Neurotrophins in bronchial asthma
© BioMed Central Ltd 2001
Received: 27 April 2001
Accepted: 11 June 2001
Published: 12 July 2001
Allergic bronchial asthma (BA) is characterized by chronic airway inflammation, development of airway hyperreactivity and recurrent reversible airway obstruction. T-helper 2 cells and their products have been shown to play an important role in this process. In contrast, the mechanisms by which immune cells interact with the cells residing in lung and airways, such as neurons, epithelial or smooth muscle cells, still remains uncertain. Sensory and motor neurons innervating the lung exhibit a great degree of functional plasticity in BA defined as 'neuronal plasticity'. These neurons control development of airway hyperresponsiveness and acute inflammatory responses, resulting in the concept of 'neurogenic inflammation'. Such quantitative and/or qualitative changes in neuronal functions are mediated to a great extent by a family of cytokines, the neurotrophins, which in turn are produced by activated immune cells, among others in BA. We have therefore developed the concept that neurotrophins such as nerve growth factor and brain-derived neurotrophic factor link pathogenic events in BA to dysfunctions of the immune and nervous system.
Keywordsbronchial asthma neurogenic inflammation neuronal plasticity neurotrophins
BA is a complex disease with several clinically well-defined pathogenic components, including recurrent reversible airway obstruction, chronic airway inflammation and development of airway hyperresponsiveness . The constituents of the inflammatory component have, in recent years, been relatively well characterized and defined. There is now overwhelming evidence that T cells play a central role in, particularly, allergic BA. Strong evidence supports the notion that T-helper 2 cells orchestrate allergic inflammation and control many important aspects of the effector phase response, including recruitment, activation and survival of eosinophils, activation of mast cells and IgE production. Reversible airway obstruction is pathogenetically related to mucus hypersecretion, development of local tissue edema as a consequence of acute inflammatory responses, and constriction of airway smooth muscle. Nonspecific bronchial hyperresponsiveness may be defined as an increase in the ease and degree of airway narrowing in response to a wide range of bronchoconstrictor stimuli. The development of airway hyperresponsiveness is mediated by multiple independent and additive pathways working in concert, which can be clinically tested using stimuli such as methacholine, histamine, exercise, cold air, capsaicin, and so on. Constriction of airway smooth muscle is largely controlled by sensory and motor neurons innervating the airways and the lung. The autonomic nerves that regulate many aspects of airway function, including airway smooth muscle tone, mucus secretion and bronchial microcirculation, can be functionally subdivided into cholinergic, adrenergic and nonadrenergic noncholinergic pathways.
Neurogenic inflammation and neuronal plasticity in BA
Sensory and motor neurons exhibit drastic functional changes in BA. These changes are defined by the term 'neuronal plasticity' . Increased levels of neuropeptides including substance P have been detected in the lungs of asthmatic patients [3,4]. Increased levels of Neurokinin A have been detected in bronchoalveolar lavage fluids of asthmatic patients following airway allergen challenge. Since cholinergic nerves represent the dominant bronchoconstrictor pathway, anticholinergic drugs are very effective bronchodilators in asthma therapy. This further underlines the importance of cholinergic mechanisms in the development of BA and airway hyperresponsiveness. The underlying mechanisms include enhanced reflex activity, increased mediator release, enhanced sensitivity of smooth muscle to neuropeptides and tachykinins, and increased density of receptor expression of both airway smooth muscle cells and neurons. In addition to qualitative changes in neuronal functions, debate still continues regarding whether quantitative changes in sensory and/or motor neurons also occur in this disease.
Neuropeptides and tachykinins are involved in several key features of BA, including airway smooth muscle constriction, vascular dilatation, increased vascular permeability, mucus hypersecretion and acceleration of airway inflammation. These effects attributed to the function of neuropeptides and tachykinins lead to the concept of 'neurogenic inflammation' in BA [5,6,7].
The functional plasticity of sensory and motor neurons is under close control of neurotrophins. The neurotrophins nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 and neurotrophin-4/neurotrophin-5 belong to a family of homologous proteins that exert their effects primarily as target-derived paracrine or autocrine neurotrophic factors. The role of the neurotrophins in survival, differentiation and maintenance of neurons is defined well . They exhibit partially overlapping but distinct patterns of expression and cellular targets. In addition to the effects in the central nervous system, neurotrophins also effect peripheral afferent and efferent neurons. The biological effects of neurotrophins are mediated by binding either to the high affinity (KD10-11) tyrosine kinese receptors (trkA, trkB, trkC) or the low affinity (KD10-9) pan-neurotrophin receptor p75NTR. Substantial biological effects of neurotrophins are mediated by the high affinity kinese receptors. The high affinity effector for NGF is trkA, that for BDNF and neurotrophin-4 is trkB, and that for neurotrophin-3 is trkC. Neurotrophin receptors are widely expressed on the neurons of the peripheral and the central nervous system, both during development and in adults. However, trk receptors as well as p75NTR are also expressed on non-neuronal cells, including immune cells, muscle cells and epithelial cells.
The traditional cellular sources of neurotrophins under physiological conditions are primarily nerve-associated cells such as glia cells, Schwann cells or fibroblasts and neurons themselves [8,9]. NGF is also produced in inflammatory processes by a wide range of hematopoetic cells, including mast cells , macrophages , T cells  and B cells . This has been shown in a well-characterized animal model system of allergic airway inflammation and airway hyperresponsiveness [11,14,15]. In addition, airway epiphilium constitutively expresses BDNF but not NGF, and BDNF production is further enhanced during inflammatory responses. Further to animal model systems, enhanced neurotrophin production has also been shown in patients with several allergic conditions. The initial report of enhanced NGF production was provided by Bonini et al, indicating that patients with severe allergic BA display high serum levels of NGF . Furthermore, increases in NGF serum levels have been demonstrated in patients with vernal ceratonconjunctivities and allergic rhinoconjunctivities . Together with the group of Virchow et al, we have more recently shown that neurotrophin production is increased in bronchoalveolar lavage fluids from patients undergoing segmental allergen provocation. BDNF and NGF levels were particularly increased 18 hours after provocation, whereas no increases were detected 20 min after provocation . These data again indicate local production and release of neurotrophins on stimulation, and increased levels of neurotrophins are associated with late-phase allergic responses, but not with the early-phase response.
In parallel, neurotrophins also exhibit profound effects on immune cells residing in airways and lung tissue. These effects are described by the term 'immunological plasticity'. In this regard, neurotrophins act as amplifiers of the locally occurring immune dysbalance. This effect has so far exclusively been demonstrated for NGF, but not for BDNF. NGF augments the production of IL-4 and IL-5 but not IFN-γ on activation of lymphocytes with allergen. Furthermore, these increases result in enhanced levels of IgE and IgG1 but not IgG2a antibodies .
It is important to note that the effects of neurotrophins are not immediate, but rather long acting. In this context, we propose the concept that neurotrophins act as intermediate or long-acting modulators of neuronal and immune functions in the pathogenesis of BA. Data on the kinetics of local neurotrophin production (manuscript in preparation) support this concept because peak levels of neurotrophin content in bronchoalveolar lavage fluid have been detected 7–10 days following local allergen challenges, and these levels return to baseline level no sooner than 3 weeks after allergen provocation.
Further experiments are certainly required to further evaluate this concept. Treatment modalities particularly need to be explored, aimed to locally antagonize increased neurotrophin production. Neurotrophins may, however, represent the 'common' trunk of immune and nerve cell modulators. This may lead to similar clinical signs and symptoms (e.g. airway hyperresponsiveness and airway obstruction owing to enhanced airway smooth muscle contractility, mucus hypersecretion and edema) observed in asthma patients, regardless of the underlying cause (e.g. allergen-induced asthma, airway hyperresponsiveness in association with viral infections, exercise-induced asthma, etc.).
brain-derived neurotrophic factor
nerve growth factor.
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