A Pilot Feasibility Study of Detection of IL-11 and Other Cytokines in the Exhaled Breath Condensate (EBC) and Blood of Healthy Volunteers

IL-11 has been proven to be highly expressed in lungs of patients with idiopathic pulmonary fibrosis (IPF), a type of interstitial lung disease (ILD). An IL-11 neutralizing antibody has been shown to diminish lung inflammation and fibrosis in bleomycin induced lung fibrosis in mice model. In this study, IL-11 has also been shown to be expressed in samples of human lungs with IPF. The mechanism had been shown to be linked to reduction of fibroblast proliferation and activity.

The identification of individuals with different sub-types of lung fibrosis can be based on symptoms, lung function tests, radiology or even lung biopsies. However, all these methods are rather subjective and sometimes invasive but yet inconclusive. So to identify individual patients whom IL-11 may play a role in their disease processes, investigators propose to use IL-11 in EBC as a biomarker to identify these patients.

The design of this pilot study is; prospective, single arm, non-interventional study involving invasive investigations

1. Procedures/ investigations
2. Blood taking (venepuncture)
3. Exhaled breath condensate (EBC) collection method- this involved breathing in and out through a disposable device (akin to breathing onto cold glass to produce condensate) with an external cooler device. The R Tube starter kit is a complete disposable EBC collection kit that is FDA approved in USA. It has been used in many research clinical investigations. Investigators prefer completely disposable kits (not just mouthpiece).

Laboratory method in detection and quantification of IL-11 (ELISA)- Investigators will use the Human IL-11 Quantikine ELISA kit (#D1100, R\&D Systems) to measure IL-11 concentrations in serum/ plasma, and EBC. This immunoassay has been used by Prof Cook's team for accurate quantification of IL-11 concentrations within the assay ranges of 31.2 - 2,000 pg/mL in studies, and possess a similar a detection range to that of another IL-11 ELISA kit used in a prior publication which quantified IL-11 concentrations in the serum and EBC. Each ELISA kit allows for simultaneous detection in up to 96 samples (including duplicates and standards). The assay employs the quantitative sandwich ELISA technique. Investigators may also use similar technique to examine the whole range of other interleukins which involved in lung fibrosis.

The use of EBC to detect IL-11 has been previously shown to be feasible and detectable in healthy volunteers. In that series, it was demonstrated that IL-11 levels were significantly increased in patients with NSCLC. Investigators first need to reproduce the feasibility of detection of IL-11 in EBC of healthy volunteers and use this as a reference range for levels of IL-11 in EBC of patients with fibrosis. IL-11 has previously been shown to be detectable in serum of human patients with pancreatitis by ELISA kits too. If this is the case, investigators can propose to use IL-11 as a screening tool, to identify patients who may benefit from IL-11 neutralizing antibody when this is available in humans.

Other interleukins which have been shown to contribute to lung fibrosis are IL-1B and IL-5, in rat animal models, by promoting inflammation. IL-9, IL-10, and IL-17 on the other hand are protective in lung fibrosis. IL-12 inhibits collagen synthesis. IL-2, IL-4, IL-6, IL-13, IL-18 and IL-37 have also been shown to contribute to lung fibrosis through cell proliferation and fibroblasts activation, rather than direct inflammation. More importantly, IL-2, IL-6, IL-8, IL-10, and IL-12 have been shown to be increased in sera of patients with IPF compared to healthy volunteers.