Phenotypic and functional characteristics of HLA‐DR+ neutrophils in Brazilians with cutaneous leishmaniasis. Issue 3 (17th October 2016)
- Record Type:
- Journal Article
- Title:
- Phenotypic and functional characteristics of HLA‐DR+ neutrophils in Brazilians with cutaneous leishmaniasis. Issue 3 (17th October 2016)
- Main Title:
- Phenotypic and functional characteristics of HLA‐DR+ neutrophils in Brazilians with cutaneous leishmaniasis
- Authors:
- Davis, Richard E.
Sharma, Smriti
Conceicão, Jacilara
Carneiro, Pedro
Novais, Fernanda
Scott, Phillip
Sundar, Shyam
Bacellar, Olivia
Carvalho, Edgar M.
Wilson, Mary E. - Abstract:
- Abstract : Lesions and peripheral blood of cutaneous leishmaniasis patients have HLA‐DR‐expressing neutrophils with antigen presenting cell‐like characteristics, which retain morphologic and functional characteristics of neutrophils. Abstract : The protozoan Leishmania braziliensis causes cutaneous leishmaniasis (CL) in endemic regions. In murine models, neutrophils (PMNs) are recruited to the site of infection soon after parasite inoculation. However, the roles of neutrophils during chronic infection and in human disease remain undefined. We hypothesized that neutrophils help maintain a systemic inflammatory state in subjects with CL. Lesion biopsies from all patients with CL tested contained neutrophils expressing HLA‐DR, a molecule thought to be restricted to professional antigen‐presenting cells. Although CL is a localized disease, a subset of patients with CL also had circulating neutrophils expressing HLA‐DR and the costimulatory molecules CD80, CD86, and CD40. PMNs isolated from a low‐density leukocyte blood fraction (LD‐PMNs) contained a higher percentage of HLA‐DR + PMNs than did normal‐density PMNs. In vitro coculture experiments suggested LD‐PMNs do not suppress T cell responses, differentiating them from MDSCs. Flow‐sorted HLA‐DR + PMNs morphologically resembled conventional PMNs, and they exhibited functional properties of PMNs. Compared with conventional PMNs, HLA‐DR + PMNs showed increased activation, degranulation, DHR123 oxidation, and phagocytic capacity. AAbstract : Lesions and peripheral blood of cutaneous leishmaniasis patients have HLA‐DR‐expressing neutrophils with antigen presenting cell‐like characteristics, which retain morphologic and functional characteristics of neutrophils. Abstract : The protozoan Leishmania braziliensis causes cutaneous leishmaniasis (CL) in endemic regions. In murine models, neutrophils (PMNs) are recruited to the site of infection soon after parasite inoculation. However, the roles of neutrophils during chronic infection and in human disease remain undefined. We hypothesized that neutrophils help maintain a systemic inflammatory state in subjects with CL. Lesion biopsies from all patients with CL tested contained neutrophils expressing HLA‐DR, a molecule thought to be restricted to professional antigen‐presenting cells. Although CL is a localized disease, a subset of patients with CL also had circulating neutrophils expressing HLA‐DR and the costimulatory molecules CD80, CD86, and CD40. PMNs isolated from a low‐density leukocyte blood fraction (LD‐PMNs) contained a higher percentage of HLA‐DR + PMNs than did normal‐density PMNs. In vitro coculture experiments suggested LD‐PMNs do not suppress T cell responses, differentiating them from MDSCs. Flow‐sorted HLA‐DR + PMNs morphologically resembled conventional PMNs, and they exhibited functional properties of PMNs. Compared with conventional PMNs, HLA‐DR + PMNs showed increased activation, degranulation, DHR123 oxidation, and phagocytic capacity. A few HLA‐DR + PMNs were observed in healthy subjects, and that proportion could be increased by incubation in either inflammatory cytokines or in plasma from a patient with CL. This was accompanied by an increase in PMN hladrb1 mRNA, suggesting a possible connection between neutrophil "priming" and up‐regulation of HLA‐DR. These data suggest that PMNs that are primed for activation and that also express surface markers of antigen‐presenting cells emerge in the circulation and infected tissue lesions of patients with CL. … (more)
- Is Part Of:
- Journal of leukocyte biology. Volume 101:Issue 3(2017)
- Journal:
- Journal of leukocyte biology
- Issue:
- Volume 101:Issue 3(2017)
- Issue Display:
- Volume 101, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 101
- Issue:
- 3
- Issue Sort Value:
- 2017-0101-0003-0000
- Page Start:
- 739
- Page End:
- 749
- Publication Date:
- 2016-10-17
- Subjects:
- Leishmania -- neutrophil -- granulocyte
Leucocytes -- Periodicals
Reticulo-endothelial system -- Periodicals
571.96 - Journal URLs:
- http://jlb.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)1938-3673/ ↗
https://academic.oup.com/jleukbio ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1189/jlb.4A0915-442RR ↗
- Languages:
- English
- ISSNs:
- 0741-5400
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5010.305000
British Library DSC - BLDSS-3PM
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- 9115.xml