Hypersensitivity pneumonitis


Hypersensitivity pneumonitis or extrinsic allergic alveolitis is a rare immune system disorder that affects the lungs. It is an inflammation of the alveoli within the lung caused by hypersensitivity to inhaled organic dusts. Sufferers are commonly exposed to the dust by their occupation or hobbies.

Signs and symptoms

Hypersensitivity pneumonitis is categorized as acute, subacute, and chronic based on the duration of the illness.

Acute

In the acute form of HP, symptoms may develop 4–6 hours following heavy exposure to the provoking antigen. Symptoms include fever, chills, malaise, cough, chest tightness, dyspnea, rash, swelling and headache. Symptoms resolve within 12 hours to several days upon cessation of exposure.
Acute HP is characterized by poorly formed noncaseating interstitial granulomas and mononuclear cell infiltration in a peribronchial distribution with prominent giant cells.
On chest radiographs, a diffuse micronodular interstitial pattern may be observed. Findings are normal in approximately 10% of patients." In high-resolution CT scans, ground-glass opacities or diffusely increased radiodensities are present. Pulmonary function tests show reduced diffusion capacity of lungs for carbon monoxide. Many patients have hypoxemia at rest, and all patients desaturate with exercise. Extrinsic allergic alveolitis may eventually lead to Interstitial lung disease.

Subacute

Patients with subacute HP gradually develop a productive cough, dyspnea, fatigue, anorexia, weight loss, and pleurisy. Symptoms are similar to the acute form of the disease, but are less severe and last longer. On chest radiographs, micronodular or reticular opacities are most prominent in mid-to-lower lung zones. Findings may be present in patients who have experienced repeated acute attacks.
The subacute, or intermittent, form produces more well-formed noncaseating granulomas, bronchiolitis with or without organizing pneumonia, and interstitial fibrosis.

Chronic

In chronic HP, patients often lack a history of acute episodes. They have an insidious onset of cough, progressive dyspnea, fatigue, and weight loss. This is associated with partial to complete but gradual reversibility. Avoiding any further exposure is recommended. Clubbing is observed in 50% of patients. Tachypnea, respiratory distress, and inspiratory crackles over lower lung fields often are present.
On chest radiographs, progressive fibrotic changes with loss of lung volume particularly affect the upper lobes. Nodular or ground-glass opacities are not present. Features of emphysema are found on significant chest films and CT scans.
Chronic forms reveal additional findings of chronic interstitial inflammation and alveolar destruction associated with dense fibrosis. Cholesterol clefts or asteroid bodies are present within or outside granulomas.
In addition, many patients have hypoxemia at rest, and all patients desaturate with exercise.

Pathophysiology

Hypersensitivity pneumonitis involves inhalation of an antigen. This leads to an exaggerated immune response. Type III hypersensitivity and type IV hypersensitivity can both occur depending on the cause.

Diagnosis

The diagnosis is based upon a history of symptoms after exposure to the allergen and clinical tests. A physician may take blood tests, seeking signs of inflammation, a chest X-ray and lung function tests. The sufferer shows a restrictive loss of lung function.
Precipitating IgG antibodies against fungal or avian antigens can be detected in the laboratory using the traditional Ouchterlony immunodiffusion method wherein 'precipitin' lines form on agar plate. The ImmunoCAP technology has replaced this time-consuming, labor-intensive method with their automated CAP assays and FEIA that can detect IgG antibodies against Aspergillus fumigatus or avian antigens.
Although overlapping in many cases, hypersensitivity pneumonitis may be distinguished from occupational asthma in that it is not restricted to only occupational exposure, and that asthma generally is classified as a type I hypersensitivity. Unlike asthma, hypersensitivity pneumonitis targets lung alveoli rather than bronchi.

Lung biopsy

Lung biopsies can be diagnostic in cases of chronic hypersensitivity pneumonitis, or may help to suggest the diagnosis and trigger or intensify the search for an allergen. The main feature of chronic hypersensitivity pneumonitis on lung biopsies is expansion of the interstitium by lymphocytes accompanied by an occasional multinucleated giant cell or loose granuloma.
When fibrosis develops in chronic hypersensitivity pneumonitis, the differential diagnosis in lung biopsies includes the idiopathic interstitial pneumonias. This group of diseases includes usual interstitial pneumonia, non-specific interstitial pneumonia and cryptogenic organizing pneumonia, among others.
The prognosis of some idiopathic interstitial pneumonias, e.g. idiopathic usual interstitial pneumonia, are very poor and the treatments of little help. This contrasts the prognosis for hypersensitivity pneumonitis, which is generally fairly good if the allergen is identified and exposures to it significantly reduced or eliminated. Thus, a lung biopsy, in some cases, may make a decisive difference.

Types

Hypersensitivity pneumonitis may also be called many different names, based on the provoking antigen. These include:
TypeSpecific antigenExposure--
Bird fancier's lung
Also called bird breeder's lung, pigeon breeder's lung, and poultry worker's lung
Avian proteinsFeathers and bird droppings--
Bagassosis
Exposure to moldy molasses
Thermophilic actinomycetesMoldy bagasse --
Cephalosporium HP CephalosporiumContaminated basements --
Cheese-washer's lungPenicillum casei or P. roquefortiCheese casings--
Chemical worker's lung – Isocyanate HPToluene diisocyanate, Hexamethylene diisocyanate, or Methylene bisphenyl isocyanate Paints, resins, and polyurethane foams--
Chemical worker's lung – Trimellitic anhydride HPTrimellitic anhydridePlastics, resins, and paints--
Coffee worker's lungCoffee bean proteinCoffee bean dust--
Compost lungAspergillusCompost--
Detergent worker's diseaseBacillus subtilis enzymesDetergent--
Familial HP
Also called Domestic HP
Bacillus subtilis, puffball sporesContaminated walls--
Farmer's lungThe molds
  • Aspergillus species
The bacteria
  • Thermophilic actinomycetes
  • Thermoactinomyces vulgaris
  • Saccharopolyspora rectivirgula
  • Absidia corymbifera
  • Eurotium amstelodami
Moldy hay--
Hot tub lungMycobacterium avium complexMist from hot tubs--
Humidifier lungThe bacteria
  • Thermoactinomyces candidus
  • Bacillus subtilis
  • Bacillus cereus, and Klebsiella oxytoca;
  • Thermophilic actinomycetes
  • The fungi
    The amoebae
    • Naegleria gruberi,
    • Acanthamoeba polyhaga, and
    • Acanthamoeba castellani.
    Mist generated by a machine from standing water--
    Japanese summer house HP Also called Japanese summer-type HPTrichosporon cutaneumDamp wood and mats--
    Laboratory worker's lungMale rat urine proteinLaboratory rats--
    LycoperdonosisPuffball sporesSpore dust from mature puffballs--
    Malt worker's lungAspergillus clavatusMoldy barley--
    Maple bark diseaseCryptostroma corticaleMoldy maple bark--
    Metalworking fluids HPNontuberculous mycobacteriaMist from metalworking fluids--
    Miller's lungSitophilus granarius Dust-contaminated grain--
    Mollusc shell HPAquatic animal proteinsMollusc shell dust--
    Mushroom worker's lungThermophilic actinomycetesMushroom compost--
    Peat moss worker's lungCaused by Monocillium sp. and Penicillium citreonigrumPeat moss--
    Pituitary snuff taker's lungPituitary snuffMedication --
    Potato peeler's lungPotatococcus, Potato skin sppPotato dipped in immune globulins--
    Sauna worker's lungAureobasidium, Graphium sppContaminated sauna water--
    SequoiosisAureobasidium, Graphium sppRedwood bark, sawdust--
    Streptomyces HPStreptomyces albusContaminated fertilizer--
    SuberosisPenicillium glabrum Moldy cork dust--
    Tap water HPUnknownContaminated tap water--
    Thatched roof diseaseSaccharomonospora viridisDried grass--
    Tobacco worker's lungAspergillus sppMoldy tobacco--
    Trombone Player's lung Mycobacterium chelonaeVarious Mycobacteria inside instruments
    Well-emptier's lungWellercoccus sppContaminated well water--
    Wine-grower's lungBotrytis cinerea moldMoldy grapes--
    Woodworker's lungAlternaria, Penicillium sppWood pulp, dust--
    Of these types, Farmer's Lung and Bird-Breeder's Lung are the most common. "Studies document 8-540 cases per 100,000 persons per year for farmers and 6000-21,000 cases per 100,000 persons per year for pigeon breeders. High attack rates are documented in sporadic outbreaks. Prevalence varies by region, climate, and farming practices. HP affects 0.4–7% of the farming population. Reported prevalence among bird fanciers is estimated to be 20-20,000 cases per 100,000 persons at risk."

    Treatment

    The best treatment is to avoid the provoking allergen, as chronic exposure can cause permanent damage. Corticosteroids such as prednisolone may help to control symptoms but may produce side-effects.

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