Rhinosinusitis in hematopoietic stem cell-transplanted patients: influence of nasosinus mucosal abnormalities?
© Ortiz et al.; licensee BioMed Central. 2014
Received: 19 March 2014
Accepted: 13 October 2014
Published: 4 December 2014
Rhinosinusitis is characterized by inflammation extending from the mucosa of the nasal cavity into the paranasal sinuses. There are some aggravating features, such as immunosuppression, that can cause the nasal mucosal inflammation to linger for a long period, resulting in chronic or recurrent episodes. Such immunosuppression is the major feature of patients undergoing a hematopoietic stem cell transplant (HSCT); rhinosinusitis prevalence is higher in this group compared to immunocompetent patients. Nasal epithelial abnormalities have been described in, and may have some influence over, recurrent sinus infections among those patients. However, it is not clear whether rhinosinusitis can trigger mucosal abnormalities or whether a preexisting vulnerability for sinusitis recurrence is more likely. The objective of the study was to verify the influence of rhinosinusitis on nasal epithelial damage in patients undergoing hematopoietic stem cell transplantation.
A total of 30 allogeneic HSCT patients were divided into two groups: 24 patients with chronic or recurrent rhinosinusitis and 6 patients without rhinosinusitis. These patients underwent a biopsy of the uncinate process that was analyzed by transmission electron microscopy and optical microscopy.
The nasal mucosa analysis by optical microscopy showed no significant abnormalities. The ciliary orientation was obviously normal in the transplanted patients without rhinosinusitis. There was a trend toward a difference in the amount of cilia (decreased) and the primary modification of the ultrastructure of transplanted patients with rhinosinusitis.
HSCT patients, with and without rhinosinusitis, showed no significant histological abnormalities, except for ciliary disorientation and a possible decrease in ciliary and ultrastructural abnormalities in HSCT patients with rhinosinusitis.
Rhinosinusitis is characterized by inflammation extending from the mucosa of the nasal cavity into the paranasal sinuses, blocking the sites of sinus drainage, especially the middle meatus. The uncinate process is a crucial anatomical structure of the middle meatus, and its mucosa may be representative of the paranasal sinuses[2, 3]. Such a blockage in the uncinate process region can trigger secretion stasis within the maxillary, frontal and ethmoid sinuses, thus altering mucociliary clearance to favor the possibility of microorganism proliferation and nasal mucosa infections[1, 3].
Certain aggravating factors can extend nasal mucosa inflammation for longer periods, constituting chronic or recurrent episodes[1, 3]. Among the factors described in the literature is immunosuppression, which constitutes the main feature of patients undergoing hematopoietic stem cell transplantation. The immunosuppression of these patients is therefore believed to be the only cause for their high frequency of rhinosinusitis[1, 3–6].
The frequency of bacterial rhinosinusitis in patients receiving hematopoietic stem cell transplants (HSCTs) is much higher (37%) than that of immunocompetent patients (5 to 15%)[2, 6–10]. The risk is further increased in HSCT patients who develop chronic graft versus host disease (GVHD), with a 4.3 times higher frequency of infection. In addition, there is a risk of developing the dreaded invasive fungal rhinosinusitis, although the frequency of this type is lower (0.3 to 3.8%)[11–15].
Histology of the nasal mucosa
HSCT with GVHD
Cilia (absence or decrease) (%)
Ciliar ultrastructure abnormalities (%)
Cytoplasmic mitochondria (decreased/absence) (%)
Cytoplasmic vacuolization (%)
Goblet cells (decreased/absence), n (%)
Moderate/severe inflammatory infiltrate, n (%)
A subsequent study showed that there was no change in the frequency of nasal epithelial damage in the presence of rhinosinusitis in patients undergoing HSCT, even among those with GVHD. Immunosuppression thus remains the main cause of the higher frequency of rhinosinusitis in HSCT and GVHD.
Nevertheless, it seems that the recurrence of nasal infection causes a progressive decrease in the number of cilia in the sinus epithelia of transplanted patients. Therefore, it is possible that epithelial damage could be an associated or aggravated feature of sinusitis recurrence or chronicity.
Because transplanted patients have histological abnormalities after the hematopoietic stem cell transplantation process, as well as in the presence of rhinosinusitis, and because the recurrence of rhinosinusitis increases this epithelial damage, the aim of this study is to verify the influence of rhinosinusitis on nasal epithelial damage in patients undergoing hematopoietic stem cell transplantation.
This exploratory prospective study includes patients who underwent a transplant of hematopoietic stem cells at the Transplantation Hematopoietic Stem Cells Unit of the HC UNICAMP/Blood Center of Campinas and who were evaluated by the Office of Rhinology of Otorhinolaryngology, FCM-UNICAMP, University of Campinas, Brazil. The study was approved by Research Ethics UNICAMP, under number 088-2002, and patients also completed the research ethics consent form to participate in this study.
We selected a total of 30 allogeneic hematopoietic stem cell-transplanted patients who were divided into two groups: 24 patients with chronic or recurrent rhinosinusitis, and six patients without rhinosinusitis. These patients underwent a biopsy of the nose to collect the samples; 24 patients underwent biopsies in the presence of rhinosinusitis. Only 22 slides for the group with rhinosinusitis were analyzable by electron microscopy, and 19 slides were examined by optical microscopy (24 patients). The biopsies of the six patients without rhinosinusitis were analyzed by electron microscopy, and five were examined by optical microscopy.
Exclusion criteria included patients with serious risks of bleeding due to thrombocytopenia and patients with cytomegalovirus or herpes virus.
Groups of transplanted hematopoietic stem cells
Myeloablative: 16 (66%)
CML: 5 (21%)
With: 16 (66%)
AML: 5 (21%)
Nonmyeloablative: 8 (33%)
MM: 3 (12.5%)
Without: 8 (33%)
CLL: 1 (4%)
AA: 3 (12.5%)
MDS: 4 (17%)
ALL: 2 (8%)
SCA: 1 (4%)
Myeloablative: 6 (100%)
ALL: 1 (17%)
With: 5 (83%)
CML: 3 (50%)
AML: 1 (17%)
Without: 1 (17%)
AA: 1 (17%)
Biopsies of the uncinate process mucosa at the middle meatus were endoscopically performed for all patients under anesthesia. Those biopsies were taken from the full thickness of the uncinate process of those patients that underwent to surgery; and two or three samples from the medial to lateral uncinate process, with cutting blaksley. Histopathological evaluations were achieved using optical microscopy and transmission electron microscopy. Hematoxylin and eosin, Periodic acid–Schiff and Masson’s trichrome staining were used to better assess each variable. The histological criteria analyzed by light microscopy of hematoxylin and eosin-stained samples were the density and composition of the epithelial and submucosal inflammatory infiltrate, the number of apoptotic bodies and intraepithelial eosinophils, and the submucosal glandular density. The intraepithelial lymphocyte counts and the density of the epithelial and submucosal inflammatory infiltrate were examined by Periodic acid–Schiff, and the basal membrane thickening, submucosal edema and fibrosis were determined by Masson’s trichrome stain. The variable counts were determined by analyzing the histological sections that were randomly selected from the best embedded glass slides using at least 10 fields per 40× high-power field. The measurements of the basal membrane were made with the aid of a micrometer eyepiece graticule (Breslow strip) in histological sections stained with Masson’s trichrome in 10 high-power fields of 40× magnification, which were randomly selected areas where the material was well embedded. The lymphocyte, eosinophil, apoptotic body and submucosal gland counts, as well as the basal membrane thickness values, were summed and divided by the number of selected fields (arithmetic average) for a comparative analysis among the groups. The inflammatory infiltrate density as well as edema and fibrosis levels were subjectively graded under optical microscopy as absent, mild, moderate or severe.
For electron microscopy, the sample was placed on a permeable thin paper card on a hard wax and cut into fine fragments approximately 0.3 mm in diameter and then placed in a container with fixative (3% glutaraldehyde solution) and maintained at 4°C for 3 hours. The samples were then processed through the wash steps and placed in a container with phosphate buffer. Various fragments of approximately 2 mm from the uncinate process were randomly selected and made into ultrathin sections 50 to 60 nm thick using an ultramicrotome diamond knife. The magnification used was 1,600 to 20,000×. The parameters subjectively evaluated by transmission electron microscopy included the following: amount of cilia (absent, decreased, normal), organization of ciliary structures, squamous metaplasia (absent or present), microvilli (present or absent), goblet cells (absent, decreased, increased or normal), intracellular mitochondria (present or absent) and cytoplasmic vacuolization (present or absent). The ciliary orientation was measured by cross-sections of at least 10 cilia, which were delineated as one perpendicular line between the central microtubules and arranged in the same direction and angle within a possible variation of 10°.
For light microscopy, all of the slides were examined by two pathologists, and for electron microscopy, all of the fragments of the biopsy were always evaluated by the same investigator.
The data collected from the biopsies were compared among the two groups using a statistical analysis of contingency (chi-squared) and the Wilcoxon test in R version 2.7.0 (© 2008 The R Foundation for Statistical Computing). The level of significance (P value) was set at 0.05, and confidence intervals were set at 95%.
The data used as a control for comparison and discussion in this study were obtained from our previous studies, the methodologies of which were identical. These studies evaluated the histological aspects of the nasal mucosa of immunocompetent patients and patients undergoing bone marrow transplants, with and without rhinosinusitis[16, 18].
Analysis of the sinonasal epithelium by optical microscopy
Moderate inflammatory infiltrate
Intraepithelial lymphocytes (n/HPF)
Apoptotic bodies (n/HPF)
Glandular density (n/HPF)
Basal membrane (mm)
Analysis of the nasal epithelium by transmission electron microscopy
Normal ciliary orientation
Goblet cells (decreased/absence)
Cytoplasmic mitochondria (decreased/absence)
A previous study found that hematopoietic stem cell-transplanted patients experience epithelial injury after transplantation, showing a reduction in the number of cilia (77%) and goblet cells (50%) and a 50% change in the ciliary ultrastructure, independent of sinonasal infections. These abnormalities would trigger mucous dryness, malfunctions of mucociliary clearance, and inadequate lubrication that prevents the surface maintenance of defense proteins (lysozymes, lactoferrins and IgA). This epithelial damage, in addition to the immunosuppression inherent in transplantations, may explain the higher rates of occurrence and recurrence of rhinosinusitis in these patients.
Chronic GVHD can affect the mucosal membranes of transplanted hematopoietic stem cell patients due to a cytotoxic reaction that results in the generation of apoptotic bodies as the end product of cellular degeneration in the epithelium. Previous studies have shown an increase in the number of apoptotic bodies in the sinonasal mucosa of HSCT with chronic GVHD. This result could also explain the greater risk of rhinosinusitis in these patients, as described in the literature.
However, a subsequent study showed no difference in the epithelial damage in HSCT patients, with or without chronic GVHD, in the presence of rhinosinusitis. The only significant finding of this study was an increase in the number of microvilli, which may have occurred due to release of proinflammatory cytokines in the nasosinal mucosa in chronic rhinosinusitis. These cytokines decrease ciliogenesis and the formation of basal bodies, preventing the elongation of the centrioles. A transplanted patient with chronic GVHD does not seem to have more severe epithelial lesions relative to other HSCT patients, although such a patient would appear to have more edema and fibrosis. In addition, these patients appear to have denser inflammatory infiltrate with eosinophils and decreased glandular density in the submucosa. It has been suggested that immunosuppression remains the main cause of the higher prevalence of rhinosinusitis among recipients, with or without GVHD.
In immunocompetent patients, chronic and/or recurrent rhinosinusitis is known to cause histological abnormalities in the sinus mucosa, disrupting the protective barrier and potentially triggering the immune response of the individual, depending on the pathogen. These abnormalities may be ultrastructural (17 to 45%), related to the leukocyte inflammatory infiltrate, the epithelial squamous metaplasia, the glandular hyperplasia or the presence of microvilli[22–25]. Aside from these abnormalities, aggravating factors – such as anatomical variations, allergy, smoking and genetic diseases – can perpetuate sinonasal inflammation or stimulate its recurrence[1, 2]. A previous study showed that rhinosinusitis recurrence in HSCT patients is associated with an absence or decrease in the number of cilia. Rhinosinusitis may thus be an aggravating factor for sinonasal epithelial damage in these patients.
In this study, rhinosinusitis did not significantly influence the nasal histology of HSCT patients, although these patients did show a more dense inflammatory infiltrate with eosinophils and intraepithelial lymphocytes, as well as increased edema and fibrosis. These features seem to result from the modification of the top of the cilia and the ciliary ultrastructure (50%), which changes the orientation of the cilia during rhinosinusitis.
The ultrastructural abnormalities found here are the same as those in chronic rhinosinusitis among immunocompetent patients, including compound cilia and triple central microtubules, which occur after the release of cytokines or toxins and proteases from the infecting microorganisms (viruses, bacteria or fungi). These abnormalities may improve over an approximately 10-week course of recovery from infection[10, 21, 26].
Epithelial damage may therefore be a consequence of the transplant process and an aggravating factor for rhinosinusitis. Rhinosinusitis recurrences can also act as an aggravating factor for this epithelial damage. Finally, immunosuppression is the main causal factor for HSCT rhinosinusitis and chronic GVHD.
HSCT patients, with and without rhinosinusitis, showed no significant histological abnormalities, except for ciliary disorientation, a possible decrease in the amount of cilia and an increase in ultrastructural abnormalities in HSCT patients with rhinosinusitis.
graft versus host disease
hematopoietic stem cell transplant.
The authors thank Roberto Zulli for statistical analysis, Adilson Abilio Piaza for the photograph and figure scans, Marilucia Rugiero Martins for elaboration of the electron microscopy samples, and Prof. Luciana Rodrigues Meirelles for cooperation on the histological analysis.
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