Pre-exposure with low-dose UVA suppresses lesion development and enhances Th1 response in BALB/c mice infected with Leishmania (Leishmania) amazonensis

Journal of Dermatological Science

Volumn 26, Issue 3, 2001, Pages 217-232

  Khaskhely, Noor Mohammad ^a   Maruno, Motoyoshi ^a   Takamiyagi, Atsushi ^a   Uezato, Hiroshi ^a   Kasem, Khan Mohammad Abul ^a   Hosokawa, Atsushi ^a   Kariya, Ken ichi ^a   Hashiguchi, Yoshihisa ^b   Landires, Eduardo A Gomez ^c   Nonaka, Shigeo ^a  

^a UNIVERSITY OF THE RYUKYUS   (Japan)

^b KOCHI MEDICAL SCHOOL   (Japan)

^c UNIVERSIDAD CATÓLICA DE SANTIAGO DE GUAYAQUIL   (Ecuador)

Author keywords

BALB c mice; L. amazonensis; Lesion development; UVA irradiation

Indexed keywords

GAMMA INTERFERON; INTERLEUKIN 10; INTERLEUKIN 12; INTERLEUKIN 4; MESSENGER RNA; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELLULAR IMMUNITY; CONTROLLED STUDY; DISEASE COURSE; DOSE TIME EFFECT RELATION; ELECTRON MICROSCOPY; ENZYME LINKED IMMUNOSORBENT ASSAY; LEISHMANIA; LEISHMANIASIS; MALE; MICROSCOPY; MOUSE; NONHUMAN; PARASITE; PRIORITY JOURNAL; PROMASTIGOTE; RADIATION DOSE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SKIN DEFECT; TH1 CELL; TH2 CELL; ULTRAVIOLET A RADIATION;

ANIMALS; DOSE-RESPONSE RELATIONSHIP, RADIATION; DOWN-REGULATION; IMMUNE SYSTEM; INTERFERON TYPE II; INTERLEUKIN-10; INTERLEUKIN-12; INTERLEUKIN-4; LEISHMANIASIS; MICE; MICE, INBRED BALB C; MICROSCOPY, ELECTRON; RNA, MESSENGER; TH1 CELLS; TUMOR NECROSIS FACTOR-ALPHA; ULTRAVIOLET RAYS; UP-REGULATION;

EID: 0035009248     PISSN: 09231811     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0923-1811(01)00098-6     Document Type: Article

References (45)

1. Herwaldt B.L. Leishmaniasis. Lancet. 354:1999;1191-1199.
2. Weigle K., Saravia N.G. Natural history, clinical evaluation, and the host-parasite interaction in New World cutaneous leishmaniasis. Clin. Dermatol. 14:1996;433-450.
3. Sher A., Coffman R.L. Regulation of immunity to parasites by T cells and T cell-derived cytokines. Ann. Rev. Immunol. 10:1992;385-409.
4. Mosmann T.R., Cherwinski H., Bond M.W., Giedlin M.A., Coffman R.L. Two types of murine helper T cell clone. 1. Defination according to profiles of lymphokines activities and secreted proteins. J. Immunol. 136:1986;2348-2357.
5. Ullrich S.E. Does exposure to UV radiation induce a shift to a Th-2 like immune reaction? Photochem. Photobiol. 64:1996;254-258.
6. Sadick M.D., Locksley R.M., Tubbs C., Raff H.V. Murine cutaneous leishmaniasis: resistance correlates with the capacity to generate interferon-gamma in response to Leishmania antigens in vitro. J. Immunol. 136:1986;655-661.
7. Heinzel F.P., Sadick D., Holaday B.J., Coffman R.L., Loclsley R.M. Reciprocal expression of interferon gamma or interleukin 4 during the rsolution or progression of murine leishmaniasis. Evidence for expansion of distinct helper T cell subsets. J. Exp. Med. 169:1989;59-72.
8. Scott P. IFN-γ modulates the early development of Th1 and Th2 responses in a murine model of cutaneous leishmaniasis. J. Immunol. 147:1991;3149-3155.
9. Locksley R.M., Louis J.A. Immunology of leishmaniasis. Curr. Opin. Immunol. 4:1992;413-418.
10. Hoffman V., Marty P., Perrin C., Saint-paul M.C., et al. The histological spectrum of Visceral leishmaniasis caused by Leishmania infantum MON-1 in acquired immunedeficiency syndrome. Hum. Pathol. 31:2000;75-84.
11. Wolday D., Berhe N., Akuffo- H., Britton S. Leishmania-HIV interaction immuno-pathogenic mechanism. Parasitol. Today. 15:1999;182-187.
12. Nonaka S., Gomez A.E.L., Hashiguchi Y. A comparative study of cutaneous changes of leishmaniasis patients from highland and lowland Ecuador. Studies on New World Leishmaniasis and Its Transmission, with Particular References to Ecuador. 1990;150-161 Kyowa Printing, Kochi Japan. Series No: 2.
13. DeFabo E.C., Noonan F.P. Photoimmunology ultraviolet radiation effects on the immune system. Zola H. Laboratory Methods in Immunology. II:1990;CRC Press, Boca Raton, FL.
14. Jeevan A., Kripke M.L. Effects of a single exposure to ultraviolet radiation on Myco-bacterium bovis Bacille Calmette Guerin infection in mice. J. Immunol. 143:1989;2837-2843.
15. Hersey P., Bradley M., Hasic E., Haren G., Edwards A., McCarthy W.H. Immunological effects of solarium exposure. Lancet. 12:1983;545-548.
16. Yoshikawa T., Rae V., Bruins-Slot W., Van Den Berg J.W., Taylor R., Streilein J.W. Susceptibility to effects of UVB radiation on induction of contact hypersensitivity as a risk factor for skin cancer in humans. J. Invest. Dermatol. 95:1990;530-536.
17. Giannini M.S. Suppression of pathogenesis in cutaneous leishmaniasis by UV irradiation. Infect. Immun. 51:1986;838-843.
18. Biessert S., Ullrich S.E., Hosoi J., Granstein R.D. Suppernants from UVB radiation-exposed keratinocytes inhibit Langerhans cell presentation of tumor-associated antigen via IL-10 content. J. Leuko. Biol. 58:1995;234-240.
19. Schwarz A., Grabbe S., Aragane Y., et al. Interleukin-12 prevents ultraviolet B-induced local immunosuppression and overcomes UVB-induced tolerance. J. Invest. Dermatol. 106:1996;1187-1191.
20. Shen J., Bao S., Reeve V.E. Modulation of IL-10, IL-12, and IFN-γ in the epidermis of hairless mice by UVA (320-400 nm) and UVB (280-320 nm) radiation. J. Invest. Dermatol. 113:1999;1059-1064.
21. Neal R.A., Hale C. A comperative study of susceptibility of inbred and outbred mouse strains compared with hamasters to infection with New World cutaneous Leishmaniasis. Prarasitology. 87:1983;7-13.
22. Inafuku K., Takamiyagi A., Oshiro M., Kinjo T., Nakashima Y., Nonaka S. Alterations of mRNA levels of δ-aminolevulinic acid synthase, Ferro-chelatase and heme oxygenase-1 in griseofulvin induced protoporphyria mice. J. Dermatol. Sci. 19:1999;189-198.
23. Takamiyagi A., Nakashima Y., Irifune H., Uezato H., Nonaka S. Quantitative analyasis of ferrocheletase mRNA in blood cells of erytheropoietic protoporphyria patients. J. Dermatol. Sci. 11:1996;154-160.
24. Howie S., Norval M., Maingay J. Exposure to low-dose ultraviolet radiation suppresses delayed-type hypersensitivity to herpes simplex virus in mice. J. Invest. Dermatol. 86:1986;125-128.
25. Jeevan A., Kripke M.L. Altration of the immune response to Mycobacterium bovis (BCG) in mice exposed chronically to low doses of UV radiation. Cell. Immunol. 130:1990;32-41.
26. Denkins Y., Fidler I.J., Kripke M.L. Exposure of mice to UV-B radiation suppresses delayed hypersensitivity to Candida albicans. Photochem. Photobiol. 49:1989;615-619.
27. Letvin N.L., Kauffman R.S., Finberg R. T lymphocyte immunity to reovirus. Cellular requirements for generation and role in clearance of primary infections. J. Immunol. 127:1981;2334-2339.
28. Veress B., Abdalla R.E., El Hassan A.M. Electron microscope investigations on the leishmaniasis in the Sudan: II, Ultrastractural morphology of macrophage-parasite interaction in human and hamaster macrophages in vitro. Ann. Trop. Med. Hyg. 75:1981;607-613.
29. Reed S.G., Scott P. T-cell and cytokine responses in leishmaniasis. Curr. Opin. Immunol. 5:1993;524-531.
30. Kenney R.T., Sacks D.L., Sypek J.P., Vilela L., Gam A.A., Evans-Davis K. Protective mmunity using recombinant human IL-12 and alum as adjuvants in a primate model of cutaneous leishmaniasis. J. Immunol. 163:1999;4481-4488.
31. Harms G., Zwingenberger K., Chehade A.K., et al. Effects of intradermal gamma-interferon in cutaneous leishmaniasis. Lancet. 1:1989;1287-1292.
32. Taylor A.P., Murray H.W. Therapeutic effects of interferon-gamma gene transfer in experimental visceral leishmaniasis. J. Infect. Dis. 178:1998;908-911.
33. Kondo S., Jimbow K. Dose dependent induction of IL-12 but not IL-10 from human keratinocytes after exposure to ultraviolet light A. J. Cell Physiol. 177:1989;93-94.
34. Afonso L.C., Scharton T.M., Vieira L.Q., Wysocka M., Trinchieri G., Scott P. The adjuvent effects of interlukin-12 in a vaccine against Leishmania major. Science. 263:1994;235-237.
35. Sadick M.D., Heinzel F.D., Holaday B.J., Pu R.T., Dawkins R.S., Locksley R.M. Cure of murine cutaneous leishmaniasis with anti-interleukin 4 monoclona antibody. Evidence for a T cell dependent, interferon γ-independent mechanism. J. Exp. Med. 171:1990;115-127.
36. Belosevic M., Finbloom D.S., van der Meide P., Slayter M.V., Nacy C.A. Administration of monoclonal anti IFN-γ antibodies in vivo abrogates natural resistance of C3H/HeN mice to infection with Leishmania major. J. Immunol. 143:1989;266-274.
37. Afonso L.C.C., Scott P. Immune responses associated with susceptibility of C57BL/10 mice to Leishmania amazonensis. Infect. Immun. 61:1993;2952-2959.
38. Ma N., Chow J.M., Gri G., et al. The interleukin-12 p40 gene promoter is primed by interferon gamma in monocytic cells. J. Exp. Med. 183:1996;147-157.
39. Schmitt D.A., Owen-Schaub L., Ulrich S.E. Effect of IL-12 on immune suppression and suppressor cell induction by ultraviolet radiation. J. Immunol. 154:1995;5114-5120.
40. Titus R.G., Sherry B., Cerami A. Tumor necrosis factor plays a protective role in experimental cutaneous leishmaniasis. J. Exp. Med. 170:1989;2097-2104.
41. Liew F.Y., Parkinson C., Millot S., Severn A., Carrier M. Tumor necrosis (TNF-α) in leishmaniasis. I. TNF-α mediates host protection against cutaneous leishmaniasis. Immunology. 69:1990;570-573.
42. Corsini E., Sangha N., Feldman S.R. Epidermal stratification reduces the effect of UVB (but not UVA) on keratinocytes cytokine production and cytotxicity. Photodermatol. Photoimmunol. Photomed. 13:1997;147-152.
43. Nakane A., Minagawa T., Kohonawa M., Chen Y., Sato H., Moriyama M., Tsuruoka N. Interactions between endogenous g interferon and tumor necrosis factor in host resistance against primary and secondary Listeria monocytogenesis infections. Infect. Immun. 57:1989;3331-3337.
44. Tsujimoto M., Yip Y.K., Vilcek J. Interferon-gamma enhances cellular receptors for tumor necrosis factor. J. Immunol. 136:1986;2441-2444.
45. Murray H.W., Hariprashad J. Treatment of experimental visceral leishmaniasis with interleukin 12. Clin. Res. 42:1994;345A.