Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by deteriorated exocrine gland function with associated lymphocytic infiltration. However, there are few pathological studies on bronchial glands in SS. In this study, we aimed to clarify pathological features of bronchial glands in SS.
Methods
We retrospectively evaluated infiltration of lymphocytes in the bronchial glands incidentally collected by transbronchial lung cryobiopsy (TBLC), which were performed for the diagnosis of diffuse lung diseases. The degrees of lymphocyte infiltration in the bronchial glands were classified into four grades (grade 0–3). We compared the degrees of infiltration of SS with those of other diffuse lung diseases.
Results
TBLC for diagnosis of diffuse lung diseases were performed on 432 cases during the study period. The samples of 50 cases included bronchial glands. Of those, 20 cases were excluded due to insufficient size or influence of therapy. The remaining 30 cases included 17 of idiopathic interstitial pneumonias, 5 of chronic hypersensitivity pneumonia, 6 of connective tissue disease (SS; n = 4, systemic sclerosis; n = 1, dermatomyositis; n = 1) and 2 of other diseases. In SS, infiltration of lymphocytes was observed in all cases; grade 1 in one, grade 2 in one, and grade 3 in two cases. In contrast, 11 of 26 in other diseases showed no lymphocytes infiltration, with the remaining 15 of grade 1 infiltration. Grade 2 or more infiltration were found only in SS but not in other diseases.
Conclusion
Our results suggested that high-grade lymphocytic infiltration of bronchial glands is a distinct characteristics in SS.
Hinweise
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
SS
Sjögren’s syndrome
TBLC
Transbronchial lung cryobiopsy
SLB
Surgical lung biopsy
IIPs
Idiopathic interstitial pneumonias
cHP
Chronic hypersensitivity pneumonia
SSc
Systemic sclerosis
DM
Dermatomyositis
GPA
Granulomatosis with polyangitis
MALT
Mucosa associated lymphoid tissue
IPF
Idiopathic pulmonary fibrosis
NSIP
Nonspecific interstitial pneumonia
COP
Cryptogenic organizing pneumonia
UCIIPs
Unclassifiable idiopathic interstitial pneumonia
Background
Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by deteriorated salivary and lacrimal gland function with lymphocytic infiltration of exocrine glands. Not only salivary and lacrimal glands but also various extraglandular organ systems such as lung and kidney are affected in SS. Bronchial glands are morphologically similar to salivary glands. Salivary gland biopsy is a technique broadly applied for the diagnosis of SS [1‐3]. High-grade lymphocyte infiltration in salivary gland is observed in SS. However, there are very few literatures that describe the characteristics of cell infiltration and histopathological changes in the bronchial glands of SS.
Recently, the utility of transbronchial lung cryobiopsy (TBLC) has been reported in the diagnosis of diffuse lung disease [4‐7]. Cryoprobe-retrieved specimens are larger than those of transbronchial forceps biopsies and less crush. TBLC tend to sample more proximal portion of the lung apart from the pleural than surgical lung biopsy (SLB). Although bronchial glands are rarely collected by SLB or transbronchial forceps biopsy, they are sometimes incidentally biopsied by TBLC. In this study, we aimed to clarify whether high-grade lymphocytic infiltration in the bronchial glands was observed as a distinct feature in SS.
Anzeige
Methods
Patients
We retrospectively reviewed all the specimens collected by TBLC, which were performed for the diagnosis of diffuse lung diseases between May 2017 and October 2018 in Kanagawa Cardiovascular and Respiratory Center. Among those, specimens incidentally including the bronchial glands were extracted (Fig. 1). The exclusion criteria of this study were as follows: (1) the size of biopsied bronchial glands was small (< 0.05mm2); (2) medication such as steroids or immunosuppressant have already been given before biopsy. Institutional review board of Kanagawa Cardiovascular and Respiratory Center approved the study protocol (KCRC-19-0032).
Fig. 1
Bronchial glands that were collected by transbronchial lung cryobiopsy. The bronchus with cartilage was biopsied. Head arrows show bronchial glands
×
The procedure of transbronchial cryobiopsy
The patients were intubated with flexible endotracheal tube using moderate to deep sedation. Sedative agents were midazolam plus fentanyl. Balloon blocker (Edwards Lifesciense, Fogarty E-80-4F) was routinely placed balloon blocker in the targeted sub-segmental bronchi. A 1.9 mm or 2.4 mm cryoprobe (Erbe Elektromedizin GmBH) was introduced through the working channel of a flexible bronchoscope under fluoroscopic guidance into the selected bronchi. Freezing time of cryoprobe was 6–7 s with 1.9 mm probe and 4–5 s with 2.4 mm probe.
Scoring of lymphocytes and plasma cells infiltration in bronchial glands
Lymphocytes and plasma cells infiltration in bronchial glands were classified into four grades from 0 to 3 (Fig. 2). A “focus” was defined an aggregate of 50 or more lymphocytes and plasma cells. More than one focus infiltration was defined as grade 3. Moderate infiltration less than one focus was defined as grade 2. Grade 1 was defined mild infiltration. Absence of lymphocyte and plasma cell infiltrate was defined as grade 0. The pathologist (T.T: specialized in diffuse lung disease) evaluated without clinical and radiological information.
Fig. 2
Scoring of lymphocyte and plasma cell infiltration in bronchial gland. a; grade 0: absent of lymphocyte and plasma cells infiltration. b; grade 1: mild infiltration. c; grade2: moderate infiltration with less than 50 lymphocytes and plasma cells. d; grade 3: severe infiltration aggregated of 50 or more lymphocytes and plasma cells
×
Diagnosis of underlying diseases
The diagnosis of idiopathic interstitial pneumonias (IIPs) and chronic hypersensitivity pneumonitis (cHP) was based on consensus using previously reported criteria at a multidisciplinary conference [8‐10]. Cases suspected with collagen diseases were consulted with rheumatologists. Patients with SS and systemic sclerosis (SSc) fulfilled the European/American International classification criteria [3, 11]. The diagnosis of dermatomyositis (DM) was based on Bohan and Peter’s [12, 13] and Sontheimer’s criteria [14, 15]. Granulomatosis with polyangitis (GPA) was diagnosed on the basis of 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides [16]. Mucosa associated lymphoid tissue (MALT) lymphoma was diagnosed in accordance with WHO classification of tumours of haematopoietic and lymphoid tissues [17].
Anzeige
Results
Baseline characteristics
TBLC was performed on 432 cases for diagnosing diffuse lung diseases during the study period. The samples of 50 cases included bronchial glands. Of those, 20 cases were excluded because sample sizes were small or steroid has already been administered before biopsy (Fig. 3). Thirty cases were included in this study. The remaining 30 cases included 17 of idiopathic interstitial pneumonias, 5 of chronic hypersensitivity pneumonia, 6 of connective tissue disease (SS; n = 4, systemic sclerosis; n = 1, dermatomyositis; n = 1) and 2 of other diseases.
Fig. 3
Patients flow diagram
×
The baseline characteristics are shown in Table 1. Median age was 65.5 years. The most frequent underlying disease was 17 of IIPs including 7 of IPF. All cases with SS were primary disease and had no other collagen diseases. The 19 of 30 cases (63.3%) including all SS cases complained cough. Moderate bleeding requiring endobronchial instillation of thrombin was observed in 12.1% of the specimens from which the bronchial gland was biopsied. There was no severe bleeding causing hemodynamic or respiratory instability, requiring tamponade or other surgical interventions, transfusions, or admission to the intensive care unit. There was one case with pneumothorax that did not require drainage.
Connective tissue disease related interstitial pneumonia
6
Sjögren’s syndrome (SS)
4
Systemic sclerosis (SSc)
1
Dermatomyositis (DM)
1
Granulomatosis with polyangitis (GPA)
1
Mucosa associated lymphoid tissue lymphoma
1
Dates are expressed as group median values or numbers of patients
Scoring of lymphocytes and plasma cells infiltration in bronchial glands
In SS, infiltration of lymphocytes and plasma cells was observed in all cases; grade 1 in one, grade 2 in one, and grade 3 in two cases. In contrast, 11 of 26 in other diseases showed no lymphocytes infiltration, with remaining 15 of grade 1 infiltration (IPF: 6 cases, NSIP: 2 cases, UCIPs: 4 cases, cHP: 2 cases, DM: 1 case). Grade 2 or more infiltration were found only in SS but not in other diseases, while mild lymphocytes infiltration classified as grade 1 were observed in the diseases other than SS. Two SS patients had duct dilation of bronchial glands. There was no case of grade 0 in SS (Table 2).
Table 2
Histopathological findings of bronchial glands
Clinical diagnosis
No. of Patients
lymphocytes and plasma cell infiltration Grade 0/1/2/3
The baseline characteristics are shown in Table 3. All cases were female and positive for anti-SS-A/Ro antibody. Three of the four SS patients had xerostomia or xerophthalmia. Case 1 did not suffer from xerostomia and xerophthalmia. This case was performed a salivary gland biopsy and other cases were diagnosed by other tests that met the diagnostic criteria. Figure 4 shows the bronchial glands of all 4 cases with SS. The bronchial glands of case 3 and 4 revealed high-grade lymphocytic infiltration. Case 2 represented grade 2 lymphocytes infiltration and duct dilation. Case 1 had mild lymphocytes infiltration and duct dilation.
Table 3
Baseline characteristics of Sjögren’s syndrome patients
Case
1
2
3
4
Age (years)
70’s
40’s
70’s
70’s
Gender
Female
Female
Female
Female
Smoking status
Never
Never
Ex
Ex
Clinical manifestations
Cough
+
+
+
+
Sputum
–
+
–
–
Dyspnea
–
+
+
+
Xerostomia
–
–
+
+
Xerophthalmia
–
+
+
+
Anti-nuclear antibody
80 (centromere)
640 (speckled, cytoplasmic)
1280 (homogenous)
1280 (speckled)
Anti-SS-A/Ro antibody
> 240
> 240
> 240
> 240
Anti-SS-B/La antibody
Negative
> 320
Negative
270.1
Pulmonary function
FVC % pred
90.9
72.1
63.9
66.4
FEV1% pred
90.3
79.4
65.5
73.3
FEV1/FVC ratio
77.2
91.4
81.4
86.7
DLCO % pred
97.7
40.1
48.3
52.6
HRCT pattern
NSIP
UIP + NSIP
UIP
NSIP+OP
Salivary gland biopsy
grade 3a
N/A
N/A
N/A
Bronchial gland
Histopathology grading
1
2
3
3
Duct dilation
+
+
–
–
aChisholm-Mason score
HRCT high-resolution computed tomography, N/A not available
Fig. 4
Bronchial glands of Sjogren’s syndrome. a Case 1 with grade 1 lymphocyte and plasma cell infiltration and duct dilation. b Case 2 with grade 2 lymphocyte and plasma cell infiltration and duct dilation. c, d Case 3and 4 with grade 3 lymphocyte and plasma cell infiltration
×
Discussion
In this study, we examined pathological characteristics of the bronchial glands collected by TBLC. Our results showed that high-grade lymphocytic infiltration in bronchial glands was a distinct characteristics in SS, although mild lymphocytes infiltrations in bronchial glands were occasionally observed in other collagen diseases or other interstitial lung diseases.
SS is characterized by B-cell hyperactivity and lymphocytic infiltration of exocrine glands and other target organs. The pulmonary manifestations of SS are xerotrachea, airway abnormalities, interstitial pneumonia, and lymphoproliferative disorders [18‐23]. Xerotrachea is associated with lymphocytic inflammation and atrophy of the submucosal gland [24]. There is only one literature that reported on a case that transbronchial forceps biopsy specimen showed a dense infiltrate of lymphocytes around the bronchial gland in SS patient, despite that the collected bronchial gland was small [25]. Others reported that the bronchial glands in SS showed significant hyperplasia, without mentioning the inflammatory cells in the bronchial glands [26]. As they studied on the autopsy lungs, their subjects may have been affected by treatment such as steroids and immunosuppressant.
SS has characteristic microscopic findings involving lymphocytic infiltration surrounding the excretory ducts in combination with the destruction of acinar tissue. In early stage or advanced phase of SS, there is often slight or none lymphocyte infiltration in the salivary glands. Dilatation of intralobular and interlobular duct is a common finding in the salivary glands of SS, regardless of the degree of lymphocyte infiltration [27]. In this study, duct dilatation in the bronchial glands was observed only in SS. Because this study was a small and retrospective study, we could not compare the degree of respiratory symptoms such as cough with the degree of lymphocytic infiltration of the bronchial glands. In patients with Sjögren’s syndrome who complain of severe persistent cough despite mild or no interstitial pneumonia, exocrine dysfunction of the bronchial glands may be involved, and a bronchial gland biopsy may prove this. Comparing the degree of lymphocytic infiltration of the bronchial glands with clinical symptoms such as cough is future work.
Cryobiopsy is a new technique for diagnosing diffuse parenchymal lung disease [4‐7]. TBLC provides larger samples than transbronchial forceps biopsy and more proximal portion of the lung apart from the pleura than SLB. We actively perform TBLC in patients with interstitial pneumonia associated collagen vascular diseases to rule out complications of other diseases such as chronic hypersensitivity pneumonia, to select therapeutic agents, and to predict treatment response and prognosis. A bronchial gland is rarely biopsied by SLB for diagnosing interstitial lung disease. In previous reports on bronchial glands, the specimens were obtained by autopsy or lung resection for localized pulmonary lesions [26, 28]. Autopsied lungs are affected by treatment during their lifetime. There was no report that examined lymphocytes infiltration in bronchial glands of collagen diseases or interstitial lung diseases by lung resection. As we excluded the cases that had been treated before biopsy, the cases of this study were not affected by treatment such as steroids or immunosuppressant. The present study is the first report focusing on lymphocytes infiltration in the bronchial glands with various interstitial lung diseases that were not affected by treatment. Complications of bleeding in the specimens including bronchial glands were not more common than previous reports, and there was no severe bleeding [6].
Anzeige
This study has several limitations. First, this was a small, retrospective study, which may have been subject to various biases. Second, bronchial glands were incidentally biopsied in this study. As we performed TBLC for the diagnosis of diffuse lung diseases, we did not intend to biopsy bronchial glands. Bronchial glands are present in trachea and bronchus with cartilage. If we evaluate focus on lymphocytes infiltration in bronchial glands, transbronchial biopsy in the central airway should be considered. Third, an adequate sample size to evaluate lymphocyte infiltration of bronchial glands is unknown. Because lymphocytes infiltration in salivary glands of SS have irregular distribution, a sufficient volume of specimen is needed in salivary gland biopsy. If a sample is small, the degree of lymphocytes infiltration may be misinterpreted. In this study, we examined the cases that had sufficient size of bronchial glands. We excluded the cases with small size of bronchial glands (< 0.05mm2), although it is necessary to examine whether this criteria is appropriate in the future. Finally, we were not able to compare the degrees of lymphocytic infiltration in the salivary glands and the bronchial glands of SS and did not evaluate SS patients without interstitial pneumonia.
Conclusion
Our results showed that mild lymphocytic infiltration is a nonspecific finding that is also seen in other diseases, but high-grade lymphocytic infiltration of bronchial glands is a distinct characteristics in SS.
Acknowledgments
We would like to acknowledge all the participants.
Ethics approval and consent to participate
The institutional review board of Kanagawa Cardiovascular and Respiratory Center, Kanagawa, Japan approved the study protocol with written or verbal informed consent waiver due to the retrospective nature of this study. Information about the research was made available to research subjects, and we ensured that they had the opportunity to refuse to allow the research to be carried out.
Anzeige
Consent for publication
Not applicable.
Competing interests
All of the authors, except one, report they have no conflict of interest to disclose. Tomohisa Baba has received lecture fee from AMCO incorporated.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
