Bronchiolitis obliterans is also known as obliterative bronchiolitis or constrictive bronchiolitis. When it occurs after lung transplantation or hematopoietic stem cell transplantation (HSCT), it is called bronchiolitis obliterans syndrome. Bronchiolitis obliterans is a type of obstructive lung disease of the small airways. It is a rare disease with characteristic features of fibrosis of terminal and distal bronchioles and spirometry showing airflow obstruction. It usually leads to a progressive decline in lung function and has variable outcomes.
Several risk factors can lead to the development of bronchiolitis obliterans. It is one of the most common noninfectious complications after lung transplant and hematopoietic stem cell transplantation. Other etiologies of bronchiolitis obliterans include exposure to inhaled toxins and gases, including sulfur mustard gas, nitrogen oxides, diacetyl (used as popcorn flavoring), fly ash, and fiberglass. Bronchiolitis obliterans is also associated with autoimmune disorders, especially rheumatoid arthritis, SLE, and less commonly with inflammatory bowel disease. It is also known to occur after a respiratory viral infection (adenovirus, respiratory syncytial virus), especially in children. Other infections associated with bronchiolitis obliterans are HIV, Postinfectious (mycoplasma, bacteria, fungi), and Human Herpes Virus (HHV) 8. Rare conditions like Castleman disease and paraneoplastic pemphigus have also been associated with bronchiolitis obliterans. Other associations include microcarcinoid tumorlets and Cryptogenic constrictive bronchiolitis.
Bronchiolitis obliterans syndrome is considered a form of chronic allograft rejection after lung transplantation. The majority of lung transplant recipients who are long term survivors develop bronchiolitis obliterans syndrome. More than 50% of recipients will develop some degree of BO by 5 years post-transplant. The average time to diagnose BO is 16 to 20 months after lung transplant but has been reported as early as 3 months after transplantation. About 5% to 14% of Hematopoietic stem cell transplantation (HSCT) recipients also develop bronchiolitis obliterans syndrome, which is pulmonary graft vs. host disease and can present several months to years later after transplantation.
There is inflammation of sub-epithelial structures and dysregulated repair in response to injury from inhalational toxins or autoimmune responses, leading to fibroproliferation and abnormal regeneration of epithelium of the small airways. Histopathology classically demonstrates the involvement of terminal and respiratory bronchioles (distal small airways) but without significant changes in alveolar spaces and distal lung parenchyma. Hypertrophy of the smooth muscles of the bronchioles, peribronchiolar inflammatory infiltrates, accumulation of mucus in the bronchiolar lumen, and bronchiolar scarring can be noted in bronchiolitis obliterans. There is a concentric narrowing of the lumen of the bronchioles by inflammatory fibrosis. There may even be complete occlusion of the lumen in some cases.
In lung transplantation, microvascular insufficiency and alloimmune responses to the transplanted lung may result in airway injury and the development of bronchiolitis obliterans syndrome. Episodes of acute cellular rejection, HLA antibodies, and gastroesophageal reflux disease with microaspiration have been shown to increase the risk of developing bronchiolitis obliterans syndrome after transplantation.
In bronchiolitis obliterans associated with paraneoplastic pemphigus, autoantibodies against desmoglein and plakin protein are found in both cutaneous and respiratory epithelium have been implicated.
Bronchiolitis obliterans characteristically presents with dyspnea and cough that is persistent and progressive. Some may also have wheezing. Symptoms usually develop over weeks to months and are not episodic, unlike asthma. History may also elicit recent exposure to toxic fumes or gases, viral infections, symptoms of joint stiffness in cases of rheumatoid arthritis, prior lung, or hematopoietic stem cell transplantation.
A physical exam may reveal decreased breath sounds and a prolonged expiratory phase with or without wheeze, usually in the inspiratory and expiratory phase. Rales may also be noted in some cases. Cases of bronchiolitis obliterans associated with Castleman’s disease may also have paraneoplastic pemphigus, which may present with oral ulcers as well as lymphadenopathy.
Pulmonary function testing is essential for diagnosis. Spirometry demonstrates airflow obstruction that does not reverse with inhaled bronchodilator challenge. Forced expiratory volume in one second (FEV1) will be reduced, and the ratio of FEV1 to forced vital capacity (FEV1/FVC) is also reduced. Hyperinflation may occur, and hence total lung capacity (TLC) may be increased with air trapping. Diffusion capacity (DLCO) is usually reduced. The degree of FEV1 decline from post-transplant value determines the stage of bronchiolitis obliterans syndrome in lung transplant.
Chest radiographs may be normal in early disease or show signs of hyperinflation. Chest CT imaging may show bronchial wall thickening, mosaic pattern with patchy areas of hypo attenuation. If there are dynamic images with inspiratory and expiratory films, a mosaic pattern persists due to air trapping from small airway disease.
Bronchoscopy can be performed if other causes of airflow obstruction are suspected like endobronchial tumors or sarcoid but might be unrevealing in bronchiolitis obliterans. A lung biopsy is usually not necessary for diagnosis in the setting of classic symptoms, air trapping on imaging, airflow obstruction on spirometry in the setting of organ transplantation, or toxic inhalational injury. If required for diagnosis, surgical lung biopsy is preferred over transbronchial biopsy since it involves distal bronchioles and not parenchyma. Also, the sensitivity by transbronchial biopsy for the diagnosis of BO is low (range 15 to 87%). In cases following lung transplantation, a biopsy is not required to diagnose bronchiolitis obliterans syndrome but may be required to exclude other causes of deterioration lung function like infection or acute rejection. Spirometry showing obstructive pattern is necessary for diagnosis.
Treatment of bronchiolitis obliterans syndrome after lung transplant involves augmenting immunosuppression since it is thought to be a form of chronic rejection. Hence, increasing or adding immunosuppressive agents like tacrolimus, cyclosporine, mycophenolate mofetil, and prednisone has been used to treat bronchiolitis obliterans syndrome after transplant. Azithromycin has also been shown to decrease the incidence of bronchiolitis obliterans syndrome and improvement in lung function. The combination of inhaled fluticasone, oral montelukast, and azithromycin triple therapy has also been shown to decrease the decline in lung function in bronchiolitis obliterans syndrome post-HSCT. In addition to these therapies, controlling gastroesophageal reflux is also recommended to decrease bronchiolitis obliterans syndrome. In cases where bronchiolitis obliterans syndrome is progressive and severe, then retransplantation of a lung may be indicated. Extracorporeal photopheresis has also been successfully used to slow the decline in lung function from bronchiolitis obliterans syndrome. In non-transplant related bronchiolitis obliterans, removal from offending agents is essential. Immunosuppression with corticosteroids and cytotoxic agents like cyclophosphamide has been used for bronchiolitis obliterans related to rheumatoid arthritis but has not been beneficial for bronchiolitis obliterans from toxic inhalation or post-infectious etiology. In these patients, symptomatic treatment should be provided with cough suppressants, inhaled bronchodilators, and oxygen supplementation if needed.
Clinical Staging System for Bronchiolitis Obliterans Syndrome (BOS)
|BOS-0||No BO||FEV1 >90% of baseline and FEF25-75% >75% of baseline|
|BOS 0-p||Potential BO||FEV1 81 to 90% of baseline and/or FEF25-75% ≤ 75% of baseline|
|BOS 1||Mild BO||FEV1 66% to 80% of baseline|
|BOS 2||Moderate BO||FEV1 51 % to 65% of baseline|
|BOS 3||Severe BO||FEV1 ≤ 50% of baseline|
Each stage is subdivided into a and b, where a is without histologic documentation of OB, and b is with histologic documentation of OB.
The prognosis of bronchiolitis obliterans depends on the underlying pathology. Some patients achieve complete improvement; however, those with constrictive disease generally demonstrate a more progressive course, but at present, there is insufficient research to provide a statistical correlation. Lung function often deteriorates over time, so patients will usually need to have repeated lung testing throughout their lives. Progressive disease may require supplemental oxygen or mechanical ventilation in very severe cases. The worst cases may require a lung transplant.
Patients with bronchiolitis obliterans demonstrate an increased risk of developing lung infections, including bronchitis and pneumonia. With bronchiolitis obliterans, these infections are more likely to become severe, resulting in baseline respiratory symptoms that are substantially worse than persons who do not have this condition.
Patients need to be counseled regarding medication and therapy adherence, to remain active within the limitations of their respiratory limitations, and to return for lung function testing to monitor for disease progression.
The diagnosis and management of bronchiolitis obliterans is done with a multidisciplinary team that includes a transplant surgeon, pulmonologist, pathologist, radiologist, internist, nurse practitioner, and a pharmacist. The condition has no cure and is progressive. Most patients need some type of medical therapy to relieve the symptoms. Retransplant is an option but most patients are frail and not fit for surgery. Patients managed with corticosteroids and cytotoxic drugs also develop a whole host of adverse drug reactions.
|||Kavaliunaite E,Aurora P, Diagnosing and managing bronchiolitis obliterans in children. Expert review of respiratory medicine. 2019 Feb 23; [PubMed PMID: 30798629]|
|||Rao U,Sharma M,Mohanakumar T,Ahn C,Gao A,Kaza V, Prevalence of antibodies to lung self-antigens (Kα1 tubulin and collagen V) and donor specific antibodies to HLA in lung transplant recipients and implications for lung transplant outcomes: Single center experience. Transplant immunology. 2019 Feb 20; [PubMed PMID: 30794945]|
|||Shabrawishi M,Qanash SA, Bronchiolitis Obliterans After Cefuroxime-Induced Stevens-Johnson Syndrome. The American journal of case reports. 2019 Feb 9; [PubMed PMID: 30737366]|
|||Chambers DC, Bronchiolitis obliterans syndrome 'endotypes' in haematopoietic stem cell transplantation. Respirology (Carlton, Vic.). 2019 Feb 7; [PubMed PMID: 30730090]|
|||Colom AJ,Teper AM, Post-infectious bronchiolitis obliterans. Pediatric pulmonology. 2019 Feb; [PubMed PMID: 30548423]|
|||Bondeelle L,Bergeron A, Managing pulmonary complications in allogeneic hematopoietic stem cell transplantation. Expert review of respiratory medicine. 2018 Dec 7; [PubMed PMID: 30523731]|
|||Wieruszewski PM,Herasevich S,Gajic O,Yadav H, Respiratory failure in the hematopoietic stem cell transplant recipient. World journal of critical care medicine. 2018 Oct 16; [PubMed PMID: 30370228]|
|||Williams KM, How I treat bronchiolitis obliterans syndrome after hematopoietic stem cell transplantation. Blood. 2017 Jan 26; [PubMed PMID: 27856461]|
|||Cheng GS,Storer B,Chien JW,Jagasia M,Hubbard JJ,Burns L,Ho VT,Pidala J,Palmer J,Johnston L,Mayer S,Crothers K,Pusic I,Lee SJ,Williams KM, Lung Function Trajectory in Bronchiolitis Obliterans Syndrome after Allogeneic Hematopoietic Cell Transplant. Annals of the American Thoracic Society. 2016 Nov; [PubMed PMID: 27513368]|
|||Sheth JS,Belperio JA,Fishbein MC,Kazerooni EA,Lagstein A,Murray S,Myers JL,Simon RH,Sisson TH,Sundaram B,White ES,Xia M,Zisman D,Flaherty KR, Utility of Transbronchial vs Surgical Lung Biopsy in the Diagnosis of Suspected Fibrotic Interstitial Lung Disease. Chest. 2017 Feb; [PubMed PMID: 27729263]|
|||Yang X,Kong J,Yang MX,Xie WP,Wang H,Rong R,Kong H, [Analysis of clinical characteristics of 21 cases of acute fibrinous and organizing pneumonia]. Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases. 2020 Aug 12; [PubMed PMID: 32727179]|
|||Ren D,Kaleekal TS,Graviss EA,Nguyen DT,Sinha N,Goodarzi A,Agboli I,Suarez EE,Loebe M,Scheinin SA,Bruckner BA, Retransplantation Outcomes at a Large Lung Transplantation Program. Transplantation direct. 2018 Nov; [PubMed PMID: 30534595]|
|||Hakim A,Cooke KR,Pavletic SZ,Khalid M,Williams KM,Hashmi SK, Diagnosis and treatment of bronchiolitis obliterans syndrome accessible universally. Bone marrow transplantation. 2018 Jul 23; [PubMed PMID: 30038355]|