Abstract

Leishmaniasis continues to afflict known and newer endemic sites despite global efforts towards its control and elimination. In this regard, the emergence of newer endemic sites with unusual disease formats is recognized wherein Leishmania donovani complex classically known to cause visceral disease is demonstrated to cause cutaneous manifestation. In this context, atypical cutaneous leishmaniasis (CL) cases caused by L. donovani genetic variants from the newer endemic state of Himachal Pradesh (HP) in India are beginning to be understood in terms of parasite determinants. The atypical CL manifestation further needs to be explored to define host immune correlates with a possible role in driving the unusual disease progression. In the given study, we performed comprehensive systemic-immune profiling of the atypical CL patients from the study area in HP, India, in comparison with the classical visceral leishmaniasis (VL) patients from the northeast region of India. The systemic immune response was studied using ELISA-based assessment of Th1, Th2, Th17, Treg, and Th22 specific plasma cytokine expression pattern and parasite-specific total serum IgG/IgG subclasses. The specified immune correlates are known to exhibit heterogeneous association with the different infecting parasite species, infection load, and co-lateral host immunopathology in classical CL and VL. In the atypical CL patient group, altered expression of IL-10 emerged as the key finding that could potentially fine-tune the Th1/Th17/Th22 effector cytokine axis towards a localized cutaneous manifestation. A reduced expression of IL-10 along with a high IFN-γ/IL-10 ratio as a readout of effective parasite killing defined atypical cutaneous outcome. In contrast, high circulatory IL-10 levels and a depressed IFN-γ/IL-10 ratio were seen in classical VL patients in line with an ineffective parasite-killing cytokine response. Overall, the study highlights new knowledge on host immune correlates in terms of cytokine expression pattern and IgG subclasses that underline atypical disease manifestation such that L. donovani, a generally visceralizing parasite species cause skin localized cutaneous lesions.

Highlights

  • Leishmaniasis is an ongoing global public health problem despite efforts towards its control and elimination over the last decade. It is a disease complex with clinical manifestations ranging from systemic visceral leishmaniasis (VL) caused by Leishmania donovani complex, cutaneous leishmaniasis (CL) with skin restricted lesions caused by Leishmania tropica complex, and mucocutaneous leishmaniasis (MCL) involving mucocutaneous membrane caused by Leishmania braziliensis complex [1]

  • We investigated systemic immune-cytokine expression profile and parasite-specific immunoglobulin G (IgG) and IgG subclasses expression patterns in L. donovani-mediated atypical CL (LdCL) patients from the endemic state of Himachal Pradesh (HP) [11]

  • An exploration of the systemic cytokine effector response comprising Th1 signature cytokines IFN-g, TNF-a, and IL-12; Th2-specific cytokine IL-4; regulatory cytokines IL-10, IL-27, and TGF-b; and Th17 and Th22 cytokines comprising IL-6, IL-23, IL-1b, IL-17A, IL-22, and TNF-a along with parasite-specific total IgG and IgG subclasses was done for the specified study groups to gauge the immunological basis of the atypical CL caused by L. donovani genetic variant circulating in the study region

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Summary

Introduction

Leishmaniasis is an ongoing global public health problem despite efforts towards its control and elimination over the last decade. It is a disease complex with clinical manifestations ranging from systemic visceral leishmaniasis (VL) caused by Leishmania donovani complex, cutaneous leishmaniasis (CL) with skin restricted lesions caused by Leishmania tropica complex, and mucocutaneous leishmaniasis (MCL) involving mucocutaneous membrane caused by Leishmania braziliensis complex [1]. The disease is emerging as an unusual cutaneous manifestation caused by L. donovani in the newer endemic sites in Sri Lanka, Nepal, and India [9,10,11]. There are few reports on genetic analysis of parasite isolates from atypical CL cases endemic in Sri Lanka, Nepal, and the states of Kerala and Himachal Pradesh (HP) in India, identified as L. donovani genetic variants distinct from the classical VL L. donovani isolates [9,10,11,12]

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