Doxycycline Treatment of Mansonella perstans–Infected Individuals Affects Immune Cell Activation and Causes Long-term T-cell Polarization. (3rd June 2022)
- Record Type:
- Journal Article
- Title:
- Doxycycline Treatment of Mansonella perstans–Infected Individuals Affects Immune Cell Activation and Causes Long-term T-cell Polarization. (3rd June 2022)
- Main Title:
- Doxycycline Treatment of Mansonella perstans–Infected Individuals Affects Immune Cell Activation and Causes Long-term T-cell Polarization
- Authors:
- Aniagyei, Wilfred
Adjei, Jonathan Kofi
Adankwah, Ernest
Seyfarth, Julia
Mayatepek, Ertan
Antwi Berko, Daniel
Sakyi, Samuel Asamoah
Batsa Debrah, Linda
Debrah, Alexander Yaw
Hoerauf, Achim
Owusu, Dorcas O
Phillips, Richard O
Jacobsen, Marc - Abstract:
- Abstract: Background: Doxycycline is used for treatment of Mansonella perstans infection. Immune modulatory effects of both M. perstans and doxycycline have been described but long-term implications on host immune response are not defined. Here we determined multiple immune parameters of M. perstans– infected individuals before and after doxycycline treatment to characterize doxycycline effects on host T-cell immunity. Methods: Immune characterization of doxycycline-treated M. perstans– infected individuals was performed as part of an open-label randomized clinical trial. Immune cell population phenotyping by flow cytometry and functional in vitro T-cell assays were performed at baseline, 6 months, and "long term" (18–24 months) after treatment start. Treatment efficacy, based on peripheral blood microfilaria (mf) burden, was correlated with immune parameters and effects on immune response against concomitant Mycobacterium tuberculosis infection were determined. Results: Immune population phenotyping indicated changes in functional T-cell responses after doxycycline treatment. Constitutive and superantigen-induced T-cell activation and polarization towards T-helper type (TH ) 1 phenotype at baseline declined after doxycycline treatment, whereas low proportions of TH 17 and TH 1* cells at baseline increased significantly at follow-up. In accordance, long-term decline in antigen-specific TH 1 responses against concomitant M. tuberculosis infection was seen. Notably, only TH 17Abstract: Background: Doxycycline is used for treatment of Mansonella perstans infection. Immune modulatory effects of both M. perstans and doxycycline have been described but long-term implications on host immune response are not defined. Here we determined multiple immune parameters of M. perstans– infected individuals before and after doxycycline treatment to characterize doxycycline effects on host T-cell immunity. Methods: Immune characterization of doxycycline-treated M. perstans– infected individuals was performed as part of an open-label randomized clinical trial. Immune cell population phenotyping by flow cytometry and functional in vitro T-cell assays were performed at baseline, 6 months, and "long term" (18–24 months) after treatment start. Treatment efficacy, based on peripheral blood microfilaria (mf) burden, was correlated with immune parameters and effects on immune response against concomitant Mycobacterium tuberculosis infection were determined. Results: Immune population phenotyping indicated changes in functional T-cell responses after doxycycline treatment. Constitutive and superantigen-induced T-cell activation and polarization towards T-helper type (TH ) 1 phenotype at baseline declined after doxycycline treatment, whereas low proportions of TH 17 and TH 1* cells at baseline increased significantly at follow-up. In accordance, long-term decline in antigen-specific TH 1 responses against concomitant M. tuberculosis infection was seen. Notably, only TH 17 and TH 1* changes after 6 months and TH 17 at baseline were negatively correlated with M. perstans microfilaria burden or reduction, whereas long-term changes were not associated with treatment efficacy. Conclusions: We found long-term immune modulatory effects of doxycycline treatment leading to decreased constitutive T-cell activation, polarization towards TH 17/TH 1*, and impaired immune response against concomitant M. tuberculosis infection. Abstract : Doxycycline caused modulation of T-cell activation and polarization with functional implications on concomitant Mycobacterium tuberculosis infection in Mansonella perstans –infected individuals. Immunological changes were detectable long term after treatment and were largely independent from anti-microfilaria treatment efficacy. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 76:Number 3(2023)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 76:Number 3(2023)
- Issue Display:
- Volume 76, Issue 3 (2023)
- Year:
- 2023
- Volume:
- 76
- Issue:
- 3
- Issue Sort Value:
- 2023-0076-0003-0000
- Page Start:
- e1399
- Page End:
- e1407
- Publication Date:
- 2022-06-03
- Subjects:
- doxycycline -- T-cell polarization -- Mansonella perstans -- Mycobacterium tuberculosis
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/ciac428 ↗
- 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
British Library HMNTS - ELD Digital store - Ingest File:
- 25748.xml