Role of neutrophils in the pathogenesis of Post Kala-azar Dermal Leishmaniasis (PKDL)

PLoS Negl Trop Dis. 2024 Nov 27;18(11):e0012655. doi: 10.1371/journal.pntd.0012655. eCollection 2024 Nov.

Abstract

Background: Post Kala-azar Dermal Leishmaniasis (PKDL) is a dermal sequel of visceral leishmaniasis (VL), poses a significant threat to the success of ongoing kala-azar elimination program, due to its potential role in sustaining transmission cycles and complicating disease management strategies. In VL, neutrophils have been identified as the 'first line of defence', having multiple roles in disease pathogenesis, but their role in PKDL, if any, still remains elusive; presenting a critical gap in knowledge, and was the aim of this study.

Methodology/principal findings: In a cohort of PKDL patients, CD66b+ neutrophils were quantified in skin biopsies, followed by immunostaining of FFPE sections to identify activated neutrophils (CD66b+/CD64+) and degranulated (CD66b+/MPO+), along with expression of neutrophil elastase (NE), matrix metalloprotease 9 (MMP9) and collagen I. Plasma levels of neutrophil chemo-attractants CXCL8/1/2/5, CCL2 and 20 and cytokines, (IL-6, IFN-γ, IL-4, IL-10, TNF-α, IL-17 and IL-22, 23) were evaluated by a multiplex assay, while lesional expression of IL-8, IL-10 and IL-17 was evaluated by immunohistochemistry. As compared to healthy individuals (control skin samples), PKDL cases at the lesional sites had an increased number of activated CD66b+ neutrophils (positive for CD64+, MPO+ and NE+). The plasma levels of neutrophil chemo-attractants, pro-inflammatory and regulatory cytokines were raised as was circulating and lesional IL-8, along with an enhanced lesional expression of IL-10 and IL-17A. An increase in circulatory and lesional MMP9 was accompanied by decreased collagen I, suggesting disintegration of matrix integrity.

Conclusions/significance: Taken together, in PKDL, activated neutrophils possibly contribute towards modulating the lesional landscape. Understanding this involvement of neutrophils in patients with PKDL, particularly in the absence of an animal model, could offer better understanding of the disease pathogenesis and provide insights into novel therapeutic strategies for the ongoing elimination program.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD
  • Cell Adhesion Molecules
  • Cytokines* / metabolism
  • Female
  • GPI-Linked Proteins
  • Humans
  • Leishmaniasis, Cutaneous* / immunology
  • Leishmaniasis, Cutaneous* / parasitology
  • Leishmaniasis, Visceral* / immunology
  • Leishmaniasis, Visceral* / parasitology
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Middle Aged
  • Neutrophils* / immunology
  • Skin / immunology
  • Skin / parasitology
  • Skin / pathology
  • Young Adult

Substances

  • Cytokines
  • Antigens, CD
  • Matrix Metalloproteinase 9
  • Cell Adhesion Molecules
  • CEACAM8 protein, human
  • GPI-Linked Proteins

Grants and funding

The work received assistance from Department of Science and Technology, Govt. of India (DST-FIST) [SR/FST/LS1-663/2016 to MC], Indian Council of Medical Research Govt. of India (6/ 9-7(151)2017-ECD II to MC), JC Bose Fellowship, Govt. of India (JCB/2019/000043 to MC) and Bill & Melinda Gates Foundation (BMGF) [INV- 048694 and Collaborator Reference No: R8291 to MC]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.