forkhead box protein 3 (FoxP3) on blood and BAL fluid lymphocytes in addition to a comprehensive set of activation markers. Differential cell counts from the alveolar lavage fraction differed significantly from calculated pooled fractions (n = 11). In contrast, marginal differences were found between atopic and non-atopic subjects. Interestingly, the BAL fluid CD4(+)/CD8(+) ratio correlated strongly with age (r2 = 0.50, P < 0.0001). We consider the bronchial and alveolar fraction to be lavage fluid from fundamentally different compartments and recommend analysis of the alveolar fraction in diagnostic work-up of ILD. In addition, our data suggest that age corrected BAL fluid CD4(+)/CD8(+) ratios should be used in the clinical evaluation of patients with interstitial lung diseases.