Photodynamic Vaccination of BALB/c Mice for Prophylaxis of Cutaneous Leishmaniasis Caused by Leishmania amazonensis

Sayonara M. Viana, Fabiana S. Celes, Laura Ramirez, Bala Kolli, Dennis K. P. Ng, Kwang P. Chang, Camila I. de Oliveira

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 ofLeishmaniaby this means renders them non-viable, but preserves their effective use as vaccines.Leishmaniacan 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 ofLeishmaniaamazonensiswas further examinedin vitroandin vivofor vaccination against cutaneous leishmaniasis (CL).Methods and Results:Leishmania amazonensispromastigotes were photodynamically inactivatedin vitroby 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 macrophagesin vitroand their infectivity to mouse ear dermisin vivo. Inactivation ofLeishmaniato 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 vaccinationin vivo. Each site was inoculated first within vitrodoubly PS-sensitized promastigotes and then spot-illuminated with white light (50 J/cm2) for their photo-inactivationin 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 virulentL. 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:Leishmaniadoubly PS-sensitized andin situphoto-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.