Neutrophils Contribute to Severity of Tuberculosis Pathology and Recovery From Lung Damage Pre- and Posttreatment. (24th August 2021)
- Record Type:
- Journal Article
- Title:
- Neutrophils Contribute to Severity of Tuberculosis Pathology and Recovery From Lung Damage Pre- and Posttreatment. (24th August 2021)
- Main Title:
- Neutrophils Contribute to Severity of Tuberculosis Pathology and Recovery From Lung Damage Pre- and Posttreatment
- Authors:
- Nwongbouwoh Muefong, Caleb
Owolabi, Olumuyiwa
Donkor, Simon
Charalambous, Salome
Bakuli, Abhishek
Rachow, Andrea
Geldmacher, Christof
Sutherland, Jayne S - Abstract:
- Abstract: Background: Despite microbiological cure, about 50% of tuberculosis (TB) patients have poor lung recovery. Neutrophils are associated with lung pathology; however, CD16/CD62L-defined subsets have not been studied in TB. Using flow cytometry, we monitored frequencies, phenotype, and function of neutrophils following stimulation with Mycobacterium tuberculosis ( Mtb ) whole cell lysate (WCL) and ESAT-6/CFP-10 fusion protein (EC) in relation to lung pathology. Methods: Fresh blood from 42 adult, human immunodeficiency virus (HIV)–negative TB patients were analyzed pre- and post-therapy, with disease severity determined using chest radiography and bacterial load. Flow cytometry was used to monitor frequencies, phenotype, and function (generation of reactive oxygen species [ROS], together with CD11b, tumor necrosis factor, and interleukin 10 [IL-10] expression) of neutrophils following 2-hour stimulation with Mtb -specific antigens. Results: Total neutrophils decreased by post-treatment compared to baseline ( P = .0059); however, CD16 br CD62L br (segmented) neutrophils increased ( P = .0031) and CD16 dim CD62L br (banded) neutrophils decreased ( P = .038). Banded neutrophils were lower in patients with severe lung damage at baseline ( P = .035). Following WCL stimulation, ROS from segmented neutrophils was higher in patients with low Mtb loads even after adjusting for sex ( P = .038), whereas IL-10–expressing CD16 dim CD62L lo cells were higher in patients withAbstract: Background: Despite microbiological cure, about 50% of tuberculosis (TB) patients have poor lung recovery. Neutrophils are associated with lung pathology; however, CD16/CD62L-defined subsets have not been studied in TB. Using flow cytometry, we monitored frequencies, phenotype, and function of neutrophils following stimulation with Mycobacterium tuberculosis ( Mtb ) whole cell lysate (WCL) and ESAT-6/CFP-10 fusion protein (EC) in relation to lung pathology. Methods: Fresh blood from 42 adult, human immunodeficiency virus (HIV)–negative TB patients were analyzed pre- and post-therapy, with disease severity determined using chest radiography and bacterial load. Flow cytometry was used to monitor frequencies, phenotype, and function (generation of reactive oxygen species [ROS], together with CD11b, tumor necrosis factor, and interleukin 10 [IL-10] expression) of neutrophils following 2-hour stimulation with Mtb -specific antigens. Results: Total neutrophils decreased by post-treatment compared to baseline ( P = .0059); however, CD16 br CD62L br (segmented) neutrophils increased ( P = .0031) and CD16 dim CD62L br (banded) neutrophils decreased ( P = .038). Banded neutrophils were lower in patients with severe lung damage at baseline ( P = .035). Following WCL stimulation, ROS from segmented neutrophils was higher in patients with low Mtb loads even after adjusting for sex ( P = .038), whereas IL-10–expressing CD16 dim CD62L lo cells were higher in patients with mild damage ( P = .0397) at baseline. Conclusions: High ROS generation, low levels of banded neutrophils, and high levels of IL-10–expressing CD16 dim CD62L lo neutrophils are associated with reduced lung pathology at diagnosis. Hence, neutrophils are potential early indicators of TB severity and promising targets for TB host-directed therapy. Abstract : Neutrophil-mediated (proportions of functional protective subtypes and reactive oxygen species generation capacity) tuberculosis susceptibility constitutes a strong scientific premise for future mechanistic and clinical studies targeting immunosuppressive host-directed therapies for tuberculosis disease progression and severity. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 74:Number 10(2022)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 74:Number 10(2022)
- Issue Display:
- Volume 74, Issue 10 (2022)
- Year:
- 2022
- Volume:
- 74
- Issue:
- 10
- Issue Sort Value:
- 2022-0074-0010-0000
- Page Start:
- 1757
- Page End:
- 1766
- Publication Date:
- 2021-08-24
- Subjects:
- tuberculosis -- neutrophils -- immunosuppression -- inflammation -- lung damage
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciab729 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.293860
British Library DSC - BLDSS-3PM
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- 21742.xml