Abstract

Background: Photosensitizers (PS), like porphyrins and phthalocyanines (PC) are excitable by light to generate cytotoxic singlet oxygen and other reactive oxygen species in the presence of atmospheric O2. Photodynamic inactivation of Leishmania by this means renders them non-viable, but preserves their effective use as vaccines. Leishmania can be photo-inactivated after PS-sensitization by loading via their endocytic uptake of PC or endogenous induction of transgenic mutants with delta-aminolevulinate (ALA) to accumulate cytosolic uroporphyrin I (URO). Here, PS-sensitization and photo-inactivation of Leishmania amazonensis was further examined in vitro and in vivo for vaccination against cutaneous leishmaniasis (CL).Methods and Results: Leishmania amazonensis promastigotes were photodynamically inactivated in vitro by PC-loading followed by exposure to red light (1–2 J/cm2) or ALA-induction of uroporphyrinogenic transfectants to accumulate cytosolic URO followed by longwave UV exposure. When applied individually, both strategies of photodynamic inactivation were found to significantly, albeit incompletely abolish the MTT reduction activities of the promastigotes, their uptake by mouse bone marrow-derived macrophages in vitro and their infectivity to mouse ear dermis in vivo. Inactivation of Leishmania to completion by using a combination of both strategies was thus used for the sake of safety as whole-cell vaccines for immunization of BALB/c mice. Different cutaneous sites were assessed for the efficacy of such photodynamic vaccination in vivo. Each site was inoculated first with in vitro doubly PS-sensitized promastigotes and then spot-illuminated with white light (50 J/cm2) for their photo-inactivation in situ. Only in ear dermis parasites were photo-inactivated beyond detection. Mice were thus immunized once in the ear and challenged 3 weeks later at the tail base with virulent L. amazonensis. Prophylaxis was noted in mice photodynamically vaccinated with doubly photo-inactivated parasites, as indicated by a significant delay in the onset of lesion development and a substantial decrease in the parasite loads.Conclusion: Leishmania doubly PS-sensitized and in situ photo-inactivated as described proved to be safe and effective when used for one-time immunization of ear dermis, as indicated by its significant protection of the inherently very susceptible BALB/c mice against CL.

Highlights

  • Cutaneous leishmaniasis (CL) is caused by protozoan parasites in the genus of Leishmania and is a wide-spread disease, with estimated 1.5 million new cases per year (WHO, 2010)

  • We have explored the principle of photodynamic therapy (PDT) as a new strategy for Leishmania inactivation in vitro to develop non-viable, but immunologically competent whole cell vaccines and vaccine carriers (Sah et al, 2002; Dutta et al, 2005; Chang and Kolli, 2016)

  • We have evaluated initially both endogenous and exogenous strategies separately for photoinactivation of L. amazonensis based on parasite viability, parasite uptake in vitro and lesion development in mice

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Summary

Introduction

Cutaneous leishmaniasis (CL) is caused by protozoan parasites in the genus of Leishmania and is a wide-spread disease, with estimated 1.5 million new cases per year (WHO, 2010). Leishmanization is, unacceptable because of its association with the development of non-healing lesions, especially in immunocompromised individuals [reviewed in (Palatnik-De-Sousa, 2008)] Attempts to overcome these difficulties included the use of parasites after attenuation via, for example, long-term in vitro cultivation (Daneshvar et al, 2003), genetic modifications (Alexander et al, 1998; Spath et al, 2000; Uzonna et al, 2004; Selvapandiyan et al, 2009; Dey et al, 2013; Bhattacharya et al, 2015) and gamma irradiation (Alexander, 1982). PS-sensitization and photoinactivation of Leishmania amazonensis was further examined in vitro and in vivo for vaccination against cutaneous leishmaniasis (CL)

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