Systematic Reporting of Eosinophils in Transbronchial Biopsies After Lung Transplantation Defines a Distinct Inflammatory Response

Author:

Darley David R.12,Sivasubramaniam Vanathi23,Qiu Min R.23,Barrett Wade A.3,Wong Stephen J.3,Martinu Tereza45,Pal Prodipto4,Thwe Le Myo1,Tonga Katrina O.267,MacDonald Peter S.4,Plit Marshall L.12

Affiliation:

1. Department of Thoracic Medicine and Lung Transplantation, St Vincent’s Hospital Sydney, University of New South Wales, Sydney, NSW, Australia.

2. St Vincent's Clinical Campus, Faculty of Medicine and Health, University of New South Wales, Sydney, NSW, Australia.

3. Department of Anatomical Pathology, St Vincent’s Hospital Darlinghurst, Sydney, NSW, Australia.

4. Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.

5. Department of Medicine, University of Toronto, Toronto, ON, Canada.

6. Department of Thoracic Medicine, St Vincent’s Hospital Darlinghurst, Sydney, NSW, Australia.

7. Department of Cardiac Transplantation, St Vincent’s Hospital Darlinghurst, Sydney, NSW, Australia.

Abstract

Background. Descriptions of eosinophils in transbronchial biopsy (TBBx) pathology reports after lung transplantation (LTx) are associated with poor long-term outcomes. The absence of routine reporting and standardization precludes accurate assessment of this histologic predictor. A systematic reporting scheme for the presence of TBBx eosinophils after LTx was implemented. This report aims to assess this scheme by describing the presence, pattern, and gradation of TBBx eosinophils and clinical associations. Methods. A prospective cross-sectional study of all TBBx reports was performed including all patients presenting for a surveillance or diagnostic TBBx between January 2020 and June 2023. Each TBBx was systematically reported in a blinded manner. Mixed-effects logistic regression was performed to measure the association between concurrent clinical and histologic features, and the presence of TBBx eosinophils. Results. A total of 410 TBBx reports from 201 patients were systematically reported. In 43.8% recipients, any TBBx eosinophils were detected and in 17.1% recipients, higher-grade eosinophils (≥3 per high power field) were present. Adjusted analysis showed that retransplantation, A- and B-grade cellular rejection, positive bronchoalveolar lavage (BAL) bacterial microbiology, and elevated blood eosinophil count were independently associated with the presence of any TBBx eosinophils. Diagnostic “for-cause” procedures were independently associated with higher quantities of TBBx eosinophils. Conclusions. Systematic reporting demonstrates that TBBx eosinophils are a distinct inflammatory response associated with rejection, infection, and peripheral eosinophilia. Although these findings require multicenter external validation, standardized reporting for TBBx eosinophils may assist in identifying recipients at risk of poor outcomes and provides a platform for mechanistic research into their role after lung transplantation.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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