The Immunology of a Healing Response in Cutaneous Leishmaniasis Treated with Localized Heat or Systemic Antimonial Therapy

• Published in: PLoS neglected tropical diseases 2015-10, Vol.9 (10), p.e0004178-e0004178
• Main Authors: Lakhal-Naouar, Ines, Slike, Bonnie M, Aronson, Naomi E, Marovich, Mary A
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Antimony - administration & dosage; Care and treatment; Cell Proliferation; Cohort Studies; Cytokines; Development and progression; Drug Therapy - methods; Female; Flow Cytometry; Humans; Hyperthermia, Induced - methods; Interferon-gamma - metabolism; Leishmania major - immunology; Leishmaniasis, Cutaneous; Leishmaniasis, Cutaneous - immunology; Leishmaniasis, Cutaneous - parasitology; Leishmaniasis, Cutaneous - therapy; Leukocytes, Mononuclear - immunology; Lymphocyte Subsets - immunology; Lymphocytes; Male; Middle Aged; Parasites; Parasitic diseases; Patient outcomes; Physiological aspects; Risk factors; T cell receptors; T cells; Young Adult
• ISSN: 1935-2735; 1935-2727; 1935-2735
• DOI: 10.1371/journal.pntd.0004178

The effectiveness of systemic antimonial (sodium stibogluconate, Pentostam, SSG) treatment versus local heat therapy (Thermomed) for cutaneous leishmaniasis was studied previously and showed similar healing rates. We hypothesized that different curative immune responses might develop with systemic and local treatment modalities. We studied the peripheral blood immune cells in a cohort of 54 cutaneous Leishmania major subjects treated with SSG or TM. Multiparameter flow cytometry, lymphoproliferative assays and cytokine production were analyzed in order to investigate the differences in the immune responses of subjects before, on and after treatment. Healing cutaneous leishmaniasis lead to a significant decline in circulating T cells and NKT-like cells, accompanied by an expansion in NK cells, regardless of treatment modality. Functional changes involved decreased antigen specific CD4+ T cell proliferation (hyporesponsiveness) seen with CD8+ T cell depletion. Moreover, the healing (or healed) state was characterized by fewer circulating regulatory T cells, reduced IFN-γ production and an overall contraction in polyfunctional CD4+ T cells. Healing from cutaneous Leishmaniasis is a dynamic process that alters circulating lymphocyte populations and subsets of T, NK and NKT-like cells. Immunology of healing, through local or systemic treatments, culminated in similar changes in frequency, quality, and antigen specific responsiveness with immunomodulation possibly via a CD8+ T cell dependent mechanism. Understanding the evolving immunologic changes during healing of human leishmaniasis informs protective immune mechanisms.