TY - JOUR
T1 - New "light" for one-world approach toward safe and effective control of animal diseases and insect vectors from leishmaniac perspectives
AU - Chang, Kwang Poo
AU - Kolli, Bala K.
AU - Batchu, Ramesh B.
AU - Chen, Hui Wen
AU - Chow, Larry Ming C
AU - Elliott, Robert
AU - Head, Jonathan F.
AU - Fan, Chia Kwung
AU - Hung, Chen Hsiung
AU - Ji, Dar Der
AU - Lun, Zhao Rong
AU - Manna, Laura
AU - Matsumoto, Yoshitsugu
AU - Ng, Dennis K P
AU - De Oliveira, Camila I.
AU - Melo, Sayonara
AU - Ozbel, Yusuf
AU - Özbilgin, Ahmet
AU - Reynolds, Joseph
AU - Sanjoba, Chizu
AU - Shiao, Shin Hong
AU - Shih, Nang Yao
AU - Tsai, Chi Wei
AU - Vicente, Maria Da Graça H
AU - Barré, Charles H.
AU - Volf, Petr
AU - Wu, Yueh Lung
AU - Yu, Chao Lan
AU - Zhou, Xiao Nong
N1 - Funding Information:
Work described has received partial support by NIH/NIAID Grant # AI097830, AI-7712375, AI-68835 and other sources.
Publisher Copyright:
© 2016 The Author(s).
PY - 2016/7/13
Y1 - 2016/7/13
N2 - Light is known to excite photosensitizers (PS) to produce cytotoxic reactive oxygen species (ROS) in the presence of oxygen. This modality is attractive for designing control measures against animal diseases and pests. Many PS have a proven safety record. Also, the ROS cytotoxicity selects no resistant mutants, unlike other drugs and pesticides. Photodynamic therapy (PDT) refers to the use of PS as light activable tumoricides, microbicides and pesticides in medicine and agriculture. Here we describe "photodynamic vaccination" (PDV) that uses PDT-inactivation of parasites, i.e. Leishmania as whole-cell vaccines against leishmaniasis, and as a universal carrier to deliver transgenic add-on vaccines against other infectious and malignant diseases. The efficacy of Leishmania for vaccine delivery makes use of their inherent attributes to parasitize antigen (vaccine)-presenting cells. Inactivation of Leishmania by PDT provides safety for their use. This is accomplished in two different ways: (i) chemical engineering of PS to enhance their uptake, e.g. Si-phthalocyanines; and (ii) transgenic approach to render Leishmania inducible for porphyrinogenesis. Three different schemes of Leishmania-based PDV are presented diagrammatically to depict the cellular events resulting in cell-mediated immunity, as seen experimentally against leishmaniasis and Leishmania-delivered antigen in vitro and in vivo. Safety versus efficacy evaluations are under way for PDT-inactivated Leishmania, including those further processed to facilitate their storage and transport. Leishmania transfected to express cancer and viral vaccine candidates are being prepared accordingly for experimental trials. We have begun to examine PS-mediated photodynamic insecticides (PDI). Mosquito cells take up rose bengal/cyanosine, rendering them light-sensitive to undergo disintegration in vitro, thereby providing a cellular basis for the larvicidal activity seen by the same treatments. Ineffectiveness of phthalocyanines and porphyrins for PDI underscores its requirement for different PS. Differential uptake of PS by insect versus other cells to account for this difference is under study. The ongoing work is patterned after the one-world approach by enlisting the participation of experts in medicinal chemistry, cell/molecular biology, immunology, parasitology, entomology, cancer research, tropical medicine and veterinary medicine. The availability of multidisciplinary expertise is indispensable for implementation of the necessary studies to move the project toward product development.
AB - Light is known to excite photosensitizers (PS) to produce cytotoxic reactive oxygen species (ROS) in the presence of oxygen. This modality is attractive for designing control measures against animal diseases and pests. Many PS have a proven safety record. Also, the ROS cytotoxicity selects no resistant mutants, unlike other drugs and pesticides. Photodynamic therapy (PDT) refers to the use of PS as light activable tumoricides, microbicides and pesticides in medicine and agriculture. Here we describe "photodynamic vaccination" (PDV) that uses PDT-inactivation of parasites, i.e. Leishmania as whole-cell vaccines against leishmaniasis, and as a universal carrier to deliver transgenic add-on vaccines against other infectious and malignant diseases. The efficacy of Leishmania for vaccine delivery makes use of their inherent attributes to parasitize antigen (vaccine)-presenting cells. Inactivation of Leishmania by PDT provides safety for their use. This is accomplished in two different ways: (i) chemical engineering of PS to enhance their uptake, e.g. Si-phthalocyanines; and (ii) transgenic approach to render Leishmania inducible for porphyrinogenesis. Three different schemes of Leishmania-based PDV are presented diagrammatically to depict the cellular events resulting in cell-mediated immunity, as seen experimentally against leishmaniasis and Leishmania-delivered antigen in vitro and in vivo. Safety versus efficacy evaluations are under way for PDT-inactivated Leishmania, including those further processed to facilitate their storage and transport. Leishmania transfected to express cancer and viral vaccine candidates are being prepared accordingly for experimental trials. We have begun to examine PS-mediated photodynamic insecticides (PDI). Mosquito cells take up rose bengal/cyanosine, rendering them light-sensitive to undergo disintegration in vitro, thereby providing a cellular basis for the larvicidal activity seen by the same treatments. Ineffectiveness of phthalocyanines and porphyrins for PDI underscores its requirement for different PS. Differential uptake of PS by insect versus other cells to account for this difference is under study. The ongoing work is patterned after the one-world approach by enlisting the participation of experts in medicinal chemistry, cell/molecular biology, immunology, parasitology, entomology, cancer research, tropical medicine and veterinary medicine. The availability of multidisciplinary expertise is indispensable for implementation of the necessary studies to move the project toward product development.
KW - Leishmania
KW - Mosquito
KW - Photodynamic insecticide
KW - Photodynamic therapy
KW - Photodynamic vaccination
KW - Photosensitizers
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UR - http://www.scopus.com/inward/citedby.url?scp=84979738925&partnerID=8YFLogxK
U2 - 10.1186/s13071-016-1674-3
DO - 10.1186/s13071-016-1674-3
M3 - Review article
C2 - 27412129
AN - SCOPUS:84979738925
SN - 1756-3305
VL - 9
JO - Parasites and Vectors
JF - Parasites and Vectors
IS - 1
M1 - 396
ER -